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Showing posts with label Activity. Show all posts
Showing posts with label Activity. Show all posts

Neuroscientists: Brain activity may mark beginning of memories

1:30 PM Posted by Rhoda , , , ,

Using lab rats on a circular track, James Knierim, professor of neuroscience in the Zanvyl Krieger Mind/Brain Institute at Johns Hopkins, and a team of brain scientists noticed that the rats frequently paused to inspect their environment with head movements as they ran. The scientists found that this behavior activated a place cell in their brain, which helps the animal construct a cognitive map, a pattern of activity in the brain that reflects the animal's internal representation of its environment.

In a paper recently published by the journal Nature Neuroscience, the researchers state that when the rodents passed that same area of the track seconds later, place cells fired again, a neural acknowledgement that the moment has imprinted itself in the brain's cognitive map in the hippocampus.

The hippocampus is the brain's warehouse for long- and short-term processing of episodic memories, such as memories of a specific experience like a trip to Maine or a recent dinner. What no one knew was what happens in the hippocampus the moment an experience imprints itself as a memory.

"This is like seeing the brain form memory traces in real time," said Knierim, senior author of the research. "Seeing for the first time the brain creating a spatial firing field tied to a specific behavioral experience suggests that the map can be updated rapidly and robustly to lay down a memory of that experience."

A place cell is a type of neuron within the hippocampus that becomes active when an animal or human enters a particular place in its environment. The activation of the cells helps create a spatial framework much like a map, that allows humans and animals to know where they are in any given location. Place cells can also act like neural flags that "mark" an experience on the map, like a pin that you drop on Google maps to mark the location of a restaurant.

"We believe that the spatial coordinates of the map are delivered to the hippocampus by one brain pathway, and the information about the things that populate the map, like the restaurant, are delivered by a separate pathway," Knierim said. "When you experience a new item in the environment, the hippocampus combines these inputs to create a new spatial marker of that experience."

In the experiments, researchers placed tiny wires in the brains of the rats to monitor when and where brain activity increased as they moved along the track in search of chocolate rewards. About every seven seconds, the rats stopped moving forward and turned their heads to the perimeter of the room as they investigated the different landmarks, behavior called "head-scanning."

"We found that many cells that were previously silent would suddenly start firing during a specific head-scanning event," Knierim said. "On the very next lap around the track, many of these cells had a brand new place field at that exact same location and this place field remained usually for the rest of the laps. We believe that this new place field marks the site of the head scan and allows the brain to form a memory of what it was that the rat experienced during the head scan."

Knierim said the formation and stability of place fields and the newly activated place cells requires further study. The research is primarily intended to understand how memories are formed and retrieved under normal circumstances, but it could be applicable to learning more about people with brain trauma or hippocampal damage due to aging or Alzheimer's.

"There are strong indications that humans and rats share the same spatial mapping functions of the hippocampus, and that these maps are intimately related to how we organize and store our memories of prior life events," Knierim said. "Since the hippocampus and surrounding brain areas are the first parts of the brain affected in Alzheimer's, we think that these studies may lend some insight into the severe memory loss that characterizes the early stages of this disease."



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Physical activity is beneficial for late life insight

8:28 PM Posted by Rhoda , , ,

Modifiable risk factors for dementia have proposed were, but further refinement of this information is essential for effective preventive intervention on high-risk groups targeted. Leisure time of physical activity (LTPA) especially in General and heart and circulatory health is a particularly important due to its larger impact on health. Previous studies led inconsistent evidence for the association between LTPA and dementia, possibly due to the short connection time, intensity of physical activity or population characteristics such as gender, body mass index, age or genetic risk factors of dementia.

Current knowledge of cardiovascular risk factors, aging and dementia (CAIDE) frequency study showed that those physical activity (LTPA) at least twice involved the leisure per week had lower risk of dementia compared to less active individuals. Although this protective effect in the entire study population, regardless of gender or genetic risk factors, were observed, they were particularly strong in overweight and obese individuals.

Always physically active after midlife can reduce the risk of dementia

More to stay physically active, or increasingly active mid life overweight obese at midlife can also reduce the dementia risk, especially in people, or. The results were not by socio-economic background, age, gender, genetic risk factors, obesity, weight loss, General State of health or work-related physical activity explains.

These results indicate that the window of opportunity for physical activity can extend interventions for the prevention of dementia from mid-life to older children. Results of ongoing studies, as the Finnish multicenter study can give more detailed information about the type of FINGER sink intensity and duration of physical activity interventions that cognitive can be used to avoid late-life.

CAIDE are participants from four separate and independent population-based samples in 1972, 1977, 1982 and 1987 in the North Karelia Project and FINMONICA study. It was at the beginning of the study 50 years. 1432 this study included participants from the region of Kuopio and Joensuu, the cognitive tests in 1998 and 2005-2008 visited. Survivor or selection into account bias, the analyses also among these were 3242 North Karelia/FINMONICA project participants, came the diagnoses from registers of Kuopio and Joensuu, but not the cognitive reviews with dementia conducted.



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Executed, heart-circulatory activity in young adulthood can keep thinking skills in the middle ages

Keep young adults who are running or other cardio-fitness activities can participate in their memory and thinking skills in middle age, according to a new study published in the April 2, 2014, online issue of Neurology®, the medical journal of the American Academy of Neurology. Middle Ages was defined as age 43 to 55.

"Many studies show the benefits to the brain or the good health of the heart," said study author David r. Jacobs, Jr., PhD, with the University of Minnesota in Minneapolis. "This is an important study that health benefits of cardio-fitness activities like swimming, cycling or cardio-fitness courses run, should remind young adult brain."

Cardio fitness is a measure of how well your body exercise transports oxygen to your muscles, and how well your muscles while absorb the oxygen.

For the study, 2,747 healthy people with an average age of 25 treadmill were tests in the first year of the study and then again 20 years later. Cognitive tests 25 years after the beginning of the study tasks measured psychomotor speed (the relationship between thinking skills and physical activity), verbal memory and executive function.

Had the treadmill test, which corresponded to a heart cardiovascular stress test, participants walked or ran as the speed and slope increases, until she could be discontinued, or symptoms such as shortness of breath. Participants at the first trial lasted an average of 10 minutes on the treadmill. Twenty years later, the number of an average 2.9 minutes decreased. For each additional minute people on the treadmill at the first test completed reminded 0.12 more words right on the memory test or 15 words and correctly replaced 0.92 more numbers with meaningless symbols in the test or psychomotor speed 25 years later also adjusted for other factors such as smoking, diabetes and high cholesterol.

People who had smaller declines in their time on the treadmill test 20 years later concluded were rather reduced on the exam as more powerful had larger executive function. In particular they could state more properly printing ink (written in green ink, the correct answer was for the word "yellow", "green").

"These changes were significant, and while they may be modest, they were greater than the effect of one year of aging," Jacobs said. "Other studies in older patients have shown that these tests to develop among the strongest predictors of dementia in the future." "One study showed that each additional word reminded the memory test with an 18 - percent decrease in the risk of developing dementia after 10 years."

"These results are likely to help us identify and therefore used to prevent or treat high risk of developing dementia", said Jacobs.

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NIH-funded Atlas Details Gene Activity of the Prenatal Human Brain

12:07 PM Posted by Rhoda , , , , , ,

A comprehensive three-dimensional atlas of the developing human brain that incorporates gene activity along with anatomical reference atlases and neuroimaging data has released its first major report online today in Nature. This National Institutes of Health (NIH)-funded resource, freely available to the public, enables researchers to answer questions related to the early roots of brain-based disorders such as autism and schizophrenia.

BrainSpan

The recently created BrainSpan Atlas of the Developing Human Brain incorporates gene activity or expression (right) along with anatomical reference atlases (left) and neuroimaging data (not shown) of the mid-gestational human brain. In this figure, the location and expression level of the gene TGIF1 is shown of a brain from 21 weeks post-conception. Knowledge of where and when particular genes are expressed will facilitate research surrounding human brain development and disease.

This big science endeavor, which highlights the transcriptome — when and where genes are turned on in the brain — and anatomy of the human brain during mid-term pregnancy, was undertaken at the Allen Institute for Brain Science in Seattle. It is the first installment of a consortium project funded by the National Institute of Mental Health (NIMH), part of the NIH, called the BrainSpan Atlas of the Developing Human Brain, which aims to profile gene activity throughout the course of brain development.

“Many neuropsychiatric diseases are likely the result of abnormal brain development during prenatal life,” said lead author Ed Lein, Ph.D., of the Allen Institute. “An anatomically precise molecular atlas of the brain during this time period is a first step to understanding how the human brain develops normally and what can go wrong.”

Although animal studies have provided invaluable insights in the basic mechanisms of brain function, there are limitations that make studies based on human tissues, which are very difficult to obtain, incredibly important. One key area is the neocortex, the outermost brain region involved in higher functions such as action and thought. The neocortex is smooth in rodents; in humans and non-human primates, it is much more complexly organized, elaborately folded into grooves and wrinkles called sulci and gyri.

Further differences in developmental compartments of this area exist between humans and non-human primates. The aim of this highly detailed atlas was to analyze all genes at this level of granularity, allowing meaningful analysis of the molecular underpinnings of human cortical development. Many psychiatric disorders show altered gene activity in the cortex, possibly highlighting changes that occurred during development of this region.

Lein and other researchers studied four donated, intact, high-quality human prenatal brains from preterm stillbirths — two from 15–16 weeks and two from 21 weeks post-conception – as a framework for their atlas. Contributing labs provided data from a variety of genomic and imaging techniques.

The BrainSpan Atlas aims to inspire new hypotheses regarding human brain development, and has already led to some surprising findings. For example, the study authors found significant differences between mouse and human brains in the subplate zone, a developmentally transient structure critical for proper cortical development. On the other hand, the researchers expected to find a unique molecular signature for the outer portion of the subventricular zone, an area which is not found in mice and which contains a hugely expanded pool of neuronal stem cells that give rise to our greatly expanded neocortex. Surprisingly, despite its much larger size, no significant differences were found between this zone and the inner portion of this layer that is conserved from mouse to human.

“The BrainSpan Atlas becomes very powerful when one can understand where and when a particular gene is used — for instance, is it active in precursor cells or in the neurons derived from them?” said Lein, who gave the example that autism candidate genes are expressed very early in in the cortex. Knowledge of the time and location of these genes may lead to future treatment targets and early interventions for this brain disorder, he added.

The BrainSpan Atlas already is making inroads in research surrounding human brain development and disease.

“Although the many genes associated with autism and schizophrenia don’t show a clear relationship to each other in the adult brain, the BrainSpan Atlas reveals how these diverse genes are connected in the developing brain,” said NIMH Director Thomas R. Insel, M.D. “Findings of what goes on early in the prenatal brain can lead to the development of biomarkers for diagnosing brain disorders and for matching patients to treatment options most likely to be successful.

“This atlas is a clear example of the progress that can be made when the public and private sectors work together,” Insel said. “On this first anniversary of the BRAIN Initiative, we are encouraged to see the impact the BrainSpan Atlas is already making on brain research.”

The resource is freely available for viewing, searching, and data mining for gene activity patterns as part of the BrainSpan Atlas of the Developing Human Brain Developing Human Brain External Web Site Policy, and can also be found via the Allen Brain Atlas data portal Allen Brain Atlas data portal External Web Site Policy.

The mission of the NIMH is to transform the understanding and treatment of mental illnesses through basic and clinical research, paving the way for prevention, recovery, and cure. For more information, visit http://www.nimh.nih.gov.

About the National Institutes of Health (NIH): NIH, the nation's medical research agency, includes 27 Institutes and Centers and is a component of the U.S. Department of Health and Human Services. NIH is the primary federal agency conducting and supporting basic, clinical, and translational medical research, and is investigating the causes, treatments, and cures for both common and rare diseases. For more information about NIH and its programs, visit www.nih.gov.

NIH...Turning Discovery Into Health®

Reference

Transcriptional landscape of the prenatal human brain. Miller JA, Ding S-L, Sunkin SM, Smith KA, Ng L, Szafer A, Ebbert A, Riley ZL, Aiona K, Arnold JM, Bennet C, Bertagnolli D, Brouner K, Butler S, Caldejon S, Carey A, Cuhaciyan C, Dalley RA, Dee N, Dolbeare TA, Facer BAC, Fend D, Fliss TP, Gee G, Goldy J, Gourley L, Gregor BW, Gu G, Howard RE, Jochim JM, Kuan CL, Lau C, Lee C-K, Lee F, Lemon TA, Lesnar P, McMurray B, Mastan N, Mosqueda NF, Naluai-Cecchini T, Ngo N-K, Nyhus J, Oldre A, Olson E, Parente J, Parker PD, Parry SE, Player AS, Pletikos M, Reding M, Royall JJ, Roll K, Sandman D, Sarreal M, Shapouri S, Shapovalova NV, Shen EH, Sjoquist N, Slaughterbeck CR, Smith M, Sodt AJ, Williams D, Zöllei L, Fischl B, Gerstein MB, Geschwind DH, Glass IA, Hawrylycz MJ, Hevner RF, Huang H, Jones AR, Knowles JA, Levitt P, Phillips JW, Sestan N, Wohnoutka P, Dang C, Bernard A, Hohmann JG, Lein ES. Nature, April 2, 2014.

Grant number: MH089921

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