A new study from the University of Colorado Anschutz Medical Campus has found that caffeine, the world’s most consumed psychoactive substances, may impair the quality of donated blood and reduce the effectiveness of transfusions – especially in recipients whose red blood cell (RBC) metabolism is influenced by a common genetic variant.
Category: 8. Health
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Middle and High School Educator Perspectives on Nicotine Use in Schools
Students vape to fit in, and cope with stress
Educators suggested a range of reasons why vaping occurs in middle and high school, including peer pressure, self-soothing, and experimentation. Students are commonly turning to vaping as they try to fit in with peers and assert independence from adults. Educators noted that vaping was common among students struggling with anxiety, stress, and depression.
“I definitely see some middle schoolers that are actually addicted to nicotine now, to the point where they’re trying to sneak it in (school) and they get caught. They get this sort of desperation about them, because they know they’re going to be struggling.” Middle School-Based Psychologist, Minnesota
“These kids are self-medicating. Vaping gives them a dopamine hit, a break from stress, a moment of comfort. It’s everywhere—their parents do it, siblings, friends. But at its core, they’re using it to escape what they’re feeling.” Middle School Assistant Principal, Ohio
“Between that [vapes] and the phones, those two addictions, irritability is a big thing. Not being able to stay focused, needing to get up and go get their fix.” High School-Based Psychologist, California
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Map of 600,000 brain cells rewrites the textbook on how the brain makes decisions
Researchers have completed the first-ever activity map of a mammalian brain in a groundbreaking duo of studies, and it has rewritten scientists’ understanding of how decisions are made.
The project, involving a dozen labs and data from over 600,000 individual mouse brain cells, covered areas representing over 95% of the brain. Findings from the research, published in two papers in the journal Nature, suggest that decision-making involves far more of the brain than previously thought.
The mammoth project was led by the International Brain Laboratory (IBL), a collaboration of experimental and theoretical neuroscientists from across Europe and the U.S. These scientists were united by a familiar, nagging feeling.
“We had a problem with the way science was done,” said Matteo Carandini, a neuroscientist at University College London and a core member of the IBL.
In previous studies of the brain, many separate labs set out to answer big questions about the organ, exploring how brain activity relates to behavior, for instance. However, each lab studied this question in different mice’s brains, and performed slightly different behavioral tasks with each set of rodents. Once you added in uncertainties around how each research group defined distinct regions within the brain, these inconsistencies muddied the results.
“We wouldn’t know whether we actually agree or disagree, because so many things were different,” Carandini told Live Science.
Related: Most detailed human brain map ever contains 3,300 cell types
So the IBL came together to design a single, robust, standardized experiment on a scale that no individual lab could tackle alone. They then paired this megatest with precision brain measuring tools and preset analysis methods to make the results as reproducible as possible. The aim of the experiment would be to overcome an enduring obstacle in the field.
“One of the longest-standing challenges in neuroscience is to decipher how variation in neural systems — both structural and functional — maps onto variation in behavior,” Federico Turkheimer, a neuroscientist at King’s College London who was not involved in the study, said in a statement to the U.K. Science Media Centre.
This project ultimately included 139 mice, spread across 12 labs around the world, that were implanted with brain-recording devices called Neuropixels probes. The probes can record up to 1,000 individual neurons simultaneously. The researchers tested the mice with a simple behavioral task that each of the dozen labs could reliably replicate: Researchers placed mice in front of a screen, and a black-and-white striped marker would flash either on the right or left. If the mice moved a small wheel in the same direction as the flash, they received a reward.
Based on what you’d read in a neuroscience textbook, said Carandini, you’d expect the brain activity that occurred during the experiment to follow a linear path. First, cells in the visual cortex that recognize images would fire up, followed by neurons in a different part of the brain, such as the prefrontal cortex, known to be involved in abstract decisions. This information might then be combined with additional activity that represented the mouse’s prior experiences — in other words, memories — before being sent to motor regions of the brain that control muscle responses.
The studies included data from more than 600,000 brain cells across 139 mice. (Image credit: Dan Birman, International Brain Laboratory) The researchers’ findings supported some of this chain reaction; the visual cortex was the first thing to activate, for example. Yet other findings clashed with the team’s expectations.
“We found decision signals and signals related to the prior information in way more brain regions than we might have thought,” Carandini said. Taken together, the activity across nearly all of the brain regions studied could be used to deduce whether or not the mouse had received a reward.
In some of the experimental trials, the researchers made the on-screen marker incredibly faint, so the mice essentially had to guess which way to move the wheel. The second Nature paper focused on how the mice used prior expectations — based on where the marker had been in previous tests — to inform their guess. The brain activity that flashed up when the mice guessed in these tasks was also far more widely distributed in the brain than the team anticipated it would be.
The IBL modeled its approach to understanding the brain on similar initiatives, such as the particle physics experiments conducted at CERN or the Human Genome Project’s work to understand our DNA. To describe the project’s impact, Carandini reaches for yet another field: astronomy.
He noted that the earliest astronomers could look up at the night sky and see every star, but in very poor detail. With the advent of the telescope, individual celestial bodies could be explored. Previous work in neuroscience, he said, was “as if somebody had pointed a telescope only to one galaxy, and then different astronomers had pointed their telescopes at different galaxies, and said, ‘My galaxy does this!’ or ‘No, my galaxy does that!” The new project, he explained, was like being able to view all the features of the night sky at once and up close.
Such work has only been possible with recent technological advances and improved collaboration across labs, but Carandini hopes that it can now be used to address other big questions about the brain. The current paper’s findings are only correlational, so it is currently not possible to say whether the observed brain activity directly causes a decision to be made or is only associated with the process.
“I think that’s the next frontier,” he said, “is to add causality to the study.”
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Cornell biologists expose bacteria’s hidden Achilles’ heel
Antibiotic resistance is considered one of the most urgent health threats of our time. Common bacteria such as E. coli and Staphylococcus aureus are evolving defenses against the drugs doctors rely on most. To combat the threat, scientists are racing to find new ways to halt bacterial growth without triggering resistance too quickly.
In recent research, Cornell biologists identified a surprising mechanism that weakens bacteria from within—an insight that could guide the next generation of antibiotics as drug resistance rises worldwide. Researchers at the Weill Institute for Cell and Molecular Biology found that when certain sugar-phosphate molecules pile up inside bacteria, they block a key step in building the bacterial cell wall. Without a strong wall, bacteria cannot survive.
The study, led by Megan Keller, postdoctoral fellow in the laboratory of Tobias Dӧrr, associate professor and director of graduate studies of Microbiology in the College of Agriculture and Life Sciences, was published in the American Society for Microbiology journal mBio in July 2025.
The team studied Vibrio cholerae, the water-borne bacterium that causes cholera disease, yet also possesses the ability to withstand specific antibiotics for an extended period of time. By engineering strains that accumulated certain sugar-phosphates, the scientists noticed dramatic growth defects. Chemical analysis revealed that these sugar-phosphates directly interfered with the enzymes that create peptidoglycan—the rigid mesh that forms the bacterial cell wall.
The interference was specific and powerful: when sugar-phosphate levels rose, the cell wall could not form properly. Instead, bacteria became fragile and prone to bursting. Importantly, the effect mimicked the action of existing antibiotics that also target cell wall synthesis, but through a completely different mechanism, one that may reduce the formation of antibiotic resistance.
The research included contributions from collaborators at Weill Cornell Medicine, with expertise spanning metabolomics, genetics, and biochemistry. The findings offer a new angle for antibiotic development. Instead of designing drugs that directly attack bacterial enzymes, scientists might create compounds that cause sugar-phosphate molecules to accumulate to toxic levels.
“In a way this is an ideal situation,” Keller said. “We shut down the bacterium’s ability to eat sugar, while at the same time, sensitize it to cell-wall targeting antibiotics. This will make it harder for them to develop resistance.” That strategy could bypass existing resistance pathways and provide a fresh line of defense against “superbugs.”
Because peptidoglycan is essential for virtually all bacteria but absent in human cells, therapies based on this mechanism could be potent—killing bacteria without harming patients. However, this therapeutic approach could also kill beneficial microbes with the same process.
“This work shows us that bacteria carry the seeds of their own destruction,” Dӧrr said. “Exploring synergies between antibiotics and metabolic perturbations is an emerging field, holding great promise for the development of novel therapies. If we can trigger this internal imbalance, we might develop therapies that bacteria will find much harder to resist.”
The Cornell team plans to test whether the same mechanism operates in other disease-causing bacteria and to screen for molecules that enhance sugar-phosphate buildup. The long-term goal is to translate the basic science into antibiotic strategies that can outpace drug resistance.
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Tackle the sugar lobby to save young teeth | Health
No one will argue against the benefits of good oral hygiene (The Guardian view on the dental divide: ministers must brush up their policy as well as children’s teeth, 2 September), but teaching toothbrushing at breakfast clubs to prevent dental decay (cavities and fillings) is a waste of time unless it is backed up by dietary advice with regard to unnecessary sugar. Why can’t this simple advice, and ways to apply it, be given to pregnant women and mothers of newborns? It can be given by a variety of healthcare professionals, costs nothing to apply at home and would save the NHS millions in a few years’ time. Children would have less pain and dentists would have a happier job.
Extending the sugar tax and challenging the aggressive marketing and lobbying tactics of the food industry, which promotes and profits from high-sugar foods, should also be considered if we are to take the problem seriously. There is “no specific correlation between the number of NHS dentists and young children with tooth decay” because the damage has been done and habits established before most children get to see a dentist.
Incidentally, a bit more advice at the earliest stages would have significant health benefits in other respects too.
Nick Hopkinson
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Timekeeper Protein Found To Regulate Daily T Cell Immunity
A newly discovered “timekeeper” for fighting infections dramatically shapes the body’s immune defenses, offering insight as to why antiviral T cell response varies throughout the day, according to UT Southwestern Medical Center researchers. Their findings, published in Science Advances, could lead to new strategies for treating infections, using immunotherapies to combat cancer, and limiting the effects of body clock disruptors such as jet lag and shift work.
The scientists found that a protein on the surface of T cells that binds to adrenaline appears to act as a timekeeper for the cells’ infection-fighting function. This pathway suppresses inflammation while also increasing vulnerability to disease. The discovery could help explain why individuals might be more susceptible to some infections or experience more severe symptoms at various times during a 24-hour period.
“The adrenaline receptor sets the internal clock of virus-specific T cells, which regulates how well they respond to viral infections at different times of the day,” said David Farrar, Ph.D., Associate Professor of Immunology and Molecular Biology at UT Southwestern. Dr. Farrar co-led the study with Drashya Sharma, Ph.D., Instructor of Immunology at UTSW.
Most organisms have biological functions that cycle on a 24-hour time frame, a phenomenon known as circadian rhythm. For humans and many other mammals, light sets these cycles by programming a region of the brain that sends chemical signals throughout the body to synchronize the circadian clocks in cells, tissues, and organs.
Although scientists have long known the immune system functions on its own daily cycle – for example, vaccines tend to elicit a greater immune response when given in the morning than at night – it has not been known which chemical signals regulate its circadian clock.
Dr. Farrar and his colleagues got their first clues in a study they published in 2022. To better understand the role of the adrenaline receptor on T cells, they used genetic engineering to remove this receptor (ADRB2) from T cell surfaces. Surprisingly, among more than 300 genes affected by this change, the researchers found several genes important for maintaining circadian rhythms.
In the new study, Drs. Farrar and Sharma and their colleagues discovered that deleting ADRB2 had an inconsistent effect on these circadian clock genes. While some lost their rhythmic expression, others adopted abnormal rhythms, either shifting when they were normally expressed within a 24-hour cycle or cycling outside a 24-hour period.
Next, healthy, normal mice and others genetically altered to remove ADRB2 from their T cells were infected with vesicular stomatitis virus, a common pathogen for this species. T cells of the mice with ADRB2 proliferated and differentiated into various subsets, as typically happens after exposure to bacterial and viral pathogens; however, T cells of the mice lacking ADRB2 had reduced proliferation and differentiation.
One subset particularly affected in the altered mice was memory T cells, which are targeted by vaccines. These cells stick around after infection, preserving a cellular memory of the pathogen so they can launch a new attack upon exposure to the same pathogen in the future.
Drs. Farrar and Sharma explained that adrenaline produced by brain cells rises upon waking and falls at bedtime, a cycle that’s the opposite of immune activity. Because some circadian clock genes in T cells continue to cycle even in the absence of ADRB2, the researchers added, adrenaline is probably just one of several chemical signals that direct circadian rhythms in T cells.
Future research in the Farrar Lab will focus on identifying other cycle-setting chemicals in these immune cells as well as how they affect T cell response to various pathogens at different times of the day.
Reference: Sharma D, Kohlbach KA, Maples R, Farrar JD. The β2-adrenergic receptor (Adrb2) entrains circadian gene oscillation and CD8+ T cell differentiation in response to virus infection. Science Advances. 2025;11(31):eady2643. doi: 10.1126/sciadv.ady2643
This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source. Our press release publishing policy can be accessed here.
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5 warnings signs of a heart attack, according to cardiologists – The Washington Post
- 5 warnings signs of a heart attack, according to cardiologists The Washington Post
- Are you always feeling tired? Cardiologist explains how fatigue can be a symptom for many cardiovascular diseases Hindustan Times
- From decreased walking pace to fatigue to stamina: CMC Vellore doctor says it could be a warning sign of h The Economic Times
- Heart attacks without chest pain: Why atypical symptoms are dangerous Moneycontrol
- Over 45% of heart attacks go unnoticed in India NewsMeter
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Congo declares new Ebola outbreak, 28 suspected cases – Reuters
- Congo declares new Ebola outbreak, 28 suspected cases Reuters
- World Health Organisation warning as several left dead from eye-bleeding horror virus Daily Star
- Ebola outbreak kills 15 in DR Congo BBC
- WHO to Speak on Suspected Hemorrhagic Fever Outbreak in DRC Bloomberg.com
- Democratic Republic of the Congo declares Ebola virus disease outbreak in Kasai Province WHO | Regional Office for Africa
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‘Shampoo’ could protect against hair loss during chemo
Researchers have developed a shampoo-like gel that has been studied in animal models and could protect hair from falling out during chemotherapy treatment.
Baldness from chemotherapy-induced alopecia causes personal, social, and professional anxiety for everyone who experiences it.
Currently, there are few solutions—the only ones that are approved are cold caps worn on the patient’s head, which are expensive and have their own extensive side effects.
Bryan Smith, an associate professor in the Michigan State University College of Engineering and with MSU’s Institute for Qualitative Health Science and Engineering, has developed a gel the consistency of shampoo that he hopes will help protect patients’ hair throughout treatment.
When Smith was a trainee at Stanford University, he learned and used a process that inverted the typical engineering process, seeking to objectively identify and completely characterize critical clinical needs prior to solving them.
“This unmet need of chemotherapy-induced alopecia appealed to me because it is adjacent to the typical needs in medicine such as better treatments and earlier, more accurate diagnostics for cancer,” Smith says.
“This is a need on the personal side of cancer care that, as an engineer, I didn’t fully recognize until I began interviewing cancer physicians and former cancer patients about it. Once I understood, it became clear to me that better solutions are very important to many cancer patients’ quality of life.”
This rigorous process of specifying the need, identifying possible solutions, developing an initial prototype, and refining and testing it led to the development of a gel described in a new paper in Biomaterials Advances.
The gel is a hydrogel, which absorbs a lot of water and provides long-lasting delivery of drugs to the patient’s scalp. The hydrogel is designed to be applied to the patient’s scalp before the start of chemotherapy and left on their head as long as the chemotherapy drugs are in their system—or until they are ready to easily wash it off.
During chemotherapy treatment, chemotherapeutic drugs circulate throughout the body. When these drugs reach the blood vessels surrounding the hair follicles on the scalp, they kill or damage the follicles, which releases the hair from the shaft and causes it to fall out. The gel, containing the drugs lidocaine and adrenalone, prevents most of the chemotherapy drugs from reaching the hair follicle by restricting the blood flow to the scalp. Dramatic reduction in drugs reaching the follicle will help protect the hair and prevent it from falling out.
To support practical use of this “shampoo,” the gel is designed to be temperature responsive. For example, at body temperatures the gel is thicker and clings to the patient’s hair and scalp surface. When the gel is exposed to slightly cooler temperatures, the gel becomes thinner and more like a liquid that can be easily washed away.
Smith and his team hope to obtain federal and/or venture funding to move this research forward into clinical trials and, eventually, to human patients.
“The research has the potential to help many people,” Smith says. “All the individual components are well-established, safe materials, but we can’t move forward with follow-up studies and clinical trials on humans without the support of substantial funding.”
Source: Michigan State University
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Listen: How trees boost your focus and mental health
In a new podcast episode, a psychologist explains how trees boost your attention, improve mental health—and even reduce crime.
University of Chicago psychologist Marc Berman’s research on “soft fascination” and nature’s cognitive effects is reshaping how we think about everything from urban planning to depression treatment.
From groundbreaking hospital studies to surprising results with plastic plants, Berman’s work uncovers the deep—and often invisible—power that natural environments hold over our minds and bodies.
Whether you’re a city planner, a parent, or just someone feeling mentally fatigued, the conversation on this episode of the Big Brains podcast may just change the way you think about a walk in the park:
Source: University of Chicago
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