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Microbiota-derived 3-Indolepropionic acid

Lactobacillus Beijerinck 1901 resmi

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: Several vector versions of this file are available. File:API → File:Microbiota-derived 3-Indolepropionic acid.svgFile:Microbiota-derived 3-Indolepropionic acid-notext.svg For more information, see Help:SVG. In other languages. Alemannischالعربيةбеларуская (тарашкевіца)българскиবাংলাcatalàнохчийнčeštinadanskDeutschΕλληνικάEnglishBritish EnglishEsperantoespañoleestieuskaraفارسیsuomifrançaisFryskgalegoעבריתhrvatskimagyarհայերենBahasa IndonesiaIdoitaliano日本語ქართული한국어lietuviųмакедонскиമലയാളംBahasa Melayunorsk bokmålPlattdüütschNederlandsnorsk nynorsknorskoccitanpolskiportuguêsportuguês do BrasilromânăрусскийsicilianuScotsslovenčinaslovenščinaсрпски / srpskisvenskaதமிழ்ไทยTürkçeтатарча/tatarçaукраїнськаvènetoTiếng Việt中文(简体)中文(繁體)+/−. : . Description: English: This diagram shows the metabolism of tryptophan to indole and indole derivatives in the colonic lumen. Clostridium sporogenes metabolizes indole into 3-indolepropionic acid (IPA), a highly potent neuroprotective antioxidant. In the intestine, IPA binds to pregnane X receptors (PXR) in intestinal cells, thereby facilitating mucosal homeostasis and barrier function. Following absorption and distribution to the brain, IPA confers a neuroprotective effect against cerebral ischemia and Alzheimer’s disease. Lactobacillus species metabolize indole into indole-3-aldehyde (I3A) which acts on the aryl hydrocarbon receptor (AhR) in intestinal immune cells, in turn increasing interleukin-22 (IL-22) production. AhR activation markedly affects in gut immunity by supporting epithelial barrier function, increasing immune tolerance to commensal microbiota, and protecting against pathogenic infections. Indole itself acts as a glucagon-like peptide-1 (GLP-1) secretagogue in intestinal L cells and as a ligand for AhR. Indole can also be metabolized by the liver to indoxyl sulfate, a compound that is detrimental to human health in high concentrations. Accumulation of indoxyl sulfate in blood plasma is toxic and associated with vascular disease and renal dysfunction. AST-120 (activated charcoal), an intestinal sorbent that is taken by mouth, adsorbs indole, in turn decreasing the concentration of indoxyl sulfate in blood plasma. Date: 21 April 2016. Source: (April 2016). "Microbial metabolism of dietary components to bioactive metabolites: opportunities for new therapeutic interventions". Genome Med 8 (1): 46. DOI:10.1186/s13073-016-0296-x. PMID 27102537. PMC: 4840492. Figure 1: Molecular mechanisms of action of indole and its metabolites on host physiology and disease. Author: Zhang LS, Davies SS.

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