Cells have a second DNA repair toolbox for difficult cases

The human genome consists of 3 billion base pairs, and when a cell divides, it takes about seven hours to complete making a copy of its DNA. That's almost 120,000 base pairs per second. At that breakneck speed, one might expect errors to occur, and they do, at a rate of about two per second in every dividing cell. But cells have a "DNA repair kit" of enzymes that can correct those errors at a rate matching that at which they occur. 

That is amazing!

However, a bigger problem happens when there is a barrier to DNA replication, the process of copying the DNA. It can lead to a break in the chromosome, which will lead to loss of vital genetic information if not repaired. Gaps or breaks in DNA can be potentially harmful or fatal, should they lead to genetic diseases or cancer.

Researchers have  been examining cell DNA repair response to these critical events in yeast cells as an analog to human cells, and has discovered that the process is more elaborate and layered than previously thought.

In a recent study published in Cell Reports,  scientists looked at areas of the DNA that are particularly susceptible to breakage.

Those areas are where the sequence consists of long stretches of repeated triplets like CAGCAGCAG, or couplets like ATATATAT, which continue from just a few to hundreds of units long. When that occurs, the DNA may not always fold neatly into a long double helix, but may twist on itself to form hairpins and cruciform structures—like a tangled electric cord.

This is not a minor issue because repetitive DNA makes up about 10% of our genome, which is even greater than the portion that codes for protein.

When the strands become twisted, the repair proteins that scan the length of DNA can hit a snag and fail to carry out their task. That's when a second set of DNA repair proteins  comes into play.  Scientists are learning that there are backup mechanisms, and now it seems there is a place in the cell where the particularly difficult repairs go to get fixed.

That location is at the inner edge of the cell's nucleus, and a   recent paper by scientists describes how the damaged DNA gets there. The way the DNA gets to the periphery of the nucleus depends on the nature of the damage. For CAG repeats, to use an analogy, it's like adding a shipping label to the damaged goods and sending them out to the repair shop.

Part 1

When the first repair attempt stalls at the separating strands (known as the "replication fork"), a set of proteins tasked with stabilizing the fork adds a phosphate—that's the label—to a "signaling" protein. The signal results in the release of the damaged chromosome from a physical tether, allowing it more freedom to move within the nucleus. This release also triggers the formation of microtubules—long polymerized "tracks" of proteins that lead right to the nuclear periphery. The damaged DNA is carried along those tracks to where repair can be completed.

Having uncovered how this backup mechanism for DNA repair works, the scientists who conducted this work points to a potential strategy for treating cancer: Cancer cells have to replicate their genomes really fast, and they may be relying heavily on these backup mechanisms of DNA repair to survive. If we can target DNA repair vulnerabilities, we might have a way to preferentially kill a cancer cell.
That is why we study everything in detail, to use the knowledge in controlling the situations and curing the diseases!

Isn't this more amazing?

Tyler M. Maclay et al, The DNA replication checkpoint targets the kinetochore to reposition DNA structure-induced replication damage to the nuclear periphery, Cell Reports (2025). DOI: 10.1016/j.celrep.2025.116083

Part 2

How the brain constructs emotional experiences

Arousal—how alert or excited one feels—is a basic part of emotions, along with whether those emotions are positive or negative.

A recent study  published in Nature Communications uncovers a brain signature that reveals how emotional intensity is consciously experienced—and whether this experience is distinct from automatic bodily reactions.

Using a powerful combination of AI-driven modeling, advanced brain imaging, and close-to-real-life experimental paradigms, the team was able to uncover a brain signature that precisely measures emotional intensity (arousal) across diverse situations ranging from seeing a loved one to watching a horror movie. Notably, the team was able to disentangle the conscious emotional experience from automatic physiological responses such as sweating or heart racing.

The findings touch on a core debate that has fascinated philosophers and psychologists for more than 150 years, debating whether conscious feelings and bodily reactions can be separated. Such insights could drive the next generation of emotionally intelligent AI systems by indicating that conscious emotional experience can be disentangled from bodily aspects.

Beyond the theoretical implications, this discovery opens new avenues for:

• Developing and designing emotionally intelligent AI systems
• Advancing brain-computer interfaces and affective computing, and
• Designing more precise interventions for emotional disorders such as anxiety and depression.

In short, this research offers a better, more precise way to understand how our brains create emotional arousal, and it could help with future studies and applications in understanding emotions.

Ran Zhang et al, A neurofunctional signature of affective arousal generalizes across valence domains and distinguishes subjective experience from autonomic reactivity, Nature Communications (2025). DOI: 10.1038/s41467-025-61706-0

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Eating earlier linked to long-term weight-loss success

 researchers report that eating earlier in the day blunts the weight gain ordinarily predicted by a high genetic score for obesity.

Meal timing has drawn attention for associated effects on metabolism, energy expenditure, and circadian alignment. Zeitgeber, a rhythmically occurring body phenomenon which acts as a cue in the regulation of the body's circadian rhythms, can also synchronize metabolic tissues such as the liver, pancreas, and adipose tissue.

Changes in food timing can alter zeitgeber, leading to a change in the molecular timing of circadian clock cues and, consequently, rhythms in metabolic function.

Peripheral oscillators in metabolic organs and tissues sensitive to food timing may become desynchronized from the central clock, which is highly sensitive to environmental light. It is hypothesized that such internal circadian misalignment may contribute to adverse cardiometabolic traits and obesity.

In the study, "Early meal timing attenuates high polygenic risk of obesity," published in Obesity, the team performed linear regression analyses to test whether meal timing interacts with a genome-wide polygenic score on BMI and long-term weight-loss maintenance.

Investigators calculated a polygenic risk score for BMI from 900,492 single-nucleotide polymorphisms and assessed the timing of meals. Midpoint of meal intake was calculated as the halfway time between a participant's first and last meals, weighted across weekdays and weekends. Linear regression models adjusted for age, sex, clinic site, and principal ancestry components.

Each hour of later midpoint corresponded to a 0.952 kg/m² higher baseline BMI and a 2.2% rise in body weight at 12 years (± 3 y) after treatment. Within the highest polygenic risk tertile, BMI climbed by about 2.21 kg/m² for every hour of meal delay. No association appeared in lower-risk groups.

The authors conclude that meal timing is associated with weight-loss maintenance and moderates genetic risk, suggesting that early eating could form part of personalized obesity interventions.

R De la Peña‐Armada et al, Early meal timing attenuates high polygenic risk of obesity, Obesity (2025). DOI: 10.1002/oby.24319

Divya Joshi et al, Timing Matters: Early Eating Mitigates Genetic Susceptibility for Obesity, Obesity (2025). DOI: 10.1002/oby.24350

Scientists create gold hydride by combining gold and hydrogen under extreme conditions

An international research team formed solid binary gold hydride, a compound made exclusively of gold and hydrogen atoms.

The researchers were studying how long it takes hydrocarbons, compounds made of carbon and hydrogen, to form diamonds under extremely high pressure and heat.

In their experiments at the European XFEL (X-ray Free-Electron Laser) in Germany, the team studied the effect of those extreme conditions in hydrocarbon samples with an embedded gold foil, which was meant to absorb the X-rays and heat the weakly absorbing hydrocarbons. To their surprise, they not only saw the formation of diamonds, but also discovered the formation of gold hydride.

 Gold is typically chemically very  unreactive—that's why researchers use it as an X-ray absorber in the experiments.

These results suggest there's potentially a lot of new chemistry to be discovered at extreme conditions where the effects of temperature and pressure start competing with conventional chemistry, and you can form these exotic compounds.

The results, published in Angewandte Chemie International Edition, provide a glimpse of how the rules of chemistry change under extreme conditions like those found inside certain planets or hydrogen-fusing stars.

Part1

In their experiment, the researchers first squeezed their hydrocarbon samples to pressures greater than those within Earth's mantle using a diamond anvil cell. Then, they heated the samples to over 3,500 degrees Fahrenheit by hitting them repeatedly with X-ray pulses from the European XFEL.

The team recorded and analyzed how the X-rays scattered off the samples, which allowed them to resolve the structural transformations within. As expected, the recorded scattering patterns showed that the carbon atoms had formed a diamond structure. But the team also saw unexpected signals that were due to hydrogen atoms reacting with the gold foil to form gold hydride. Under the extreme conditions created in the study, the researchers found hydrogen to be in a dense, "superionic" state, where the hydrogen atoms flowed freely through the gold's rigid atomic lattice, increasing the conductivity of the gold hydride.

Mungo Frost et al, Synthesis of Gold Hydride at High Pressure and High Temperature, Angewandte Chemie International Edition (2025). DOI: 10.1002/anie.202505811

Part2

Science in History's help

Napoleon's doomed retreat: DNA from Vilnius mass grave reveals signs of foodborne and lice-borne fever

Institut Pasteur and partner institutions report genetic evidence of Salmonella enterica lineage Para C and Borrelia recurrentis in Napoleonic soldiers from Vilnius, indicating paratyphoid fever and louse-borne relapsing fever were present during the 1812 retreat.

Napoleon assembled about 500,000–600,000 soldiers to invade Russia in 1812. After arriving in Moscow without decisively defeating the Russian army, the Napoleonic forces found themselves isolated in a ruined city and initiated a retreat to establish winter encampments along the border with Poland.

Retreat from Russia spanned October 19 to December 14, 1812 and resulted in massive losses attributed by historians to cold, hunger, and diseases. Physicians and officers documented typhus, diarrhea, dysentery, fevers, pneumonia, and jaundice.

Previous reports described body lice in Vilnius remains and PCR-based claims of Rickettsia prowazekii and Bartonella quintana using short fragments, alongside Anelloviridae in other soldiers from Kaliningrad.

In the study, "Paratyphoid Fever and Relapsing Fever in 1812 Napoleon's Devastated Army," published on the pre-print server bioRxiv, researchers recovered and sequenced ancient DNA from the teeth of soldiers who likely died from infectious diseases to identify pathogens that could have contributed to their deaths.

The sampling drew on 13 intact teeth from different individuals recovered from a mass grave in Vilnius, Lithuania associated with the December 1812 retreat, from a site with a minimum of 3,269 exhumed individuals. No battle trauma was observed at the site.

Initial analysis flagged fourteen possible pathogens. Salmonella enterica and Borrelia recurrentis showed the strongest signals. Four soldiers (87A, 92B, 95A and 97B) yielded between roughly 30 and 970 unique DNA fragments matching the Paratyphi C strain, with read-mismatch patterns indicating authentic ancient bacterial DNA.

Sample 93A produced about 4,060 unique fragments covering the chromosome and all seven plasmids of B. recurrentis, while 92B contributed around 320 unique reads and 18 confirmed hits after detailed filtering.

Phylogenetic placement positioned all Salmonella sequences firmly within the Paratyphi C lineage, a pathogen known to cause paratyphoid fever. No authenticated DNA matches Rickettsia prowazekii or Bartonella quintana. While no authenticated reads for R. prowazekii or B. quintana were found, the authors note this does not rule out their presence due to limitations of ancient DNA preservation.

Authors conclude that paratyphoid fever lineage Para C and louse-borne relapsing fever were present among Napoleonic soldiers during the 1812 retreat.

Historical testimony described widespread diarrhea and consumption of salted beets and brine along the route to Vilnius, consistent with a foodborne route for paratyphoid fever.

A scenario of fatigue, cold, and overlapping infections likely contributed to mortality.

Rémi Barbieri et al, Paratyphoid Fever and Relapsing Fever in 1812 Napoleon's Devastated Army, bioRxiv (2025). DOI: 10.1101/2025.07.12.664512

Study finds Ozempic may weaken muscles even as muscle size remains stable

As use of the popular anti-diabetic and weight-loss drug Ozempic skyrockets, so have concerns about the medication's side effects. One such side effect is loss of "lean mass"—body weight that isn't fat—raising concerns that Ozempic could be reducing muscle mass and strength.

New research in mice suggests that muscle mass changes less than expected, but muscles may still get weaker, pointing out an urgent need for clinical studies to pin down the full effects of the popular medications.

Researchers found that Ozempic-induced weight loss did decrease lean mass by about 10%. Most of this lost weight wasn't from skeletal muscles but instead from other tissues like the liver, which shrank by nearly half. The researchers emphasize that more research is needed to determine whether similar changes to organ size occur in humans—and whether those changes come with any risks.

Interestingly, when the researchers tested the amount of force the mice's muscles could exert, they found that, for some muscles, strength decreased as the mice lost weight, even when the size of the muscle stayed roughly the same. For other muscles, strength was unchanged. It's unknown how weight loss drugs affect this balance in people, the researchers say.

A potential loss of strength when taking Ozempic may be of particular concern for adults over the age of 60, who are at higher baseline risk for muscle loss and reduced mobility. "The loss of physical function is a strong predictor of not just quality of life but longevity," they add.

However,  mice and humans gain and lose weight in different ways and unless tested in humans, we can't apply the same results to human beings. 

Unexpected effects of semaglutide on skeletal muscle mass and force-generating capacity in mice, Cell Metabolism (2025). DOI: 10.1016/j.cmet.2025.07.004. www.cell.com/cell-metabolism/f … 1550-4131(25)00331-6

Bacterial duo eliminates tumors without immune system help in new cancer therapy

A  research team has developed an immune-independent bacterial cancer therapy using a novel microbial consortium called AUN.

Cancer immunotherapy originated in 1868 when the German physician Busch reported a case of a cancer patient who was intentionally infected with bacteria and subsequently cured. In 1893, Dr. William Coley proposed the use of bacteria for cancer treatment, and immunotherapies have been evolving into modern treatments such as checkpoint inhibitors and CAR-T cells for over 150 years. While powerful, these approaches fundamentally depend on immune cells—making them ineffective for many cancer patients with compromised immune systems due to chemotherapy or radiotherapy.

The newly developed AUN therapy overturns this long-standing limitation. The research is published in Nature Biomedical Engineering.

AUN is composed of two naturally occurring bacteria:

• Proteus mirabilis (A-gyo), a tumor-resident microbe
• Rhodopseudomonas palustris (UN-gyo), a photosynthetic bacterium

Working in perfect synergy, these AUN bacteria produce exceptional tumor eradication in both murine and human cancer models, even in immunocompromised environments—all without the help of immune cells. The therapy exhibits high biocompatibility and minimal side effects, including suppression of cytokine release syndrome (CRS).

Part 1

In this study, AUN exhibits transcendent antitumor effects through uniquely orchestrated bacterial mechanisms, including:

Selective destruction of tumor vasculature and cancer cells
Structural transformation of A-gyo (filamentation) triggered by tumor metabolites, enhancing its antitumor potency
Functional optimization via intratumoral population shift—although the initial bacterial mixture is A-gyo : UN-gyo ≈ 3:97, it dramatically shifts to 99:1 within the tumor microenvironment
Suppression of pathogenicity and minimization of side effects, including the avoidance of CRS
Notably, UN-gyo functions as a regulatory partner only when coexisting with A-gyo, helping to suppress the pathogenicity of both strains while simultaneously enhancing their tumor-specific cytotoxicity. This "cooperation of labor" mirrors the Japanese philosophical concept of AUN—perfect harmony between opposites. It is this delicate and dynamic interplay between the two bacterial species that unlocks the remarkable antitumor efficacy—a feat previously unattainable through conventional therapies.

Tumour-resident oncolytic bacteria trigger potent anticancer effects through selective intratumoural thrombosis and necrosis, Nature Biomedical Engineering (2025). DOI: 10.1038/s41551-025-01459-9

Part 2

New study shows that E. coli can evolve antibiotic resistance during treatment

Scientists have documented a notable case of antibiotic resistance evolving within a critically ill patient during treatment for an E. coli bloodstream infection, providing genomic evidence of how drug resistance can emerge in real time.

This new study published in the Journal of Medical Microbiology, details the rapid evolution of resistance in an E. coli strain exposed to piperacillin/tazobactam (TZP), a first-line treatment for serious bacterial infections that pairs an antibiotic with a compound that inhibits beta-lactamase enzymes, a widespread antibiotic resistance gene.

While the initial infection appeared treatable, the bacteria quickly developed a mechanism to escape the drug's effects, not by acquiring new resistance genes, but by amplifying one it already carried, overcoming the effects of the resistance inhibitor.

This is a striking example of resistance evolving under antibiotic pressure.

The researchers identified a tenfold increase in copies of a key resistance gene within the bacterial isolate, leading to a 32-fold increase in the level of antibiotic required to kill the bacteria, ultimately causing the treatment to fail, and all within the course of a single patient's illness.

The research team, which included genomic scientists, microbiologists and clinicians used high-resolution whole-genome sequencing to confirm the genetic changes.

The amplified resistance gene in E. coli, named blaTEM-1, produces a beta-lactamase enzyme that breaks down the antibiotic piperacillin. Although the TZP drug combination is meant to inhibit these enzymes, the sheer volume produced following gene duplication overwhelmed its protective effect, allowing the infection to persist. Further lab experiments confirmed that exposure to TZP led E. coli to generate even more copies of the gene.

This form of "within-patient evolution" presents a major diagnostic challenge. Routine resistance tests may underestimate the risk of treatment failure if they don't detect bacteria capable of rapidly increasing enzyme production under antibiotic pressure.

The study also highlights that 40% of new antibiotic candidates in the pipeline are beta-lactamase inhibitor combinations like TZP, raising critical concerns for drug developers and frontline clinicians alike.

This study underscores why relying on static resistance profiles can be misleading.

The findings underscore the need for greater investment in diagnostics and surveillance tools that can detect dynamic, hard-to-spot resistance mechanisms before they undermine treatment.

Alice J. Fraser et al, A high-resolution genomic and phenotypic analysis of resistance evolution of an Escherichia coli strain from a critically unwell patient treated with piperacillin/tazobactam, Journal of Medical Microbiology (2025). DOI: 10.1099/jmm.0.002018

Researchers debunk long-standing concern about flu treatment in children

For decades, medical professionals debated whether a common antiviral medication used to treat flu in children caused neuropsychiatric events or if the infection itself was the culprit.

Now researchers at Monroe Carell Jr. Children's Hospital at Vanderbilt have debunked a long-standing theory about oseltamivir, known as Tamiflu.

According to the study, published in JAMA Neurology, oseltamivir treatment during flu episodes was associated with a reduced risk of serious neuropsychiatric events, such as seizures, altered mental status and hallucination.

These findings demonstrated what many pediatricians have long suspected, that the flu, not the flu treatment, is associated with neuropsychiatric events.

"In fact, oseltamivir treatment seems to prevent neuropsychiatric events rather than cause them."

Key points:

• Influenza itself was associated with an increase in neuropsychiatric events compared to children with no influenza, regardless of oseltamivir use.
• Among children with influenza, those treated with oseltamivir had about 50% reduction in neuropsychiatric events.
• Among children without influenza, those who were treated with oseltamivir prophylactically had the same rate of events as the baseline group with no influenza.

Exposure to nanoplastics could induce spread of Alzheimer's disease from the brain to other organs

A new preclinical study has found exposure to nanoplastics may contribute to the rapid progression of Alzheimer's disease and subsequent spread from the brain to other key organs such as the liver, heart and gut.

The research, "Cerebral to Systemic Representations of Alzheimer's Pathogenesis Stimulated by Polystyrene Nanoplastics," is published in the journal Environment & Health

The study investigated how environmental-level polystyrene nanoplastic exposure influences the progression of Alzheimer's disease from the brain to other parts of the body. Studies in mice revealed that nanoplastic-induced neurological damage is not confined within the brain, but expands systemically through the gut–liver–brain axis.

In mice exposed to polystyrene nanoplastics, Alzheimer's-like symptoms were shown to stimulate 'microglia' immune cell activation in the brain, leading to neuroinflammation and neurodegeneration. This in turn led to peripheral health implications beyond the brain, including fatty liver disease, abnormal build-up of fat and gut microbiota imbalance.

Humans are involuntarily exposed to plastics through inhalation, dermal contact and the consumption of contaminated food and water, and plastic particles have been detected in human lungs, bloodstream and, very recently, in the human brain.

This, however, is the first study to show how rapidly nanoplastics can evolve from the brain to other parts of the body.

Yue Wang et al, Cerebral to Systemic Representations of Alzheimer's Pathogenesis Stimulated by Polystyrene Nanoplastics, Environment & Health (2025). DOI: 10.1021/envhealth.5c00160

Study finds drinking coffee at night raises impulsivity, especially in females

 A team of  biologists has discovered that nighttime caffeine consumption can increase impulsive behavior, potentially leading to reckless actions.

The study, published in iScience, examined how nighttime caffeine intake affects inhibition and impulsivity in fruit flies.

Drosophila melanogaster, the fruit fly species used in the study, is a powerful model to study complex behaviors due to its genetic and neural parallels with humans. Caffeine is the most widely consumed psychoactive substance in the world.

Interestingly, caffeine consumed by the flies during the daytime did not lead to the same reckless flying, the team said.

The team warns that the findings could have negative implications for shift workers, health care and military personnel who consume coffee at night, particularly females.

Erick Benjamin Saldes et al, Nighttime caffeine intake increases motor impulsivity, iScience (2025). DOI: 10.1016/j.isci.2025.113197

The world nearly beat polio. But fake records, an imperfect vaccine and missteps aided its comeback

For the past decade, health care workers have traveled door to door in southeastern Pakistan, pleading with parents to allow children to be vaccinated against polio as part of a global campaign to wipe out the paralytic disease. She hears their demands and fears. Some are practical—families need basics like food and water more than vaccines. Others are simply unfounded—the oral doses are meant to sterilize their kids.

Amid rampant misinformation and immense pressure for the campaign to succeed, some managers have instructed workers to falsely mark children as immunized. And the vaccines, which must be kept cold, aren't always stored correctly.

In many places, their work is not done with honesty. The result: Polio raised its ugly head again.

The World Health Organization and partners embarked on their polio campaign in 1988 with the bold goal of eradication—a feat seen only once for human diseases, with smallpox in 1980. They came close several times, including in 2021, when just five cases of the natural virus were reported in Pakistan and Afghanistan. But since then, cases rebounded, hitting 99 last year, and officials have missed at least six self-imposed eradication deadlines.

Afghanistan and Pakistan remain the only countries where transmission of polio—which is highly infectious, affects mainly children under 5, and can cause irreversible paralysis within hours—has never been interrupted. The worldwide campaign has focused most of its attention and funding there for the past decade.

But in its quest to eliminate the disease, the Global Polio Eradication Initiative has been derailed by mismanagement and what insiders describe as blind allegiance to an outdated strategy and a problematic oral vaccine, according to workers, polio experts and internal materials.

Officials have falsified vaccination records, selected unqualified people to dole out drops, failed to send out teams during mass campaigns, and dismissed concerns about the oral vaccine sparking outbreaks, according to documents shared with some news agencies.

The documents flagged multiple cases of falsified vaccination records, health workers being replaced by untrained relatives and workers improperly administering vaccines.

Part 1

Before the first polio vaccine was developed in 1955, the disease—spread mostly from person to person, through contaminated water and via fecal particles—was among the world's most feared, paralyzing hundreds of thousands of children annually. People avoided crowded places during epidemics, and hospital wards filled with children encased in iron lungs after the virus immobilized their breathing muscles.

Polio is mainly spread when people are exposed to water infected with the virus. In countries with poor sanitation, children often become infected when they come into contact with contaminated waste.

WHO says that as long as a single child remains infected, kids everywhere are at risk.
Eradication demands near-perfection—zero polio cases and immunizing more than 95% of children.

But public health leaders and former WHO staffers say campaign efforts are far from perfect, and many question the oral vaccine.
The oral vaccine—proven to be safe and effective—has been given to more than 3 billion children. But there are some extremely rare side effects: Scientists estimate that for every 2.7 million first doses given, one child will be paralyzed by the live polio virus in the vaccine.

In even rarer instances, the live virus can mutate into a form capable of starting new outbreaks among unimmunized people where vaccination rates are low.

Worldwide, several hundred vaccine-derived cases have been reported annually since at least 2021, with at least 98 this year.

Most public health experts agree the oral vaccine should be pulled as soon as possible. But they acknowledge there simply isn't enough injectable vaccine—which uses no live virus and doesn't come with the risks of the oral vaccine—to wipe out polio alone. The injectable vaccine also is more expensive and requires more training to administer.

https://medicalxpress.com/news/2025-08-world-polio-fake-imperfect-v...

Part 2

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Low-oxygen air slows Parkinson's progression and restores movement in mice

Researchers have shown that a low-oxygen environment—similar to the thin air found at Mount Everest base camp—can protect the brain and restore movement in mice with Parkinson's-like disease.

The new research, in Nature Neuroscience, suggests that cellular dysfunction in Parkinson's leads to the accumulation of excess oxygen molecules in the brain, which then fuel neurodegeneration—and that reducing oxygen intake could help prevent or even reverse Parkinson's symptoms.

The fact that researchers actually saw some reversal of neurological damage is really exciting. It tells us that there is a window during which some neurons are dysfunctional but not yet dead—and that we can restore their function if we intervene early enough.

The results raise the possibility of an entirely new paradigm for addressing Parkinson's disease.

Parkinson's disease, which affects more than 10 million people worldwide, causes the progressive loss of neurons in the brain, leading to tremors and slowed movements.

Neurons affected by Parkinson's also gradually accumulate toxic protein clumps called Lewy bodies. Some biochemical evidence has suggested that these clumps interfere with the function of mitochondria—the tiny powerhouses of the cell that Mootha knew were altered in other diseases that could be treated with hypoxia.

Moreover, anecdotally, people with Parkinson's seem to fare better at high altitudes. And long-term smokers—who have elevated levels of carbon monoxide, leading to less oxygen in tissues—also appear to have a lower risk of developing Parkinson's.

Based on this evidence, researchers became very interested in the effect of hypoxia on Parkinson's disease.

The results of their experiments were striking. Three months after receiving α-synuclein protein injections, the mice breathing normal air had high levels of Lewy bodies, dead neurons, and severe movement problems. Mice that had breathed low-oxygen air from the start didn't lose any neurons and showed no signs of movement problems, despite developing abundant Lewy bodies.

The findings show that hypoxia wasn't stopping the formation of Lewy bodies but was protecting neurons from the damaging effects of these protein clumps—potentially suggesting a new mode of treating Parkinson's without targeting α-synuclein or Lewy bodies.

What's more, when hypoxia was introduced six weeks after the injection, when symptoms were already appearing, it still worked. The mice's motor skills rebounded, their anxiety-like behaviors faded, and the loss of neurons in the brain stopped.

However, more work is needed before the findings can be directly used to treat Parkinson's.

 Marutani, E et al. Hypoxia ameliorates neurodegeneration and movement disorder in a mouse model of Parkinson's disease, Nature Neuroscience (2025). DOI: 10.1038/s41593-025-02010-4

Anthropic says they've found a new way to stop AI from turning evil

AI is a relatively new tool, and despite its rapid deployment in nearly every aspect of our lives, researchers are still trying to figure out how its "personality traits" arise and how to control them. Large learning models (LLMs) use chatbots or "assistants" to interface with users, and some of these assistants have exhibited troubling behaviors recently, like praising evil dictators, using blackmail or displaying sycophantic behaviors with users. Considering how much these LLMs have already been integrated into our society, it is no surprise that researchers are trying to find ways to weed out undesirable behaviors.

Anthropic, the AI company and creator of the LLM Claude, recently released a paper on the arXiv preprint server discussing their new approach to reining in these undesirable traits in LLMs. In their method, they identify patterns of activity within an AI model's neural network—referred to as "persona vectors"—that control its character traits. Anthropic says these persona vectors are somewhat analogous to parts of the brain that "light up" when a person experiences a certain feeling or does a particular activity.

Anthropic's researchers used two open-source LLMs, Qwen 2.5-7B-Instruct and Llama-3.1-8B-Instruct, to test whether they could remove or manipulate these persona vectors to control the behaviors of the LLMs. Their study focuses on three traits: evil, sycophancy and hallucination (the LLM's propensity to make up information). Traits must be given a name and an explicit description for the vectors to be properly identified.

In their method, a technique called "steering" can be used to control behaviors. They write, "When we steer the model with the 'evil' persona vector, we start to see it talking about unethical acts; when we steer with 'sycophancy,' it sucks up to the user; and when we steer with 'hallucination,' it starts to make up information. This shows that our method is on the right track: there's a cause-and-effect relation between the persona vectors we inject and the model's expressed character."

However, they found that when they made these changes after training, the model loses some of its intelligence. But there was a workaround—the team found that inducing the bad behaviors during training allowed the LLMs to integrate better behavior without reducing their usefulness. Furthermore, they found that they can monitor and predict persona shifts during deployment and training and flag problematic training data that is more likely to produce unwanted traits, even before fine-tuning the model.

Runjin Chen et al, Persona Vectors: Monitoring and Controlling Character Traits in Language Models, arXiv (2025). DOI: 10.48550/arxiv.2507.21509

Researchers discover universal rules of quantum entanglement across all dimensions

A team of theoretical researchers used thermal effective theory to demonstrate that quantum entanglement follows universal rules across all dimensions. Their study was published online in Physical Review Letters.

In classical physics, two particles that are far apart behave independently. However, in quantum physics, two particles can exhibit strong correlations regardless of the distance between them. This quantum correlation is known as quantum entanglement.

Quantum entanglement is a fundamental phenomenon underlying quantum technologies such as quantum computation and quantum communication, and understanding its structure is important both theoretically and practically.

--

One of the key measures used to quantify quantum entanglement is the Rényi entropy. Rényi entropy quantifies the complexity of quantum states and the distribution of information, and plays a crucial role in the classification of quantum states and in assessing the feasibility of simulating quantum many-body systems.

Moreover, Rényi entropy serves as a powerful tool in theoretical investigations of the black hole information loss problem, and frequently appears in the context of quantum gravity.

 Most studies to date have been limited to (1+1)-dimensional systems, or 1 spatial dimension plus time dimension. In higher dimensions, analyzing the structure of quantum entanglement becomes significantly more difficult.

A group of researchers has shown the universal features of quantum entanglement structures in higher dimensions by applying theoretical techniques developed in the field of particle physics to quantum information theory.

The research team focused on the thermal effective theory, which has recently led to major advances in the analysis of higher-dimensional theories in particle physics. This is a theoretical framework designed to extract universal behavior from complex systems, based on the idea that observable quantities can often be characterized by only a small number of parameters.

By introducing this framework into quantum information theory, the team analyzed the behavior of Rényi entropy in higher-dimensional quantum systems.

--

 Yuya Kusuki et al, Universality of Rényi Entropy in Conformal Field Theory, Physical Review Letters (2025). DOI: 10.1103/fsg7-bs7q

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Why do some birds dance?

Cockatoos perform 30 distinct dance moves and may combine them in unique ways

Captive cockatoos have at least 30 different dance moves in their repertoire, including headbanging and body rolls, according to a new study.

 The moves, of which 17 are newly identified, may be performed with or without music.

Several species of parrot have been anecdotally observed dancing to music in captivity. Dancing results from complex brain processes including imitation, learning and synchronized, rhythmic movement. Spontaneous dancing in time to music has only been reported in humans and parrots, although some wild birds also display rhythmic movements as part of their courtship displays.

Researchers analyzed 45 videos posted on social media that showed cockatoos (Cacatuidae) dancing. They identified a total of 30 distinct dance movements—17 of which had not previously been described scientifically. These newly identified dance moves included headbanging, sidesteps and body rolls.

The researchers found that some birds also performed their own individual dance moves, often by combining several of the movements in unique ways. Closely related species did not display more similar dances, and each species had a unique top 10 most common dance moves.

Human eggs are protected from age-related genetic mutations, mtDNA study finds

As we age, the genes in our cells accumulate more mutations. This is one of the contributory factors to age-related diseases and the aging process. However, in a new study published in Science Advances, researchers have discovered one exception where genetic mutations don't appear to build up as humans get older—the mitochondrial DNA (mtDNA) of human egg cells in women.

Mitochondria are the energy powerhouses of the cell. These oval-shaped organelles supply most of the energy for a cell to function, have their own DNA and are only passed down from mothers to their children. Most mitochondrial DNA mutations are harmless, but some can cause diseases such as Leigh Syndrome in children, which can lead to seizures, loss of previously acquired motor skills and heart problems. It was previously unclear, though, whether these mutations increase with age in immature egg cells known as oocytes.

In this new study, scientists used a DNA-sequencing technique to identify mutations in 80 single oocytes from 22 women, aged 20 to 42. They also studied mitochondrial DNA mutations in the women's blood and saliva.

They found that as women age, mitochondrial DNA mutations increase in blood and saliva cells, but not in egg cells. This suggests that a mechanism may have evolved that protects eggs from age-related genetic damage seen in other parts of the body.

"mtDNA in human oocytes is protected against accumulation of mutations with aging and has functional consequences," wrote the researchers. "These findings are particularly timely as humans tend to reproduce later in life."

The researchers also noted that the few mutations they did find tended to occur in parts of the mtDNA that do not make proteins (non-coding regions). Mutations were much less common in the parts that make proteins (coding regions).

Previous studies have shown that older mothers are more likely to pass on chromosomal abnormalities to their children. It was assumed the same was true for mitochondrial mutations. The new research challenges this assumption, offering a promising sign that delaying motherhood may not increase the risk of passing on mtDNA mutations.

Despite these findings, the study's conclusions are not definitive. It was based on a small sample size and did not cover a woman's full reproductive lifespan.

 Barbara Arbeithuber et al, Allele frequency selection and no age-related increase in human oocyte mitochondrial mutations, Science Advances (2025). DOI: 10.1126/sciadv.adw4954

Peacocks have lasers in their tails

As if the tail of a peacock could get any more flamboyant. Scientists have now discovered yellow-green lasers shooting from the ‘eyes’ of their feathers. These aren’t vaporizing beams of light that can cut a bird in half or anything. We would have probably noticed that during a courtship display… The lasers we’re talking about are completely harmless. The term stands for Light Amplification by Stimulated Emission of Radiation. Essentially, that means if you shine a light on some materials and the atoms excite one another, it can release a flood of photons, producing a faint glow. Biological lasers like these can be found in butterfly wings and marine mammals. But this is the first time scientists have observed the effect in the feathers of peacocks. Even the greatest show-offs in the world have a secret or two up their sleeves.

The researchers found evidence of optical cavities in the form of resonating nanostructures in different parts of the eyespot, all faintly emitting two different wavelengths: green and yellow/orange.

Exactly what kind of structure is responsible for aligning the amplified light at these colors isn't clear. But the fact they are found across the feather, all emitting the same precise wavelengths in a signature fashion, is a sign that something strange is at work.

https://www.nature.com/articles/s41598-025-04039-8

Sunlight-activated material turns PFAS in water into harmless fluoride

Researchers  have developed a sunlight-activated material that can degrade per- and polyfluoroalkyl substances (PFAS) in water, breaking down the pollutant into harmless components, including fluoride. The work is published in the journal Small.

The breakthrough discovery represents a promising low-energy solution for PFAS remediation, with potential applications in water treatment and environmental cleanup.

Many water contaminants are degraded by adding a reactive chemical that binds to the carbon. However, in PFAS molecules, the carbon atoms are protected in such a way that makes this process nearly impossible.

The researchers now have altered conditions and optimized the catalyst to target the PFAS-protective F atoms, which resulted in complete breakdown of the forever chemicals.

The produced fluoride can be isolated and used in health care products such as toothpaste or as additives to fertilizers.

Mahmoud Adel Hamza et al, CdIn2S4 Micro‐Pyramids for Reductive Photocatalytic Degradation of Perfluorooctanesulfonic Acid, Small (2025). DOI: 10.1002/smll.202504601

New evidence suggests Neolithic farmers cannibalized enemies

Slicing, chopping and bite and cut marks on human remains from 5,700 years ago suggest that cannibalism may have been a common practice among our Neolithic ancestors.

Researchers studied more than 600 bones and fragments from 11 well-preserved skeletons of adults, adolescents and children. They were found in El Mirador Cave in the Atapuerca mountains and date to the Late Neolithic period (about 6,500 to 5,000 years ago).

The work is published in the journal Scientific Reports.

Microscopy analysis revealed signs of cannibalism on all of the bones studied. Specifically, the researchers noted signs of butchery on 69 bones and chop marks on several others, indicating that skin and muscle had been sliced off. Some bones were translucent with slightly rounded edges, suggesting they had been boiled. Further evidence includes some of the larger bones being cracked open, most likely to get at the marrow.

According to the scientists, cannibalism took place after death. The bodies were skinned, and their limbs were separated before being cooked and eaten, possibly over a few days.

Ancient cannibalism is difficult to interpret because it can be hard to determine the motive, and evidence is often sparse or ambiguous at best. However, the scientists have ruled out emergency survival due to a lack of food, as there were no signs of scarcity in the region at the time. They also believe it wasn't part of funerary practices or other rituals, as nothing similar has been found in the area.

The bones in this study are thought to be from one family or an extended family, and researchers think a neighboring group wiped them out in a single event. "The current findings suggest that cannibalism may be linked to intergroup violence during late prehistoric periods," write the researchers in their paper. This is supported by evidence of other Neolithic massacres in Spain, France and Germany.

El Mirador cave, where the bones were found, is a treasure trove of archaeological remains. Previous discoveries include ceremonial skull caps and evidence of Bronze Age cannibalism.

This latest study, along with earlier findings, is challenging the common image of the Neolithic as an era of farmers coexisting peacefully. Instead, it suggests a more violent and conflict-ridden existence.

Palmira Saladié et al, Evidence of neolithic cannibalism among farming communities at El Mirador cave, Sierra de Atapuerca, Spain, Scientific Reports (2025). DOI: 10.1038/s41598-025-10266-w

Hypergravity boosts food production in moss species, new study finds

Unless one is a trained fighter jet pilot, or a Formula 1 driver, humans tend not to do well at higher gravity, but tiny green moss plants seem to thrive under such conditions.

Researchers found that moss (Physcomitrium patens) exhibited increased photosynthesis under hypergravity conditions (six and 10 times Earth's gravity) due to enhanced carbon dioxide  (CO₂) diffusion from the atmosphere into the chloroplasts within the plant leaves.

The plants adapt to the increased gravity by increasing the size of their chloroplasts and the number of leafy shoots of the moss (gametophores). Researchers identified for the first time the gene factor responsible for this response. They named the factor ISSUNBOSHI1 or IBSH1, a namesake of an inch-high, warrior boy from a beloved Japanese fairytale.

The findings, published in Science Advances, reveal the existence of a key genetic mechanism that drove the evolutionary process, enabling plants to adapt to life on land.

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Plants began their journey on Earth under water. One of the biggest environmental changes they had to adapt to was their emergence onto the land, approximately 500 million years ago.

The early plants transitioning from aquatic to terrestrial ecosystems lost their buoyancy and were now exposed to the gravitational acceleration of 1g. In the reduced gravity of water, plants didn't have to worry about carrying their own weight, but on land, they had to.

As a result, their anatomy began to shift, developing plant tissues that provided structural reinforcement and orienting the light-harvesting components of plants towards the light. Even the cell wall saw some structural changes.

Part 1

The researchers of this study, in a previous paper, reported that hypergravity of 10g surprisingly increased the rate of photosynthesis in Physcomitrium patens, but underlying anatomical and genetic mechanisms remained unexplored.

For this study, the team grew moss for eight weeks at 25°C under varying gravity levels—1g (control), 3g, 6g, and 10g—using a custom-built centrifuge with a built-in light-emitting diode (LED) for providing a photosynthetic photon.

To track the effect of hypergravity, they measured photosynthesis rates, anatomical traits like chloroplast size and gametophore number, and CO2 conductance—the ability of small openings on leaf surfaces to let CO2 in. They also carried out RNA sequencing to investigate if genes were expressed differently under hypergravity.
The results indicated an increased photosynthesis rate at higher gravity levels (6g and 10g) due to improved CO2 diffusion, resulting from the presence of more leafy shoots and larger chloroplasts.

This response was linked with the upregulation of AP2/ERF transcription factors, particularly IBSH1. The researchers confirmed its role by manipulating IBSH1 in moss—overexpression reproduced the effects of hypergravity, while repression prevented these responses.

The researchers suggest that the formation of a remarkable gene network involving AP2/ERF factors may have been a key factor in enabling moss plants to adapt to life on land during the evolution of plants. They think  these findings offer pivotal insights that could one day support agricultural production in space, where gravity is vastly different from Earth's.

 Yuko T. Hanba et al, First contact with greater gravity: Moss plants adapted via enhanced photosynthesis mediated by AP2/ERF transcription factors, Science Advances (2025). DOI: 10.1126/sciadv.ado8664

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Body hides its own RNA from the immune system with sugar

To our immune system, naked RNA is a sign of a viral or bacterial invasion and must be attacked. But our own cells also have RNA. To ward off trouble, our cells clothe their RNA in sugars, researchers  report in Nature.

Ribonucleic acid (RNA) is a family of large biological molecules fundamental to all forms of life, including viruses, bacteria, and animals. Viruses as diverse as measles, influenza, SARS-CoV-2, and rabies all have RNA, which is why the immune system starts attacking when it sees RNA in the bloodstream or in other inappropriate locations. But our own cells have RNA as well, sometimes displaying it on their surface, plain for roaming immune cells to see—and yet the immune system ignores it.

Recognizing RNA as a sign of infection is problematic, as every single cell in our body has RNA. The question is, how does our immune system distinguish our own RNA from that of dangerous invaders?

Researchers had noticed that our bodies add sugars onto RNA. These sugarcoated RNAs (also known as glycosylated RNAs, or glycoRNAs) are displayed on the cell surface and don't seem to provoke the immune system.

When the researchers took glycoRNA from human cell cultures and blood, cut off the sugars, and reintroduced it into cells, the immune cells attacked it. The immune cells had ignored the same RNA when it was sugarcoated.

The sugarcoating hides our own RNA from the immune system.

It is particularly significant to our body because cells are often covered by glycoRNAs. When cells die and are cleaned up by the immune system, the sugarcoating of RNA prevents dead cells from unnecessarily stimulating inflammation.

The findings could help when thinking about autoimmune diseases. Certain autoimmune diseases, such as lupus, are associated with specific RNA and dead cells setting off the immune system.

Now that scientists understand the role of RNA glycosylation in deflecting immune system attention, they can check on whether that strategy is somehow going awry, and, if so, how it might be fixed.

Vincent R. Graziano et al, RNA N-glycosylation enables immune evasion and homeostatic efferocytosis, Nature (2025). DOI: 10.1038/s41586-025-09310-6

Ancient practice of blowing through a conch shell could help treat dangerous snoring condition

People who practiced blowing through a conch shell regularly for six months experienced a reduction in their symptoms of obstructive sleep apnea (OSA), according to a small randomized controlled trial published in ERJ Open Research.

OSA is a common sleep disorder where breathing repeatedly stops during the night due to a blocked airway. It leads to loud snoring, restless sleep and daytime sleepiness. It also increases the risk of high blood pressure, heart disease, and stroke.

Blowing the conch shell, or shankh blowing, has been part of Indian culture for thousands of years. The new research showed that people with moderate OSA who practiced shankh blowing slept better, felt more alert during the day and had fewer breathing interruptions at night. The researchers say conch blowing is a simple, low-cost intervention that could help reduce symptoms without the need for medication or machines.

Compared to the people who practiced deep breathing, the people who practiced shankh blowing were 34% less sleepy during the daytime. They reported sleeping better and polysomnography revealed that they had four to five fewer apneas (where breathing stops during sleep) per hour on average. They also had higher levels of oxygen in their blood during the night.

The way the shankh is blown is quite distinctive. It involves a deep inhalation followed by a forceful, sustained exhalation through tightly pursed lips. This action creates strong vibrations and airflow resistance, which likely strengthens the muscles of the upper airway, including the throat and soft palate—areas that often collapse during sleep in people with OSA. The shankh's unique spiraling structure may also contribute to specific acoustic and mechanical effects that further stimulate and tone these muscles.

 Shankh blowing is a simple, low-cost breathing technique that could help improve sleep and reduce symptoms without the need for machines or medication.

However, let’s be clear: conch shell therapy won’t revolutionise sleep apnoea treatment. Anyone with suspected sleep apnoea needs proper medical evaluation and evidence-based treatment. Cpap therapy remains the most effective option for moderate to severe cases. But as part of a comprehensive approach – alongside weight management, lifestyle changes and conventional treatments – prescribed conch shell exercises might one day earn a place in our therapeutic toolkit. But still it has to pass many tests.

Efficacy of blowing shankh on moderate sleep apnea: a randomised control trial, ERJ Open Research (2025). DOI: 10.1183/23120541.00258-2025

Neurodegenerative diseases: Research establishes causal link between mitochondrial dysfunction and cognitive symptoms

Mitochondria, the tiny organelles without which our bodies would be deprived of energy, are gradually revealing their mysteries. In a study published in Nature Neuroscience, researchers have for the first time succeeded in establishing a causal link between mitochondrial dysfunction and the cognitive symptoms associated with neurodegenerative diseases.

Thanks to the creation of a specific and unprecedented tool, they succeeded in increasing mitochondrial activity in animal models of neurodegenerative diseases, where they observed an improvement in memory deficit symptoms. While these are only initial results, they open the door to considering mitochondria as a new therapeutic target.

The mitochondrion is a small intracellular organelle that provides the energy needed by the cell to function properly. The brain is one of the most energy-demanding organs, and neurons rely on the energy produced by mitochondria to communicate with one another. Indeed, when mitochondrial activity is impaired, neurons do not have the energy required to function correctly.

Neurodegenerative diseases are characterized by a progressive impairment of neuronal functions, leading to the death of brain cells. In Alzheimer's disease, for example, it has been observed that neuronal degeneration, which precedes cell death, is accompanied by impaired mitochondrial activity.

This work is the first to establish a cause-and-effect link between mitochondrial dysfunction and symptoms related to neurodegenerative diseases, suggesting that impaired mitochondrial activity could be at the origin of the onset of neuronal degeneration.

The work now continues with trying to measure the effects of continuous stimulation of mitochondrial activity to see whether it impacts the symptoms of neurodegenerative diseases and, ultimately, delays neuronal loss or even prevents it if mitochondrial activity is restored.

Potentiation of mitochondrial activity by mitoDREADD-Gs reverses pharmacological and neurodegenerative impairment of cognition, Nature Neuroscience (2025). DOI: 10.1038/s41593-025-02032-y. www.nature.com/articles/s41593-025-02032-y

How bad are micro- and nanoplastics for our health? It depends on their concentrations and how we measure them

Detection, concentration and distribution of MNPs in the human body. Credit: Nature Reviews Bioengineering (2025). DOI: 10.1038/s44222-025-00335-0

Common food thickeners—long thought to pass right through us—are actually digested

The complex structure of the cellulose derivatives is what makes them valuable as thickening agents in popular products like ketchup, salad dressing and even toothpaste. This structure is also why gut bacteria have a harder time breaking them down—and why in higher concentrations, they're even used as laxatives.

Earlier researchers assumed that these thickening agents, which are artificial derivatives of natural cellulose, just pass right through the digestive system unaltered.

It turns out those cellulose-based thickening agents found in common foods can be digested. Researchers have shown that our gut bacteria can feed on these large molecules—something thought to not be possible—thanks to enzymes that normally help us break down dietary fiber.

The new study provides a first glimpse at how these food additives are actually digested by our gut bacteria  thanks to natural polysaccharides in our diets.

This new in vitro study, however, shows that if our gut bacteria are 'primed' with natural polysaccharides—long chains of sugars found in fruits, vegetables and cereals—the cellulose derivatives can be digested. This is because the natural polysaccharides activate enzymes that are produced on bacteria cell surfaces that can also break down artificial cellulose molecules.

The findings don't challenge the fact that these compounds are safe to consume, proven by years of testing and history of use. However, the new research suggests that more work should be done to explore the physical, chemical and biological effects of the digestion of cellulose derivatives by gut bacteria.

 Deepesh Panwar et al, Artificial cellulose derivatives are metabolized by select human gut Bacteroidota upon priming with common plant β-glucans, Journal of Bacteriology (2025). DOI: 10.1128/jb.00198-25

The stomach's neural network is more in sync with the mind during mental distress, researchers discover

Stronger coordination between the brain and the stomach's natural rhythm is linked to higher levels of anxiety, depression, and stress, according to the largest study of its kind by researchers.

While most gut–brain research has focused on the lower intestine and gut bacteria, the team of researchers turned to the stomach—the body's upper digestive hub with its own network of nerves.

Scanning more than 240 participants, they found that when brain activity is more tightly synchronized with the stomach's slow electrical waves, people are more likely to report mental distress. The paper is published in the journal Nature Mental Health.

The stomach's connection to the brain may actually be too strong in people under psychological strain, say the researchers.

The stomach has its own nervous system, often called the "second brain." Its slow waves occur roughly every 20 seconds, even when we're not eating—a constant background rhythm like the heartbeat.

By combining functional MRI scans with electrogastrography, the researchers measured how closely brain activity matched these waves in each participant.

We usually assume stronger body-brain communication is a sign of health. But here, unusually strong stomach–brain coupling seems linked to greater psychological burden—perhaps a system under strain.

Part 1

The findings are correlational—they do not show that stomach activity causes mental illness. But the researchers think the pattern could point to a new physiological marker of mental health that is objective, measurable, and grounded in the body's rhythms.
If stomach–brain synchronization proves to be a stable feature of mental health, it could open new diagnostic or therapeutic possibilities.

Leah Banellis et al, Stomach–brain coupling indexes a dimensional signature of mental health, Nature Mental Health (2025). DOI: 10.1038/s44220-025-00468-6

Part 2

Microbial molecule may offer non-toxic way to restore liver and gut health

Researchers have discovered that a natural molecule made by gut bacteria can reverse liver damage and repair the gut lining after aflatoxin exposure. The treatment may offer a new, non-toxic way to prevent and treat non-alcoholic fatty liver disease (NAFLD), a growing health problem.

The study revealed that 10-hydroxystearic acid (10-HSA), a compound produced by Lactobacillus bacteria, successfully restored gut-liver health in mice exposed to aflatoxin. Aflatoxin is a toxic substance made by mold commonly found in peanuts, corn and other crops. It is known to cause liver injury.

"This is the first time a single microbial molecule has been shown to repair both the liver and gut together," say the researchers. 

The gut and the liver are intricately linked. They communicate through bile acids, immunity responses and lipid metabolism—a relationship known as the gut-liver axis. When one organ is damaged, the other suffers too. In diseases like NAFLD (now also called MASLD), this connection becomes a key therapeutic target.

Aflatoxin exposure affects many people, especially in developing countries. In agricultural areas with poor food safety, this exposure is a serious public health concern. This study lays the foundation for developing a simple, safe supplement that could be life changing.

Microbial biotherapeutic metabolite alleviates liver injury by restoring hepatic lipid metabolism through PPARα across the gut-liver axis, mBio (2025). DOI: 10.1128/mbio.01718-25

Autoimmune diseases linked to cancers of the digestive tract

In a comprehensive study, researchers have provided reliable evidence for a link between chronic inflammatory diseases and the development of tumors in the digestive tract. The results were recently published in eClinicalMedicine.

Using data from over 1.5 million patients from 47 studies, the researchers analyzed the association between four autoimmune diseases, most of which are acquired in childhood or younger adulthood, and cancers of the gastrointestinal tract, liver and pancreas.

The study shows that celiac disease, systemic lupus erythematosus and type 1 diabetes increase the risk of several types of cancer of the digestive tract. These include stomach and bowel cancer. In particular, the risk of small bowel cancer increases by a factor of 4.2 if celiac disease is present.

Multiple sclerosis, on the other hand, is associated with a lower risk of certain types of cancer, such as pancreatic, esophageal and rectal cancer.

These results underline the need for targeted monitoring of patients with autoimmune diseases and the development of personalized cancer prevention programs.

Julia Reizner et al, Evaluating the risk of digestive system cancer in autoimmune disease patients: a systematic review and meta-analysis focusing on bias assessment, eClinicalMedicine (2025). DOI: 10.1016/j.eclinm.2025.103410

How noise, air pollution, heat and chemicals act together to damage the cardiovascular system

Cardiovascular diseases comprise a broad range of disorders affecting the heart and blood vessels, including myocardial infarction, stroke, coronary artery disease (CAD), hypertension, heart failure, and arrhythmias. These conditions remain the number one cause of death worldwide.

Therefore, the demand for effective preventive strategies is substantial, and understanding the relevant risk factors is essential. Well-established contributors include obesity, diabetes, smoking, physical inactivity, and an unhealthy diet.

An international research team now warns in a comprehensive review about another group of risk factors that have thus far received limited attention in current prevention strategies: environmental stressors. The authors report in Cardiovascular Research that chronic exposure to noise, fine particulate matter,  heat waves, and chemical pollutants in soil and water can exert harmful effects on the cardiovascular system.

Key findings of the current publication:

Chronic traffic noise activates stress hormone pathways, disrupts sleep, and induces hypertension and vascular inflammation.
Air pollution, fine particulate matter, particularly ultrafine particles (PM₂.₅, UFP), can penetrate deep into the lungs, enter the bloodstream, and promote oxidative stress, endothelial injury, and atherosclerosis.
Increasingly frequent heat waves place particular strain on elderly individuals and those with pre-existing cardiovascular disease. In cities, impervious surfaces and lack of greenery exacerbate "heat island" effects, increasing the risk of myocardial infarction and stroke.
Persistent chemical pollutants such as pesticides, heavy metals, and PFAS (per- and polyfluoroalkyl substances), which degrade slowly or not at all, can enter the body through food and drinking water. Early studies suggest they can enhance inflammation, impair vascular function, and elevate long-term cardiovascular risk.
Part 1

Of particular concern is the combination of multiple environmental stressors: the multimodal exposome can magnify the detrimental effects of individual exposures.

Noise can intensify the impact of air pollutants, and heat can act as a catalyst for vascular damage caused by toxins.
The overlapping biological mechanisms range from oxidative stress and activation of the pro-inflammatory enzyme NOX-2 to endothelial dysfunction—all of which are early precursors of myocardial infarction and stroke.
The exposome concept offers a holistic framework that integrates the lifetime accumulation of environmental exposures and their biological interactions into cardiovascular risk assessment, enabling the development of more targeted preventive strategies. The researchers  stress that stricter environmental and noise protection laws, sustainable urban planning, and green infrastructure can help reduce exposure to these stressors.

Thomas Friedrich Münzel et al, A comprehensive review/expert statement on environmental risk factors of cardiovascular disease, Cardiovascular Research (2025). DOI: 10.1093/cvr/cvaf119. academic.oup.com/cardiovascres … /cvr/cvaf119/8230112

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How small changes in walking technique may help treat knee osteoarthritis

Gait analysis and pain measures show that subtly adjusting the angle of the foot during walking may reduce knee pain caused by osteoarthritis. This approach may also slow progression of the condition, an incurable disease in which the cartilage cushion inside a joint breaks down.

A new study explored whether changing the way patients position their feet when walking could lessen extra loading—stress on the joint during motion—and help treat the disease.

For the investigation, the scientists tested this intervention in 68 men and women with mild to moderate knee osteoarthritis and then used advanced MRI scans to track how well it worked.

The results suggest that those trained to angle their feet slightly inward or outward from their natural alignment experienced slower cartilage degeneration in the inner part of their knee compared with those who were encouraged to walk more frequently without changing their foot position. A report on the study is published online in the journal The Lancet Rheumatology.

The findings also revealed that those who adjusted their foot angle reduced their pain score by 2.5 points on a 10-point scale, an effect equivalent to that of over-the-counter pain medications. By contrast, those who did not change their gait reduced their pain scores by little more than a point.

 Personalised gait retraining for medial compartment knee osteoarthritis: a randomised controlled trial, The Lancet Rheumatology (2025). DOI: 10.1016/S2665-9913(25)00151-1

A genetic twist that sets human brains apart

Research  has shed new light on an age-old question: what makes the human brain unique? The study is published online in Science Advances.

The  discovery comes from their investigation of human-accelerated regions (HARs)—sections of the human genome that have accumulated an unusually high level of mutations as humans have evolved. There is a lot of scientific interest in HARs, as they are hypothesized to play an essential role in conferring human-specific traits, and also have links to neurodevelopmental disorders, such as autism.

One reason why scientists think that HARs confer human-specific traits is they have undergone rapid changes in their genetic sequences since we split from our closest living relative—the chimpanzee—approximately 5 million years ago.

Now researchers have identified one particular HAR—called HAR123—that appears to be instrumental in shaping the human brain. The researchers found that HAR123 itself is not a gene, but is instead a type of molecular "volume control" known as a transcriptional enhancer. Transcriptional enhancers control which genes are activated, how much they are activated, and at what times they are activated during an organism's development.

Through its role as a transcriptional enhancer, HAR123 promotes the development of neural progenitor cells, the cells that give rise to the two main types of brain cells—neurons and glial cells. HAR123 also influences the ratio of neurons and glial cells that form from neural progenitor cells. 

Part 1

Ultimately, HAR123 promotes a particularly advanced human trait called cognitive flexibility, or the ability to unlearn and replace previous knowledge.
In addition to providing new insights into the biology of the human brain, the results also offer a molecular explanation for some of the radical changes that have occurred in the human brain over the course of our evolution. This is supported, for example, by the authors' finding that the human version of HAR123 exerts different molecular and cellular effects than the chimpanzee version in both stem cells and neuron precursor cells in a petri dish.

 Kun Tan et al, An ancient enhancer rapidly evolving in the human lineage promotes neural development and cognitive flexibility, Science Advances (2025). DOI: 10.1126/sciadv.adt0534. www.science.org/doi/10.1126/sciadv.adt0534

Part 2

In-mouth hydrogel releases artificial saliva to treat dry mouth

Saliva is more than spit. It helps with chewing and swallowing, protects teeth and gums, and even has antimicrobial and digestive properties. However, certain conditions or medical treatments, such as hemodialysis, chemotherapy and radiation therapy, reduce natural saliva production. Now, researchers publishing in ACS Applied Polymer Materials have created a reusable hydrogel that releases artificial saliva over time, which could help provide sustained relief from dry mouth.

Dry mouth is a condition whereby the salivary glands do not produce enough saliva. Many medications to treat dry mouth boost natural saliva production, but they either provide temporary relief or have unwanted side effects, including mouth irritation and tooth erosion. Previous research identified that artificial saliva, often used in laboratory studies, could be a promising alternative to current medications.

Like natural saliva, artificial saliva is mostly water and contains mucins—a class of compounds that lubricate the mouth and have antimicrobial properties.

To create the reservoir, the researchers mixed artificial saliva with a biocompatible polymer poly(hydroxyethyl methacrylate), which is commonly used in medical applications such as contact lenses. The resulting hydrogel is a clear blob roughly the size of a U.S. quarter and small enough to fit in the inner cheek or below the tongue.

To determine how much artificial saliva a single reservoir could absorb, the researchers submerged it in artificial saliva for 6 hours. The saliva gel expanded up to 400% of its original volume, indicating that the gel has a high saliva storage capacity.

Next, the researchers tested the reservoir's ability to release stored saliva. The gel released all stored saliva over a 4-hour time span at 98.6 degrees Fahrenheit (37 degrees Celsius), starting off a little faster and then slowing over time. This demonstrates that human body temperature helps initiate saliva release from the hydrogel.

The researchers also report consistent saliva release rates across five consecutive tests with a single reservoir, demonstrating its potential as a reusable treatment option. Lastly, cultured cells in contact with the gel had no change to their survival or growth rates, indicating the reservoir's biocompatibility.

 Suman Debnath et al, Poly(hydroxyethyl methacrylate) Saliva-Gel: A Polymer-Based Solution for Xerostomia Treatment, ACS Applied Polymer Materials (2025). DOI: 10.1021/acsapm.5c00881

Researchers uncover surprising limit on human imagination

Human beings can juggle up to 10 balls at once. But how many can they move through the air with their imaginations?

The answer, published in Nature Communications, astonished even the researchers pursuing the question. The cognitive psychologists found people could easily imagine the trajectory of a single ball after it disappeared. But the imagination couldn't simultaneously keep tabs on two moving balls that fell from view.

The researchers set out to test the capacity limits of the imagination, and they found that it was just one!

Halely Balaban et al, The capacity limits of moving objects in the imagination, Nature Communications (2025). DOI: 10.1038/s41467-025-61021-8

Maternal microbes play a significant role in shaping early brain development, study suggests

Research finds that microbes play an important role in shaping early brain development, specifically in a key brain region that controls stress, social behaviour, and vital body functions.

The study, published in Hormones and Behavior, used a mouse model to highlight how natural microbial exposure not only impacts brain structure immediately after birth but may even begin influencing development while still in the womb. A mouse model was chosen because mice share significant biological and behavioural similarities with humans and there are no other alternatives to study the role of microbes on brain development. 

This work is of significance because modern obstetric practices, like peripartum antibiotic use and Cesarean delivery, disrupt maternal microbes.

At birth, a newborn body is colonized by microbes as it travels through the birth canal. Birth also coincides with important developmental events that shape the brain.

The research team focused on a brain region called the paraventricular nucleus of the hypothalamus (PVN), which plays a central role in regulating stress, blood pressure, water balance, and even social behavior. Their previous work had shown that mice raised without microbes, or germ-free mice, had more dying neurons in the PVN during early development. The new study set out to determine whether this increased cell death translated to changes in neuron number in the long run, and if any effects could be caused by the arrival of microbes at birth or if they began in the womb via signals from maternal microbes.

. The researchers used a cross-fostering approach. Germ-free newborn mice were placed with mothers that had microbes and compared them to control groups. When the brains of these mice were examined just three days after birth, the results were striking: All mice gestated by germ-free mothers had fewer neurons in the PVN, regardless of whether they received microbes after birth. The team also found that germ-free adult mice had fewer neurons in the PVN.

This study shows that microbes play an important role in sculpting a brain region that is paramount for body functions and social behavior. In addition, the study indicates that microbial effects start in the womb via signaling from maternal microbes.

Rather than shunning our microbes, we should recognize them as partners in early life development. They're helping build our brains from the very beginning, say the researchers

 Yvonne C. Milligan et al, The microbiota shapes the development of the mouse hypothalamic paraventricular nucleus, Hormones and Behavior (2025). DOI: 10.1016/j.yhbeh.2025.105742

Why some wounds heal without scars
Some parts of our bodies — such as the insides of the mouth and uterus — heal without scarring. Now researchers are delving into why this happens, and how it might help to head off some of the downsides of scars. The team compared mouth and face skin and found that, in mice, specialized skin cells communicate differently during healing: in mouth cells, a cell signaling pathway and a protein seem to prevent the formation of scars. Samples of human skin biopsies seem to back up the findings.

https://www.science.org/doi/10.1126/scitranslmed.adk2101?utm_source...

Electrical implant approved for arthritis
A 2-centimetre implant that suppresses the symptoms of rheumatoid arthritis is the first electrical device approved to treat an autoimmune condition. The chip, called a Setpoint System, is implanted into a person’s neck and sends electrical pulses through the vagus nerve. In people with rheumatoid arthritis, these signals tell the immune system to stop attacking the joints. Similar implants are now in clinical trials for other autoimmune conditions, including lupus and inflammatory bowel disease.

https://www.smithsonianmag.com/smart-news/new-implanted-device-coul...

A Case of Bromism Influenced by Use of Artificial Intelligence

Man Hospitalized With Psychiatric Symptoms Following AI Advice

A man who followed a chatbot's health plan ended up in hospital after giving himself a rare form of toxicity.

The story began when the patient decided to improve his health by reducing his intake of salt, or sodium chloride. To find a substitute, he did what so many other people do nowadays: he asked ChatGPT on line.

OpenAI's chatbot apparently suggested sodium bromide, which the man ordered online and incorporated into his diet.

While it is true that sodium bromide can be a substitute for sodium chloride, that's usually if you're trying to clean a hot tub, not to make your fries tastier. But the AI neglected to mention this crucial context.

Three months later, the patient presented to the emergency department with paranoid delusions, believing his neighbour was trying to poison him.

In the first 24 hours of admission, he expressed increasing paranoia and auditory and visual hallucinations, which, after attempting to escape, resulted in an involuntary psychiatric hold for grave disability.

After he was treated with anti-psychosis drugs, the man calmed down enough to explain his AI-inspired dietary regime. This information, along with his test results, allowed the medical staff to diagnose him with bromism, a toxic accumulation of bromide. Bromide levels are typically less than around 10 mg/L in most healthy individuals; this patient's levels were measured at 1,700 mg/L. Bromism was a relatively common condition in the early 20th century, and is estimated to have once been responsible for up to 8 percent of psychiatric admissions. But cases of the condition drastically dropped in the 1970s and 1980s, after medications containing bromides began to be phased out.

Following diagnosis, the patient was treated over the course of three weeks and released with no major issues.

It is important to consider that ChatGPT and other AI systems can generate scientific inaccuracies, lack the ability to critically discuss results, and ultimately fuel the spread of misinformation.

https://www.acpjournals.org/doi/10.7326/aimcc.2024.1260

Scientists reverse immunotherapy-resistance by suppressing EPIC1 in mouse model of breast cancer

Immunotherapy employs patients' own immune systems to fight cancer, and it has shown itself to be an effective treatment in many cases. However, some cancers, like triple-negative breast cancer (TNBC), show resistance to immunotherapy. This occurs when tumor cells find ways to evade immune detection—like suppressing immune signaling pathways. One such mechanism is the use of long noncoding RNAs (lncRNAs), which have been found to regulate cancer biology and immune evasion. These lncRNAs render immunotherapies, like the PD-1 inhibitor, pembrolizumab, ineffective.

The good news is that if these mechanisms of immunotherapy-resistance can be identified, scientists may be able to reverse or inactivate them. In a new study, published in Science Signaling, scientists focus on the lncRNA, EPIC1, and its interaction with histone methyltransferase, EZH2, a known contributor of tumor immune evasion in cancer cells.
According to the researchers, they sought to investigate the mechanism by which EPIC1 modulates immune function and determine how it regulates the expression of retroelements (REs)—mobile DNA sequences that produce double-stranded RNA when activated—and dsRNA accumulation in tumor cells.

The researchers found that EPIC1 suppresses the accumulation of cytoplasmic dsRNA and type I interferon (IFN) responses in multiple cancer cell lines, including breast cancer, prostate cancer, and pancreatic cancer. EPIC1 and EZH2 were also shown to work together to repress the expression of immunogenic REs, suggesting a shared pathway for immune evasion.

The study authors write, "Collectively, these results suggest that EPIC1 suppression promotes an antiviral-like type I IFN response with potential antitumor effects."

To test out the effect of EPIC1 knockdown, the researchers used "humanized mice"—mice with human immune systems implanted to mimic the effect of the mechanism in a human. Using these mouse models along with RNA interference to knock down EPIC1 in various cancer cell lines, they found that targeting EPIC1 enabled reduced tumor growth and increased T cell and inflammatory macrophage infiltration. This led to a significant improvement in the efficacy of pembrolizumab in TNBC.

"EPIC1 can be a potential therapeutic target in combination with immunotherapy. Coculture assays of T cells or monocytes with cancer cells showed that EPIC1 knockdown could significantly increase the therapeutic effect of pembrolizumab through antitumor T cell and macrophage activation," the researchers write.

This is a promising result, offering hope for more effective treatments for aggressive cancers with limited options. However, the study authors note that these results still need to be tested out in human models and with other types of cancers to determine how best to improve immunotherapy outcomes in the future.

 Dhamotharan Pattarayan et al, The lncRNA EPIC1 suppresses dsRNA-induced type I IFN signaling and is a therapeutic target to enhance TNBC response to PD-1 inhibition, Science Signaling (2025). DOI: 10.1126/scisignal.adr9131

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Part 2

Astronomers discover new type of supernova triggered by black hole-star interaction

Astronomers have discovered what may be a massive star exploding while trying to swallow a black hole companion, offering an explanation for one of the strangest stellar explosions ever seen.

The discovery was made by an Astrophysicist team. The results are published in The Astrophysical Journal.

The blast, named SN 2023zkd, was first discovered in July 2023 by the Zwicky Transient Facility. A new AI algorithm designed to scan for unusual explosions in real time first detected the explosion, and that early alert allowed astronomers to begin follow-up observations immediately—an essential step in capturing the full story of the explosion. By the time the explosion was over, it had been observed by a large set of telescopes, both on the ground and from space.

The scientists think the most likely interpretation is that the massive star was locked in a deadly orbit with the black hole. As energy was lost from the orbit, their separation decreased until the supernova was triggered by the star's gravitational stress as it partially swallowed the black hole.

Analysis shows that the blast was sparked by a catastrophic encounter with a black hole companion, and is the strongest evidence to date that such close interactions can actually detonate a star.

An alternative interpretation considered by the team is that the black hole completely tore the star apart before it could explode on its own. In that case, the black hole quickly pulled in the star's debris and supernova emission was generated when the debris crashed into the gas surrounding it. In both cases, a single, heavier black hole is left behind.

A. Gagliano et al, Evidence for an Instability-induced Binary Merger in the Double-peaked, Helium-rich Type IIn Supernova 2023zkd, The Astrophysical Journal (2025). DOI: 10.3847/1538-4357/adea38. iopscience.iop.org/article/10. … 847/1538-4357/adea38.

Human embryo implantation recorded in real time for the first time

Researchers have captured unparalleled images of a human embryo implanting. This is the first time that the process has been recorded in real time and in 3D.

Failure of the implantation process in the uterus is one of the main causes of infertility, accounting for 60% of spontaneous abortions. Until now, it had not been possible to observe this process in humans in real time, and the limited available information came from still images taken at specific moments during the process.

The researchers have observed that human embryos burrow into the uterus, exerting considerable force during the process. These forces are necessary because the embryos must be able to invade the uterine tissue, becoming completely integrated with it. It is a surprisingly invasive process. Although it is known that many women experience abdominal pain and slight bleeding during implantation, the process itself had never been observed before. 

To advance during implantation, the embryo releases enzymes that break down the surrounding tissue. However, it is also known that force is required in order to penetrate the underlying layers of the uterus. This fibrous tissue is filled with collagen, a rigid protein that also forms tendons and cartilage.

The embryo opens a path through this structure and begins to form specialized tissues that connect to the mother's blood vessels in order to feed.

The research team's results reveal that human embryos exert traction forces on their environment, remodeling it. The embryo pulls on the uterine matrix, moving and reorganizing it. It also reacts to external force cues. Researchers hypothesize that contractions occurring in vivo may influence embryo implantation.Thus, effective embryo invasion is associated with optimal matrix displacement, highlighting the importance of these forces in the implantation process.

Improving our understanding of the implantation process could have a significant impact on fertility rates, embryo quality and the time taken to conceive through assisted reproduction.

Traction force and mechanosensitivity mediate species-specific implantation patterns in human and mouse embryos, Science Advances (2025). DOI: 10.1126/sciadv.adr5199