砷代谢中宿主与微生物群的相互作用:对宿主葡萄糖稳态的影响。

IF 5.4 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Chemico-Biological Interactions Pub Date : 2025-01-25 Epub Date: 2024-12-12 DOI:10.1016/j.cbi.2024.111354
Dinakaran Vasudevan , Buvaneswari Gajendhran , Krishnan Swaminathan , Ganesan Velmurugan
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引用次数: 0

摘要

砷(As)是一种具有独特性质的天然元素,已被世界卫生组织(世卫组织)认定为世界上最大的集体中毒。由于自然和人为活动,全世界约有2亿人接触到有毒水平的砷。这种广泛的接触需要更深入地了解微生物与砷的相互作用及其对宿主接触和健康风险的潜在影响。它是包括糖尿病在内的代谢性疾病的主要致病因素。砷暴露与多种细胞类型和组织的功能障碍有关,特别是对胰岛细胞的影响。在体外和体内条件下,已经确定了许多机制来负责砷暴露。这些机制有助于调节潜在糖尿病病因的过程,如葡萄糖刺激胰腺β细胞分泌胰岛素。与其他有毒元素不同,砷会在包括微生物、植物和动物在内的生物体中代谢。其他有毒元素,如铅(Pb)和汞(Hg)在微生物、植物和动物体内的代谢方式通常与砷不同。在这篇综述中,我们通过回顾微生物-砷相互作用的已知方面,并将其置于影响宿主暴露和健康风险的潜在背景下,努力发起对话。这篇综述提供了关于人体及其相关微生物群的砷代谢的最新见解,以及在糖尿病病因中连接不同种类砷的破译分子途径。此外,还讨论了转化医学中砷的缓解和解毒的未来前景以及当前情况下的局限性。本文的综合综述强调了探索砷代谢、宿主-微生物群相互作用之间的复杂相互作用及其对葡萄糖稳态和代谢性疾病的影响的重要性。它强调需要继续进行研究,以制定有效战略,减轻与砷有关的健康风险,并促进更好的转化医学方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Host-microbiota interplay in arsenic metabolism: Implications on host glucose homeostasis
Arsenic (As), a naturally occurring element with unique properties, has been recognized as the largest mass poisoning in the world by the World Health Organization (WHO). Approximately 200 million people worldwide are exposed to toxic levels of arsenic due to natural and anthropogenic activities. This widespread exposure necessitates a deeper understanding of microbe-arsenic interactions and their potential influence on host exposure and health risks. It is a major causative factor for metabolic diseases, including diabetes. Arsenic exposure has been linked to dysfunction in various cell types and tissues, notably affecting pancreatic islet cells. Numerous mechanisms have been identified to be responsible for arsenic exposure under both in vitro and in vivo conditions. These mechanisms contribute to the regulation of processes underlying diabetes etiology, such as glucose-stimulated insulin secretion from pancreatic beta cells. Unlike other toxic elements, arsenic undergoes metabolism by living organisms, including microbes, plants, and animals. Other toxic elements like Lead (Pb) and mercury (Hg) are generally not metabolized in the same way as Arsenic in microbes, plants and animals. In this review, we strive to initiate a dialogue by reviewing known aspects of microbe-arsenic interactions and placing it in the context of the potential for influencing host exposure and health risks. This review provides an up-to-date insight into arsenic metabolism by the human body and its associated microbiota, as well as the deciphered molecular pathways linking the different species of arsenic in the etiology of diabetes. Additionally, the future perspectives of mitigation and detoxification of arsenic in translational medicine and limitations in current scenarios are discussed. The comprehensive review presented here underscores the importance of exploring the complex interplay between arsenic metabolism, host-microbiota interactions, and their implications on glucose homeostasis and metabolic diseases. It emphasizes the need for continued research to develop effective strategies for mitigating arsenic-related health risks and fostering better translational medicine approaches.
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来源期刊
CiteScore
7.70
自引率
3.90%
发文量
410
审稿时长
36 days
期刊介绍: Chemico-Biological Interactions publishes research reports and review articles that examine the molecular, cellular, and/or biochemical basis of toxicologically relevant outcomes. Special emphasis is placed on toxicological mechanisms associated with interactions between chemicals and biological systems. Outcomes may include all traditional endpoints caused by synthetic or naturally occurring chemicals, both in vivo and in vitro. Endpoints of interest include, but are not limited to carcinogenesis, mutagenesis, respiratory toxicology, neurotoxicology, reproductive and developmental toxicology, and immunotoxicology.
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