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|    Gut-brain link grabs neuroscientists Ide    |
|    02 Mar 15 03:38:27    |
      From: hounddog23x@gmail.com              Gut–brain link grabs neuroscientists        Idea that intestinal bacteria affect mental health gains ground.               Sara Reardon        12 November 2014        Article tools        PDFRights & Permissions               Lester V. Bergman/Corbis        Feeding mice the bacterium Bacteroides fragilis can reverse autism-like       symptoms.        Companies selling ‘probiotic’ foods have long claimed that cultivating the       right gut bacteria can benefit mental well-being, but neuroscientists have       generally been sceptical. Now there is hard evidence linking conditions such       as autism and        depression to the gut’s microbial residents, known as the microbiome. And       neuroscientists are taking notice — not just of the clinical implications       but also of what the link could mean for experimental design.                      “The field is going to another level of sophistication,” says Sarkis       Mazmanian, a microbiologist at the California Institute of Technology in       Pasadena. “Hopefully this will shift this image that there’s too much       commercial interest and data from        too few labs.”               This year, the US National Institute of Mental Health spent more than US$1       million on a new research programme aimed at the microbiome–brain       connection. And on 19 November, neuroscientists will present evidence for the       link in a symposium at the annual        Society for Neuroscience meeting in Washington DC called ‘Gut Microbes and       the Brain: Paradigm Shift in Neuroscience’.               Although correlations have been noted between the composition of the gut       microbiome and behavioural conditions, especially autism1, neuroscientists are       only now starting to understand how gut bacteria may influence the brain. The       immune system almost        certainly plays a part, Mazmanian says, as does the vagus nerve, which       connects the brain to the digestive tract. Bacterial waste products can also       influence the brain — for example, at least two types of intestinal       bacterium produce the        neurotransmitter γ-aminobutyric acid (GABA)2.               The microbiome is likely to have its greatest impact on the brain early in       life, says pharmacologist John Cryan at University College Cork in Ireland. In       a study to be presented at the neuroscience meeting, his group found that mice       born by caesarean        section, which hosted different microbes from mice born vaginally, were       significantly more anxious and had symptoms of depression. The animals’       inability to pick up their mothers’ vaginal microbes during birth — the       first bacteria that they would        normally encounter — may cause lifelong changes in mental health, he says.               Similarly, a 2013 study from Mazmanian’s lab found that a mouse model with       some features of autism had much lower levels of a common gut bacterium called       Bacteroides fragilis than did normal mice3. The animals were also stressed,       antisocial and had        gastrointestinal symptoms often seen in autism. Feeding B. fragilis to the       mice reversed the symptoms. The group also found that the mice with these       symptoms had higher levels of a bacterial metabolite called 4-et       ylphenylsulphate (4EPS) in their blood,        and that injecting that chemical into normal mice caused the same behavioural       problems.               Related stories        Microbiome therapy gains market traction        Bacterium can reverse autism-like behaviour in mice        Friendly bacteria cheer up anxious mice        More related stories        The mechanism for these effects is still unclear. At the meeting, Mazmanian       will present data showing that feeding 4EPS to mice causes behavioural       problems only if the gut is leaky, presumably because that allows the chemical       to seep into the body        through the intestinal wall. That observation raises the possibility that some       people with autism could be supported with therapies, such as probiotics, that       target the gut instead of the brain, which is a much more complex and       inaccessible organ.               Yet even those at the forefront of the research remain sceptical that the       findings will translate into treatments for humans. The evidence that       probiotics affect human behaviour “is minimal to say the least”, Mazmanian       acknowledges. Still, he says, a        growing number of researchers are starting to look at some mental illnesses       through a microbial lens.               There are implications for basic research too. In another study to be       presented at the meeting, veterinarian Catherine Hagan at the University of       Missouri in Columbia compared the gut bacteria in laboratory mice of the same       genetic strain that had been        bought from different vendors. Their commensals differed widely, she found:       mice from the Jackson Laboratory in Bar Harbor, Maine, for instance, had fewer       bacterial types in their guts than did mice from Harlan Laboratories, which is       headquartered in        Indianapolis, Indiana.               Such differences could present a major complication for researchers seeking to       reproduce another lab’s behavioural experiments, Hagan says. When her team       transplanted bacteria from female Harlan mice into female Jackson mice, the       animals became less        anxious and had lower levels of stress-related chemicals in their blood. Hagan       notes that when a lab makes a mouse by in vitro fertilization, the animal will       pick up microbes from its surrogate mother, which might differ greatly from       those of its genetic        mother. “If we’re going to kill animals for research, we want to make sure       they’re modelling what we think they’re modelling,” she says.               Nature 515, 175–177 (13 November 2014) doi:10.1038/515175a        References               Kang, D.-W. et al. PLoS ONE 8, e68322 (2013).        ArticlePubMedChemPort        Show context        Barrett, E. et al. J. Appl. Microbiol. 113, 411–417 (2012).        ArticlePubMedChemPort        Show context        Hsiao, E. Y. et al. Cell 155, 1451–1463 (2013).        ArticlePubMedISIChemPort        Show context        Related stories and links               From nature.com        Microbiome therapy gains market traction        13 May 2014        Bacterium can reverse autism-like behaviour in mice        05 December 2013        Friendly bacteria cheer up anxious mice        30 August 2011        From elsewhere        Society for Neuroscience Annual Meeting 2014                                    http://www.nature.com/news/gut-brain-link-grabs-neuroscientists-1.16316              --- SoupGate-Win32 v1.05        * Origin: you cannot sedate... all the things you hate (1:229/2)    |
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