Professional Documents
Culture Documents
Paul-Michael R. Lowey
Editor, BNLC News and Research Blurb
William & Mary Law School, 2017
Williamsburg, VA
prlowey@email.wm.edu
Page 1 of 6
Page 2 of 6
Page 3 of 6
those who did not. One possible exception was a marginal increase in risk with one drug,
risperidone (Risperdal), which the authors said will require further study. (August 18, 2016).
http://tinyurl.com/hck8myr
Scientists Engineer An Opioid That May Reduce Pain With Less Risk. NPR. The recent opioid epidemic
has spurred a search for a painkiller that relieves pain without triggering the euphoria, dependence
and life-threatening respiratory suppression that causes deadly overdoses. That wasn't thought
possible until 2000, when a scientist named Laura Bohn found out something about a protein called
beta-arrestin, which sticks to the opioid receptor when something like morphine activates it. When
she gave morphine to mice that couldn't make beta-arrestin, they were still numb to pain, but a lot
of the negative side effects of the drug were missing. They didn't build tolerance to the drug. At
certain dosages, they had less withdrawal. Their breathing was more regular, and they weren't as
constipated as normal mice on morphine. After Bohn's discovery, a number of people, including a
team that includes Manglik, started looking for a drug that could connect to the mu-opioid receptor
in a way that avoids the negative effects of beta-arrestin. . To do that, they mapped the receptor's
structure in a computer program and started looking for chemicals that would stick to it. "We tried
to look for molecules that would still bind to this 3-D structure, but are as far away from morphine
and codeine as possible," Manglik says. The team ran 3 million possibilities through the computer
and picked the 23 best candidates to test in a lab. One chemical, PZM21, seems to do what they
hoped: Turn the opioid receptor on without using much beta-arrestin. (August 17, 2016).
http://tinyurl.com/ze36f4f
Neurodegenerative Disorders
Parkinson's Could Potentially Be Detected By An Eye Test. BBC. Scientists at University College London
believe the results from animal tests could eventually lead to a cheap and non-invasive way to spot
Parkinsons. "Although the research is in its infancy and is yet to be tested on people with
Parkinson's, a simple non-invasive test - such as an eye test - could be a significant step forward in
the search for treatments that can tackle the underlying causes of the condition rather than masking
its symptoms," he added. "Having a biomarker for Parkinson's would help diagnose Parkinson's
earlier, when people are most likely to benefit from the new treatments aimed at slowing
progression," he explained. Their research is published in Acta Neuropathologica Communications.
(August 18, 2016).
http://www.bbc.com/news/health-37107189
Zika Kills Brain Cells In Adult Mice. SCIENCE NEWS. The virus, which can cause brain damage in
infants infected in the womb, kills stem cells and stunts their numbers in the brains of adult mice,
researchers report August 18 in Cell Stem Cell. Though scientists have considered Zika primarily a
threat to unborn babies, the new findings suggest that the virus may cause unknown and potentially
long-term damage to adults as well. In adults, Zika has been linked to Guillain-Barr syndrome, a
rare neurological disorder. But for most people, infection is typically mild: a headache, fever and
rash lasting up to a week, or no symptoms at all. In mice infected with Zika, the virus hit the
forebrain and hippocampus hard. Nerve cells died and the regions generated one-fifth to one-half as
many new cells compared with those of uninfected mice. The results might not translate to humans;
the mice were genetically engineered to have weak immune systems, making them susceptible to
Zika. (August 18, 2016).
https://www.sciencenews.org/article/zika-kills-brain-cells-adult-mice?tgt=nr
BNLC BlurbAugust 2016
Page 4 of 6
Do Schizophrenic Brains Repair Themselves? THE SCIENTIST. A number of psychiatrists have noticed that
some patients with schizophrenia seem to improve over time, unlike those with degenerative
neurological disorders such as Alzheimers disease, Huntingtons, or Parkinsons. So far, most
research has focused on the neurological decline associated with schizophreniatypically involving
a loss of brain tissue. Lena Palaniyappan and his colleagues wondered whether there might be
something happening in the brain [that] helps them come to a state of stability. To get at this
question, he and his colleagues performed MRI scans to assess the cortical thickness of 98
schizophrenia patients at various stages of illness. Sure enough, the researchers noted that, while
patients who were less than two years removed from their diagnosis had significantly thinner tissue
than healthy controls, those patients whod had the disease for longer tended to show less deviation
in some brain regions, suggesting some sort of cortical amelioration. Some brain regions are
regaining or normalizing while other brain regions continue to show deficits, Palaniyappan says. To
better understand how the brain changes over time in this disease, it will be necessary to follow
individual patients, taking multiple brain scans over the course of their illness, he says. Palaniyappan
is anxious to understand if the reparatory effect he and his colleagues observed is replicable, and if
so, to study what factors might be contributing. All of Palaniyappans study subjects were on
antipsychotics at the time of their MRI scans, he notes, so whether the same changes would have
been seen without treatment remains unclear. But we never used to think that the schizophrenic
brain can recover, he says. (August 1, 2016).
http://tinyurl.com/hgf4o9m
Neuroscientific Research & Technology
A Simple Phone Game Could Diagnose Autism. REAL CLEAR SCIENCE. Researchers from Jagiellonian
University in Poland and the University of Strathclyde in the United Kingdom hope they have found
a cheap and effective way to diagnose autism spectrum disorder (ASD).They aim to diagnose autism
with a simple game played on a phone or tablet. Prior research has hinted that children diagnosed
with ASD demonstrate distinct patterns in motor control, particularly with their hands. With this in
mind, authors Anna Anzulewicz, Krzysztof Sobota, and Jonathan T. Delafield-Butt recruited 37
children between the ages of three and six years old and matched them with 45 typically-developing
controls of equal age at the same gender ratio. One-by-one, each child was brought into a room, sat
in front of an iPad mini affixed to a table, and instructed to play two basic games for seven minutes
each. In those short and painless moments, the researchers collected heaps of data on the children's
finger movements extracted via inertial sensors and the tablet's touchscreen. As predicted, their
results showed children with autism touched the screen with more impact force and greater pressure
compared to controls. They also swiped faster and tapped the screen more quickly. Utilizing those
touch patterns, the algorithm devised diagnostic criteria for autism based on the children's gameplay.
The criteria successfully identified the autistic children with an impressive 93 percent accuracy. The
study is an exciting proof-of-concept, the researchers say, but more work needs to be done. Next,
they aim to test their approach on many more subjects in order to refine the algorithm's diagnostic
criteria and eliminate potential confounding variables. (August 25, 2016).
http://tinyurl.com/hlyfg7u
Seeing Through to a Mouses Nervous System. NEW YORK TIMES. Neuroscientists have developed a way
to turn an entire mouse, including its muscles and internal organs, transparent while illuminating the
nerve paths that run throughout its body. The process, called uDisco, provides an alternate way for
researchers to study an organisms nervous system without having to slice into sections of its organs
or tissues. It allows researchers to use a microscope to trace neurons from the rodents brain and
BNLC BlurbAugust 2016
Page 5 of 6
spinal cord all the way to its fingers and toes. So far, the technique has been conducted only in mice
and rats, but the scientists think it could one day be used to map the human brain. They also said it
could be particularly useful for studying the effects of mental disorders like Alzheimers disease or
schizophrenia. Researchers often study these diseases by examining thin slices of brain tissue under a
microscope. That is not a good way to study neurons because if you slice the brain, you slice the
network, Dr. Ertrk said. The best way to look at it is to look at the entire organism, not only the
brain lesion but beyond that. We need to see the whole picture. (August 22, 2016).
http://tinyurl.com/hrhaak6
Sleep Deprivation Hits Some Brain Areas Hard. SCIENCE NEWS. Pulling consecutive all-nighters makes
some brain areas groggier than others. Regions involved with problem solving and concentration
become especially sluggish when sleep-deprived, a new study using brain scans reveals. Other areas
appear to be less affected by a mounting sleep debt. Dijk and collaborators at the University of Liege
in Belgium assessed the cognitive function of 33 young adults who went without sleep for 42 hours.
Over the course of this sleepless period, the participants performed some simple tasks testing
reaction time and memory. The sleepy subjects also underwent 12 brain scans during their ordeal
and another scan after 12 hours of recovery sleep. Throughout the study, the researchers also
measured participants levels of the sleep hormone melatonin, which served as a way to track the
hands on their master circadian clocks. Activity in some brain areas, such as the thalamus, a central
hub that connects many other structures, waxed and waned in sync with the circadian clock. But in
other areas, especially those in the brains outer layer, the effects of this master clock were
overridden by the bodys drive to sleep. Brain activity diminished in these regions as sleep debt
mounted, the scans showed. While the brains circadian clock signal is known to originate in a
cluster of nerve cells known as the suprachiasmatic nucleus, it is not clear where the drive to sleep
comes from, says Charles Czeisler, a sleep expert at Harvard Medical School. The need to sleep
might grow as toxic metabolites build up after a days worth of brain activity, or be triggered when
certain regions run out of fuel. (August 11, 2016).
https://www.sciencenews.org/article/sleep-deprivation-hits-some-brain-areas-hard
New Ways To Mass Produce Human Neurons For Studying Neuropsychiatric Disorders. MEDICAL XPRESS.
Scientists from Singapore have streamlined the process of using human stem cells to mass produce
GABAergic neurons (GNs) in the laboratory. GNs are inhibitory neurons that reduce neuronal
activation, and make up roughly 20 per cent of the human brain. They work alongside excitatory
neurons (ENs) to ensure balanced neural activity for normal brain function. The coordinated
interplay between GNs and ENs orchestrate specific activation patterns in the brain, which are
responsible for our behavior, emotions, and higher reasoning. Functional impairment of GNs results
in imbalanced neural activity, thereby contributing to the symptoms observed in many psychiatric
disorders. The availability of high quality, functional human GN populations would facilitate the
development of good models for studying psychiatric disorders, as well as for screening drug effects
on specific populations of neurons. Drugs and small molecules may now be screened at an
unparalleled rate to discover the next blockbuster treatment for autism, schizophrenia, and epilepsy.
(August 4, 2016).
http://medicalxpress.com/news/2016-08-ways-mass-human-neurons-neuropsychiatric.html
Additional permissions may be required for access to some sites/articles. Please feel encouraged
to contact Committee Chair Eric Drogin for assistance.
Page 6 of 6