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Adjusting Proteins Increases Ozempics Effectiveness – Neuroscience News
Summary: Adjusting melanocortin proteins in the brain enhances the effectiveness of GLP-1 diabetes and weight-loss drugs. By inhibiting MC3R or activating MC4R, mice showed increased sensitivity to these drugs, leading to more significant weight loss and reduced feeding without additional side effects.
This discovery could improve treatment outcomes for patients using GLP-1 drugs. Further research and clinical trials are needed to confirm these findings in humans.
Key Facts:
Source: University of Michigan
A network of proteins found in the central nervous system could be harnessed to increase the effectiveness and reduce the side effects of popular diabetes and weight-loss drugs, according to new research from the University of Michigan.
The study, appearing today in theJournal of Clinical Investigation, focused on two proteins called melanocortin 3 and melanocortin 4 found primarily on the surface of neurons in the brain that play a central role in regulating feeding behavior and maintaining the bodys energy balance.
Melanocortin 3 and melanocortin 4 impact everything from sensing long-term energy stores to processing signals from the gut regarding short-term fullness, or satiety, said U-M physiologistRoger Cone, who led the study.
The class of drugs known as GLP-1 agonists, which includes semaglutides (e.g., Ozempic) and tirzepatides (e.g., Mounjaro), have received substantial attention recently for their effectiveness in treating not only type 2 diabetes, but also obesity, heart disease and potentially addiction. They work by mimicking a natural hormone that the gut produces when it is full, triggering the brain to reduce feeding behavior.
So the obvious question for us was: How do these GLP-1 drugs, which work by manipulating satiety signals, function when we prime the melanocortin system? said Cone, professor of molecular and integrative physiology at the U-M Medical School and director of the U-M Life Sciences Institute where his lab is located.
Working in mouse models, Cone and his colleagues tested the effects of several hormones that reduce food intake. They compared the results in normal mice with mice that genetically lacked the MC3R protein, in mice that were given chemicals to block the activity of MC3R, and in mice that were given a drug to increase the activity of MC4R. (Because MC3R is a natural negative regulator of MC4R, meaning it decreases the activity of MC4R, blocking MC3R and increasing MC4R activity has similar effects.)
In all cases, Naima Dahir, first author of the study and a postdoctoral research fellow in Cones lab, and colleagues found that adjusting the melanocortin systemeither by inhibiting MC3R or increasing MC4R activitymade the mice more sensitive to GLP-1 drugs and other hormones that affect feeding behavior.
The mice that were given a GLP-1 drug in combination with an MC4R agonist or MC3R antagonist showed up to five times more weight loss and reduced feeding than mice receiving only the GLP-1 drugs.
We found that activating the central melanocortin system hypersensitizes animals to the effects of not just GLP-1s, but to every anti-feeding hormone we tested, Cone said.
The researchers also measured activity in parts of the brain thought to trigger nausea in response to GLP-1 drugs and observed no increased activation when GLP-1 drugs were combined with alterations to the melanocortin system. In contrast, priming of the melanocortin neurons significantly increased GLP-1 drug activation of neurons in hypothalamic feeding centers in the brain.
The findings indicate that pairing the existing GLP-1 drugs with an MC4R agonist could increase sensitivity to the desired effects of the drugs by up to fivefold, without increasing unwanted side effects.
Ultimately, this approach could enable patients who are sensitive to the side effects to take a lower dose, or could improve the results in patients who have not responded to the existing drug dosages. Further drug development and clinical testing are needed before this can occur.
While this research has been conducted only in mouse models, Cone is optimistic that the results will translate well to humans.
The melanocortin system is highly conserved in humans, he said. Everything weve observed in the mouse over the past decades studying these proteins has also been found in humans, so I suspect that these results would also be translatable to patients.
This research was funded by the National Institutes of Health and Courage Therapeutics.
Study authors are: Naima Dahir, Yijun Gui, Yanan Wu, Alix Rouault, Savannah Williams, Luis Gimenez, Stephen Joy, Anna K. Mapp and Roger Cone, University of Michigan; Patrick Sweeney, University of Illinois; and Tomi Sawyer, Courage Therapeutics.
Author: Morgan Sherburne Source: University of Michigan Contact: Morgan Sherburne University of Michigan Image: The image is credited to Neuroscience News
Original Research: Open access. Subthreshold activation of the melanocortin system causes generalized sensitization to anorectic agents in mice by Roger Cone et al. JCI
Abstract
Subthreshold activation of the melanocortin system causes generalized sensitization to anorectic agents in mice
The melanocortin-3 receptor (MC3R) regulates GABA release from agouti-related protein (AgRP) nerve terminals and thus tonically suppresses multiple circuits involved in feeding behavior and energy homeostasis.
Here, we examined the role of the MC3R and the melanocortin system in regulating the response to various anorexigenic agents.
The genetic deletion or pharmacological inhibition of the MC3R, or subthreshold doses of an MC4R agonist, improved the dose responsiveness to glucagon-like peptide 1 (GLP1) agonists, as assayed by inhibition of food intake and weight loss.
An enhanced anorectic response to the acute satiety factors peptide YY (PYY3-36) and cholecystokinin (CCK) and the long-term adipostatic factor leptin demonstrated that increased sensitivity to anorectic agents was a generalized result of MC3R antagonism.
We observed enhanced neuronal activation in multiple hypothalamic nuclei using Fos IHC following low-dose liraglutide in MC3R-KO mice (Mc3r/), supporting the hypothesis that the MC3R is a negative regulator of circuits that control multiple aspects of feeding behavior.
The enhanced anorectic response inMc3r/mice after administration of GLP1 analogs was also independent of the incretin effects and malaise induced by GLP1 receptor (GLP1R) analogs, suggesting that MC3R antagonists or MC4R agonists may have value in enhancing the dose-response range of obesity therapeutics.
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Adjusting Proteins Increases Ozempics Effectiveness - Neuroscience News
Low-Calorie Diets Harm Athletes Performance and Health – Neuroscience News
Summary: Female athletes consuming only half their caloric needs for 14 days experienced significant drops in performance and muscle mass. This low energy availability also weakened their immune systems.
The harmful effects couldnt be reversed by short-term refeeding, highlighting the risks of weight loss practices in sports. The findings emphasize the need for awareness and better support for athletes.
Key Facts:
Source: University of Copenhagen
Whether selected to swim, row or run in the Olympics, or gearing up to ride in the Tour de France, achieving the right weight has been a focal point of many elite athletes for decades. It could be to look lean and mean in a swimsuit or jersey, or to qualify for a certain weight category. But there is also a belief that losing weight enhances performance.
As such, it is a widespread phenomenon among athletesespecially inendurance sportslike running, swimming, cycling and rowingto reduce theirdietary intakein the run-up to competition.
It is particularly problematic among female endurance athletes. Many athletes focus heavily on weight in their respective sports. Consequently, they tend to go into short-term, but intense periods of weight loss with the expectation of performing better, says Professor Ylva Hellsten of the University of Copenhagens Department of Nutrition, Exercise and Sports.
She and Ph.D. student Jan Sommer Jeppesen are two of the researchers behinda new studyon the effects of low energy availability amongfemale athletes.
The paper is published in the journalRedox Biology.
We know that the phenomenon of not eating enough is associated with many things that are harmful to healthincluding missed periods, compromised bone health and changes in metabolism. But there is still plenty that we dont know. As such, we investigated some of the possible consequences more closely, says Jeppesen, who is the studys lead author.
For the study, the researchers recruited twelve female triathletes, all of whom had a normal energy intake. During one part of the trial, the athletes were given enough calories for 14 days, after which their performance was tested. The same athletes also went through a 14-day period during which they consumed only about 50% of their energy needs while sticking to their normal intensive training schedule.
During the period with insufficient calories, athletes lost an average of roughly 4% of their body weight, about half of which was muscle mass. And they experienced a loss in performance:
The fourteen days of insufficient food intake reduced their performance by 7.7% in a 20-minute time trial on a bike, which is quite significant. And during a more intense short-term test, their performance slid by as much as 18%. So there is no doubt that this practice greatly impairs ones performance as an athlete, even over shorter periods of time, says Jeppesen.
In addition to sports performance, the researchers examined the effects on athletes immune function.
Among other things, we saw that insufficient energy intake was associated with increased systemic stress. The athletes had a large increase in cortisol, a stress hormone, and a dramatically increased stress level in immune cells. This suggests that there is a quite severe impact on several aspects of the immune system if one doesnt eat enough. This may potentially contribute to athletes being more exposed to illness, says Jeppesen.
The researchers hope that the results of the study will help create more awareness of the phenomenon.
Many coaches continue to pressure athletes to lose weight. For many years, it has been a part of the culture in the sports worldand remains so. We need to shed light on the phenomenon and ask critically: What are we actually doing to our athletes both physically and psychologically? says Hellsten.
Team Denmark, the Danish elite sport organization, welcomes the new research results with open arms.
It focuses on a really important topic and challenges the attitude that lighter is always better. The theory and culture remains prevalent in many sports. I experience many athletes who trim their weight in the weeks leading up to a competition, but without understanding the consequences of doing so, says Majke Jrgensen, a sports nutritionist and manager at Team Denmark.
She sees the results as useful knowledge that can support a message that Team Denmark has been trying to promote:
My experience is that elite athletes and coaches are curious, but need research that backs up any critiques of the phenomenon. Here, the fact that thetest subjectsare actual athletes is a major strength, so that the results can be transferred to the athletes and coaches that Team Denmark supports.
We will use these results to support what we are already trying to communicate, both when we sit down with athletes one-on-one, as well as during workshops and presentations in these types of contexts, says Jrgensen.
After fourteen days of low energy availability (LEA), the athletes underwent a three-day refeeding period as part of the trial, during which they were provided plenty to eat.
We had expected that the three days of enough food would restore their performanceand maybe even improve itbut there was absolutely no effect. Their performance was just as degraded as prior to the three days. This tells us that the negative effects cannot be reversed by quickly replenishing energy stores, which is a strategy used by many athletes, says Jeppesen.
According to the research literature, men tend to be more resilient when it comes to insufficient energy intake.
Based upon the rather limited research in this area, it seems that men are able to tolerate reduced energy intake before it affects us negatively. This indicates that women in particular are a vulnerable population in this respect, says Jeppesen.
The gender difference is partly due to the fact that low energy availability can cause a womans estrogen levels to drop drastically. Since estrogen protects the circulatory system, muscles and bones, etc., estrogen loss has extensive effects on a womans physiology.
Hellsten points out that theharmful effectsof not eating enough for long periods of time, especially in women, can therefore also be lifelong.
Author: Ylva Hellsten Source: University of Copenhagen Contact: Ylva Hellsten University of Copenhagen Image: The image is credited to Neuroscience News
Original Research: Open access. Low energy availability increases immune cell formation of reactive oxygen species and impairs exercise performance in female endurance athletes by Ylva Hellsten et al. Redox Biology
Abstract
Low energy availability increases immune cell formation of reactive oxygen species and impairs exercise performance in female endurance athletes
The effects of low energy availability (LEA) on the immune system are poorly understood. This study examined the effects of 14 days of LEA on immune cell redox balance and inflammation at rest and in response to acute exercise, and exercise performance in female athletes.
Twelve female endurance athletes (age: 26.83.4yrs, maximum oxygen uptake (O2max): 55.25.1 mLmin1kg1) were included in a randomized, single-blinded crossover study. They were allocated to begin with either 14 days of optimal energy availability diet (OEA, 522kcalkg fat free mass (FFM)1day1) or LEA diet (222kcalkg FFM1day1), followed by 3 days of refueling (OEA) with maintained training volume. Peripheral blood mononuclear cells (PBMCs) were isolated, and plasma obtained at rest before and after each dietary period. The PBMCs were used for analysis of mitochondrial respiration and H2O2emission and specific proteins. Exercise performance was assessed on cycle by a 20-min time trial and time to exhaustion at an intensity corresponding to 110%O2max).
LEA was associated with a 94% (P=0.003) increase in PBMC NADPH oxidase 2 protein content, and a 22% (P=0.013) increase in systemic cortisol. LEA also caused an alteration of several inflammatory related proteins (P<0.05). Acute exercise augmented H2O2emission in PBMCs (P<0.001) following both OEA and LEA, but to a greater extent following LEA. LEA also reduced the mobilization of white blood cells with acute exercise. After LEA, performance was reduced in both exercise tests (P<0.001), and the reduced time trial performance remained after the 3 days of refueling (P<0.001).
14 days of LEA in female athletes increased cortisol levels and had a pronounced effect on the immune system, including increased capacity for ROS production, altered plasma inflammatory proteome and lowered exercise induced mobilization of leukocytes. Furthermore, LEA resulted in a sustained impairment in exercise performance.
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Low-Calorie Diets Harm Athletes Performance and Health - Neuroscience News
Reflective Thinking Boosts Teen Brain Resilience to Violence – Neuroscience News
Summary: Teens who engage in transcendent thinking can counteract the negative effects of violence exposure on brain development. This type of thinking involves considering broader ethical and societal implications of social issues.
The study showed that such reflective thinking leads to brain growth even in teens from high-violence communities. These findings emphasize the importance of fostering reflective thinking skills in adolescents.
Key Facts:
Source: USC
These latest findings from CANDLE (USC Center for Affective Neuroscience, Development, Learning and Education) researchers show that teens who think about social issues and violence in more reflective ways show greater resilience to the effects of violence exposure on their brain development.
The study was published in theJournal of Research on Adolescence.
Mary Helen Immordino-Yang and a team of CANDLE researchers have found that teens who engage in more transcendent thinking, that is thinking that moves beyond reacting to the specifics of social situations to also consider broader ethical, personal and societal implications, can counteract the negative impacts exposure to violence has on theirbrain development.
The study built onan earlier oneby Immordino-Yang that showed the disturbing link between adolescents exposure to violence in their community and their brain development.
In both studies, MRI brain scans of teens who grew up in communities with high levels of violenceshowed thinner cortex in parts of the brain that are involved in feeling stress and pain as well as motivation, judgment and emotional processing.
This new study confirms these links exist even in older teens, around age 1618 when they witness violence, but also offers a possible antidote. The 55 participants were all from low socioeconomic status backgrounds and lived in urban settings. The teens were asked about their exposure to community violence and underwent two MRI brain scans, one at the beginning of the study and one two years later.
At the time of the initial scans, participants also watched mini-documentaries about teens in compelling situations and discussed their reactions in a recorded interview which was later assessed for transcendent thinking.
The final MRI scans showed that the more a teen had engaged in transcendent thinking, the greater the brain growth in various areas across the two years, including those areas most impacted by the violence.
The findings suggest that teens transcendent thinking may be helping them to counteract the effect of exposure to violence on their brain development.
These findings reveal that as adolescents work to contextualize and make sense of the violence they are exposed to, this complex thinking builds resilience and thus grows their brains despite the violence they witness.
When the teens were able to reflect on such things as why violence happens and what can be done to get to the root of the problems, they showed a form of neural resilience in theiranterior cingulate cortex, among other regions.
Let me be clearwe found that witnessing community violence and crime, even in older teens, was associated with key regions of their brain losing volume over time. In effect, witnessing violence made regions of their brains shrink a bit, which is a pattern seen in people suffering from PTSD and in soldiers deployed to war, said Immordino-Yang.
At the same time, the kids were not passively being impactedwhen they showed us that they were thinking hard about why these things happen, and what could be done to make the world better for everyone involved, this kind of thinking grew their brain volume in these same brain regions. Violence was bad for them, but transcendent and civically oriented thinking was a kind of antidote, neurologically speaking.
The study builds on a body of research spearheaded by Immordino-Yang that investigates the effects of transcendent thinking on adolescent brain development. A recentlandmark studypublished by Immordino-Yang showed that transcendent thinking in adolescents can predict future brain growth and that this brain growth, in turn, predicts life satisfaction when youth transition to adulthood.
Immordino-Yangs teams findings underline the vulnerability of adolescents in communities impacted by high levels of violence while also emphasizing the importance of fostering skills like transcendent thinking in teens.
These skills cannot only helpteensmake sense of the violence they witness but also help them counteract the negative impact of thisviolenceon their developing brains.
Author: Kianoosh Hashemzadeh Source: USC Contact: Kianoosh Hashemzadeh USC Image: The image is credited to Neuroscience News
Original Research: Open access. Transcendent thinking counteracts longitudinal effects of midadolescent exposure to community violence in the anterior cingulate cortex by XiaoFei Yang et al. Journal of Research on Adolescence
Abstract
Transcendent thinking counteracts longitudinal effects of midadolescent exposure to community violence in the anterior cingulate cortex
Adolescence involves extensive brain maturation, characterized by social sensitivity and emotional lability, that co-occurs with increased independence. Mid-adolescence is also a hallmark developmental stage when youths become motivated to reflect on the broader personal, ethical, and systems-level implications of happenings, a process we term transcendent thinking.
Here, we examine the confluence of these developmental processes to ask, from a transdisciplinary perspective, how might community violence exposure (CVE) impact brain development during mid-adolescence, and how might youths dispositions for transcendent thinking be protective?
Fifty-five low-SES urban youth with no history of delinquency (32 female; 27 Latinx, 28 East Asian) reported their CVE and underwent structural MRI first at age 1418, and again 2years later.
At the studys start, participants also discussed their feelings about 40 minidocumentaries featuring other teens compelling situations in a 2-h private interview that was transcribed and coded for transcendent thinking.
Controlling for CVE and brain structure at the start: (1) New CVE during the 2-year inter-scan interval was associated with greater gray matter volume (GMV) reduction over that interval in the anterior cingulate cortex (ACC), a central network hub whose reduced volume has been associated with posttraumatic stress disorder, and across multiple additional cortical and subcortical regions; (2) participants transcendent thinking in the interview independently predicted greater GMV increase during the 2-year inter-scan interval in the ACC.
Findings highlight the continued vulnerability of mid-adolescents to community violence and the importance of supporting teens dispositions to reflect on the complex personal and systems-level implications and affordances of their civic landscape.
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Reflective Thinking Boosts Teen Brain Resilience to Violence - Neuroscience News
Neuroscience Says Olympians Like Simone Biles Use the Autopilot Trick to Achieve Peak Performance. So Can You – Inc.
What well-being is (and isnt), according to neuroscience – Big Think
Cultivating your own well-being does not mean getting rid of discomfort, according to neuroscientist Mary Helen Immordino-Yang.
Immordino-Yang is a professor of education, psychology, and neuroscience at the University of Southern California, and she has spent years researching what makes one well.
Turns out, true well-being comes from balance and flexibility, not just from filling your life with positive experiences. Immordino-Yang suggests a few practical tips for maintaining this balance, such as prioritizing quality relationships, monitoring our social media usage, and engaging in activities that bring joy and reflection.
We cant fully eradicate suffering, but we can accept it and choose to grow through it. By welcoming healthy levels of discomfort and taking agency over our own activities and habits, we can achieve wellness as it was meant to be achieved as a state of being, not a destination.
Mary Helen Immordino-Yang:Often we think about well-being as the absence of disease, the absence of mental illness, the absence of strife. But neuroscience and developmental social science help us understand that the origins of well-being are really about balance. It's about an ability and a flexibility to manage oneself. Well-being is both a capacity and a state.
The brain data really help us understand the contributions to that capacity and state. A concept like well-being is not applied to a person; it's conjured within the person by their own actions and dispositions of mind. This shifts the way in which we support a person in developing well-being and becoming well.
I think there are practical things that you can do to support your own well-being strategically. Prioritizing the quality of the relationships that you have with the people around you, whom you care about. Setting yourself up to have control over certain kinds of social media use, certain kinds of scrollingthese addictive things that suck you into a pattern of wanting more and pull you out of a space where you can reflect and just sort of be.
Construct meaningful stories about how that's happening and what that feels like. Privilege the things that you really enjoy doing with the people you really enjoy being with. Taking the time to reflect and think about what it's all for, and then enact that. Giving to others and being engaged with otherswe reap back the benefits of that.
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What well-being is (and isnt), according to neuroscience - Big Think
Brain Areas Take Micro-Naps While the Rest Stays Awake – Neuroscience News
Summary: New research shows sleep can be detected by brain activity patterns just milliseconds long. This study found small brain regions can momentarily flicker awake or asleep, challenging traditional views on sleep and wake states.
Using advanced neural network analysis, researchers uncovered high-frequency patterns that define sleep. These findings could help study neurodevelopmental and neurodegenerative diseases linked to sleep disturbances.
Key Facts:
Source: UC Santa Cruz
Sleep and wake: theyre totally distinct states of being that define the boundaries of our daily lives. For years, scientists have measured the difference between these instinctual brain processes by observing brain waves, with sleep characteristically defined by slow, long-lasting waves measured in tenths of seconds that travel across the whole organ.
For the first time, scientists have found that sleep can be detected by patterns of neuronal activity just milliseconds long, 1000 times shorter than a second, revealing a new way to study and understand the basic brain wave patterns that govern consciousness.
They also show that small regions of the brain can momentarily flicker awake while the rest of the brain remains asleep, and vice versa from wake to sleep.
These findings, described ina new study published in the journalNature Neuroscience, are from a collaboration between the laboratories of Assistant Professor of Biology Keith Hengen at Washington University in St. Louis and Distinguished Professor of Biomolecular Engineering David Haussler at UC Santa Cruz. The research was carried out by Ph.D. students David Parks (UCSC) and Aidan Schneider (WashU).
Over four years of work, Parks and Schneider trained a neural network to study the patterns within massive amounts of brain wave data, uncovering patterns that occur at extremely high frequencies that have never been described before and challenge foundational, long-held conceptions of the neurological basis of sleep and wake.
With powerful tools and new computational methods, theres so much to be gained by challenging our most basic assumptions and revisiting the question of what is a state? Hengen said.
Sleep or wake is the single greatest determinant of your behavior, and then everything else falls out from there. So if we dont understand what sleep and wake actually are, it seems like weve missed the boat.
It was surprising to us as scientists to find that different parts of our brains actually take little naps when the rest of the brain is awake, although many people may have already suspected this in their spouse, so perhaps a lack of male-female bias is what is surprising, Haussler quipped.
Understanding sleep
Neuroscientists study the brain via recordings of the electrical signals of brain activity, known as electrophysiology data, observing voltage waves as they crest and fall at different paces. Mixed into these waves are the spike patterns of individual neurons.
The researchers worked with data from mice at the Hengen Lab in St. Louis. The freely-behaving animals were equipped with a very lightweight headset that recorded brain activity from 10 different brain regions for months at a time, tracking voltage from small groups of neurons with microsecond precision.
This much input created petabytes which are one million times larger than a gigabyte of data. David Parks led the effort to feed this raw data into an artificial neural network, which can find highly complex patterns, to differentiate sleep and wake data and find patterns that human observation may have missed.
A collaboration with theshared academic compute infrastructurelocated at UC San Diego enabled the team to work with this much data, which was on the scale of what large companies like Google or Facebook might use.
Knowing that sleep is traditionally defined by slow-moving waves, Parks began to feed smaller and smaller chunks of data into the neural network and asked it to predict if the brain was asleep or awake.
They found that the model could differentiate between sleep and wake from just milliseconds of brain activity data. This was shocking to the research team it showed that the model couldnt have been relying on the slow-moving waves to learn the difference between sleep and wake.
Just as listening to a thousandth of a second of a song couldnt tell you if it had a slow rhythm, it would be impossible for the model to learn a rhythm that occurs over several seconds by just looking at random isolated milliseconds of information.
Were seeing information at a level of detail thats unprecedented, Haussler said. The previous feeling was that nothing would be found there, that all the relevant information was in the slower frequency waves.
This paper says, if you ignore the conventional measurements, and you just look at the details of the high frequency measurement over just a thousandth of a second, there is enough there to tell if the tissue is asleep or not. This tells us that there is something going on a very fast scale thats a new hint to what might be going on in sleep.
Hengen, for his part, was convinced that Parks and Schneider had missed something, as their results were so contradictory to bedrock concepts drilled into him over many years of neuroscience education. He asked Parks to produce more and more evidence that this phenomena could be real.
This challenged me to ask myself to what extent are my beliefs based on evidence, and what evidence would I need to see to overturn those beliefs? Hengen said.
It really did feel like a game of cat and mouse, because Id ask David [Parks] over and over to produce more evidence and prove things to me, and hed come back and say check this out! It was a really interesting process as a scientist to have my students tear down these towers brick by brick, and for me to have to be okay with that.
Local patterns
Because an artificial neural network is fundamentally a black box and does not report back on what it learns from, Parks began stripping away layers of temporal and spatial information to try to understand what patterns the model could be learning from.
Eventually, they got down to the point where they were looking at chunks of brain data just a millisecond long and at the highest frequencies of brain voltage fluctuations.
Wed taken out all the information that neuroscience has used to understand, define, and analyze sleep for the last century, and we asked can the model still learn under these conditions? Parks said. This allowed us to look into signals we havent understood before.
By looking at these data, they were able to determine that the hyper-fast pattern of activity between just a few neurons was the fundamental element of sleep that the model was detecting. Crucially, such patterns cannot be explained by the traditional, slow and widespread waves.
The researchers hypothesize that the slow moving waves may be acting to coordinate the fast, local patterns of activity, but ultimately reached the conclusion that the fast patterns are much closer to the true essence of sleep.
If the slow moving waves traditionally used to define sleep are compared to thousands of people in a baseball stadium doing the wave, then these fast-moving patterns are the conversations between just a few people deciding to participate in the wave. Those conversations occurring are essential for the overall larger wave to take place, and are more directly related to the mood of the stadium the wave is a secondary result of that.
Observing flickers
In further studying the hyperlocal patterns of activity, the researchers began to notice another surprising phenomenon.
As they observed the model predicting sleep or wake, they noticed what looked at first like errors, in which for a split second the model would detect wake in one region of the brain while the rest of the brain remained asleep. They saw the same thing in wake states: for a split second, one region would fall asleep while the rest of the regions were awake. They call these instances flickers.
We could look at the individual time points when these neurons fired, and it was pretty clear that [the neurons] were transitioning to a different state, Schneider said. In some cases, these flickers might be constrained to the area of just an individual brain region, maybe even smaller than that.
This compelled the researchers to explore what flickers could mean about the function of sleep, and how they affect behavior during sleep and wake.
Theres a natural hypothesis there; lets say a small part of your brain slips into sleep while youre awake does that mean your behavior suddenly looks like youre asleep? We started to see that that was often the case, Schneider said.
In observing the behavior of mice, the researchers saw that when a brain region would flicker to sleep while the rest of the brain was awake, the mouse would pause for a second, almost like it had zoned out. A flicker during sleep (one brain region wakes up) was reflected by an animal twitching in its sleep.
Flickers are particularly surprising because they dont follow established rules dictating the strict cycle of the brain moving sequentially between wake to non-REM sleep to REM sleep.
We are seeing wake to REM flickers, REM to non-REM flickers we see all these possible combinations, and they break the rules that you would expect based on a hundred years of literature, Hengen said.
I think they reveal the separation between the macro-state sleep and wake at the level of the whole animal, and the fundamental unit of state in the brain the fast and local patterns.
Impact
Gaining a deeper understanding of the patterns that occur at high-frequencies and the flickers between wake and sleep could help researchers better study neurodevelopmental and neurodegenerative diseases, which are both associated with sleep dysregulation.
Both Haussler and Hengens lab groups are interested in understanding this connection further, with Haussler interested in further studying these phenomena in cerebral organoid models, bits of brain tissue grown on a laboratory bench.
This gives us potentially a very, very sharp scalpel with which to cut into these questions of diseases and disorders, Hengen said. The more we understand fundamentally about what sleep and wake are, the more we can address pertinent clinical and disease related problems.
On a foundational level, this work helps push forward our understanding of the many layers of complexity of the brain as the organ that dictates behavior, emotion, and much more.
Author: Emily Cerf Source: UC Santa Cruz Contact: Emily Cerf UC Santa Cruz Image: The image is credited to Neuroscience News
Original Research: Closed access. A nonoscillatory, millisecond-scale embedding of brain state provides insight into behavior by David Haussler et al. Nature Neuroscience
Abstract
A nonoscillatory, millisecond-scale embedding of brain state provides insight into behavior
The most robust and reliable signatures of brain states are enriched in rhythms between 0.1 and 20Hz. Here we address the possibility that the fundamental unit of brain state could be at the scale of milliseconds and micrometers.
By analyzing high-resolution neural activity recorded in ten mouse brain regions over 24h, we reveal that brain states are reliably identifiable (embedded) in fast, nonoscillatory activity.
Sleep and wake states could be classified from 100to 101ms of neuronal activity sampled from 100m of brain tissue. In contrast to canonical rhythms, this embedding persists above 1,000Hz.
This high-frequency embedding is robust to substates, sharp-wave ripples and cortical on/off states. Individual regions intermittently switched states independently of the rest of the brain, and such brief state discontinuities coincided with brief behavioral discontinuities.
Our results suggest that the fundamental unit of state in the brain is consistent with the spatial and temporal scale of neuronal computation.
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Brain Areas Take Micro-Naps While the Rest Stays Awake - Neuroscience News