Neuroscience

Articles and news from the latest research reports.

Posts tagged science

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New formula predicts if scientists will be stars
A new Northwestern Medicine study offers the first formula that accurately predicts a young scientist’s success up to 10 years into the future and could be useful for hiring and funding decisions.
Currently, hiring decisions are made using the instincts and research of search committees. Universities are increasingly complementing this with a measure of the quality and quantity of papers published, called the h index.
But the new formula is more than twice as accurate as the h index for predicting future success for researchers in the life sciences. It considers other important factors that contribute to a scientist’s trajectory including the number of articles written, the current h index, the years since publishing the first article, the number of distinct journals one has published in and the number of articles in high impact journals.

New formula predicts if scientists will be stars

A new Northwestern Medicine study offers the first formula that accurately predicts a young scientist’s success up to 10 years into the future and could be useful for hiring and funding decisions.

Currently, hiring decisions are made using the instincts and research of search committees. Universities are increasingly complementing this with a measure of the quality and quantity of papers published, called the h index.

But the new formula is more than twice as accurate as the h index for predicting future success for researchers in the life sciences. It considers other important factors that contribute to a scientist’s trajectory including the number of articles written, the current h index, the years since publishing the first article, the number of distinct journals one has published in and the number of articles in high impact journals.

Filed under prediction formula scientists neuroscience psychology researchers success career science

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New research from the Hebrew University of Jerusalem shows that a carefully scheduled high-fat diet can lead to a reduction in body weight and a unique metabolism in which ingested fats are not stored, but rather used for energy at times when no food is available.
The results were published in FASEB Journal under the title ‘Timed high-fat diet resets circadian metabolism and prevents obesity.’  Previous research has established that disrupting mammals’ daily rhythms, or feeding them a high-fat diet, disrupts metabolism and leads to obesity. The researchers wanted to determine the effect of combining a high-fat diet with long-term feeding on a fixed schedule. They hypothesized that careful scheduling of meals would regulate the biological clock and reduce the effects of a high-fat diet that, under normal circumstances, would lead to obesity.

New research from the Hebrew University of Jerusalem shows that a carefully scheduled high-fat diet can lead to a reduction in body weight and a unique metabolism in which ingested fats are not stored, but rather used for energy at times when no food is available.

The results were published in FASEB Journal under the title ‘Timed high-fat diet resets circadian metabolism and prevents obesity.’

Previous research has established that disrupting mammals’ daily rhythms, or feeding them a high-fat diet, disrupts metabolism and leads to obesity. The researchers wanted to determine the effect of combining a high-fat diet with long-term feeding on a fixed schedule. They hypothesized that careful scheduling of meals would regulate the biological clock and reduce the effects of a high-fat diet that, under normal circumstances, would lead to obesity.

Filed under circadian rhythms obesity weight loss nutrition neuroscience psychology brain science

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Stem Cells Turn Hearing Back On
Scientists have enabled deaf gerbils to hear again—with the help of transplanted cells that develop into nerves that can transmit auditory information from the ears to the brain. The advance, reported in Nature, could be the basis for a therapy to treat various kinds of hearing loss.
In humans, deafness is most often caused by damage to inner ear hair cells—so named because they sport hairlike cilia that bend when they encounter vibrations from sound waves—or by damage to the neurons that transmit that information to the brain. When the hair cells are damaged, those associated spiral ganglion neurons often begin to degenerate from lack of use. Implants can work in place of the hair cells, but if the sensory neurons are damaged, hearing is still limited.
"Obviously the ultimate aim is to replace both cell types," says Marcelo Rivolta of the University of Sheffield in the United Kingdom, who led the new work. "But we already have cochlear implants to replace hair cells, so we decided the first priority was to start by targeting the neurons."
In the past, scientists have tried to isolate so-called auditory stem cells from embryoid bodie—aggregates of stem cells that have begun to differentiate into different types. But such stem cells can only divide about 25 times, making it impossible to produce them in the quantity needed for a neuron transplant.
Rivolta and his colleagues knew that during embryonic development, a handful of proteins, including fibroblast growth factor (FGF) 3 and 10, are required for ears to form. So they exposed human embryonic stem cells to FGF3 and FGF10. Multiple types of cells formed, including precursor inner-ear hair cells, but they were also able to identify and isolate the cells beginning to differentiate into the desired spiral ganglion neurons. Then, they implanted the neuron precursor cells into the ears of gerbils with damaged ear neurons and followed the animals for 10 weeks. The function of the neurons was restored.
"We’ve only followed the animals for a very limited time," Rivolta says. "We want to follow them long-term now"—both to assess the possibility of increased cancer risk and to observe the long-term function of the new neurons, he adds.
"It’s very exciting," says neuroscientist Mark Maconochie of Sussex University in the United Kingdom, who was not involved in the new work. "In the past, there has been work where someone makes a single hair cell or something that looks like one neuron [from stem cells], and even that gets the field excited. This is a real step change."
The question now, he says, is whether the procedure can be fine-tuned to allow more efficient production of the relay neurons—currently, fewer than 20% of the stem cells treated develop into those ear neurons. By combining growth factors other than FGF3 and FGF10 with the stem cell mix, researchers could harvest even more ear progenitor cells, he hypothesizes.
"The next big challenge will be to do something as effective as this for the hair cells," Maconochie adds.

Stem Cells Turn Hearing Back On

Scientists have enabled deaf gerbils to hear again—with the help of transplanted cells that develop into nerves that can transmit auditory information from the ears to the brain. The advance, reported in Nature, could be the basis for a therapy to treat various kinds of hearing loss.

In humans, deafness is most often caused by damage to inner ear hair cells—so named because they sport hairlike cilia that bend when they encounter vibrations from sound waves—or by damage to the neurons that transmit that information to the brain. When the hair cells are damaged, those associated spiral ganglion neurons often begin to degenerate from lack of use. Implants can work in place of the hair cells, but if the sensory neurons are damaged, hearing is still limited.

"Obviously the ultimate aim is to replace both cell types," says Marcelo Rivolta of the University of Sheffield in the United Kingdom, who led the new work. "But we already have cochlear implants to replace hair cells, so we decided the first priority was to start by targeting the neurons."

In the past, scientists have tried to isolate so-called auditory stem cells from embryoid bodie—aggregates of stem cells that have begun to differentiate into different types. But such stem cells can only divide about 25 times, making it impossible to produce them in the quantity needed for a neuron transplant.

Rivolta and his colleagues knew that during embryonic development, a handful of proteins, including fibroblast growth factor (FGF) 3 and 10, are required for ears to form. So they exposed human embryonic stem cells to FGF3 and FGF10. Multiple types of cells formed, including precursor inner-ear hair cells, but they were also able to identify and isolate the cells beginning to differentiate into the desired spiral ganglion neurons. Then, they implanted the neuron precursor cells into the ears of gerbils with damaged ear neurons and followed the animals for 10 weeks. The function of the neurons was restored.

"We’ve only followed the animals for a very limited time," Rivolta says. "We want to follow them long-term now"—both to assess the possibility of increased cancer risk and to observe the long-term function of the new neurons, he adds.

"It’s very exciting," says neuroscientist Mark Maconochie of Sussex University in the United Kingdom, who was not involved in the new work. "In the past, there has been work where someone makes a single hair cell or something that looks like one neuron [from stem cells], and even that gets the field excited. This is a real step change."

The question now, he says, is whether the procedure can be fine-tuned to allow more efficient production of the relay neurons—currently, fewer than 20% of the stem cells treated develop into those ear neurons. By combining growth factors other than FGF3 and FGF10 with the stem cell mix, researchers could harvest even more ear progenitor cells, he hypothesizes.

"The next big challenge will be to do something as effective as this for the hair cells," Maconochie adds.

Filed under hearing hearing loss auditory cortex deafness implants stem cells neuron neuroscience brain psychology science

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A team of Australian researchers, led by University of Melbourne has developed a genetic test that is able to predict the risk of developing Autism Spectrum Disorder, ASD.
Lead researcher Professor Stan Skafidas, Director of the Centre for Neural Engineering at the University of Melbourne said the test could be used to assess the risk for developing the disorder.
 
“This test could assist in the early detection of the condition in babies and children and help in the early management of those who become diagnosed,” he said.
 
“It would be particularly relevant for families who have a history of Autism or related conditions such as Asperger’s Syndrome,” he said. 
 
Autism affects around one in 150 births and is characterized by abnormal social interaction, impaired communication and repetitive behaviours.

The test correctly predicted ASD with more than 70 per cent accuracy in people of central European descent. Ongoing validation tests are continuing including the development of accurate testing for other ethnic groups.

A team of Australian researchers, led by University of Melbourne has developed a genetic test that is able to predict the risk of developing Autism Spectrum Disorder, ASD.

Lead researcher Professor Stan Skafidas, Director of the Centre for Neural Engineering at the University of Melbourne said the test could be used to assess the risk for developing the disorder.
 
“This test could assist in the early detection of the condition in babies and children and help in the early management of those who become diagnosed,” he said.
 
“It would be particularly relevant for families who have a history of Autism or related conditions such as Asperger’s Syndrome,” he said. 
 

Autism affects around one in 150 births and is characterized by abnormal social interaction, impaired communication and repetitive behaviours.

The test correctly predicted ASD with more than 70 per cent accuracy in people of central European descent. Ongoing validation tests are continuing including the development of accurate testing for other ethnic groups.

Filed under ASD autism brain neuroscience psychology genetic test science

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Scientists discover how the brain ages

Researchers at Newcastle University have revealed the mechanism by which neurons, the nerve cells in the brain and other parts of the body, age.

The research, published in Aging Cell, opens up new avenues of understanding for conditions where the ageing of neurons are known to be responsible, such as dementia and Parkinson’s disease.

The ageing process has its roots deep within the cells and molecules that make up our bodies. Experts have previously identified the molecular pathway that react to cell damage and stems the cell’s ability to divide, known as cell senescence.

However, in cells that do not have this ability to divide, such as neurons in the brain and elsewhere, little was understood of the ageing process. Now a team of scientists at Newcastle University, led by Professor Thomas von Zglinicki have shown that these cells follow the same pathway.

This challenges previous assumptions on cell senescence and opens new areas to explore in terms of treatments for conditions such as dementia, motor neuron disease or age-related hearing loss.

Newcastle University’s Professor Thomas von Zglinicki who led the research said: “We want to continue our work looking at the pathways in human brains as this study provides us with a new concept as to how damage can spread from the first affected area to the whole brain.”

Working with the University’s special colony of aged mice, the scientists have discovered that ageing in neurons follows exactly the same rules as in senescing fibroblasts, the cells which divide in the skin to repair wounds.

DNA damage responses essentially re-program senescent fibroblasts to produce and secrete a host of dangerous substances including oxygen free radicals or reactive oxygen species (ROS) and pro-inflammatory signalling molecules. This makes senescent cells the ‘rotten apple in a basket’ that can damage and spoil the intact cells in their neighbourhood.  However, so far it was always thought that ageing in cells that can’t divide - post-mitotic, non-proliferating cells - like neurons would follow a completely different pathway.

Now, this research explains that in fact ageing in neurons follows exactly the same rules as in senescing fibroblasts.

Professor von Zglinicki, professor of Cellular Gerontology at Newcastle University said: “We will now need to find out whether the same mechanisms we detected in mouse brains are also associated with brain ageing and cognitive loss in humans. We might have opened up a short-cut towards understanding brain ageing, should that be the case.”

Dr Diana Jurk, who did most of this work during her PhD in the von Zglinicki group, said: “It was absolutely fascinating to see how ageing processes that we always thought of as completely separate turned out to be identical.  Suddenly so much disparate knowledge came together and made sense.”

(Source: ncl.ac.uk)

Filed under brain neuron neuroscience psychology aging neurodegenerative diseases science

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As humans, we create life. And we’re all familiar with the idea of artificial intelligence. But what about artificial life? What is it, and why should we care?
Artificial Life is a recently labelled but truly ancient field in which technology is used to imitate biological life. From the earliest stone and clay figurines, to puppets, through hydraulic and pneumatic creations, on to clockwork, through electrical robots and even to flesh, artificial life has a long history that now also extends into the abstract computational realm.
My own interest is as much in the current examples of this phenomenon as in its earliest examples, a prevailing fascination with not only “life-as-we-know-it”, but “life-as-we-have-interpretted-it”.
Since the very earliest days of humankind, we have represented life using whatever technology was available. This has allowed us to observe the traits of life, even our own, in devices over which we have control.
In this way we have embodied our theories of life’s vital principles in artefacts, and tinkered like any Creator from poetry and fiction.
In short, artificial life is central to our attempts to understand who we are.

As humans, we create life. And we’re all familiar with the idea of artificial intelligence. But what about artificial life? What is it, and why should we care?

Artificial Life is a recently labelled but truly ancient field in which technology is used to imitate biological life. From the earliest stone and clay figurines, to puppets, through hydraulic and pneumatic creations, on to clockwork, through electrical robots and even to flesh, artificial life has a long history that now also extends into the abstract computational realm.

My own interest is as much in the current examples of this phenomenon as in its earliest examples, a prevailing fascination with not only “life-as-we-know-it”, but “life-as-we-have-interpretted-it”.

Since the very earliest days of humankind, we have represented life using whatever technology was available. This has allowed us to observe the traits of life, even our own, in devices over which we have control.

In this way we have embodied our theories of life’s vital principles in artefacts, and tinkered like any Creator from poetry and fiction.

In short, artificial life is central to our attempts to understand who we are.

Filed under A-Life artificial life mechanical devices philosophy technology science

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The brain is a notoriously difficult organ to treat, but Johns Hopkins researchers report they are one step closer to having a drug-delivery system flexible enough to overcome some key challenges posed by brain cancer and perhaps other maladies affecting that organ.
In a report published online on August 29 in Science Translational Medicine, the Johns Hopkins team says its bioengineers have designed nanoparticles that can safely and predictably infiltrate deep into the brain when tested in rodent and human tissue.
“We are pleased to have found a way to prevent drug-embedded particles from sticking to their surroundings so that they can spread once they are in the brain,” says Justin Hanes, Ph.D., Lewis J. Ort Professor of Ophthalmology, with secondary appointments in chemical and biomolecular engineering, biomedical engineering, oncology, neurological surgery and environmental health sciences, and director of the Johns Hopkins Center for Nanomedicine.

The brain is a notoriously difficult organ to treat, but Johns Hopkins researchers report they are one step closer to having a drug-delivery system flexible enough to overcome some key challenges posed by brain cancer and perhaps other maladies affecting that organ.

In a report published online on August 29 in Science Translational Medicine, the Johns Hopkins team says its bioengineers have designed nanoparticles that can safely and predictably infiltrate deep into the brain when tested in rodent and human tissue.

“We are pleased to have found a way to prevent drug-embedded particles from sticking to their surroundings so that they can spread once they are in the brain,” says Justin Hanes, Ph.D., Lewis J. Ort Professor of Ophthalmology, with secondary appointments in chemical and biomolecular engineering, biomedical engineering, oncology, neurological surgery and environmental health sciences, and director of the Johns Hopkins Center for Nanomedicine.

Filed under brain neuroscience drug-delivery system nanoparticles psychology science

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Mr. Abicca, a 17-year-old from San Diego, is essentially wearing a robot. His bionic suit consists of a pair of mechanical braces wrapped around his legs and electric muscles that do much of the work of walking. It is controlled by a computer on his back and a pair of crutches held in his arms that look like futuristic ski poles.
Since an accident involving earth-moving equipment three years ago that damaged his spinal cord, Mr. Abicca has been unable to walk on his own. The suit, made by a company called Ekso Bionics, is an effort to change that.

Mr. Abicca, a 17-year-old from San Diego, is essentially wearing a robot. His bionic suit consists of a pair of mechanical braces wrapped around his legs and electric muscles that do much of the work of walking. It is controlled by a computer on his back and a pair of crutches held in his arms that look like futuristic ski poles.

Since an accident involving earth-moving equipment three years ago that damaged his spinal cord, Mr. Abicca has been unable to walk on his own. The suit, made by a company called Ekso Bionics, is an effort to change that.

Filed under artificial limbs bionics exoskeleton neuroscience paraplegics robotics robots spinal cord injury science

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“Doctor” or “Darling”: The Subtle Differences of Speech
Human speech comes in countless varieties: When people talk to close friends or partners, they talk differently than when they address a physician. These differences in speech are quite subtle and hard to pinpoint. In a recent special issue of the journal Frontiers in Human Neuroscience, Johanna Derix, Dr. Tonio Ball, and their colleagues from the Bernstein Center and the University Medical Center in Freiburg report that they were able to tell from brain signals who a person was talking to. This discovery could contribute to the further development of speech synthesizers for patients with severe paralysis.
In contrast to the experimental research common in human neuroscience, the scientists studied natural, non-experimental behavior. Patients who, for medical reasons, had electrodes implanted underneath their skull allowed their brain activity to be recorded during daily life in the hospital. The Freiburg researchers compared data recorded during natural conversations that the patients had with their physicians and their life partners. They found pronounced differences in the anterior temporal lobe, a brain area well known for its significance in social interaction. Several components of neural signals that are detectable on the brain surface can convey such information.
“This study is only the first step towards elucidating the neural basis of human everyday behavior,” explains the neuroscientist and physician Tonio Ball. “Such investigations will become especially important in developing new neurotechnological treatment options for patients with impaired motor and language functions that work in real life situations.” The restoration of speech production becomes necessary in some forms of neurological diseases and chronic paralysis. A computer could synthesize speech for patients suffering from such conditions by using their brain signals. Information on who the patient is addressing could help the device to select the degree of formality – and to prevent it from calling the doctor “darling.”

“Doctor” or “Darling”: The Subtle Differences of Speech

Human speech comes in countless varieties: When people talk to close friends or partners, they talk differently than when they address a physician. These differences in speech are quite subtle and hard to pinpoint. In a recent special issue of the journal Frontiers in Human Neuroscience, Johanna Derix, Dr. Tonio Ball, and their colleagues from the Bernstein Center and the University Medical Center in Freiburg report that they were able to tell from brain signals who a person was talking to. This discovery could contribute to the further development of speech synthesizers for patients with severe paralysis.

In contrast to the experimental research common in human neuroscience, the scientists studied natural, non-experimental behavior. Patients who, for medical reasons, had electrodes implanted underneath their skull allowed their brain activity to be recorded during daily life in the hospital. The Freiburg researchers compared data recorded during natural conversations that the patients had with their physicians and their life partners. They found pronounced differences in the anterior temporal lobe, a brain area well known for its significance in social interaction. Several components of neural signals that are detectable on the brain surface can convey such information.

“This study is only the first step towards elucidating the neural basis of human everyday behavior,” explains the neuroscientist and physician Tonio Ball. “Such investigations will become especially important in developing new neurotechnological treatment options for patients with impaired motor and language functions that work in real life situations.” The restoration of speech production becomes necessary in some forms of neurological diseases and chronic paralysis. A computer could synthesize speech for patients suffering from such conditions by using their brain signals. Information on who the patient is addressing could help the device to select the degree of formality – and to prevent it from calling the doctor “darling.”

Filed under brain neuroscience speech brain signals psychology behavior science

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