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|    Message 6,013 of 8,931    |
|    ScienceDaily to All    |
|    Fecal transplants reverse hallmarks of a    |
|    04 May 22 22:30:48    |
      MSGID: 1:317/3 6273531b       PID: hpt/lnx 1.9.0-cur 2019-01-08       TID: hpt/lnx 1.9.0-cur 2019-01-08        Fecal transplants reverse hallmarks of aging                Date:        May 4, 2022        Source:        University of East Anglia        Summary:        In the search for eternal youth, fecal transplants may seem like        an unlikely way to reverse the aging process. However, scientists        have provided evidence, from research in mice, that transplanting        fecal microbiota from young into old mice can reverse hallmarks        of aging in the gut, eyes, and brain. In the reverse experiment,        microbes from aged mice induced inflammation in the brain of        young recipients and depleted a key protein required for normal        vision. These findings show that gut microbes play a role in the        regulating some of the detrimental effects of ageing and open up        the possibility of gut microbe-based therapies to combat decline        in later life.                            FULL STORY       ==========================================================================       In the search for eternal youth, fecal transplants may seem like an       unlikely way to reverse the ageing process.                     ==========================================================================       However, scientists at the Quadram Institute and the University of East       Anglia have provided evidence, from research in mice, that transplanting       faecal microbiota from young into old mice can reverse hallmarks of       ageing in the gut, eyes, and brain.              In the reverse experiment, microbes from aged mice induced inflammation       in the brain of young recipients and depleted a key protein required       for normal vision.              These findings show that gut microbes play a role in the regulating some       of the detrimental effects of ageing and open up the possibility of gut       microbe-based therapies to combat decline in later life.              Prof Simon Carding, from UEA's Norwich Medical School and head of the       Gut Microbes and Health Research Programme at the Quadram Institute,       said: "This ground-breaking study provides tantalising evidence for the       direct involvement of gut microbes in ageing and the functional decline       of brain function and vision and offers a potential solution in the       form of gut microbe replacement therapy." It has been known for some       time that the population of microbes that we carry around in our gut,       collectively called the gut microbiota, is linked to health.              Most diseases are associated with changes in the types and behaviour of       bacteria, viruses, fungi and other microbes in an individual's gut.                            ==========================================================================       Some of these changes in microbiota composition happen as we age,       adversely affecting metabolism and immunity, and this has been associated       with age- related disorders including inflammatory bowel diseases,       along with cardiovascular, autoimmune, metabolic and neurodegenerative       disorders.              To better understand the effects of these changes in the microbiota in old       age, scientists from the Quadram Institute transferred the gut microbes       from aged mice into healthy young mice, and vice versa. They then looked       at how this affected inflammatory hallmarks of ageing in the gut, brain       and eye, which suffer from declining function in later life.              The study, published in the journal Microbiome, found that the microbiota       from old donors led to loss of integrity of the lining of the gut,       allowing bacterial products to cross into the circulation, which results       in triggering the immune system and inflammation in the brain and eyes.              Age-related chronic inflammation, known as inflammageing, has       been associated with the activation of specific immune cells found       in brain. These cells were also over-activated in the young mice who       received aged microbiome transplants.              In the eye, the team also found specific proteins associated with retinal       degeneration were elevated in the young mice receiving microbiota from       old donors.                            ==========================================================================       In old mice, these detrimental changes in the gut, eye and brain could       be reversed by transplanting the gut microbiota from young mice.              In ongoing studies, the team are now working to understand how long these       positive effects can last, and to identify the beneficial components of       the young donor microbiota and how they impact on organs distant from       the gut.              The microbiota of young mice, and the old mice who received young       microbiota transplants were enriched in beneficial bacteria that have       previously been associated with good health in both mice and humans.              The researchers have also analysed the products which these bacteria       produce by breaking down elements of our diet. This has uncovered       significant shifts in particular lipids (fats) and vitamin metabolism,       which may be linked to the changes seen in inflammatory cells in the       eye and brain.              Similar pathways exist in humans, and the human gut microbiota also       changes significantly in later life, but the researchers caution about       extrapolating their results directly to humans until similar studies in       elderly humans can be performed.              A new facility for Microbiota Replacement Therapy (MRT), also known as       Faecal Microbiota Transplantation (FMT) is being built in the Quadram       Institute that will facilitate such trials, as well as other trials for       microbiota-related conditions.              Lead author of the study, Dr Aimee Parker from the Quadram Institute said:       "We were excited to find that by changing the gut microbiota of elderly       individuals, we could rescue indicators of age-associated decline commonly       seen in degenerative conditions of the eye and brain.              "Our results provide more evidence of the important links between microbes       in the gut and healthy ageing of tissues and organs around the body. We       hope that our findings will contribute ultimately to understanding how we       can manipulate our diet and our gut bacteria to maximise good health in       later life." The research was funded by the Biotechnology and Biological       Sciences Research Council, part of UK Research and Innovation.              'Fecal microbiota transfer between young and aged mice reverses hallmarks       of the aging gut, eye, and brain' is published in the journal Microbiome.                     ==========================================================================       Story Source: Materials provided by University_of_East_Anglia. Note:       Content may be edited for style and length.                     ==========================================================================       Journal Reference:        1. Aime'e Parker, Stefano Romano, Rebecca Ansorge, Asmaa Aboelnour,        Gwenaelle Le Gall, George M. Savva, Matthew G. Pontifex, Andrea        Telatin, David Baker, Emily Jones, David Vauzour, Steven Rudder,        L. Ashley Blackshaw, Glen Jeffery, Simon R. Carding. Fecal        microbiota transfer between young and aged mice reverses hallmarks        of the aging gut, eye, and brain. Microbiome, 2022; 10 (1) DOI:        10.1186/s40168-022-01243-w       ==========================================================================              Link to news story:       https://www.sciencedaily.com/releases/2022/05/220504082622.htm              --- up 9 weeks, 2 days, 10 hours, 51 minutes        * Origin: -=> Castle Rock BBS <=- Now Husky HPT Powered! (1:317/3)       SEEN-BY: 15/0 106/201 114/705 123/120 129/330 331 153/7715 218/700       SEEN-BY: 229/110 111 317 400 426 428 470 664 700 292/854 298/25 305/3       SEEN-BY: 317/3 320/219 396/45       PATH: 317/3 229/426           |
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