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首页> 外文期刊>Microbial Ecology in Health and Disease >Short-chain fatty acid fermentation products of the gut microbiome: implications in autism spectrum disorders
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Short-chain fatty acid fermentation products of the gut microbiome: implications in autism spectrum disorders

机译:肠道微生物组的短链脂肪酸发酵产物:对自闭症谱系障碍的影响

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摘要

Recent evidence suggests potential, but unproven, links between dietary, metabolic, infective, and gastrointestinal factors and the behavioral exacerbations and remissions of autism spectrum disorders (ASDs). Propionic acid (PPA) and its related short-chain fatty acids (SCFAs) are fermentation products of ASD-associated bacteria (Clostridia, Bacteriodetes, Desulfovibrio). SCFAs represent a group of compounds derived from the host microbiome that are plausibly linked to ASDs and can induce widespread effects on gut, brain, and behavior. Intraventricular administration of PPA and SCFAs in rats induces abnormal motor movements, repetitive interests, electrographic changes, cognitive deficits, perseveration, and impaired social interactions. The brain tissue of PPA-treated rats shows a number of ASD-linked neurochemical changes, including innate neuroinflammation, increased oxidative stress, glutathione depletion, and altered phospholipid/acylcarnitine profiles. These directly or indirectly contribute to acquired mitochondrial dysfunction via impairment in carnitine-dependent pathways, consistent with findings in patients with ASDs. Of note, common antibiotics may impair carnitine-dependent processes by altering gut flora favoring PPA-producing bacteria and by directly inhibiting carnitine transport across the gut. Human populations that are partial metabolizers of PPA are more common than previously thought. PPA has further bioactive effects on neurotransmitter systems, intracellular acidification/calcium release, fatty acid metabolism, gap junction gating, immune function, and alteration of gene expression that warrant further exploration. These findings are consistent with the symptoms and proposed underlying mechanisms of ASDs and support the use of PPA infusions in rats as a valid animal model of the condition. Collectively, this offers further support that gut-derived factors, such as dietary or enteric bacterially produced SCFAs, may be plausible environmental agents that can trigger ASDs or ASD-related behaviors and deserve further exploration in basic science, agriculture, and clinical medicine.
机译:最近的证据表明,饮食,代谢,感染性和胃肠道因素与自闭症谱系障碍(ASD)的行为恶化和缓解之间存在潜在但未经证实的联系。丙酸(PPA)及其相关的短链脂肪酸(SCFA)是与ASD相关的细菌(Clostridia,Bacteriodetes,Desulfovibrio)的发酵产物。 SCFA代表了一组源自宿主微生物组的化合物,这些化合物似乎与ASD相连,并且可以诱导对肠道,大脑和行为的广泛影响。对大鼠进行PPA和SCFA的脑室内给药会诱发异常的运动动作,重复性兴趣,电描记图变化,认知缺陷,坚持不懈和社交互动受损。经PPA治疗的大鼠的脑组织显示出许多与ASD相关的神经化学变化,包括先天性神经炎症,氧化应激增加,谷胱甘肽耗竭以及磷脂/酰基肉碱的变化。这些都通过肉碱依赖性途径的损伤直接或间接地导致获得性线粒体功能障碍,这与ASD患者的发现一致。值得注意的是,常见的抗生素可能会通过改变有利于生产PPA的细菌的肠道菌群以及直接抑制肉碱在肠道内的运输而损害肉碱依赖性过程。作为PPA的部分代谢产物的人群比以前认为的更为普遍。 PPA对神经递质系统,细胞内酸化/钙释放,脂肪酸代谢,间隙连接门控,免疫功能以及基因表达的改变具有进一步的生物活性,值得进一步研究。这些发现与ASD的症状和拟议的潜在机制相一致,并支持在大鼠中使用PPA输注作为该病的有效动物模型。总的来说,这进一步支持了肠源性因素,例如饮食或肠内细菌产生的SCFA,可能是可能触发ASD或ASD相关行为的环境因素,值得在基础科学,农业和临床医学中进行进一步探索。

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