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By Eryn Brown, On March 30, 1981, 25-year-old John W. Hinckley Jr. shot President Ronald Reagan and three other people. The following year, he went on trial for his crimes. Defense attorneys argued that Hinckley was insane, and they pointed to a trove of evidence to back their claim. Their client had a history of behavioral problems. He was obsessed with the actress Jodie Foster, and devised a plan to assassinate a president to impress her. He hounded Jimmy Carter. Then he targeted Reagan. In a controversial courtroom twist, Hinckley’s defense team also introduced scientific evidence: a computerized axial tomography (CAT) scan that suggested their client had a “shrunken,” or atrophied, brain. Initially, the judge didn’t want to allow it. The scan didn’t prove that Hinckley had schizophrenia, experts said—but this sort of brain atrophy was more common among schizophrenics than among the general population. It helped convince the jury to find Hinckley not responsible by reason of insanity. Nearly 40 years later, the neuroscience that influenced Hinckley’s trial has advanced by leaps and bounds—particularly because of improvements in magnetic resonance imaging (MRI) and the invention of functional magnetic resonance imaging (fMRI), which lets scientists look at blood flows and oxygenation in the brain without hurting it. Today neuroscientists can see what happens in the brain when a subject recognizes a loved one, experiences failure, or feels pain. Despite this explosion in neuroscience knowledge, and notwithstanding Hinckley’s successful defense, “neurolaw” hasn’t had a tremendous impact on the courts—yet. But it is coming. Attorneys working civil cases introduce brain imaging ever more routinely to argue that a client has or has not been injured. Criminal attorneys, too, sometimes argue that a brain condition mitigates a client’s responsibility. Lawyers and judges are participating in continuing education programs to learn about brain anatomy and what MRIs and EEGs and all those other brain tests actually show. © 2019 Scientific American

Related chapters from BN: Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System; Chapter 16: Psychopathology: Biological Basis of Behavior Disorders
Related chapters from MM:Chapter 1: Cells and Structures: The Anatomy of the Nervous System; Chapter 12: Psychopathology: The Biology of Behavioral Disorders
Link ID: 26587 - Posted: 09.09.2019

Jon Hamilton In mice, scientists have used a variety of drugs to treat brain disorders including murine versions of Alzheimer's disease, depression and schizophrenia. But in people, these same treatments usually fail. And now researchers are beginning to understand why. A detailed comparison of the cell types in mouse and human brain tissue found subtle but important differences that could affect the response to many drugs, a team reports Wednesday in the journal Nature. "If you want to develop a drug that targets a specific receptor in a specific disease, then these differences really matter," says Christof Koch, an author of the study and chief scientist and president of the Allen Institute for Brain Science in Seattle. One key difference involved genes that cause a cell to respond to the chemical messenger serotonin, says Ed Lein, a study author and investigator at the institute. "They're expressed in both mouse and human, but they're not in the same types of cells," Lein says. As a result, "serotonin would have a very different function when released into the cortex of the two species." That's potentially a big deal because antidepressants like Prozac act on the brain's serotonin system. So testing these drugs on mice could be misleading, Lein says. The comparison was possible because of new technology that allows scientists to quickly identify which of the hundreds of types of brain cells are present in a particular bit of brain tissue. © 2019 npr

Related chapters from BN: Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System; Chapter 6: Evolution of the Brain and Behavior
Related chapters from MM:Chapter 1: Cells and Structures: The Anatomy of the Nervous System
Link ID: 26530 - Posted: 08.22.2019

Laura Sanders The golf ball–sized chunk of brain is not cooperating. It’s thicker than usual, and bloodier. One side has a swath of tissue that looks, to my untrained eye, like gristle. Nick Dee, the neuroscientist charged with quickly cutting the chunk into neat pieces, confers with his colleagues. “We can trim off that ugliness on the side,” he says. The “ugliness” is the brain’s connective tissue called white matter. To produce useful slices for experiments, the brain tissue must be trimmed, superglued to a lipstick-sized base and then fed into a lab version of a deli slicer. But this difficult chunk isn’t cutting nicely. Dee and colleagues pull it off the base, trim it again and reglue. Half an hour earlier, this piece of neural tissue was tucked inside a 41-year-old woman’s head, on her left side, just above the ear. Surgeons removed the tissue to reach a deeper part of her brain thought to be causing severe seizures. Privacy rules prevent me from knowing much about her; I don’t know her name, much less her first memory, favorite meal or sense of humor. But within this piece of tissue, which the patient generously donated, are clues to how her brain — all of our brains, really — create the mind. Dee’s team is working fast because this piece of brain is alive. Some of the cells can still behave as if they are a part of a person’s brain, which means they hold enormous potential for scientists who want to understand how we remember, plan, behave and feel. After Dee and his team do their part, pieces of the woman’s brain will be whisked into the hands of eager scientists, where the cells will be photographed, zapped with electricity, relieved of their genetic material and even infected with viruses that make them glow green and red. © Society for Science & the Public 2000 - 2019

Related chapters from BN: Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System; Chapter 6: Evolution of the Brain and Behavior
Related chapters from MM:Chapter 1: Cells and Structures: The Anatomy of the Nervous System
Link ID: 26490 - Posted: 08.12.2019

Ian Sample Science editor Doctors have turned the brain signals for speech into written sentences in a research project that aims to transform how patients with severe disabilities communicate in the future. The breakthrough is the first to demonstrate how the intention to say specific words can be extracted from brain activity and converted into text rapidly enough to keep pace with natural conversation. In its current form, the brain-reading software works only for certain sentences it has been trained on, but scientists believe it is a stepping stone towards a more powerful system that can decode in real time the words a person intends to say. A neuroscientist explains: the need for ‘empathetic citizens’ - podcast Doctors at the University of California in San Francisco took on the challenge in the hope of creating a product that allows paralysed people to communicate more fluidly than using existing devices that pick up eye movements and muscle twitches to control a virtual keyboard. “To date there is no speech prosthetic system that allows users to have interactions on the rapid timescale of a human conversation,” said Edward Chang, a neurosurgeon and lead researcher on the study published in the journal Nature. The work, funded by Facebook, was possible thanks to three epilepsy patients who were about to have neurosurgery for their condition. Before their operations went ahead, all three had a small patch of tiny electrodes placed directly on the brain for at least a week to map the origins of their seizures. © 2019 Guardian News & Media Limited

Related chapters from BN: Chapter 19: Language and Lateralization; Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System
Related chapters from MM:Chapter 15: Language and Lateralization; Chapter 1: Cells and Structures: The Anatomy of the Nervous System
Link ID: 26472 - Posted: 07.31.2019

Abby Olena For years, scientists thought the brain lacked a lymphatic system, raising questions about how fluid, macromolecules, and immune cells escape the organ. In 2015, two studies in mice provided evidence that the brain does in fact have a traditional lymphatic system in the outermost layer of the meninges—the coverings that protect the brain and help keep its shape—but scientists hadn’t yet figured out the exact exit route cerebrospinal fluid (CSF) and molecules take. In a study published today (July 24) in Nature, researchers show that there is a hot spot of meningeal lymphatic vessels at the base of the rodent skull that is specialized to drain CSF and allow proteins and other large molecules to leave the brain. “What they showed very nicely is that the system of meningeal lymphatics is the drainage system of the CSF of the central nervous system,” says Jonathan Kipnis, a neuroscientist at the University of Virginia who did not participate in the new study, but coauthored the first 2015 study. “We’re just scratching really the surface of understanding what these vessels are doing.” “I’m actually quite relieved because when we published in 2015 . . . we got a lot of contrasting comments and some people were not convinced that the lymphatics really can be involved in cerebrospinal fluid drainage because there was a lot of literature telling otherwise,” Kari Alitalo of the University of Helsinki tells The Scientist. Alitalo coauthored the second 2015 paper describing the brain’s lymphatic system, but was not involved in the current study. © 1986–2019 The Scientist

Related chapters from BN: Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System
Related chapters from MM:Chapter 1: Cells and Structures: The Anatomy of the Nervous System
Link ID: 26452 - Posted: 07.26.2019

Ian Sample Science editor Brain scans of US embassy staff who became ill in mysterious circumstances while serving in Cuba have found potential abnormalities that may be related to their symptoms. The scans taken from 40 US government workers who suffered strange concussion-like symptoms during their deployment to Havana revealed that particular brain features looked different to those in healthy volunteers. Images of the diplomats’ brains found that on average they had lower volumes of white matter, the tissue made from nerve bundles that send messages around the brain. They also showed micro-structural differences and other changes that could affect auditory and visuospatial processing, doctors said. But the medical team that performed the scans said the findings were not conclusive. They do not match what is normally seen in brain injuries and the severity of symptoms did not vary with the extent of the brain differences spotted. “It’s a unique presentation that we have not seen before,” said Ragini Verma, a professor of biomedical imaging on the team at the University of Pennsylvania. “What caused it? I’m completely unequipped to answer that.” Independent experts agreed the findings were inconclusive and said it was still unclear whether the diplomats were victims of any attack or had suffered related brain injuries. The apparent abnormalities might have pre-dated the attacks, they said, and could have more mundane explanations such as anxiety or depression. One said the study did not meet the usual standards for publication. © 2019 Guardian News & Media Limited

Related chapters from BN: Chapter 19: Language and Lateralization; Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System
Related chapters from MM:Chapter 15: Language and Lateralization; Chapter 1: Cells and Structures: The Anatomy of the Nervous System
Link ID: 26446 - Posted: 07.24.2019

Ed Yong On July 22, 2009, the neuroscientist Henry Markram walked onstage at the TEDGlobal conference in Oxford, England, and told the audience that he was going to simulate the human brain, in all its staggering complexity, in a computer. His goals were lofty: “It’s perhaps to understand perception, to understand reality, and perhaps to even also understand physical reality.” His timeline was ambitious: “We can do it within 10 years, and if we do succeed, we will send to TED, in 10 years, a hologram to talk to you.” If the galaxy-brain meme had existed then, it would have been a great time to invoke it. It’s been exactly 10 years. He did not succeed. One could argue that the nature of pioneers is to reach far and talk big, and that it’s churlish to single out any one failed prediction when science is so full of them. (Science writers joke that breakthrough medicines and technologies always seem five to 10 years away, on a rolling window.) But Markram’s claims are worth revisiting for two reasons. First, the stakes were huge: In 2013, the European Commission awarded his initiative—the Human Brain Project (HBP)—a staggering 1 billion euro grant (worth about $1.42 billion at the time). Second, the HBP’s efforts, and the intense backlash to them, exposed important divides in how neuroscientists think about the brain and how it should be studied. Markram’s goal wasn’t to create a simplified version of the brain, but a gloriously complex facsimile, down to the constituent neurons, the electrical activity coursing along them, and even the genes turning on and off within them. From the outset, the criticism to this approach was very widespread, and to many other neuroscientists, its bottom-up strategy seemed implausible to the point of absurdity.

Related chapters from BN: Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System
Related chapters from MM:Chapter 1: Cells and Structures: The Anatomy of the Nervous System
Link ID: 26440 - Posted: 07.23.2019

By Tanya Lewis Late on Tuesday evening, Elon Musk, the charismatic and eccentric CEO of SpaceX and Tesla, took to the stage at the California Academy of Sciences to make a big announcement. This time, he was not unveiling a new rocket or electric car but a system for recording the activity of thousands of neurons in the brain. With typical panache, Musk talked about putting this technology into a human brain by as early as next year. The work is the product of Neuralink, a company Musk founded in 2016 to develop a high-bandwidth, implantable brain-computer interface (BCI). He says the initial goal is to enable people with quadriplegia to control a computer or smartphone using just their thoughts. But Musk’s vision is much more ambitious than that: he seeks to enable humans to “merge” with AI, giving people superhuman intelligence—an objective that is much more hype than an actual plan for new technology development. Neuralink prototype device. Credit: Neuralink On a more practical note, “the goal is to record from and stimulate [signals called] spikes in neurons” with an order of magnitude more bandwidth than what has been done to date and to have it be safe, Musk said at Tuesday’s event, which was livestreamed. Advertisement The system unveiled last night was a long way from Musk’s sci-fi vision. But it was nonetheless marked an impressive technical development. The team says it has now developed arrays with a very large number of “channels”—up to 3,072 flexible electrodes—which can be implanted in the brain’s outer layer, or cortex, using a surgical robot (a version of which was described as a “sewing machine” in a preprint paper posted on bioRxiv earlier this year). The electrodes are packaged in a small, implantable device containing custom-built integrated circuits, which connects to a USB port outside the brain (the team hopes to ultimately make the port wireless). © 2019 Scientific American

Related chapters from BN: Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System; Chapter 11: Motor Control and Plasticity
Related chapters from MM:Chapter 1: Cells and Structures: The Anatomy of the Nervous System; Chapter 5: The Sensorimotor System
Link ID: 26427 - Posted: 07.18.2019

Laura Sanders Over 100 hours of scanning has yielded a 3-D picture of the whole human brain that’s more detailed than ever before. The new view, enabled by a powerful MRI, has the resolution potentially to spot objects that are smaller than 0.1 millimeters wide. “We haven’t seen an entire brain like this,” says electrical engineer Priti Balchandani of the Icahn School of Medicine at Mount Sinai in New York City, who was not involved in the study. “It’s definitely unprecedented.” The scan shows brain structures such as the amygdala in vivid detail, a picture that might lead to a deeper understanding of how subtle changes in anatomy could relate to disorders such as post-traumatic stress disorder. To get this new look, researchers at Massachusetts General Hospital in Boston and elsewhere studied a brain from a 58-year-old woman who died of viral pneumonia. Her donated brain, presumed to be healthy, was preserved and stored for nearly three years. Before the scan began, researchers built a custom spheroid case of urethane that held the brain still and allowed interfering air bubbles to escape. Sturdily encased, the brain then went into a powerful MRI machine called a 7 Tesla, or 7T, and stayed there for almost five days of scanning. |© Society for Science & the Public 2000 - 2019.

Related chapters from BN: Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System
Related chapters from MM:Chapter 1: Cells and Structures: The Anatomy of the Nervous System
Link ID: 26401 - Posted: 07.09.2019

By Knvul Sheikh The tiny, transparent roundworm known as Caenorhabditis elegans is roughly the size of a comma. Its entire body is made up of just about 1,000 cells. A third are brain cells, or neurons, that govern how the worm wriggles and when it searches for food — or abandons a meal to mate. It is one of the simplest organisms with a nervous system. The circuitry of C. elegans has made it a common test subject among scientists wanting to understand how the nervous system works in other animals. Now, a team of researchers has completed a map of all the neurons, as well as all 7,000 or so connections between those neurons, in both sexes of the worm. “It’s a major step toward understanding how neurons interact with each other to give rise to different behaviors,” said Scott Emmons, a developmental biologist at the Albert Einstein College of Medicine in New York who led the research. Structure dictates function in several areas of biology, Dr. Emmons said. The shape of wings provided insight into flight, the helical form of DNA revealed how genes are coded, and the structure of proteins suggested how enzymes bind to targets in the body. It was this concept that led biologist Sydney Brenner to start cataloging the neural wiring of worms in the 1970s. He and his colleagues preserved C. elegans in agar and osmium fixative, sliced up their bodies like salami and photographed their cells with a powerful electron microscope. © 2019 The New York Times Company

Related chapters from BN: Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System; Chapter 7: Life-Span Development of the Brain and Behavior
Related chapters from MM:Chapter 1: Cells and Structures: The Anatomy of the Nervous System; Chapter 4: Development of the Brain
Link ID: 26389 - Posted: 07.04.2019

Sara Reardon A medical imaging device that can create 3D renderings of the entire human body in as little as 20 seconds could soon be used for a wide variety of research and clinical applications. The modified positron emission tomography (PET) scanner is faster than conventional PET scans — which can take an average of 20 minutes — and requires less radiation exposure for the person being imaged. Researchers presented video taken by the device last week at the US National Institutes of Health’s High-Risk, High-Reward Research Symposium in Bethesda, Maryland. The machine could be especially helpful for imaging children, who tend to wiggle around inside a scanner and ruin the measurements, as well as for studies of how drugs move through the body, says Sanjay Jain, a paediatrician and infectious-disease physician at Johns Hopkins University in Baltimore, Maryland. Standard PET scanners detect γ-rays from radioactive tracers that doctors inject into the person being imaged. The person’s cells take up the molecule and break it down, releasing two γ-rays. A ring-shaped detector positioned around the person measures the angle and speed of the rays and reconstructs their origin, creating a 3D map of the cells that are metabolizing the molecule. The ring is just 25 centimetres thick, however, so physicians can image only a small portion of the body at a time. Capturing larger areas requires them to dose the person with more of the radioactive molecule ― it decays quickly, which means the signal fades fast ― and move them back and forth through the ring. © 2019 Springer Nature Publishing AG

Related chapters from BN: Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System
Related chapters from MM:Chapter 1: Cells and Structures: The Anatomy of the Nervous System
Link ID: 26328 - Posted: 06.14.2019

By Kelly Servick For a hair-thin probe penetrating the brain to listen in on neurons' electrical chatter, finesse is key. It's easy to rip tissue on the way in. And once in place, a probe can do further damage that muffles the signals it aims to detect. But recent reports describe a generation of finer probes that should prove less damaging. Just a few micrometers thick—comparable to neurons themselves—these tools may soon capture unprecedented long-term recordings from hard-to-reach parts of animal brains. And they may lead to more sophisticated brain-computer interfaces for people. Improved material fabrication techniques have helped labs create the exquisitely fine probes, says neural engineer Timothy Hanson, who developed a system for inserting tiny electrodes while at the University of California, San Francisco (UCSF). And lab tests have shown that brain research using ultrasmall electrodes "can be done, and that it's worthwhile." Conventional brain probes are already vanishingly tiny. Stiff electrodes known as Michigan probes, commonly used in neuroscience research, are pointed, ribbonlike shafts that can be as thin as 15 micrometers and are usually 60 micrometers wide or more. In a standard grid known as the Utah array, each spike is roughly 200 micrometers thick at its base. But in the months after either device is implanted, its connection to neurons typically weakens and its signal fades. A key reason is that the probe provokes an immune reaction in the brain. Its initial plunge into the tissue can tear blood vessels. And even after that damage heals, the probe continues to push and pull on surrounding tissue. In response, nonneuronal cells called glia multiply and form scars that push neurons away from the electrode. © 2019 American Association for the Advancement of Science.

Related chapters from BN: Chapter 3: Neurophysiology: The Generation, Transmission, and Integration of Neural Signals
Related chapters from MM:Chapter 2: Neurophysiology: The Generation, Transmission, and Integration of Neural Signals
Link ID: 26200 - Posted: 05.02.2019

By Karen Weintraub Stroke, amyotrophic lateral sclerosis and other medical conditions can rob people of their ability to speak. Their communication is limited to the speed at which they can move a cursor with their eyes (just eight to 10 words per minute), in contrast with the natural spoken pace of 120 to 150 words per minute. Now, although still a long way from restoring natural speech, researchers at the University of California, San Francisco, have generated intelligible sentences from the thoughts of people without speech difficulties. The work provides a proof of principle that it should one day be possible to turn imagined words into understandable, real-time speech circumventing the vocal machinery, Edward Chang, a neurosurgeon at U.C.S.F. and co-author of the study published Wednesday in Nature, said Tuesday in a news conference. “Very few of us have any real idea of what’s going on in our mouth when we speak,” he said. “The brain translates those thoughts of what you want to say into movements of the vocal tract, and that’s what we want to decode.” But Chang cautions that the technology, which has only been tested on people with typical speech, might be much harder to make work in those who cannot speak—and particularly in people who have never been able to speak because of a movement disorder such as cerebral palsy. Chang also emphasized that his approach cannot be used to read someone’s mind—only to translate words the person wants to say into audible sounds. “Other researchers have tried to look at whether or not it’s actually possible to decode essentially just thoughts alone,” he says.* “It turns out it’s a very difficult and challenging problem. That’s only one reason of many that we focus on what people are trying to say.” © 2019 Scientific American

Related chapters from BN: Chapter 19: Language and Lateralization; Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System
Related chapters from MM:Chapter 15: Language and Lateralization; Chapter 1: Cells and Structures: The Anatomy of the Nervous System
Link ID: 26170 - Posted: 04.24.2019

By Kelly Servick The machines that scan our brains are usually monstrous contraptions, locked away in high-end research centers. But smaller, cheaper technologies may soon enter the field, like an MRI scanner built for the battlefield and a lightweight, wearable magnetoencephalography system that records magnetic fields generated by the brains of people in motion. If such devices become widespread, they’ll raise new ethical questions, says Francis Shen, a law professor and neuroethicist at the University of Minnesota (UMN) in Minneapolis and Massachusetts General Hospital in Boston. How should researchers share results with the far-flung populations they may soon be able to study? Could direct-to-consumer neuroimaging become an industry alongside personal genetic testing? With a grant from the federal Brain Research through Advancing Innovative Neurotechnologies (BRAIN) Initiative, Shen has teamed up with three UMN colleagues, including MRI physicist Michael Garwood, to start a conversation about the ethical implications of portable neuroimaging. Garwood is part of a multicenter team building an MRI machine powerful enough to be used in medical diagnostic tests that weighs just 400 kilograms—less than a tenth of traditional scanners. He expects the new scanner to take its first images in 3 years. And if market demand can bring down the cost of a key component, he thinks it could eventually cost $200,000 or less, versus millions of dollars for current scanners. Shen and Garwood discussed the ethical issues at play with Science, after presenting their work at a meeting of BRAIN Initiative investigators last week in Washington, D.C. This interview has been edited for brevity and clarity. © 2019 American Association for the Advancement of Science

Related chapters from BN: Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System
Related chapters from MM:Chapter 1: Cells and Structures: The Anatomy of the Nervous System
Link ID: 26149 - Posted: 04.17.2019

By Kelly Servick At age 16, Danielle Bassett spent most of her day at the piano, trying to train her fingers and ignoring a throbbing pain in her forearms. She hoped to pursue a career in music and had been assigning herself relentless practice sessions. But the more she rehearsed Johannes Brahms's feverish Rhapsody in B Minor on her family's Steinway, the clearer it became that something was wrong. Finally, a surgeon confirmed it: Stress fractures would force her to give up the instrument for a year. "What was left in my life was rather bleak," Bassett says. Her home-schooled upbringing in rural central Pennsylvania had instilled a love of math, science, and the arts. But by 17, discouraged by her parents from attending college and disheartened at her loss of skill while away from the keys, she expected that responsibilities as a housewife and mother would soon eclipse any hopes of a career. "I wasn't happy with that plan," she says. Instead, Bassett catapulted herself into a life of research in a largely uncharted scientific field now known as network neuroscience. A Ph.D. physicist and a MacArthur fellow by age 32, she has pioneered the use of concepts from physics and math to describe the dynamic connections in the human brain. "She's now the doyenne of network science," says theoretical neuroscientist Karl Friston of University College London. "She came from a formal physics background but was … confronted with some of the deepest questions in neuroscience." © 2019 American Association for the Advancement of Science.

Related chapters from BN: Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System; Chapter 7: Life-Span Development of the Brain and Behavior
Related chapters from MM:Chapter 1: Cells and Structures: The Anatomy of the Nervous System; Chapter 4: Development of the Brain
Link ID: 26133 - Posted: 04.12.2019

By Lydia Denworth The vast majority of neuroscientific studies contain three elements: a person, a cognitive task and a high-tech machine capable of seeing inside the brain. That simple recipe can produce powerful science. Such studies now routinely yield images that a neuroscientist used to only dream about. They allow researchers to delineate the complex neural machinery that makes sense of sights and sounds, processes language and derives meaning from experience. But something has been largely missing from these studies: other people. We humans are innately social, yet even social neuroscience, a field explicitly created to explore the neurobiology of human interaction, has not been as social as you would think. Just one example: no one has yet captured the rich complexity of two people’s brain activity as they talk together. “We spend our lives having conversation with each other and forging these bonds,” neuroscientist Thalia Wheatley of Dartmouth College says. “[Yet] we have very little understanding of how it is people actually connect. We know almost nothing about how minds couple.” That is beginning to change. A growing cadre of neuroscientists is using sophisticated technology—and some very complicated math—to capture what happens in one brain, two brains, or even 12 or 15 at a time when their owners are engaged in eye contact, storytelling, joint attention focused on a topic or object, or any other activity that requires social give and take. Although the field of interactive social neuroscience is in its infancy, the hope remains that identifying the neural underpinnings of real social exchange will change our basic understanding of communication and ultimately improve education or inform treatment of the many psychiatric disorders that involve social impairments. © 2019 Scientific American

Related chapters from BN: Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System; Chapter 19: Language and Lateralization
Related chapters from MM:Chapter 1: Cells and Structures: The Anatomy of the Nervous System; Chapter 15: Language and Lateralization
Link ID: 26128 - Posted: 04.11.2019

By Emily Mullin About noon most days, the Lieber Institute for Brain Development in East Baltimore gets a case — that is, a brain. It arrives in an inconspicuous red cooler. Almost immediately, resident neuropathologist Rahul Bharadwaj gets to work, carefully inspecting it for any abnormalities, such as tumors or lesions. Often, the brains come from the Maryland Medical Examiner’s Office, just a 15-minute drive across town. On other days, they are flown in — packed on dry ice — from around the country. Since opening in 2011, the institute has amassed more than 3,000 of these post-mortem brains that they are studying to better understand the biological mechanisms behind such neuropsychiatric disorders as schizophrenia, major depression, substance abuse, bipolar disorder and post-traumatic stress disorder. About 100 brain banks exist across the country for all sorts of brain diseases. But Lieber, founded with the support and funding of a wealthy couple whose daughter suffered a psychotic break in her 20s, is the biggest collection dedicated specifically to mental conditions. Current therapies for neuropsychiatric disorders — antipsychotics and antidepressants — treat symptoms rather than the underlying cause of illness, which remains largely unknown. And while they can be lifesaving for certain people, they can cause unpleasant and sometimes serious side effects. In some cases, they won't work at all. Most of these drugs were also discovered by accident. Lieber’s goal is to unravel what happens biologically in the brain to make these conditions occur and then to develop therapies to treat these conditions at their root cause, or even prevent them from happening in the first place. © 1996-2019 The Washington Post

Related chapters from BN: Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System; Chapter 16: Psychopathology: Biological Basis of Behavior Disorders
Related chapters from MM:Chapter 1: Cells and Structures: The Anatomy of the Nervous System; Chapter 12: Psychopathology: The Biology of Behavioral Disorders
Link ID: 26121 - Posted: 04.08.2019

Corey Hill Allen and Eyal Aharoni Brain evidence is playing an increasing role in criminal trials in the United States. An analysis indicates that brain evidence such as MRI or CAT scans – meant to provide proof of abnormalities, brain damage or disorder in defendants – was used for leniency in approximately 5 percent of murder cases at the appellate level. This number jumps to an astounding 25 percent in death penalty trials. In these cases, the evidence is meant to show that the defendant lacked the capacity to control his action. In essence, “My brain made me do it.” But does evidence of neurobiological disorder or abnormality tend to help or hurt the defendant? Legal theorists have previously portrayed physical evidence of brain dysfunction as a double-edged sword. On the one hand, it might decrease a judge’s or juror’s desire to punish by minimizing the offender’s perceived responsibility for his transgressions. The thinking would be that the crime resulted from disordered brain activity, not any choice on the part of the offender. On the other hand, brain evidence could increase punitive motivations toward the offender by making him seem more dangerous. That is, if the offender’s brain truly “made him” commit the crime, there is an increased risk such behavior could occur again, even multiple times, in the future. To tease apart these conflicting motivations, our team of cognitive neuroscientists, a medical bioethicist and a philosopher investigated how people tend to weigh neurobiological evidence when deciding on criminal sentences. © 2010–2019, The Conversation US, Inc.

Related chapters from BN: Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System; Chapter 18: Attention and Higher Cognition
Related chapters from MM:Chapter 1: Cells and Structures: The Anatomy of the Nervous System; Chapter 14: Attention and Higher Cognition
Link ID: 26111 - Posted: 04.03.2019

By Adrian Cho BOSTON—MRI scanners can map a person's innards in exquisite detail, but they say little about composition. Now, physicists are pushing MRI to a new realm of sensitivity to trace specific biomolecules in tissues, a capability that could aid in diagnosing Alzheimer's and other diseases. The advance springs not from improved scanners, but from better methods to solve a notoriously difficult math problem and extract information already latent in MRI data. The new techniques, described this month at a meeting of the American Physical Society here, could soon make the jump to the clinic, says Shannon Kolind, a physicist at the University of British Columbia (UBC) in Vancouver, Canada, who is using them to study multiple sclerosis (MS). "I don't think I'm being too optimistic to say that will happen in the next 5 years," she says. Sean Deoni, a physicist at Brown University, says that "any scanner on the planet can do this." An MRI scanner uses magnetic fields and radio waves to tickle the nuclei of hydrogen atoms—protons—in molecules of water, which makes up more than half of soft tissue. The protons act like little magnets, and the scanner's strong magnetic field makes them all point in one direction. A pulse of radio waves then tips the protons away from the magnetic field, causing them to twirl en masse, like so many gyroscopes. The protons then radiate radio waves of their own. © 2019 American Association for the Advancement of Scienc

Related chapters from BN: Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System; Chapter 3: Neurophysiology: The Generation, Transmission, and Integration of Neural Signals
Related chapters from MM:Chapter 1: Cells and Structures: The Anatomy of the Nervous System; Chapter 2: Neurophysiology: The Generation, Transmission, and Integration of Neural Signals
Link ID: 26059 - Posted: 03.21.2019

By David Grossman The brain remains famously remains one of the most mysterious parts of the human body. The challenges of neuroscience are among the most daunting in the medical field. Expansion microscopy is a crucial element of that study, a chemical technique that expands a small specimen to make it more observable at the molecular level. A new technique allows scientists to expand microscopy so instead of focusing a single sell, it can explore full neural circuits, at a speed around 1,000 times faster than before. A struggle in studying live cells is watching them without altering their actions. Scientists work around this problem by using thin sheets of light to illuminate cells with a piece of complex technology called a lattice light sheet microscope. By combining this microscope with expansion microscopy, scientists at the Howard Hughes Medical Institute (HHMI) were able to expand the possibility of how they could study insect brains. “I thought they were full of it,” says Eric Betzig, now an HHMI investigator at the University of California, Berkeley, in a press statement. "They" refers to Ruixuan Gao and Shoh Asano of MIT, who wanted to use Betzig's lab to attempt their combining of the two practices. While a complex procedure involving high-end scientific equipment, at its heart “the idea does sound a bit crude,” Gao says. “We’re stretching tissues apart." When the experiment was over, Betzig says, “I couldn’t believe the quality of the data I was seeing. You could have knocked me over with a feather.” ©2019 Hearst Magazine Media, Inc

Related chapters from BN: Chapter 2: Functional Neuroanatomy: The Cells and Structure of the Nervous System
Related chapters from MM:Chapter 1: Cells and Structures: The Anatomy of the Nervous System
Link ID: 25886 - Posted: 01.21.2019