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<title>AgnosticWeb.com - brain plasticity: how adults learn a language</title>
<link>https://agnosticweb.com/</link>
<description>An Agnostic&#039;s Brief Guide to the Universe</description>
<language>en</language>
<item>
<title>brain plasticity: how adults learn a language (reply)</title>
<content:encoded><![CDATA[<p>Certainly not like kids and it takes both sides:</p>
<p><a href="https://cosmosmagazine.com/health/body-and-mind/how-adults-learn-a-new-language/?utm_source=Cosmos+-+Master+Mailing+List&amp;utm_campaign=a8596dfaad-RSS_EMAIL_CAMPAIGN&amp;utm_medium=email&amp;utm_term=0_3f5c04479a-a8596dfaad-180344213&amp;mc_cid=a8596dfaad&amp;mc_eid=b072569e0b">https://cosmosmagazine.com/health/body-and-mind/how-adults-learn-a-new-language/?utm_so...</a></p>
<p>&quot;Learning languages is a breeze for young children, but once that window of opportunity closes it becomes notoriously difficult. Now, Spanish scientists have shed more light on how we get around this.</p>
<p>&quot;While it’s thought that language is specialised in the left side of the brain, the researchers found that the right side also helps out when learning a new language as an adult, providing further evidence of the brain’s remarkable flexibility.</p>
<p>“'The left hemisphere is widely considered to be more or less hardwired for language, but there is plenty of evidence that it is not quite as simple as that,” says Kshipra Gurunandan from the Basque Centre on Cognition, Brain and Language, lead author of a paper published in the Journal of Neurology.</p>
<p>***</p>
<p>“'Reading, listening and speaking activate common ‘language’ regions in the brain,” Gurunandan explains, “but they also involve the visual, auditory and motor regions, respectively, and we wanted to study the consequences for language learning.”</p>
<p>&quot;To test this, they recruited 48 healthy native Spanish speakers aged 17 to 60 from language schools. The study consisted of two experiments: one compared basic and advanced level learners of the Basque language and the second looked at Spanish-Basque natives before and after a three-month language course in intermediate-level English.</p>
<p>***</p>
<p>&quot;While speaking primarily activated language regions in the left hemisphere, results showed much greater variation in which hemisphere was activated while reading and, to a lesser degree, listening. The switch was most apparent in more advanced learners.</p>
<p>&quot;This suggests reading and listening are more flexible throughout adulthood, which makes them easier to learn as people become more proficient, according to Gurunandan. It could also explain why adults can often understand a new language but struggle to speak it to the same skill level.</p>
<p>&quot;It’s striking, she adds, that the switch from a native language to a new one that’s being actively learned recruits the brain’s left hemisphere but lateralises to both hemispheres with greater proficiency, which might also help people separate the two languages.&quot;</p>
<p>Comment: Makes sense since language involves eyes and ears.</p>
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<link>https://agnosticweb.com/index.php?id=36828</link>
<guid>https://agnosticweb.com/index.php?id=36828</guid>
<pubDate>Wed, 11 Nov 2020 00:09:52 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<title>brain plasticity: almost no optical cortex but he sees! (reply)</title>
<content:encoded><![CDATA[<p>An amazing case report of a seven year old with good vision but missing most of his optical cortex:</p>
<p><a href="https://medicalxpress.com/news/2017-12-mysterious-case-boy-visual-cortex.html">https://medicalxpress.com/news/2017-12-mysterious-case-boy-visual-cortex.html</a></p>
<p>&quot;The boy, the researchers told the audience, suffered major damage to his visual cortex as a result of medium-chain acyl-Co-A dehydrogenase deficiency at just two weeks old—a rare condition that results in severe damage to nerve cells due to an inability to convert some types of fats into energy. That meant the boy, who the researchers referred to as B.I., wound up without most of his visual cortex, a condition that for most people would result in cortical blindness. Cortical blindness is an odd condition in which the brain can still receive visual input, but cannot process what is seen, leaving the person with the sensation of sight without being able to actually see. But oddly enough, B.I. can see almost as well as any other boy his age.</p>
<p>&quot;B.I. caught the attention of the team at Monash due to his medical history—intrigued, they sought to test the boy and his vision, and find out why he could see despite his brain injury.</p>
<p>&quot;In testing B.I.'s vision, the researchers found that he was somewhat near-sighted but was otherwise fine, except for the occasional lapse when faced with false-colored objects such as a blue banana. He could play soccer, for example, and video games, and make out the difference in emotions on a person's face.</p>
<p>&quot;To find out why the boy could still see, the researchers observed him in an MRI machine and watched what happened as he processed images. By focusing on the middle temporal visual area, the researchers found an enlarged visual pathway of neural fibers that ran through two areas on the back of the brain where the visual cortex resides. One of the areas called the pulvinar is normally involved in managing sensory signals, the other, called the middle temporal area, is normally involved in detecting motion. In B.I.'s case, the pathway had grown larger than normal to allow it to do the work that his visual cortex was supposed to do, allowing him to see—a form of neuroplasticity. </p>
<p>An image of his brain is shown here:</p>
<p><a href="https://www.newscientist.com/article/2155639-a-boy-is-missing-the-vision-bit-of-his-brain-but-can-still-see/">https://www.newscientist.com/article/2155639-a-boy-is-missing-the-vision-bit-of-his-bra...</a></p>
<p>Comment: The amazing ability of  the brain's neuroplasticity is shown by this boy's brain, by adapting a totally new area to receive the signals and interpret them.</p>
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<link>https://agnosticweb.com/index.php?id=27023</link>
<guid>https://agnosticweb.com/index.php?id=27023</guid>
<pubDate>Sat, 09 Dec 2017 00:48:13 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<title>brain plasticity: blind use optical cortex for language (reply)</title>
<content:encoded><![CDATA[<p>New research shows this:</p>
<p><a href="https://www.newscientist.com/article/2147696-blind-people-repurpose-the-brains-visual-areas-for-language/">https://www.newscientist.com/article/2147696-blind-people-repurpose-the-brains-visual-a...</a></p>
<p>&quot;People who are blind use parts of their brain that normally handle for vision to process language, as well as sounds – highlighting the brain’s extraordinary ability to requisition unused real estate for new functions.</p>
<p>&quot;Neurons in the part of the brain normally responsible for vision synchronise their activity to the sounds of speech in blind people, says Olivier Collignon at the Catholic University of Louvain (UCL) in Belgium. “It’s a strong argument that the organisation of the language system… is not constrained by our genetic blueprint alone,” he says.</p>
<p>&quot;The finding builds on previous research showing that the parts of the brain responsible for vision can learn to process other kinds of information, including touch and sound, in people who are blind.</p>
<p>***</p>
<p>&quot;While they were being scanned, groups of sighted and blind volunteers were played three clips from an audio book. One recording was clear and easy to understand; another was distorted but still intelligible; and the third was modified so as to be completely incomprehensible.</p>
<p>&quot;Both groups showed activity in the brain’s auditory cortex, a region that processes sounds, while listening to the clips. But the volunteers who were blind showed activity in the visual cortex, too.</p>
<p>&quot;While they were being scanned, groups of sighted and blind volunteers were played three clips from an audio book. One recording was clear and easy to understand; another was distorted but still intelligible; and the third was modified so as to be completely incomprehensible.</p>
<p>&quot;Both groups showed activity in the brain’s auditory cortex, a region that processes sounds, while listening to the clips. But the volunteers who were blind showed activity in the visual cortex, too.</p>
<p>&quot;The blind volunteers also appeared to have neurons in their visual cortex that fired in sync with speech in the recording – but only when the clip was intelligible. This suggests that these cells are vital for understanding language, says Collignon.</p>
<p>&quot;The visual cortex contains the relevant architecture, he says, to go from sound processing to language comprehension.</p>
<p>“'The new finding is perhaps not surprising, but it is groundbreaking,” says Daniel-Robert Chebat at the Israeli Ariel University in the West Bank. “It shows that these parts of the brain are not only recruited [to receive new kinds of input], but can adapt and modulate their response.”</p>
<p>&quot;The discovery highlights how malleable our brains are, says Collignon, but he thinks there may be a limit to this. It’s unlikely that any part of the brain can eventually learn any function, he says. Instead, there may be a set of rules, laid down in our genes, which brain regions can follow.&quot;</p>
<p>Comment: This is further evidence of how the human brain can modify its functional areas. It allows a highly complex organ to adapt to almost any function presented to it. The brain enlarged and developed this capacity over an eight million year period, rather speedily for evolution. It development looks designed and driven.</p>
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<link>https://agnosticweb.com/index.php?id=26286</link>
<guid>https://agnosticweb.com/index.php?id=26286</guid>
<pubDate>Mon, 18 Sep 2017 22:40:38 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<item>
<title>brain plasticity: molecular controls (reply)</title>
<content:encoded><![CDATA[<p>Definite protein molecular controls have been found:</p>
<p><a href="https://medicalxpress.com/news/2017-07-neurons-everyday-life.html">https://medicalxpress.com/news/2017-07-neurons-everyday-life.html</a></p>
<p>&quot;Researchers from King's College London have discovered a molecular mechanism that enables neuronal connections to change through experience, thus fuelling learning and memory formation.</p>
<p>&quot;One of the most remarkable features of our brain is its ability to sense and interpret the complex environment of everyday life. To accomplish this, brain circuits undergo a process that involves experience-dependent plasticity, a fundamental mechanism through which the nervous system adapts to sensory experience and which is at the root of our capacity to learn as well as encode and retain memories. </p>
<p>&quot;Previous studies have shown that a special group of neurons present in the cerebral cortex called PV+ interneurons (a population of neurons that communicate with each other through deactivating chemical and electrical signals and express a protein called parvalbumin), are able to change in response to stimulus from the environment. However, until now the cellular and molecular mechanisms regulating this adaptability were largely unknown.</p>
<p>&quot;In their new study, the multidisciplinary team of researchers ...found that this adaptability is shaped by a specific protein called Brevican. Moreover, loss of this protein leads to deficits in short-term spatial memory, the part of memory responsible for remembering different locations as well as spatial relations between objects.</p>
<p>&quot;Most PV+ interneurons are wrapped by a mesh of proteins called perineural nets and several studies have shown that these proteins play a critical role in the regulation of experience-dependent plasticity, learning and memory. However, the mechanisms through which these proteins mediate this process remained a mystery. In this new study, the researchers found that one of these proteins called Brevican, which is also one of the most abundant proteins found in the brain, influences neuronal plasticity, orchestrating a dedicated molecular program in response to changes from the environment. The researchers also found that this protein shapes the intrinsic properties of PV+ interneurons and sculpts their connections to other neurons. These novel findings show that Brevican is dynamically regulated by experiences coming from the environment and is fundamentally required for spatial working memory and short-term memories.</p>
<p>&quot;'Perineuronal net proteins regulate cortical plasticity by acting on interneurons. When we identified some of the mechanisms underlying this regulation, I was amazed by how a single protein can act as an activity sensor, orchestrate such a complex molecular program and simultaneously influence several key cellular processes', said Dr Emilia Favuzzi.&quot;</p>
<p>Comment: It is one thing to have brains appear as the result of evolution, but this mechanism is highly complex, could not have happened through  chance. It must be designed.</p>
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<link>https://agnosticweb.com/index.php?id=25660</link>
<guid>https://agnosticweb.com/index.php?id=25660</guid>
<pubDate>Thu, 13 Jul 2017 22:06:50 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<title>brain plasticity: uses new neurons from stem cells (reply)</title>
<content:encoded><![CDATA[<p>This happens all through life:</p>
<p><a href="https://www.sciencedaily.com/releases/2017/06/170616102136.htm">https://www.sciencedaily.com/releases/2017/06/170616102136.htm</a></p>
<p>&quot;Stem cells persist in the adult mammalian brain and generate new neurons throughout life. A research group ...reports in the current issue of &quot;Science&quot; that long-distance brain connections can target discrete pools of stem cells in their niche and stimulate them to divide and produce specific subtypes of olfactory bulb neurons. This allows the &quot;on-demand&quot; generation of particular types of neurons in the adult brain.</p>
<p>&quot;Our brain generates new neurons throughout life. A diversity of stimuli promotes stem cells in their niche to form neurons that migrate to their place of action. In an animal model Prof. Fiona Doetsch's team has now been able to show that feeding-related neurons in the hypothalamus, a brain control center for many physiological functions, stimulate a distinct type of stem cell to proliferate and mature into specific nerve cells in response to feeding.</p>
<p>&quot;Stem cells reside in only a few areas of the brain. The largest reservoir is the subventricular zone, where quiescent stem cells lie closely packed together. Signals from the environment can trigger stem cells to start dividing. The stem cells in the subventricular zone supply the olfactory bulb with neurons. In rodents, almost 100,000 new neurons migrate from the stem cell niche to the olfactory bulb each day. Olfactory stimuli reaching the nose are processed in the olfactory bulb and the information is then sent to other brain regions. The closely interwoven network of diverse olfactory bulb neurons is important for distinguishing odors.</p>
<p>&quot;Each stem cell has its own identity, depending on its location in the subventricular zone. While new neurons are continuously generated, whether niche signals act to control different pools of stem cells is unknown. &quot;We have uncovered a novel long-distance and regionalized connection in the brain between the hypothalamus and the subventricular zone, and show that physiological states such as hunger and satiety can regulate the recruitment of specific pools of stem cells and in turn the formation of certain neuron subtypes in the olfactory bulb,&quot; explains Doetsch. When the animals fasted, the activity of the nerve cells in the hypothalamus decreased and with it also the rate of proliferation in the targeted stem cell population. This returns to normal levels when the animals feed again. The division of stem cells can be controlled by changing the activity of feeding-related neurons.</p>
<p>&quot;The researchers reported further that the targeted stem cell subpopulation gives rise to deep granule cells in the olfactory bulb, which may provide a substrate for adaptive responses to the environment. The results of the study raise the exciting possibility that neural circuits from diverse brain regions can regulate different pools of stem cells in response to various stimuli and states.&quot;</p>
<p>Comment: The brain is precisely able to adapt to the animal or human activity. As an example, in the olfactory bulb new neurons are needed as odors are experienced and remembered. I assume this ability began when the first true brains formed earlier in evolution. The brain is more changeable than liver, kidney, lung, etc. It has to have this capacity in order to accommodate developing personality and thought processes handled through consciousness.</p>
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<link>https://agnosticweb.com/index.php?id=25442</link>
<guid>https://agnosticweb.com/index.php?id=25442</guid>
<pubDate>Fri, 16 Jun 2017 23:52:03 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<item>
<title>brain plasticity: develops modules of control in kids (reply)</title>
<content:encoded><![CDATA[<p>A study of adolescents shows development of controls throughout the brain, not just the frontal cortex:</p>
<p><a href="https://cosmosmagazine.com/biology/networks-form-as-brains-develop">https://cosmosmagazine.com/biology/networks-form-as-brains-develop</a></p>
<p>&quot;As children grow up – moving through adolescence and into young adulthood – their ability to control their impulses, stay organised and make decisions improves dramatically.</p>
<p>&quot;According to a new study published in Current Biology, those improvements result from the development of distinct networks within the brain.<br />
 <br />
&quot;In adolescence the brain networks become increasingly divided into distinct parts, called modules. Modules are parts of a network that are tightly connected to each other, and less connected to other parts of the network. The new evidence shows that the degree to which executive function develops during this period in part depends on the degree to which these modules are present. </p>
<p>&quot;Researcher Graham Baum says the results show the brain uses “specialized units that can work together to support advanced cognitive abilities'”.</p>
<p>Full story:  <a href="http://www.cell.com/current-biology/fulltext/S0960-9822(17)30496-7">http://www.cell.com/current-biology/fulltext/S0960-9822(17)30496-7</a></p>
<p>Summary: &quot;The human brain is organized into large-scale functional modules that have been shown to evolve in childhood and adolescence. However, it remains unknown whether the underlying white matter architecture is similarly refined during development, potentially allowing for improvements in executive function. In a sample of 882 participants (ages 8–22) who underwent diffusion imaging as part of the Philadelphia Neurodevelopmental Cohort, we demonstrate that structural network modules become more segregated with age, with weaker connections between modules and stronger connections within modules. Evolving modular topology facilitates global network efficiency and is driven by age-related strengthening of hub edges present both within and between modules. Critically, both modular segregation and network efficiency are associated with enhanced executive performance and mediate the improvement of executive functioning with age. Together, results delineate a process of structural network maturation that supports executive function in youth.&quot;</p>
<p>Comment: This study shows the intimate interconnection of our developing 'self' and how our brain changes to accommodate the integration of experience and responses. These changes are automatic bot also cooperative as personality develops. We do develop ourselves. Consciousness and personality are immaterial, but based on the plasticity of the brain to fully develop and experience.</p>
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<link>https://agnosticweb.com/index.php?id=25255</link>
<guid>https://agnosticweb.com/index.php?id=25255</guid>
<pubDate>Fri, 26 May 2017 14:05:27 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<title>brain plasticity: how it can br speedy (reply)</title>
<content:encoded><![CDATA[<p>Neurons store extra RNA so newly needed proteins to respond rapidly can be made on the quick:</p>
<p><a href="https://www.sciencedaily.com/releases/2016/12/161221125505.htm">https://www.sciencedaily.com/releases/2016/12/161221125505.htm</a></p>
<p>&quot;Neurons in the brain store RNA molecules -- DNA gene copies -- in order to rapidly react to stimuli. This storage dramatically accelerates the production of proteins. This is one of the reasons why neurons in the brain can adapt quickly during learning processes. </p>
<p>***</p>
<p>&quot;The research group of Prof. Peter Scheiffele at the Biozentrum, University of Basel, has demonstrated that neurons store a reserve stock of RNA molecules, copies of the DNA, in the cell's nucleus. These RNA molecules form the blueprint for new proteins. After a neuronal stimulus, the stored RNA molecules are mobilized in order to adjust the function of the neuron. The process of RNA synthesis (DNA copying) is very slow, especially for large genes. Thus, this newly uncovered mechanism for mobilization of stored RNAs saves time and provides new insights regarding the fast adaptation of the brain during learning processes.</p>
<p>&quot;The RNA blueprint for proteins is produced by a sophisticated copying process: First, a basic RNA copy of the DNA is generated. From this copy, individual sections, so-called introns, are subsequently cut out to provide a finalized blueprint for the production of a specific protein. This process is called RNA splicing.</p>
<p>&quot;So far, it was assumed, that neuronal stimuli trigger the complete process for the production of new RNA molecules. However, the team of Peter Scheiffele now discovered that neurons in the brain pre-manufacture certain immature RNA copies which are only partially spliced. These RNA molecules still contain some introns and are stored in the cell nucleus. Signals induced by neuronal stimulation trigger the splicing completion of the immature RNA molecules.</p>
<p>&quot;'The copying process of the DNA, the so-called transcription, is already finalized in advance by the neurons. Hence, mature RNA molecules can be produced within minutes,&quot; explains Oriane Mauger, the first author.</p>
<p>&quot;For large genes, the production of the initial version of the RNAs itself takes dozens of hours. &quot;The fact that the RNA molecules are already available in an immature form and only need to be completed, shortens the whole process to a few minutes,&quot; says Mauger. &quot;Since the transcription is very time-consuming, the storage of RNA means a significant time saving. This enables neurons to quickly adapt their function.&quot;</p>
<p>&quot;'This study reveals a completely new regulatory mechanism for the brain,&quot; declares Scheiffele. &quot;The results provide us with a further explanation of how neurons steer rapid plasticity processes.&quot;</p>
<p>Comment: Quickly learning new habits is necessary for survival in the wild. I assume this is an old mechanism in evolution, but the article does not comment. From that standpoint the process may have been implanted in the first brains since rapid adaptation is vital for survival. Saltation?</p>
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<link>https://agnosticweb.com/index.php?id=23803</link>
<guid>https://agnosticweb.com/index.php?id=23803</guid>
<pubDate>Thu, 22 Dec 2016 16:56:26 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<item>
<title>brain plasticity: early development mechanics (reply)</title>
<content:encoded><![CDATA[<p>Mouse brain studies show how new neurons are developed in young mice and presumed to be present in humans:</p>
<p><a href="http://www.the-scientist.com/?articles.view/articleNo/47364/title/How-Experience-Shapes-Adult-Neurogenesis/&amp;utm_campaign=NEWSLETTER_TS_The-Scientist-Daily_2016&amp;utm_source=hs_email&amp;utm_medium=email&amp;utm_content=36656261&amp;_hsenc=p2ANqtz-9RcnLBB5SaByJJTXGPWtKRd7Ag00IR8qrJEyBTzj957RLVRAcivaJsxebcTlJF5Yiw9hCYRacp8zyjE2aV1ZEWfc_ajQ&amp;_hsmi=36656261">http://www.the-scientist.com/?articles.view/articleNo/47364/title/How-Experience-Shapes...</a></p>
<p>&quot;Newly made cells in the brains of mice adopt a more complex morphology and connectivity when the animals encounter an unusual environment than if their experiences are run-of-the-mill. Researchers have now figured out just how that happens. According to a study published today (October 27) in Science, a particular type of cell—called an interneuron—in the hippocampus processes the animals’ experiences and subsequently shapes the newly formed neurons.</p>
<p>***</p>
<p>&quot;Newborn dentate gyrus neurons, which are called granule cells, take six weeks to fully develop and integrate into the mouse brain’s existing neural networks, said Schinder. To examine these cells’ development, the team labeled newborn granule cells with red fluorescent protein in the brains of mice and then either left the animals in their regular cages (controls) or exposed them to enriched environments—cages with tunnels and other unusual objects—for different 48 hour periods. Three weeks after the new cells were labeled, the team examined their morphology and activity.</p>
<p>&quot;The researchers found that in animals who had been exposed to the enriched environment during a particular period (9 to 11 days after labeling), the young granule cells had longer dendrites with evidence of increased connections with other neurons. Specifically, these cells had a greater number of dendritic spines, the sites of incoming synapses, and more detectable electrical inputs.</p>
<p>&quot;Granule cells receive different inputs from surrounding neurons at different stages of their development, Schinder said, which may explain why they are apparently receptive to experiential input only within a short period (day 9 to 11), rather than throughout their development.</p>
<p>&quot;The team went on to analyze these neuronal inputs more closely. Through a series of optogenetic and chemogenetic experiments, the researchers showed that mature granule cells activated their younger counterparts via intermediary cells called interneurons. Artificially stimulating either the mature granule cells or the interneurons could recapitulate the effects of environmental enrichment on the young granule cells. Moreover, the team showed that blocking the activity of the interneurons during the animals’ exposure to enriched environments prevented the expected experience-induced morphology in the young granule cells.</p>
<p>&quot;'The take home message is that experience can change how these young cells are incorporating into the brain and how they are contributing to brain circuitry,” said Hongjun Song, who studies neurogenesis at the Johns Hopkins University School of Medicine in Baltimore.&quot;</p>
<p>Comment: This shows how experience in young animals can shape the brain's function. The amazing malleable brain. The arrival of the first. It is such an unusual cell, how did it happen? The first neuron in evolution was a major event. Saltation.</p>
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<link>https://agnosticweb.com/index.php?id=23322</link>
<guid>https://agnosticweb.com/index.php?id=23322</guid>
<pubDate>Fri, 28 Oct 2016 16:25:58 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<item>
<title>brain plasticity: gene content of each neuron can vary (reply)</title>
<content:encoded><![CDATA[<p>Another article on this topic discussing transposons and their role: - <a href="http://www.the-scientist.com/?articles.view/articleNo/47069/title/Sequencing-Reveals-Genomic-Diversity-of-the-Human-Brain/&amp;utm_campaign=NEWSLETTER_TS_The-Scientist-Daily_2016&amp;utm_source=hs_email&amp;utm_medium=email&amp;utm_content=34545838&amp;_hsenc=p2ANqtz--NImLYqGTPyNnN1aOEXf4QREqw_PsuOF_w6HjcJ7uMrjuYSG1XxwxPH_i_mun4rAs7i48rYJXe-mfGR31o8sf-lPe4CA&amp;_hsmi=34545838">http://www.the-scientist.com/?articles.view/articleNo/47069/title/Sequencing-Reveals-Ge...</a> - &amp;quot;Somatic mosaicism&amp;#151;the variation of the genome between individual cells&amp;#151;is particularly consequential in the brain. Neuroscientists have found that small changes to the genome of even a few neurons can have neurological consequences. In a study published in Nature Neuroscience this week (September 12), scientists set their sights on one source of this variation. Using single-cell sequencing and machine learning algorithms, they have examined the extent of long interspersed element-1 (LINE-1, or L1) retrotransposition in the healthy human brain. - &amp;quot;In the 1940s, Barbara McClintock and colleagues discovered transposons, or &amp;#147;jumping genes,&amp;#148; scraps of DNA able to move from one position in the genome to another. By 2005, Fred &amp;#147;Rusty&amp;#148; Gage of the Salk Institute for Biological Studies and colleagues identified L1 transposons as a source of genomic mosaicism in human neurons. Now, Gage and his colleagues have shown that L1s don&amp;apos;t just jump around: these mobile elements can also spontaneously trigger the deletion of certain genes.&amp;#13;&amp;#10;&amp;#147;The main aspect that&amp;apos;s new in this paper is that there seems to be increased changes in these LINE elements that may not be due to insertional changes. . . . They may be something that serve as a potential target for somatic changes,&amp;#148; said Jerold Chun of the Scripps Research Institute in La Jolla, California, who was not involved in the present study. &amp;#147;That&amp;apos;s an interesting concept, and I think it will be interesting to see what that entails.&amp;#148; - *** - &amp;quot;L1 transposons create unique alterations to neuronal genomes, on the order of 0.5 to one alteration per cell, and L1-associated changes can be found in 44 percent to 63 percent of cells in the healthy brain, the researchers found. But when the researchers sought to confirm these L1 insertions using direct molecular methods, they could not find around half of the supposed changes. Upon closer inspection of the stretches of DNA around where the algorithm had flagged a unique change to the genomes, the researchers instead found evidence of large genetic deletions.&amp;#13;&amp;#10;L1 elements contain genes for endonucleases, proteins that cleave DNA, which are part of the toolkit they use to splice into new locations. The thought, explained Gage, is that these endonucleases sometimes continue cutting after an insertion, lopping off segments of DNA. If confirmed, this would be a previously unrecognized source of genomic mosaicism in the brain caused by L1 elements.&amp;#160; - *** - &amp;quot;<strong>The precise roles of L1 transposons in somatic mosaicism of the human brain remain unclear. Neurons are unique among the body&amp;apos;s cells because they do not regularly turn over, but instead can stay with a person for his or her entire life. Genetic changes that occur when a neuron is formed can therefore have permanent effects.&amp;quot; </strong> (my bold) - Comment: This is a major way brain plasticity occurs. Note these changes last a lifetime as each of us makes use of our brain to form it to our needs. There is an evolutionary aspect to this. Our DNA is 98% similar in overall appearance when total bases are counted compared to chimps, but our brains are vastly different. I think we are looking one of the reasons. Chimp brain genetic mosaic changes will be found to not be equal to this finding.</p>
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<link>https://agnosticweb.com/index.php?id=22906</link>
<guid>https://agnosticweb.com/index.php?id=22906</guid>
<pubDate>Tue, 20 Sep 2016 14:12:59 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<title>brain plasticity: gene content of each neuron can vary (reply)</title>
<content:encoded><![CDATA[<p>To make the brain as responsive as possible to our needs each neuron can vary its own instructions:-http://www.the-scientist.com/?articles.view/articleNo/46399/title/Single-Cell-RNA-Sequencing-Reveals-Neuronal-Diversity/&amp;utm_campaign=NEWSLETTER_TS_The-Scientist-Daily_2016&amp;utm_source=hs_email&amp;utm_medium=email&amp;utm_content=30975475&amp;_hsenc=p2ANqtz--bFYZlFXBRhtY3gEshC8Bbq3WER9bcpJK9Gak9VTw2Sa5HbJB3b8vJLZdI7FDTTnbCSYSOQwIaOOqJh5gw7nif1PvRRg&amp;_hsmi=30975475/-&amp;quot;Neurons within a single brain can differ from one another in genomic content&amp;#151;a phenomenon known as mosaicism. But the extent to which those differences are reflected in gene expression has remained uncertain, in large part because of the difficulty associated with analyzing transcription in individual cells. Now, a team led by researchers at the Scripps Research Institute in La Jolla, California, and the University of California, San Diego (UCSD), has developed a high-throughput pipeline to analyze the transcriptomes of thousands of single neuronal nuclei, revealing considerable variation in gene expression across the human cerebral cortex.-***-&amp;quot;Previous attempts to resolve differences in gene expression among neurons have been limited in scope by the small samples obtainable from fresh brains, and by the challenge of physically disentangling individual cells from one other. &amp;#147;All these neurons in the human adult brain, they&amp;apos;re highly, highly connected,&amp;#148; explained UCSD&amp;apos;s Kun Zhang, a bioengineer and collaborator on the National Institute of Health&amp;apos;s Single Cell Analysis Program (SCAP). &amp;#147;It&amp;apos;s very difficult to dissociate individual neurons from human brains.&amp;#148;-***-&amp;quot;By sequencing messenger RNA (mRNA) transcripts within these nuclei, the team generated 3,227 single-cell transcriptome datasets across the six regions: &amp;#147;more than an order of magnitude more than what&amp;apos;s been looked at previously,&amp;#148; Chun told The Scientist. Not only did these datasets identify cells as either inhibitory or excitatory (consistent with previous work in mice), they also revealed 16 distinct neuronal subtypes divided between these two categories that tended to be localized in one or a few Brodmann areas, indicating that the composition of neuronal types varies among regions of the brain.-&amp;#147;&amp;apos;One of the major findings is that the composition in the visual cortex is very different from the other five areas that we sampled,&amp;#148; Zhang said, adding that further transcriptome differences were observable within subtypes as well as between them. &amp;#147;With these subtypes, we can start to ask, &amp;#145;What are the differences across these six brain areas, and do particular subtypes contribute to these differences?&amp;quot;-Comment: This is a human study. At some point ape brains will have this same study, and I can guess the result: no where near the variability. This is part of the reason why our brains are so helpful to our needs. One can only wonder how this developed in evolution without purposeful planning.</p>
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<link>https://agnosticweb.com/index.php?id=22262</link>
<guid>https://agnosticweb.com/index.php?id=22262</guid>
<pubDate>Sun, 26 Jun 2016 22:44:16 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<title>brain plasticity: easily adapts to new activities (reply)</title>
<content:encoded><![CDATA[<p>Any primate can take up new activities not foreseen by evolution and readily adapt to it as the brain has feedback circuits to enhance adaptation: - <a href="http://phys.org/news/2016-06-primate-brain-pre-adapted-potentially-situation.html">http://phys.org/news/2016-06-primate-brain-pre-adapted-potentially-situation.html</a> - &amp;quot;Scientists have shown how the brain anticipates all of the new situations that it may encounter in a lifetime by creating a special kind of neural network that is &amp;quot;pre-adapted&amp;quot; to face any eventuality. - *** - &amp;quot;Human and non-human primates can learn an astonishing variety of novel behaviors that could not have been directly anticipated by evolution&amp;#151;we now understand that this ability to cope with new situations is due to the &amp;quot;pre-adapted&amp;quot; nature of the primate brain. - &amp;quot;This study shows that this seemingly miraculous pre-adaptation comes from connections between neurons that form recurrent loops where inputs can rebound and mix in the network, like waves in a pond, thus called &amp;quot;reservoir&amp;quot; computing. This mix of the inputs allows a potentially universal representation of combinations of the inputs that can then be used to learn the right behaviour for a new situation. - &amp;quot;The authors demonstrate this by training a reservoir network to perform a novel problem solving task. They then compared the activity of neurons in the model with activity of neurons in the prefrontal cortex of a research primate that was trained to perform the same task. Remarkably, there were striking similarities in the activation of neurons in both the reservoir model and the primate. - &amp;quot;This breakthrough shows that we have taken big step towards understanding the local recurrent connectivity in the brain that prepares primates to face unlimited situations. This research shows that by allowing essentially unlimited combinations of internal representations in the network of the brain, one of them is always on hand for the given situation.&amp;quot; - Comment: Once again we find our brain setup as readily very adequate to help us in every new physical or mental usage. Consider sports or musical instruments. Cricket for apes? Or chimps playing the violin. The brain is an instrument that is built to help us.</p>
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<link>https://agnosticweb.com/index.php?id=22186</link>
<guid>https://agnosticweb.com/index.php?id=22186</guid>
<pubDate>Sat, 11 Jun 2016 00:54:49 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<title>brain plasticity: scientist awards (reply)</title>
<content:encoded><![CDATA[<blockquote><p>David&amp;apos;s comment: <em>The bolded comment is the key point. Our personalities develop on a continuum, while the working brain adapts to our needs in functional areas. We &amp;apos;r us, not what the brain makes us</em>.&amp;#13;&amp;#10;&gt; &amp;#13;&amp;#10;&gt; dhw: I&amp;apos;m not at all sure that our personality and behaviours remain fixed. Experience can change people quite drastically. And of course we all know that drugs and diseases can affect the brain and thereby change both personality and behaviour. But under normal circumstances, I also feel that I am &amp;#147;me&amp;#148; and not what my brain makes &amp;#147;me&amp;#148;, and that &amp;#147;I&amp;#148; use my brain and am not used by it. We have already had several discussions about the problem of identity: just what does this &amp;#147;I/me&amp;#148; consist of? We can see the influences of nature, nurture, heredity, experience, cells etc., but ultimately, I think it boils down to materialism versus dualism. Another endlessly fascinating question, but unless there is an afterlife, I fear we shall never know the answer!-No, we won&amp;apos;t until/if the afterlife, but the key thought still remains, we are allowed to make what our brain becomes in structure and connections.</p>
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<link>https://agnosticweb.com/index.php?id=22126</link>
<guid>https://agnosticweb.com/index.php?id=22126</guid>
<pubDate>Sat, 04 Jun 2016 13:57:39 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<title>brain plasticity: scientist awards (reply)</title>
<content:encoded><![CDATA[<p>DAVID: <em>The latest Kavli awards for advances:</em>-http://www.the-scientist.com/?articles.view/articleNo/46233/title/2016-Kavli-Prize-Winn... -QUOTE: &amp;quot;<strong><em>Our brains have a remarkable capacity to adapt to changes in the environment, [and yet] our personality and behaviors typically remain fixed as we pass through life</em></strong>.&amp;#148; -David&amp;apos;s comment: <em>The bolded comment is the key point. Our personalities develop on a continuum, while the working brain adapts to our needs in functional areas. We &amp;apos;r us, not what the brain makes us</em>.-I&amp;apos;m not at all sure that our personality and behaviours remain fixed. Experience can change people quite drastically. And of course we all know that drugs and diseases can affect the brain and thereby change both personality and behaviour. But under normal circumstances, I also feel that I am &amp;#147;me&amp;#148; and not what my brain makes &amp;#147;me&amp;#148;, and that &amp;#147;I&amp;#148; use my brain and am not used by it. We have already had several discussions about the problem of identity: just what does this &amp;#147;I/me&amp;#148; consist of? We can see the influences of nature, nurture, heredity, experience, cells etc., but ultimately, I think it boils down to materialism versus dualism. Another endlessly fascinating question, but unless there is an afterlife, I fear we shall never know the answer!</p>
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<link>https://agnosticweb.com/index.php?id=22121</link>
<guid>https://agnosticweb.com/index.php?id=22121</guid>
<pubDate>Sat, 04 Jun 2016 10:11:26 +0000</pubDate>
<category>Introduction</category><dc:creator>dhw</dc:creator>
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<title>brain plasticity: scientist awards (reply)</title>
<content:encoded><![CDATA[<p>The latest Kavli awards for advances:-http://www.the-scientist.com/?articles.view/articleNo/46233/title/2016-Kavli-Prize-Winners/&amp;utm_campaign=NEWSLETTER_TS_The-Scientist-Daily_2016&amp;utm_source=hs_email&amp;utm_medium=email&amp;utm_content=30231742&amp;_hsenc=p2ANqtz-91j493wszK_68isLvQVgYyYHeKenTIZDZOBxaqIPrhK0oZSAUR4Wg1uuoPV-i_TFR-lIAO0_oeyE8yeRFn89YwIkBhdQ&amp;_hsmi=30231742/-&amp;quot;Eve Marder of Brandeis University in Waltham, Massachusetts; Michael Merzenich of the University of California, San Francisco; and Carla Shatz of Stanford University have won the 2016 Kavli Prize in neuroscience in recognition of their discoveries of mechanisms that enable experience and neural activity to remodel the brain.-&amp;quot;<strong>&amp;#147;Our brains have a remarkable capacity to adapt to changes in the environment, [and yet] our personality and behaviors typically remain fixed as we pass through life,&amp;#148; </strong>Ole Petter Ottersen, chair of the Kavli neuroscience committee, said during today&amp;apos;s prizes announcement at the Norwegian Academy of Science and Letters in Oslo. (my bold)-&amp;quot;Marder studies simple brain circuits in crustaceans to discover how neurotransmitters work. Merzenich has shown how circuits in the sensory cortex (known as the homunculus) are remodeled by experience&amp;#151;in particular, how the auditory system adapts to hearing damage and cochlear implants. Shatz has shown how visual development commences before birth.&amp;quot;-Comment: The bolded comment is the key point. Our personalities develop on a continuum, while the working brain adapts to our needs in functional areas. We &amp;apos;r us, not what the brain makes us.</p>
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<link>https://agnosticweb.com/index.php?id=22116</link>
<guid>https://agnosticweb.com/index.php?id=22116</guid>
<pubDate>Fri, 03 Jun 2016 13:50:09 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<title>brain plasticity: new neurons, more then pruned (reply)</title>
<content:encoded><![CDATA[<p>As the brain develops new networks, more neurons are produced then needed, so some are pruned back. This makes sense to me as the brain is responsive to our needs, and must be prepared to go as far as the new use is expanded, but not overextending the network which will require more energy than is necessary.-http://www.salk.edu/news-release/adult-brain-prunes-branched-connections-of-new-neurons/-&amp;quot;New brain cells began with a period of overgrowth, sending out a plethora of neuronal branches, before the brain pruned back the connections. The observation, described May 2, 2016 in Nature Neuroscience, suggests that new cells in the adult brain have more in common with those in the embryonic brain than scientists previously thought.-***-&amp;quot;While most of the brain&amp;apos;s billions of cells are formed before birth, Gage and others previously showed that in a few select areas of the mammalian brain, stem cells develop into new neurons during adulthood. In the new study, Gage&amp;apos;s group focused on cells in the dentate gyrus, an area deep in the brain thought to be responsible for the formation of new memories. The scientists used a new microscopy technique to observe new cells being formed in the dentate gyrus of adult mice.-&amp;quot;What was really surprising was that the cells that initially grew faster and became bigger were pruned back so that, in the end, they resembled all the other cells,&amp;#148; says Gon&amp;#231;alves. He and his colleagues went on to show that changing signaling pathways could mimic some of the effects of the complex environment&amp;#151;cells grew more initially, but also pruned back earlier.-&amp;quot;Over a period of over a month, the Salk team kept track of each new neural branch, called a dendrite, on the growing neurons, as well as each dendrite that was pruned away. -&amp;quot;So why would the brain spend energy developing more dendrites than needed? The researchers suspect that the more dendrites a neuron starts with, the more flexibility it has to prune back exactly the right branches.-&amp;#147;&amp;apos;The results suggest that there is <strong>significant biological pressure </strong>to maintain or retain the dendrite tree of these neurons,&amp;#148; says Gage.&amp;quot;-Comment: Note the last paragraph bold (mine). This will be managed by a molecular feedback loop for tight control. In this way as we try to learn new knowledge or physical maneuvers the brain carefully follows our needs.</p>
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<link>https://agnosticweb.com/index.php?id=21839</link>
<guid>https://agnosticweb.com/index.php?id=21839</guid>
<pubDate>Wed, 04 May 2016 18:33:01 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<title>brain plasticity: how neurons grow dendrites (reply)</title>
<content:encoded><![CDATA[<p>In order for the brain to have plasticity new neurons must grow dendrite connections and create networks of connectivity. The genes and molecules driving this process have been found:-http://medicalxpress.com/news/2016-04-biologists-brain-cells-message-network.html-&amp;quot;Biologists at the University of Iowa have determined a group of genes associated with neurons help regulate dendrites&amp;apos; growth. But there&amp;apos;s a catch: These genes, called gamma-protocadherins, must be an exact match for each neuron for the cells to correctly grow dendrites.-***-&amp;quot;Gamma-protocadherins are called &amp;quot;adhesion molecules&amp;quot; because they stick out from a cell&amp;apos;s membrane to bind and hold cells together. The researchers learned about their role by giving a developing brain cell in a mouse the same gamma-protocadherin as in surrounding cells. When they did, the cells grew longer, more complex dendrites. But when the researchers outfitted a mouse neuron with a different gamma-protocadherin than the cells around it, dendritic growth was stunted.-***-&amp;quot;Gamma-protocadherins act like molecular Velcro, binding neurons together and instructing them to grow their dendrites. Weiner and his team figured out their role when they observed paltry dendritic growth in mouse brain cells where the gamma-protocadherins had been silenced.-&amp;quot;The researchers went further in the new study. Using mice, they expressed the same type of gamma-protocadherin (labeled either as A1 or C3) in neurons in the cerebral cortex, a region of the brain that processes language and information. After five weeks, the neurons had sizeable dendritic networks, indicative of a healthy, normally functioning brain. Likewise, when they turned on a gamma-protocadherin gene in a neuron different from the gamma-protocadherin gene with the cells surrounding it, the mice had limited dendrite growth after the same time period.-&amp;quot;That&amp;apos;s important because human neurons carry up to six gamma-protocadherins, meaning there are many combinations potentially in play. Yet, it seems the &amp;quot;grow your dendrite&amp;quot; signal only happens when neurons carrying the the same gamma-protocadherin gene pair up.-&amp;quot;The neurons actually care who they match with,&amp;quot; says Weiner, associate professor in the Department of Biology, part of the College of Liberal Arts and Sciences. &amp;quot;It takes what we knew from biochemical studies in a dish and shows that protocadherins really mediate these matching interactions in the developing brain.&amp;quot;-&amp;quot;The team reports that star-looking cells called astrocytes also play a role in neurons&amp;apos; dendrite development. Astrocytes are glial (Greek for &amp;quot;glue&amp;quot;) cells that help to bridge the gap between neurons and speed signals along. When the molecular binding between an astrocyte and neurons is an exact match, the neurons grow fully formed dendrites, the researchers report.-&amp;quot;&amp;apos;Our data indicate that g-Pcdhs (gamma-protocadherins) act locally to promote dendrite arborization via homophilic matching and confirm that connectivity in vivo depends on molecular interactions between neurons and between neurons and astrocytes,&amp;quot; the authors write.&amp;quot;-Comment: Again we see the controls and the complexity of these processes. Not by chance.</p>
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<link>https://agnosticweb.com/index.php?id=21784</link>
<guid>https://agnosticweb.com/index.php?id=21784</guid>
<pubDate>Wed, 27 Apr 2016 18:21:07 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<title>brain plasticity: brain EEG's like finger prints (reply)</title>
<content:encoded><![CDATA[<p>The proof of my contention that we control our brains (Romansh take note) is shown in this study of EEG&amp;apos;s on 50 volunteers who could be identified 100% by the patterns elicited by challenges:-https://www.sciencedaily.com/releases/2016/04/160418120608.htm-&amp;quot;A team of researchers has recorded the brain activity of 50 people wearing an electroencephalogram headset while they looked at a series of 500 images designed specifically to elicit unique responses from person to person, for instance, a slice of pizza, a boat, Anne Hathaway, the word &amp;apos;conundrum.&amp;apos; They found that participants&amp;apos; brains reacted differently to each image, enough that a computer system was able to identify each volunteer&amp;apos;s &amp;apos;brainprint&amp;apos; with 100 percent accuracy.-***-&amp;quot;In their original study, titled &amp;quot;Brainprint,&amp;quot; published in 2015 in Neurocomputing, the research team was able to identify one person out of a group of 32 by that person&amp;apos;s responses, with only 97 percent accuracy, and that study only incorporated words, not images.-&amp;quot;&amp;apos;It&amp;apos;s a big deal going from 97 to 100 percent because we imagine the applications for this technology being for high-security situations, like ensuring the person going into the Pentagon or the nuclear launch bay is the right person,&amp;quot; said Laszlo. &amp;quot;You don&amp;apos;t want to be 97 percent accurate for that, you want to be 100 percent accurate.&amp;quot;-&amp;quot;According to Laszlo, brain biometrics are appealing because they are cancellable and cannot be stolen by malicious means the way a finger or retina can. The results suggest that brainwaves could be used by security systems to verify a person&amp;apos;s identity.&amp;quot;-Comment: I&amp;apos;m not interested in the security aspect, but the fact that we are born with malleable instrument that we fashion after ourselves as we develop.</p>
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<link>https://agnosticweb.com/index.php?id=21660</link>
<guid>https://agnosticweb.com/index.php?id=21660</guid>
<pubDate>Mon, 18 Apr 2016 17:56:53 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<title>brain plasticity: more evidence (reply)</title>
<content:encoded><![CDATA[<p>Teaching sighted persons braille induces marked plasticity:-https://www.sciencedaily.com/releases/2016/03/160315085940.htm-&amp;quot;It was already known that the brain can reorganize after a massive injury or as a result of massive sensory deprivation such as blindness. The visual cortex of the blind, deprived of its input, adapts for other tasks such as speech, memory, and reading Braille by touch. There has been speculation that this might also be possible in the normal, adult brain, but there has been no conclusive evidence.-&amp;quot;&amp;apos;For the first time we&amp;apos;re able to show that large-scale reorganization is a viable mechanism that the sighted, adult brain is able to recruit when it is sufficiently challenged,&amp;quot; says Szwed.-&amp;quot;Over nine months, 29 volunteers were taught to read Braille while blindfolded. They achieved reading speeds of between 0 and 17 words per minute. Before and after the course, they took part in a functional Magnetic Resonance Imaging (fMRI) experiment to test the impact of their learning on regions of the brain. This revealed that following the course, areas of the visual cortex, particularly the Visual Word Form Area, were activated and that connections with the tactile cortex were established.-***-&amp;quot;In an additional experiment using transcranial magnetic stimulation, scientists applied magnetic field from a coil to selectively suppress the Visual Word Form Area in the brains of nine volunteers. This impaired their ability to read Braille, confirming the role of this site for the task. The results also discount the hypothesis that the visual cortex could have just been activated because volunteers used their imaginations to picture Braille dots.-&amp;quot;&amp;apos;We are all capable of retuning our brains if we&amp;apos;re prepared to put the work in,&amp;quot; says Szwed.-&amp;quot;&amp;apos;He asserts that the findings call for a reassessment of our view of the functional organization of the human brain, which is more flexible than the brains of other primates.-&amp;quot;&amp;apos;The extra flexibility that we have uncovered might be one those features that made us human, and allowed us to create a sophisticated culture, with pianos and Braille alphabet,&amp;quot; he says.&amp;quot;-Comment: So much for the philosophy of determinism as it regards the brain. The brain is under our control and command to adapt to our various needs for new areas of activity and new connections. Free will survives.</p>
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<link>https://agnosticweb.com/index.php?id=21349</link>
<guid>https://agnosticweb.com/index.php?id=21349</guid>
<pubDate>Tue, 15 Mar 2016 20:00:40 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<title>brain plasticity: migratory birds show it (reply)</title>
<content:encoded><![CDATA[<p>Scientists have shown that areas of a migratory bird&amp;apos;s brain are larger to handle the knowledge of travel:-https://www.sciencedaily.com/releases/2016/02/160224070056.htm-&amp;quot;Birds that migrate the greatest distances have more new neurons in the regions of the brain responsible for navigation and spatial orientation, suggests a new paper published in Scientific Reports.-***-&amp;quot; In reed warblers, birds that migrate as individuals at night, new neurons were found mainly in the hippocampus -- a region associated with navigation. In turtle doves, a species that migrates as a group, the new neurons were found mainly in the nidopallium caudolateral, an area associated with communication skills.-***-&amp;quot;Then, these migration distances were compared with the amount of new neurons incorporated into the birds&amp;apos; brains. This was done by selectively colouring brain cells in several relevant regions: once -- for identifying new cells, and then a few weeks again for identifying neuron cells. Those coloured twice were identified as new neurons. The researchers discovered that both species show a trend of increasing new neurons in line with migration distance and that different brain regions were affected.-***-&amp;quot;What we humans do during the day may actually make us more &amp;quot;brainy&amp;quot; as our regular activities may actually determine how our brains adapt and in which areas. In the long term, there are implications for how species evolve. For example, other research already suggests that birds that hoard food in particular periods incorporate new neurons in brain regions responsible for memory and spatial orientation. This latest paper builds on that work, suggesting that birds that need greater navigational help have more new neurons in that part of the brain while those that need to keep up with the flock incorporate new neurons in a different area.&amp;apos;&amp;quot;-Comment: Same story. Brains will develop new neurons to help with new activity. Same pattern for all animals with brain, I&amp;apos;ll bet.</p>
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<link>https://agnosticweb.com/index.php?id=21179</link>
<guid>https://agnosticweb.com/index.php?id=21179</guid>
<pubDate>Wed, 24 Feb 2016 21:32:49 +0000</pubDate>
<category>Introduction</category><dc:creator>David Turell</dc:creator>
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<title>brain plasticity: identical twin's brains differ (reply)</title>
<content:encoded><![CDATA[<blockquote><p>Mono-zygote twins start out identical but their brains are different even at birth:&amp;#13;&amp;#10;&gt; &amp;#13;&amp;#10;&gt; <a href="http://www.wsj.com/articles/brain-mutations-guarantee-our-individuality-1455810936&amp;#13;&amp;#10;&gt;">http://www.wsj.com/articles/brain-mutations-guarantee-our-individuality-1455810936&amp;...</a> &amp;#13;&amp;#10;&gt;&amp;#13;&amp;#10;&gt; Comment:... The brain is our servant, not a controller.  - Our servant or the vessel in which we inhabit? It would seem to me if it were our servant we could fully control (or learn to fully control) every aspect of our being with the brain by our wishes alone.</p>
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<link>https://agnosticweb.com/index.php?id=21160</link>
<guid>https://agnosticweb.com/index.php?id=21160</guid>
<pubDate>Sun, 21 Feb 2016 21:21:30 +0000</pubDate>
<category>Introduction</category><dc:creator>BBella</dc:creator>
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