Visuals increase attention: science explains why

"Look at me!" we might say while attempting to engage  children. It turns out there is a neurochemical explanation for why looking at mom or dad or teacher actually helps kids pay better attention.

in a paper published recently scientists report that norepinephrine, a fundamental chemical for brain performance, is locally regulated in a brain region called the visual cortex.

Norepinephrine is known to be involved in paying attention. A certain amount of this chemical needs to be released for optimum brain performance and ability to pay attention. So, if there is either too much of it or too little of it, it may affect how we process information.

Disease states in which norepinephrine is known to be altered include substance use disorders, Alzheimer's disease, post-traumatic stress disorder (PTSD) and attention-deficit/hyperactivity disorder (ADHD). In some substance use, Alzheimer's and ADHD, the release of norepinephrine is reduced, resulting in lower attention. In other substance use and PTSD, the level is too high.

The team's findings also extend to cells called astrocytes that function as helper cells in the brain and central nervous system.

"When a person makes a movement, such as turning the head to listen to a parent, and that is combined with visual stimulation, then more norepinephrine is released where visual information is processed.

Astrocytes can reliably detect the rate of norepinephrine release. 

They are sensitive to it, in other words. Astrocytes alter their response accordingly, which is expected to change brain performance.

Understanding norepinephrine release, its local regulation and the astrocyte response may represent a mechanism by which one could enhance sensory-specific attention.

Shawn R. Gray et al, Noradrenergic terminal short-term potentiation enables modality-selective integration of sensory input and vigilance state, Science Advances (2021). DOI: 10.1126/sciadv.abk1378. www.science.org/doi/10.1126/sciadv.abk1378

https://medicalxpress.com/news/2021-12-visuals-attention-science.ht...

Pain and anxiety impact breathing on a cellular level

You're startled by a threatening sound, and your breath quickens; you smash your elbow and pant in pain. Why a person's breathing rate increases dramatically when they're hurting or anxious was not previously understood. Now, a team of Salk scientists has uncovered a neural network in the brain that coordinates breathing rhythm with feelings of pain and fear. Along with contributions to the fields of pain management, psychological theories of anxiety, and philosophical investigations into the nature of pain, their findings could lead to development of an analgesic that would prevent opioid-induced respiratory depression (OIRD), the disrupted breathing that causes overdose deaths.

Scientists  focused on a group of neurons in the brainstem called the lateral parabrachial nucleus, which is arranged in a core-shell configuration. They found that neurons in the core project to the amygdala, an area of the brain that processes fear and the emotional experience of pain. Neurons in the shell project to the pre-Bötzinger complex, a region that generates breathing rhythm. The core and shell neurons influence each other according to inputs from these areas, making us breathe faster when we experience pain or anxiety.

SungHan, Divergent brainstem opioidergic pathways that coordinate breathing with pain and emotions, Neuron (2021). DOI: 10.1016/j.neuron.2021.11.029. www.cell.com/neuron/fulltext/S0896-6273(21)00990-9

https://medicalxpress.com/news/2021-12-pain-anxiety-impact-cellular...

In last 15 years, deforestation made outdoor work unsafe for millions

The tropics is becoming hotter due to a combination of warming associated with deforestation and climate change—and that can reduce the ability of outdoor workers to perform their jobs safely. Researchers reporting in the journal One Earth on December 17 estimate how many safe working hours people living in the tropics have lost due to local temperature change associated with loss of trees during the past 15 years.

There is a huge disproportionate decrease in safe work hours associated with heat exposure for people in deforested locations versus people in forestated locations just over the past 15 or 20 years.

There is a small amount of climate change that has happened over the same 15-year period, but the increase in humid heat exposure for people living in deforested relative to forested locations was much larger than that from recent climate change.

Previous research has revealed deforestation is associated with an increase in local temperature. Trees block out the sun's radiation and provide shade. They also cool down the air via evapotranspiration, a process when plants transport water from the soil then evaporate water from the leaf surface, similar to how sweating cools the skin.

"The trees in the tropics seem to limit the maximum temperatures that the air can reach. Once we cut those trees down, we lose that cooling service from the trees, and it can get really, really hot. In the Brazilian Amazon, for example, where huge swaths of the rainforest have been cleared in the last 15 or 20 years, the afternoons can be up to 10 degrees Celsius warmer than forested regions.

The One Earth study went a step further and estimated the number of people who live in locations affected by warming associated with deforestation. Using satellite data and meteorological observations, Parsons and his team tracked the local temperature and humidity in 94 low-latitude countries with tropical forests, including countries in the Americas, Africa, and Asia, from 2003 to 2018.

They estimated that in recently deforested locations, almost 5 million people lost at least half an hour of safe work time per day—when the weather outside is too hot and humid to safely conduct heavy labor. Among them, at least 2.8 million people are outdoor workers that perform heavy physical work in the agriculture and construction sectors. Heavy physical work increases heat generated within the human body, which when combined with hot and humid environments, increases the risk of heat strain and heat-related illnesses, including heat stroke, which can be fatal.

Luke AParsons, Tropical deforestation accelerates local warming and loss of safe outdoor working hours, One Earth (2021). DOI: 10.1016/j.oneear.2021.11.016. www.cell.com/one-earth/fulltex … 2590-3322(21)00664-3

https://phys.org/news/2021-12-years-deforestation-outdoor-unsafe-mi...

Scientists unveil drug discovery tool to screen more than 11 billion compounds

Scientists unveil drug discovery tool to screen more than 11 billion compounds

On the surface of our cells are docking stations called receptors. All kinds of compounds from caffeine and dopamine to heroin, THC and LSD bind to these receptors. In fact, G protein-coupled receptors are the intended targets of more than 30 percent of pharmaceutical products currently on the market. But these drugs often hit unintended targets—think carpet bombing the nervous system—leading to the laundry list of side effects commonly heard at the end of pharmaceutical commercials.

What we need are more precise and less harmful treatments that are just as effective.

But creating these better drugs isn't easy. Drug developers need to know the exact chemical structure of a drug and the intended receptor to produce the exact chemical reaction we want inside cells. The kicker is to make sure the drug doesn't affect other receptors or bind to the target receptors but bind in such a way to trigger unintended consequences inside cells.

In the past, scientists would test molecules in a one-by-one fashion against a therapeutic target in a lengthy and expensive operation. So scientists created virtual libraries of molecules and fancy computer programs to test hundreds of thousands of molecules at a time. By "test" we mean that the computer program scoured a database of molecules that theoretically could be created and theoretically could bind with the proper affinity to a given cell receptor. And then scientists could tinker with chemical bonds in a computer program to optimize a molecule's structure. Then scientists could physically make a tiny sliver of these molecules and test them in cell cultures.

The creation of virtual libraries was a giant leap in the field. Testing hundreds of thousands of possible molecules, some of which might be candidates with properties worth investigating, sounds like a lot. But there are billions upon billions of possible chemical combinations that could theoretically lead to the creation of a near infinite number of molecules or potential drugs. As a result, scientists wound up creating vast libraries of theoretical compounds, billions of mostly "undiscovered" and unexplored molecules that may or may not bind to a given cellular target; they may or may not have therapeutic value at all.

Unfortunately, chemical space is vast. It has been estimated that there exists, theoretically, more chemicals than there are actual molecules in the universe. And only a small sliver of the potential chemicals can be physically tested.

Researchers to validate V-SYNTHES, a new type of computational method that allows scientists to first identify the best combinations of chemical building blocks called synthons – hypothetical units within molecules – to serve as seeds that can grow into a hierarchy of molecules with the best predicted ability to bind to the receptor targets. This approach allows researchers to computationally test billions of compounds against a therapeutic target.

As described in their Nature paper, scientists tested 11 billion theoretical compounds against a cannabinoid receptor (CB2) that marijuana's active ingredient THC targets.

https://www.nature.com/articles/s41586-021-04220-9

https://www.med.unc.edu/pharm/scientists-unveil-drug-discovery-tool...

https://researchnews.cc/news/10594/Scientists-unveil-drug-discovery...

How organs evolve

Fuel Cell Cars

Chasing an Asteroid's Shadow

Harnessing viruses to fight bacteria and reduce antibiotic use

New research has moved a step closer to harnessing viruses to fight bacterial infection, reducing the threat of antibiotic resistance.

A growing number of infections, including pneumonia, tuberculosis, gonorrhea, and salmonellosis, are developing antibiotic resistance, which means they becoming harder to treat, resulting in higher death rates, longer hospital stays and higher costs.

Phage therapy is the concept of using viruses (known as phage) that are harmless to humans to kill bacteria. Phage therapy can be used in combination with antibiotics to cure infections more effectively, and reduce the opportunity for bacteria to develop antibiotic resistance. However, bacteria can also evolve resistance to phages.

Part 1

The new study by the University of Exeter, published in Cell Host Microbe, has cast new light on how to best combine antibiotics and phage therapy. Researchers conducted laboratory experiments on Pseudomonas aeruginosa a bacterium which causes disease in immunocompromised and cystic fibrosis patients. They exposed the bacterium to eight types of antibiotics—and found differences in the mechanisms by which the bacteria evolve resistance to phages, which affect how harmful they are.

Viruses penetrate molecules on the cell surface to infect bacteria. Like the human immune system, bacteria have their own CRISPR defense system, made up of proteins that fight off infection. As in human immune responses, this means that the virus infects the bacteria, and is then killed. In the process, the bacteria's CRISPR system learns to recognize and attack the virus in future.

However, the bacteria have a second defense option. They can also change their own cell surface to ward off infection, losing the receptor to which phages normally attach. This option comes with a cost to bacteria—the bacteria become less virulent, meaning they no longer cause disease, or the disease becomes less severe.

In the study, four of the eight antibiotics tested caused a dramatic increase in the levels of CRISPR-based immunity. These antibiotics are all bacteriostatic—they do not directly kill cells  but act by slowing down cell growth.

 Phage therapy could be an important part of the toolkit, in reducing antibiotic use, and in using them in combination to increase their efficiency. We found that by changing the type of antibiotics that are used in combination with phage, we can manipulate how bacteria evolve phage resistance, increasing the chances that treatment is effective. These effects should be considered during phage-antibiotic combination therapy, given their important consequences for pathogen virulence.

The researchers show that the effect of bacteriostatic antibiotics triggering CRISPR-Cas immunity results from slower phage replication inside the cell, which provides more time for the CRISPR-Cas system to acquire immunity and clear the phage infection. The research therefore identifies the speed of phage replication as a crucial factor controlling the possibility for CRISPR-Cas systems to defend against viruses.

Part 2

Bacteriostatic antibiotics promote CRISPR-Cas adaptive immunity by enabling increased spacer acquisition, Cell Host Microbe, 2021.

https://phys.org/news/2021-12-closer-harnessing-viruses-bacteria-an...

Part 3

Your seat on public transportation determines level of exposure to exhaled droplets

The COVID-19 pandemic has revealed the urgency of understanding how public transportation ventilation systems transmit viruses and how exhaled droplets evolve in ventilated spaces. Researchers have wondered if those ventilation systems can be improved to mitigate virus transmission.

In Physics of Fluids, researchers at IBM Research Europe developed a model with an unprecedented level of detail and focused on conditions that are more characteristic of asymptomatic transmission. The multiphysics model involved air and droplet dynamics, heat transfer, evaporation, humidity, and effects of ventilation systems.

"By visualizing the droplets and the flow, you realize the number of physical phenomena taking place around us that go unnoticed, such as the complex interactions between natural body plumes, exhalation, and ventilation.

Part 1

**

When it comes to preventing risk of infection, this is precisely what makes it difficult to contain."

The researchers analyzed what happens when speech droplets are exhaled from a row of sitting passengers in a ventilated space, like those in public transportation vehicles. In some of these systems, air is injected at the top and extracted at the bottom through the vents near the window seats.

This generates an internal recirculation to enhance thermal comfort and remove contaminants, but the researchers were interested in whether certain seat positions affect the circulation adversely.

The team found droplets from the window seat rose more and invaded the space of other passengers to a lesser extent shortly after exhalation. Moreover, droplets released from the middle seat contaminated the aisle passengers more, indicating the downward flow of personal ventilation in aisle seats could move droplets down and increase the risk of infection.

Droplets released from the aisle were dragged down by the ventilation system immediately.

Part 2

The researchers modeled various scenarios in close detail, such as a situation where passengers in different seats were pronouncing a vowel for a few seconds. By creating detailed representation of the flow field and tracking every single droplet, they were able to reconstruct their ventilation paths.

In the future, the team will reproduce conditions that more closely represent the diverse human activity on public transport vehicles to help inform actions, design, and operation of future ventilation systems for safer environments.

"These high-resolution simulations were focused on public transportation vehicles, but they could be extended to commercial or residential buildings, health care facilities, offices, or schools.

"Numerical investigation of droplets in a cross-ventilated space with sitting passengers under asymptomatic virus transmission conditions" Physics of Fluids, DOI: 10.1063/5.0070625

https://phys.org/news/2021-12-seat-exposure-exhaled-droplets.html?u...

Part 3

**

No mountain is high enough for microplastics

From Mount Everest to the Mariana Trench, microplastics are everywhere—even high in the Earth's troposphere where wind speeds allow them to travel vast distances, a study showed recently. 

Microplastics are tiny fragments—measuring less than 5 millimeters—that come from packaging, clothing, vehicles and other sources and have been detected on land, in water and in the air.

Scientists sampled air 2,877 meters above sea level at the Pic du Midi Observatory in the French Pyrenees, a so-called "clean station" because of the limited influence exerted on it by the local climate and environment.

There they tested 10,000 cubic meters of air per week between June and October of 2017 and found all samples contained microplastics.

Using weather data they calculated the trajectories of different air masses preceding each sample and discovered sources as far away as North Africa and North America.

The study's main author Steve Allen of Dalhousie University in Canada told AFP that the particles were able to travel such distances because they were able to reach great altitudes.

The research also points to microplastic sources in the Mediterranean Sea and the Atlantic Ocean.

Once in the air or ocean, it is moving around and around in an indefinite cycle.

Steve Allen, Evidence of free tropospheric and long-range transport of microplastic at Pic du Midi Observatory, Nature Communications (2021). DOI: 10.1038/s41467-021-27454-7. www.nature.com/articles/s41467-021-27454-7

https://phys.org/news/2021-12-microplastic-pristine-pyrenees-mounta...

What is the UV index? 

You've probably seen the UV index in the day's weather forecast, and you know it tells you when you need to cover up and wear sunscreen.

The Sun showers Earth with light at a huge spectrum of different wavelengths, and each wavelength can have a slightly different effect on human skin.

An important part of the spectrum is ultraviolet or UV radiation: light with wavelengths too short for our eyes to see, from around 400 nanometres to 10 nanometres.

There are two important kinds of UV radiation: UV-A, with wavelengths from 400–315 nanometres, and UV-B with wavelengths from 315–280 nanometres. (Shorter wavelengths are called UV-C, but are mainly blocked by the atmosphere so we don't need to worry about it.)

UV-A and UV-B both contribute to skin damage, aging and skin cancer. But UV-B is the more dangerous: it is the major cause of sunburn, cataracts and skin cancer.

The UV index tells you how much ultraviolet radiation is around at ground level on a given day, and its potential to harm your skin.

UV radiation is a component of sunlight that can cause tanning and sunburn in the short term. In the longer term, too much exposure to UV can cause cataracts and skin cancer.

In 2002, the World Health Organization devised the UV index in an effort to make people around the world more aware of the risks.

The index boils down several factors into a single number that gives you an idea of how careful you need to be in the sun. A score of 1 or 2 is low, 3–5 is moderate, 6 or 7 is high, 8–10 is very high, and 11 and above is extreme.

Part 1

The UV index takes into account how much UV radiation of different wavelengths is around and how each of those wavelengths affects our skin.

ARPANSA has a network of sensors around Australia measuring sunlight at different wavelengths to determine the UV index, with the information available online in real time.

This data is combined with other information about location, cloud cover and atmospheric conditions to produce maps and forecasts of the UV index for the whole country.

The UV index you see reported is usually the daily maximum—that's the highest it will be all day.

How high it gets depends on lots of factors, including your location, the time of year, the amount of cloud cover, and ozone and pollution in the atmosphere.

The index tends to be higher closer to the Equator and at high altitudes, as the sunlight has to pass through less air before it reaches the ground.

https://theconversation.com/what-is-the-uv-index-an-expert-explains...

Part 2

**

Hubble and Webb: A New Golden Age of Astronomy

Fire and Ice: The Puzzling Link Between Western Wildfires & Arctic Sea Ice

Researchers identify mechanism that explains how tissues form complex shapes that enable organ function

Our bodies are made of tissues arranged in complex shapes that aid in performing specific functions.

But how do cells fold themselves so precisely into such complicated configurations during development? What are the fundamental forces driving this process?

Now, researchers at Harvard Medical School have discovered a mechanical process by which sheets of cells morph into the delicate, looping semicircular canals of the inner ear.

The research reveals that the process involves a combination of hyaluronic acid, produced by cells, that swells with water, and thin connectors between cells that direct the force of this swelling to shape the tissue.

The conventional thinking is that the proteins actin and myosin act as tiny motors inside cells, pushing and pulling them in different directions to fold a tissue into a specific shape. However, the researchers discovered that zebrafish semicircular canals form through a markedly different process. During development, the cells produce hyaluronic acid, which is perhaps most well known as an antiwrinkle agent in beauty products. Once in the extracellular matrix the acid swells up, not unlike a diaper in a swimming pool. This swelling creates enough force to physically move nearby cells, but since the pressure is the same in all directions, the researchers wondered how the tissue ends up stretching in one direction and not another to form an elongated shape. The team found that this is accomplished by thin connectors between cells—dubbed cytocinches—that constrain the force.

It's like if you were to put a corset on a water balloon and deform it into an oblong structure. This combination of swelling and cinching progressively shapes an initially flat sheet of cells into tubes.

Although conducted in zebrafish, the work reveals a basic mechanism for how tissues take on shapes—one that is likely to be conserved across vertebrates, the researchers say, and may also have implications for bioengineering.

The genes that control hyaluronic acid production in zebrafish semicircular canals are also present in the semicircular canals  of mammals, suggesting that a similar process may be occurring. Moreover, hyaluronic acid is found in multiple parts of the human body, including skin and joints, indicating that it may play a role in shaping many tissues and organs—an avenue for future research.

If that does turn out to be the case, then studying the genes involved in hyaluronic acid production could help researchers understand congenital defects in organs where hyaluronic acid drives development.

Sean G. Megason, Extracellular hyaluronate pressure shaped by cellular tethers drives tissue morphogenesis, Cell (2021). DOI: 10.1016/j.cell.2021.11.025. www.cell.com/cell/fulltext/S0092-8674(21)01373-8

https://phys.org/news/2021-12-mechanism-tissues-complex-enable-func...

Scientists Just Identified a Brand New Muscle Layer in The Human Jaw

Undoubtedly there are still exciting new discoveries to be made in a field as well-studied as human anatomy: researchers have confirmed the existence of a layer of muscle in the human jaw that has until now eluded anatomists.

This new muscle is a deeper, third section of the masseter muscle. It's the most prominent jaw muscle: press your hand against the back of your jaw while you chew and you'll feel it moving.

Typically represented as having just two layers, there has been suspicions based on animal studies that there is more to its structure. However until now, attempts to describe it have been contradictory and confusing.

Through an analysis of more than two dozen human heads – including one living subject and 12 heads preserved in formaldehyde – it's been established through a new study that the masseter muscle does indeed have three distinct sections, not two.

This deep section of the masseter muscle is clearly distinguishable from the two other layers in terms of its course and function.

The name Musculus masseter pars coronidea, or the coronoid section of the masseter, has been proposed for the new muscle layer by the researchers, because it attaches to the muscular (coronoid) process of the lower jaw – the mandible bone.

https://www.sciencedirect.com/science/article/pii/S0940960221002053

https://www.sciencealert.com/scientists-just-identified-a-new-muscl...

Alarming Levels of Microplastics in The Feces of People With Irritable Bowel Diseases or IDB

A recent investigation by a team of researchers in Nanjing, China, has uncovered worrying signs that elevated levels of microplastics could be inflaming our digestive systems.

Feces collected from 52 individuals diagnosed with inflammatory bowel disease (IBD) were found to contain around 1.5 times the number of plastic particles smaller than 5 millimeters (about 0.2 inches) than similar samples from volunteers without any chronic illnesses.

The vast majority of plastic particles were smaller than 300 micrometers, with a few detectable pieces coming in below a minuscule 5 micrometers across. The researchers noticed those with IBD also tended to have a greater proportion of smaller flakes of microplastic.

What's more, the greater the plastic load, the more severe the individual's IBD symptoms. 

A survey revealed nothing unusual about the origins of the plastic, suggesting it was the kinds of particles we all might ingest by drinking from PET bottles or eating out of single-use disposable containers.

As an observational study, the research doesn't establish cause and effect. Nobody can claim the difference in microplastic load is solely, or even partially responsible for the symptoms of diarrhea, rectal bleeding, and abdominal cramping associated with the illness.

It's even possible having IBD might make it harder to clear the build-up of plastic detritus that accumulates in our diets.

But the mere possibility of a connection is concerning enough to warrant further investigation, especially given the shocking rate at which plastic waste is spreading virtually unabated.

Part 1

Seven million people globally were diagnosed with IBD in 2017, a condition distinguished by regular bouts of discomfort and changes in bowel motion produced by a hair-trigger system overreacting to otherwise benign materials in the gut. 

The illness usually falls into one of two main diagnoses: Crohn's disease, which is typically characterized by an inflamed lining throughout the deeper layers of the digestive tract, and ulcerative colitis, which is marked by ulcers in the large intestine's lining.

In either case, the ultimate source of the errant immune response isn't yet fully understood, though suspicions lie with the complex way our guts negotiate diplomatic relations with our microflora, particularly during an infection.

Whether plastic particles might somehow involve themselves with a link in this chain has never been fully made clear, though animal studies have previously pointed to gut inflammation as a possible side effect of microplastic exposure.

Part 2

Circumstantially, microplastics have also been shown to stir up trouble by generating reactive oxygen species that are known to play a role in inflammation.

With that in mind, it's not at all surprising to imagine an increase in gut exposure to microplastic particles might play a similar role to certain microbes in sensitizing the lining to an exaggerated immune reaction.

Further studies will be needed before we can claim with any confidence that our dietary supplement of plastic dust is putting us at increased risk of any health problems. There are still too many unknowns.

But that doesn't mean we shouldn't be taking action. Evidence that the rising tide of plastic waste is affecting everything from the climate to the distribution of species to the health of marine life is mounting.

That our health might be just one more consequence is just more reason to wean ourselves off our dependence on this pervasive pollutant.

https://pubs.acs.org/doi/10.1021/acs.est.1c03924

https://www.sciencealert.com/inflammatory-bowel-disease-feces-found...

Part 3

**

Comets' heads can be green, but never their tails. We finally know now why.

 Every so often, the Kuiper Belt and Oort Cloud throw galactic snowballs made up of ice, dust and rocks our way: 4.6-billion-year-old leftovers from the formation of the solar system.

These snowballs – or as we know them, comets – go through a colourful metamorphosis as they cross the sky, with many comets’ heads turning a radiant green colour that gets brighter as they approach the Sun.

But strangely, this green shade disappears before it reaches the one or two tails trailing behind the comet.

Astronomers, scientists and chemists have been puzzled by this mystery for almost a century. In the 1930s, physicist Gerhard Herzberg theorised the phenomenon was due to sunlight destroying diatomic carbon (also known as dicarbon or C2), a chemical created from the interaction between sunlight and organic matter on the comet’s head – but as dicarbon isn’t stable, this theory has been hard to test.

A new UNSW Sydney-led study, published in Proceedings of the National Academy of Sciences (PNAS), has finally found a way to test this chemical reaction in a laboratory – and in doing so, has proven this 90-year-old theory correct.

This explains why the green coma – the fuzzy layer of gas and dust surrounding the nucleus – shrinks as a comet gets closer to the Sun, and also why the tail of the comet isn’t green.

The key player at the centre of the mystery, dicarbon, is both highly reactive and responsible for giving many comets their green colour. It’s made up of two carbon atoms stuck together and can only be found in extremely energetic or low oxygen environments like stars, comets and the interstellar medium.

Dicarbon doesn’t exist on comets until they get close to the Sun. As the Sun starts to warm the comet up, the organic matter living on the icy nucleus evaporates and moves to the coma. Sunlight then breaks up these larger organic molecules, creating dicarbon.

The UNSW-led team have now shown that as the comet gets even closer to the Sun, the extreme UV radiation breaks apart the dicarbon molecules it recently created in a process called ‘photodissociation’. This process destroys the dicarbon before it can move far from the nucleus, causing the green coma to get brighter and shrink – and making sure the green tinge never makes it into the tail.

This is the first time this chemical interaction has been studied here on Earth.

1. Jasmin Borsovszky, Klaas Nauta, Jun Jiang, Christopher S. Hansen, Laura K. McKemmish, Robert W. Field, John F. Stanton, Scott H. Kable, Timothy W. Schmidt. Photodissociation of dicarbon: How nature breaks an unusual multiple bond. Proceedings of the National Academy of Sciences, 2021; 118 (52): e2113315118 DOI: 10.1073/pnas.2113315118

Mind-controlled robots now one step closer

A special microbe turns oil into gases all by itself

Microorganisms can convert oil into natural gas, i.e. methane. Until recently, it was thought that this conversion was only possible through the cooperation of different organisms. In 2019, Rafael Laso-Pérez and Gunter Wegener from the Max Planck Institute for Marine Microbiology suggested that a special archaeon can do this all by itself, as indicated by their genome analyses. Now, in collaboration with a team from China, the researchers have succeeded in cultivating this “miracle microbe” in the laboratory. This enabled them to describe exactly how the microbe achieves the transformation. They also discovered that it prefers to eat rather bulky chunks of food.

Underground oil deposits on land and in the sea are home to microorganisms that use the oil as a source of energy and food, converting it into methane. Until recently, it was thought that this conversion was only possible in a complicated teamwork between different organisms: certain bacteria and usually two archaeal partners. Now the researchers have managed to cultivate an archaeon called Methanoliparia from a settling tank of an oil production facility that handles this complex reaction all by itself.

This “miracle microbe” breaks down oil into methane and carbon dioxide. Now that the researchers have succeeded in cultivating these microorganisms in the laboratory, they were able to investigate the underlying processes in detail. They discovered that its genetic make-up gives Methanoliparia unique capabilities. “In its genes it carries the blueprints for enzymes that can activate and decompose various hydrocarbons. In addition, it also has the complete gear kit of a methane producer.

n their laboratory cultures, the researchers offered the microbes various kinds of food and used a variety of different methods to keep a close eye on how Methanoliparia deal with it. What was particularly surprising to see was that this archaeon activated all the different hydrocarbons with one and the same enzyme.

Zhuo Zhou, Cui-jing Zhang, Peng-fei Liu, Lin Fu, Ra­fael Laso-Pérez, Lu Yang, Li-ping Bai, Ji­ang Li, Min Yang, Jun-zhang Lin, Wei-dong Wang, Gunter We­gener, Meng Li, Lei Cheng (2021): Non-syn­trophic meth­ano­genic hy­dro­car­bon de­grad­a­tion by an ar­chaeal spe­cies. Nature (2021)

DOI: 10.1038/s41586-021-04235-2 

https://researchnews.cc/news/10687/A-special-microbe-turns-oil-into...

Frog cells transform into tiny living robots

A Scent of Space

Study shows robotic-assisted bladder removal reduces blood loss and enhances post-operative recovery

 Robotic-assisted radical cystectomy (RARC), the complete removal of the bladder with the use of surgical robots, has gained increasing acceptance worldwide. After the removal of the bladder, patients need to undergo a urinary diversion, such as the reconstruction of a “new bladder”. In the past, a urinary diversion had to be performed through an open approach, i.e. extracorporeal urinary diversion (ECUD). Recently, an intracorporeal urinary diversion (ICUD) approach has been introduced, and the whole procedure can be performed in a minimally invasive manner.

The Chinese University of Hong Kong’s Faculty of Medicine has led a...

https://www.med.cuhk.edu.hk/press-releases/study-led-by-cuhk-shows-...

https://researchnews.cc/news/10723/Study-shows-robotic-assisted-bla...

What makes an mRNA vaccine so effective against severe COVID-19?

The first two vaccines created with mRNA vaccine technology—the Pfizer/BioNTech and Moderna COVID-19 vaccines—are arguably two of the most effective COVID vaccines developed to date. In clinical trials, both were more than 90% effective at preventing symptomatic infection, easily surpassing the 50% threshold the Food and Drug Administration had set for COVID-19 vaccines to be considered for emergency use authorization.

While breakthrough infections have increased with the emergence of the delta and omicron variants, the vaccines remain quite effective at preventing hospitalizations and deaths. The success of the new technology has led scientists to try to figure out why mRNA vaccines are so effective and whether the protection they provide is likely to endure as new variants arise.

A new study from researchers at Washington University School of Medicine in St. Louis and St. Jude Children's Research Hospital shines light on the quality of the immune response triggered by mRNA vaccines. The study shows that the Pfizer vaccine strongly and persistently activates a kind of helper immune cell that assists antibody-producing cells in creating large amounts of increasingly powerful antibodies, and also drives the development of some kinds of immune memory. Known as T follicular helper cells, these cells last for up to six months after vaccination, helping the body crank out better and better antibodies. Once the helper cells decline, long-lived antibody-producing cells and memory B cells help to provide protection against severe disease and death, the researchers said.

Further, many of the T follicular helper cells are activated by a part of the virus that doesn't seem to pick up mutations, even in the highly mutated omicron variant. The findings, published online in the journal Cell, help explain why the Pfizer vaccine elicits such high levels of neutralizing antibodies and suggests that vaccination may help many people continue producing potent antibodies even as the virus changes.

The longer the T follicular helper cells provide help, the better the antibodies are and the more likely you are to have a good memory response. In this study, researchers found that these T follicular helper cell responses just keep going and going. And what's more, some of them are responding to one part of the virus's spike protein that has very little variation in it. With the variants, especially delta and now omicron, we've been seeing some breakthrough infections, but the vaccines have held up very nicely in terms of preventing severe disease and death. This strong T follicular helper response is part of the reason why the mRNA vaccines continue to be so protective.

1. Philip A. Mudd, Anastasia A. Minervina, Mikhail V. Pogorelyy, Jackson S. Turner, Wooseob Kim, Elizaveta Kalaidina, Jan Petersen, Aaron J. Schmitz, Tingting Lei, Alem Haile, Allison M. Kirk, Robert C. Mettelman, Jeremy Chase Crawford, Thi H.O. Nguyen, Louise C. Rowntree, Elisa Rosati, Katherine A. Richards, Andrea J. Sant, Michael K. Klebert, Teresa Suessen, William D. Middleton, Joshua Wolf, Sharlene A. Teefey, Jane A. O’Halloran, Rachel M. Presti, Katherine Kedzierska, Jamie Rossjohn, Paul G. Thomas, Ali H. Ellebedy. SARS-CoV-2 mRNA vaccination elicits a robust and persistent T follicular helper cell response in humans. Cell, 2021; DOI: 10.1016/j.cell.2021.12.026

https://researchnews.cc/news/10732/What-makes-an-mRNA-vaccine-so-ef...

Real-space subfemtosecond imaging of quantum electronic coherences in molecules

" It has been a long-time dream of scientists to capture image of electron moving inside the atoms. For this scientist have been using two techniques to track the movement of an electron inside a molecule. One of the techniques of attosecond science enables to generate and trace the consequences of this motion in real time, but not in real space. On the other hand, another technique Scanning tunneling microscopy, can locally probe the valence electron density in molecules, but cannot alone provide dynamical information at this ultrafast timescale.

These results are a major boon for the scientific research world because it will facilitate understanding of chemical reactions. With the help of these understandings, scientists can gain new insights into the most elementary processes such as photosynthesis in plants and the biochemical processes on our retina which are also triggered by light. These experimental achievements can enable the manipulation of electron movements which will allow unprecedented control over chemical reactions and biological processes. The scientists have now come a huge step closer to achieving this goal."

Tracking electron motion in molecules is the key to understanding and controlling chemical transformations. Contemporary techniques in attosecond science are able to generate and trace the consequences of this motion in real time, but not in real space. Scanning tunnelling microscopy, on the other hand, can locally probe the valence electron density in molecules, but cannot alone provide dynamical information at this ultrafast timescale. Here researchers show that, by combining scanning tunnelling microscopy and attosecond technologies, quantum electronic coherences induced in molecules by <6-fs-long carrier-envelope-phase-stable near-infrared laser pulses can be directly visualized at ångström-scale spatial and subfemtosecond temporal resolutions. They demonstrate concurrent real-space and -time imaging of coherences involving the valence orbitals of perylenetetracarboxylic dianhydride molecules, and full control over the population of the involved orbitals. This approach opens the way to the unambiguous observation and manipulation of electron dynamics in complex molecular systems.

https://www.nature.com/articles/s41566-021-00929-1

Parasitic worms in dogs, cats may jump into people

Parasitic worms that infect companion animals such as dogs and cats are more likely to make the leap into humans than other worm species, according to new research.

The study also identified three species of worms that don't currently infect people but have a more than 70% chance of crossing into humans in the future.

The close relationships that we have with pets is the predominant reason why people might become infected with new species of parasitic worms.

Parasitic worms, or helminths, are estimated to infect 1.5 billion people globally, according to the World Health Organization. Many of these parasites infect humans, causing a number of serious illnesses, including schistosomiasis and filariasis.

Published in The Royal Society journal Philosophical Transactions B, the study focused on 737 parasitic worm species that predominantly infect wild and domesticated mammals. Of these, 137 are known to be able to infect people.

The researchers categorized the worm species' traits and built a machine learning model to determine which characteristics were most commonly associated with transmission into humans.

They found that worms that can infect companion animals or fish are more likely to cause human infection than worms that infect other animal species. Geographically widespread parasites were also more likely to make the jump from animals into people.

The analyses showed that three worm species not currently known to infect people have traits that make them very likely to be able to do so: Paramphistomum cervi, a flatworm mostly found in livestock and some wild animals; Schistocephalus solidus, a fish-based tapeworm that also infects birds and rodents; and Strongyloides papillosus, a pinworm found largely in livestock.

The study marks the first time these species have been identified as likely to infect humans, suggesting they are candidates for surveillance and further study.

It's relatively easy for dogs and cats to become infected with parasitic worms, particularly if they're allowed to wander during the day.

Dogs and cats aren't the only transmission route, though.

Fish also host a variety of parasitic worms. People can easily become infected by eating raw, undercooked or improperly prepared fish. The roundworm that causes herring worm disease, for example, infects thousands of people each year, largely in areas where eating raw fish is common, like Japan and parts of Europe.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450625/

https://researchnews.cc/news/10746/Parasitic-worms-in-dogs--cats-ma...

Oral and gut microbes can inactivate an antidiabetic drug

Acarbose is a commonly prescribed antidiabetic drug that helps control blood sugar levels by inhibiting human enzymes that break down complex carbohydrates. Now, new research  demonstrates that some bacteria in the mouth and gut can inactivate acarbose and potentially affect the clinical performance of the drug and its impact on bacterial members of the human microbiome. The paper appeared online and in the December 2, 2021 issue of the journal Nature.

Acarbose was originally isolated from bacteria that live in soil. These bacteria secrete acarbose to hinder the growth of other types of bacteria in their environment, giving themselves a competitive advantage. Both the natural bacterial version and the drug acarbose inhibit a-glucosidases, enzymes expressed by humans and bacteria to break down complex sugars into a form that can be metabolized for energy.

But acarbose-producing bacteria also express an antidote to it—an enzyme called acarbose kinase that modifies acarbose, rendering it inactive. 

This mechanism may accidentally affect the response of diabetic patients to this drug as well as shape its impact on the microbiome.

https://www.nature.com/articles/s41586-021-04091-0?proof=t+target%3D

https://researchnews.cc/news/10757/Oral-and-gut-microbes-can-inacti...

James Webb Telescope

Researchers pinpoint blood factors linked to severe COVID

Scientists have identified unique "indicators" in the blood of patients with severe and fatal COVID, paving the way for simple diagnostic tests to help doctors identify who will go on to become critically ill.

The scientists analyzed blood samples from hospitalized COVID patients. They detected markers in the blood associated with patients becoming so ill they needed treatment in intensive care.

The findings may lead to new ways for triaging and assessing the risk of COVID patients, relieving the pressure from hospitals during infection spikes.

Since the start of the pandemic, researchers have been working to understand how and why COVID affects individuals differently. Even patients hospitalized with the disease have diverse treatment needs, with some milder cases simply requiring extra oxygen while others need invasive ventilation in intensive care.

This new study identified factors in the blood that are uniquely correlated with severe and fatal outcomes for hospitalized COVID patients. These findings support the observation that COVID is a disease that develops in stages and have the potential to provide doctors with vital information, allowing them to tailor treatments according to severity of disease and identify high-risk patients early.

The research, published in the journal iScience, involved testing blood samples from over 160 patients admitted to hospital during the first and second wave of the pandemic and was carried out in collaboration with York and Scarborough Teaching Hospitals NHS Foundation Trust, Manchester University and four NHS Trusts in Greater Manchester.

The researchers measured levels of cytokines and chemokines—the proteins in the blood that drive the overwhelming immune response observed in patients with COVID—as well as tiny RNAs, called microRNAs—which reflect the state of diseased tissues and are already known to be good indicators of severity and stage in several other diseases. They identified a set of cytokines, chemokines, and microRNAs linked to fatal outcomes from COVID.

Part 1

Early in the pandemic, researchers observed high levels of inflammatory cytokines—molecules which adjust or alter the immune system response—in COVID patients with poor outcomes. However, this so called 'cytokine storm' was also present in hospitalized patients with a milder version of the disease. We set out to fine tune our knowledge of which factors in the blood correlate with severe disease with more insight and accuracy.

These  findings provide a scientific foundation for the development of blood tests that could provide doctors with vital information on which treatments will be most effective for a patient.

Julie C. Wilson et al, Integrated miRNA/cytokine/chemokine profiling reveals severity-associated step changes and principal correlates of fatality in COVID-19, iScience (2021). DOI: 10.1016/j.isci.2021.103672

https://medicalxpress.com/news/2021-12-blood-factors-linked-severe-...

Part 2 

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Explained: Where is James Webb Telescope going and why do we need to send it so far away

This location lets the telescope stay in line with the Earth as it moves around the Sun allowing its large sunshield to protect the telescope from the light and heat of the Sun and Earth (and Moon). The position is named in honour of Italian-French mathematician Josephy-Louis Lagrange.

There are five special points where a small satellite can orbit in a constant portion with two big masses. At these five positions part of the Earth-Sun system, three (L1, L2 and L3) lie along the line connecting the two large masses. Meanwhile, L4 and L5 form the apex.

According to Nasa, the L1 point of the Earth-Sun system affords an uninterrupted view of the sun and is currently home to the Solar and Heliospheric Observatory Satellite SOHO. The L2, where the James Webb Space Telescope is going, is ideal for astronomy because a spacecraft is close enough to readily communicate with Earth, can keep Sun, Earth and Moon behind the spacecraft for solar power and (with appropriate shielding) provides a clear view of deep space.

It is to be noted that L1 and L2 points are unstable and satellites functioning from this location need to go through regular course corrections. Meanwhile, L3 remains behind the Sun and is unlikely to be used.

WHY WAS THIS PARTICULAR LOCATION SELECTED FOR THE TELESCOPE?

The location was chosen since James Webb will be observing the universe in infrared vision which can sometimes be fe... and since it is looking for the faintest signals, it needs to be safeguarded from any bright, hot sources, the biggest being our Sun.

The telescope itself will be operating at about -225 degrees Celsius and the temperature difference between the front and back of the spacecraft will be huge. To protect the telescope, the location needs to be such that light and heat from the Sun, Moon and Earth needs to come from just one direction. The second lagrange point is the optimum location from where Sun, Moon and Earth are in the one-line direction.

Part 2

Animation: The James Webb Space Telescope's Orbit

Part 3

The telescope is on a 30-day long journey to cover the 15,00,000 kilometers distance between Earth and its intended orbit. It will reach the location by the end of January.

Source: https://www.indiatoday.in/science/story/where-is-james-webb-telesco...

Part 4

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Mountain spring water isn't as clean as you think it is

 Mountain spring water is often touted as the cleanest water you can drink. But a new study revealed this isn't the case.

Using data collected over 40 years, researchers detailed how water quality in high-elevation streams has been negatively affected by a combination of historical events and modern changes, namely sediment from rural roads and agricultural runoff.

Unpaved roads are just one of several factors contributing to sediment runoff.

When streams carry a lot of sediment, it makes it more difficult for animals to see food in the water, and it affects fish growth and disease resistance. Sediment also continues to flow downstream and into public water supplies, where it costs cities and towns more to filter.

The landscape you see now isn't what it was like in 1900. For generations, people farmed the valleys  and left the hillsides forested, for hunting and gathering. But the new settlers cut the forests and even tried to farm the hills, causing erosion and sediment to move into the streams. Today, stream beds continue to show evidence of sediment deposited more than a century ago, even as new sediment pushes through the waters.

Many years later, a new kind of development in the region created a different kind of land disturbance. For generations, residents considered the steep mountain slopes undevelopable. But the 1980s and '90s brought a desire for mountain getaway homes with views.

By building homes on mountain ridges, he said, it created more land disturbance through carving out unpaved roads and cutting into hillsides, sometimes creating landslides.

"Roadside ditches and unpaved roads produce a lot of sediment, and their sediment production increases as roads get steeper and as gravel roads get more use. in areas with both mountain and valley development, the researchers found sediment concentrations four to six times higher.

Farming also takes its toll. The studies researchers analyzed found many streams in the area to have high nutrient concentrations—particularly nitrate. When a stream flowing through a pasture loses its buffer of trees, it loses a natural protection against nutrient runoff.

Streams without shade also have higher water temperatures.

The paper was published earlier this month in the journal Bioscience.

C Rhett Jackson et al, Distinctive Connectivities of Near-Stream and Watershed-Wide Land Uses Differentially Degrade Rural Aquatic Ecosystems, BioScience (2021). DOI: 10.1093/biosci/biab098

https://researchnews.cc/news/10775/Mountain-spring-water-isn-t-as-c...

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Snapshots from high in the sky allow new insight into ecosystems around the world

Heavy metals have a reputation for being dangerous, but some are essential nutrients that you can't live without.

Rethinking how drugs are administered: A breakthrough in microneedle patches

The painful feeling of receiving an injection through a hypodermic needle or with the unpleasant sensation of swallowing a large pill is a globally familiar sensation. But what if a revolutionary and gentler way of administering drugs was in the works? For over two decades, researchers have been investigating various types of microneedles as a minimally invasive method for transdermal drug delivery. Arrays of microneedles can be designed to be loaded with a drug or chemical, which they then release over time onto the blood stream after piercing slightly beyond the skin layers.

Microneedles offer several advantages compared to other types of drug delivery. First, they are painless and cause virtually no damage to the skin nor bleeding. Second, they can be self-administered. Third, unlike traditional needles, the disposal of microneedles is much easier as they don't leave behind hazardous waste. Unfortunately, there are still a few challenges that need to be addressed before microneedles become the next big thing in healthcare. One is their fabrication cost, which generally involves expensive molds, materials, and machinery. Another issue is the aggregation and degradation of proteins when microneedles are pre-loaded with a protein-based medicine, as these molecules are quite sensitive to external conditions such as temperature, acidity and salt concentration.

In a recent study published in Biomacromolecules, two research teams from Japan and Thailand collaborated to address the main limitations of existing microneedles.

One team developed and applied a functional polymer that effectively suppresses protein aggregation. The other team perfected a microneedle fabrication method suitable for the industrial scale based on photolithography. By combining these two efforts, the teams managed to produce microneedles patches with several attractive properties and potential scalability to clinical settings.

Part 1

The microneedles themselves are made of a non-degradable, biocompatible hydrogel that also contains zwitterionic poly-sulfobetaine (poly-SPB). As reported in previous studies by the same authors, this polymer suppresses protein aggregation. Thus, the researchers incorporated it during the fabrication process and showed that the proteins pre-loaded in the microneedles were stable even when subjected to various external stresses.

Additionally, the scientists developed a straightforward and cost-effective way to fabricate microneedle arrays made from the abovementioned materials. They resorted to photolithography, a process in which a photomask is used to selectively block UV light from reaching a target surface to control chemical reactions locally.

To test the performance of these microneedle arrays for drug delivery, the researchers loaded them with 50 microliters of drug solutions containing rhodamine B as a dye alongside lysozyme and insulin as example proteins. Through various experiments on porcine skin, the teams verified that their microneedle patches offered both high drug-loading capacity and high drug-release rate. Moreover, they confirmed that the microneedles could both load and preserve various water-soluble drugs and proteins simultaneously, eliminating the need for refrigeration.

Overall, the proposed microneedle arrays seem to be a remarkably promising platform for administering therapeutic drugs and vaccines.

Harit Pitakjakpipop et al, Facile Photolithographic Fabrication of Zwitterionic Polymer Microneedles with Protein Aggregation Inhibition for Transdermal Drug Delivery, Biomacromolecules (2021). DOI: 10.1021/acs.biomac.1c01325

https://medicalxpress.com/news/2021-12-rethinking-drugs-breakthroug...

Part 2

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Quantum Computers, Explained With Quantum Physics

The Final moments: Brain Death and the process of stopping it

For years, scientists have researched what happens to your brain when you die, but despite everything we've found out, progress has been stymied by an inability to easily monitor human death – since physicians are conventionally obliged to prevent death if they can, not monitor it as it takes hold. What this means is most of our understanding of the processes involved in brain death come from animal experiments, strengthened with what we can glean from the accounts of resuscitated patients disclosing their near-death experiences. But in 2018, an international team of scientists made a breakthrough. In animals, within 20 to 40 seconds of oxygen deprivation, the brain enters an 'energy-saving mode' where it becomes electrically inactive and neurons cease communicating with one another. After a few minutes, the brain begins to break down as ion gradients in cells dissipate, and a wave of electrochemical energy – called a spreading depolarisation (or 'brain tsunami') spreads throughout the cortex and other brain regions, ultimately causing irreversible brain damage.

A team of neurologists  – who monitored these processes taking place in nine patients with devastating brain injuries (under Do Not Resuscitate – Comfort Care orders) – say the tsunami of brain death may actually be capable of being stopped.

After circulatory arrest, spreading depolarisation marks the loss of stored electrochemical energy in brain cells and the onset of toxic processes that eventually lead to death. But it is reversible – up to a point – when the circulation is restored.

Using neuro-monitoring technology called subdural electrode strips and intraparenchymal electrode arrays, the researchers monitored spreading depolarisation in the patients' brains, and they suggest it's not a one-way wave – as long as circulation (and thus oxygen supply) can be resumed to the brain.

"Anoxia-triggered [spreading depolarisation] is fully reversible without any signs of cellular damage, if the oxidative substrate supply is re-established before the so-called commitment point, defined as the time when neurons start dying under persistent depolarisation. For patients at risk of brain damage or death incurred through cerebral ischemia or other kinds of stroke, the findings could one day be a life-saver, although the researchers explain a lot more work is needed before physicians will be able to take advantage of these discoveries.

https://onlinelibrary.wiley.com/doi/full/10.1002/ana.25147

https://www.sciencealert.com/death-bringing-brain-tsunamis-have-bee...

Scientists digitally 'unwrap' mummy of pharaoh Amenhotep I for the first time in 3,000 years

All the royal mummies found in the 19th and 20th centuries have long since been opened for study. With one exception: egyptologists have never been bold enough to open the mummy of Pharaoh Amenhotep I. Not because of any mythical curse, but because it is perfectly wrapped, beautifully decorated with flower garlands, and with face and neck covered by an exquisite lifelike facemask inset with colorful stones. But now for the first time, scientists from Egypt have used three-dimensional CT (computed tomography) scanning to 'digitally unwrap' this royal mummy and study its contents. They report their findings in Frontiers in Medicine.

This was the first time in three millennia that Amenhotep's mummy has been opened. The previous time was in the 11th century BCE, more than four centuries after his original mummification and burial. Hieroglyphics have described how during the later 21st dynasty, priests restored and reburied royal mummies from more ancient dynasties, to repair the damage done by grave robbers.

"This fact that Amenhotep I's mummy had never been unwrapped in modern times gave us a unique opportunity: not just to study how he had originally been mummified and buried, but also how he had been treated and reburied twice, centuries after his death.

By digitally unwrapping of the mummy and 'peeling off' its virtual layers—the facemask, the bandages, and the mummy itself—researchers could study this well-preserved pharaoh in unprecedented detail.

The things that were found during the study:  

Amenhotep I was approximately 35 years old when he died. He was approximately 169cm tall, circumcized, and had good teeth. Within his wrappings, he wore 30 amulets and a unique golden girdle with gold beads."

Amenhotep I seems to have physically resembled his father: he had a narrow chin, a small narrow nose, curly hair, and mildly protruding upper teeth. Researchers couldn't find any wounds or disfigurement due to disease to justify the cause of death, except numerous mutiliations post mortem, presumably by grave robbers after his first burial. His entrails had been removed by the first mummifiers, but not his brain or heart.

at least for Amenhotep I, the priests of the 21^st dynasty lovingly repaired the injuries inflicted by the tomb robbers, restored his mummy to its former glory, and preserved the magnificent jewelry and amulets in place.

Sahar N. Saleem et al, Digital Unwrapping of the Mummy of King Amenhotep I (1525–1504 BC) Using CT, Frontiers in Medicine (2021). DOI: 10.3389/fmed.2021.778498

https://phys.org/news/2021-12-scientists-digitally-unwrap-mummy-pha...

In a neuroprosthetic first, ALS patient sends social media message via brain-computer interface

A 62-year-old amyotrophic lateral sclerosis (ALS) patient in Australia recently became the first person to post a message on social media using only his thoughts. On December 23, he posted an initial brief message, "Hello World," on Twitter.

The technology that allowed the patient  to send his message was developed by a brain computer interface company,  and the device is called the Stentrode Brain Computer Interface (SBCI); a type of endovascular brain implant. It was implanted into the patient's brain without opening his skull—instead, it was inserted through his jugular vein. The tiny (8 mm) brain implant was designed to allow people who have lost the ability to speak to communicate using only their thoughts. The SBCI is wireless and works by reading brainwaves and translating them to words—the motor neuroprosthesis was placed into the patient's brain using techniques that have been used for several years to treat people with strokes. Human clinical trials have been underway  for over a year—currently, the device has been implanted in just one other person, but more are planned.

The patient e is now able to compose messages by thinking of words or actions (such as mouse clicks), which are translated to activity on a computer screen.

https://techxplore.com/news/2021-12-neuroprosthetic-als-patient-soc...

Ubiquitin and Parkinson's Disease