炎症、氧化应激和肠道微生物群扰乱:酒精宿醉的机制和治疗方法综述。

IF 3 Q2 SUBSTANCE ABUSE
Benedict R. H. Turner, Poppy I Jenkinson, Marc Huttman, Benjamin H. Mullish
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引用次数: 0

摘要

酒精是世界上最广泛滥用的物质,是 15-49 岁人群死亡的主要原因,也是心脏病、肝病、糖尿病和癌症的主要风险因素。尽管如此,酒精在更广泛的社会中仍经常被滥用。饮酒过量的人通常会出现一系列不良症状,即宿醉。然而,临床医生或消费者并不认为酒精宿醉具有长期的临床意义。我们对文献进行了严格审查,以证明酒精宿醉的病理生理机制。此后,我们采用布拉德福德-希尔(Bradford-Hill)标准,将酒精宿醉重新定义为继发于酒精诱发炎症的病态行为表现,以证明因果关系高于相关关系。酒精通过氧化应激和内毒素血症引起炎症。酒精代谢具有氧化性,摄入量增加会导致组织相对缺氧,自由基生成增加。随后,通过脂质过氧化和 DNA/蛋白质加合物的形成造成组织损伤。酒精代谢的副产物(如乙醛和同系物)、睡眠不足以及酒精暴露组织中非特异性诱导型 CYP2E1 的激活都会加剧自由基的生成。组织损伤和细胞死亡会导致炎症,但在肠道中,上皮细胞的丧失会导致肠道通透性,使病原菌转移到全身循环(内毒素血症)。这将导致一连串特征明显的全身性炎症,并激活收费样受体 4,诱发疾病行为。考虑到这些证据,宿醉的频率和严重程度可能是日后酒精相关疾病发展的预测因素,值得在前瞻性研究中正式确认。鉴于酒精介导炎症的机制,对肠道渗透性和肠道微生物组的研究可能是未来预防宿醉和其他酒精相关疾病的一个令人兴奋的治疗途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Inflammation, oxidative stress and gut microbiome perturbation: A narrative review of mechanisms and treatment of the alcohol hangover

Inflammation, oxidative stress and gut microbiome perturbation: A narrative review of mechanisms and treatment of the alcohol hangover

Inflammation, oxidative stress and gut microbiome perturbation: A narrative review of mechanisms and treatment of the alcohol hangover

Alcohol is the most widely abused substance in the world, the leading source of mortality in 15–49-year-olds, and a major risk factor for heart disease, liver disease, diabetes, and cancer. Despite this, alcohol is regularly misused in wider society. Consumers of excess alcohol often note a constellation of negative symptoms, known as the alcohol hangover. However, the alcohol hangover is not considered to have long-term clinical significance by clinicians or consumers. We undertook a critical review of the literature to demonstrate the pathophysiological mechanisms of the alcohol hangover. Hereafter, the alcohol hangover is re-defined as a manifestation of sickness behavior secondary to alcohol-induced inflammation, using the Bradford-Hill criteria to demonstrate causation above correlation. Alcohol causes inflammation through oxidative stress and endotoxemia. Alcohol metabolism is oxidative and increased intake causes relative tissue hypoxia and increased free radical generation. Tissue damage ensues through lipid peroxidation and the formation of DNA/protein adducts. Byproducts of alcohol metabolism such as acetaldehyde and congeners, sleep deprivation, and the activation of nonspecific inducible CYP2E1 in alcohol-exposed tissues exacerbate free radical generation. Tissue damage and cell death lead to inflammation, but in the intestine loss of epithelial cells leads to intestinal permeability, allowing the translocation of pathogenic bacteria to the systemic circulation (endotoxemia). This leads to a well-characterized cascade of systemic inflammation, additionally activating toll-like receptor 4 to induce sickness behavior. Considering the evidence, it is suggested that hangover frequency and severity may be predictors of the development of later alcohol-related diseases, meriting formal confirmation in prospective studies. In light of the mechanisms of alcohol-mediated inflammation, research into gut permeability and the gut microbiome may be an exciting future therapeutic avenue to prevent alcohol hangover and other alcohol-related diseases.

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