Effects of dietary acrylamide on kidney and liver health: Molecular mechanisms and pharmacological implications.

Q1 Environmental Science
Toxicology Reports Pub Date : 2024-12-10 eCollection Date: 2025-06-01 DOI:10.1016/j.toxrep.2024.101859
Mohammed Nazish Quasmi, Dinesh Kumar, Ashok Jangra
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引用次数: 0

Abstract

Acrylamide (AA) has raised concerns throughout the world in recent years because of its potential negative effects on human health. Numerous researches on humans and animals have connected a high dietary exposure to AA to a possible risk of cancer. Additionally, higher consumption of acrylamide has also been associated with dysfunctioning of various organ systems from nervous system to the reproductive system. Acrylamide is primarily metabolised into the glycidamide inside the body which gets accumulated in different tissues including kidney and liver, and chronic exposure to this can lead to the nephrotoxicity and hepatotoxicity through different molecular mechanisms. This review summarizes the various sources, formation and metabolism of the dietary acrylamide along with the different molecular mechanisms such as oxidative stress, inflammation, DNA damage, autophagy, mitochondrial dysfunction and morphological changes in nephron and hepatocytes through which acrylamide exerts its deleterious effect on kidney and liver causing nephrotoxicity and hepatotoxicity. This review summarizes various animal and cellular studies that demonstrate AA-induced nephrotoxicity and hepatotoxicity. Lastly, the article emphasizes on underlying protective molecular mechanisms of various pharmacological interventions against acrylamide induced hepatotoxicity and nephrotoxicity.

膳食丙烯酰胺对肾脏和肝脏健康的影响:分子机制和药理意义。
近年来,丙烯酰胺(AA)因其对人体健康的潜在负面影响而引起了全世界的关注。对人类和动物的大量研究表明,饮食中大量摄入AA与癌症的可能风险有关。此外,过量摄入丙烯酰胺还与从神经系统到生殖系统的各种器官系统功能失调有关。丙烯酰胺主要在体内代谢成缩水甘油酰胺,在不同的组织中积累,包括肾脏和肝脏,长期接触丙烯酰胺可通过不同的分子机制导致肾毒性和肝毒性。本文综述了膳食丙烯酰胺的来源、形成和代谢,以及丙烯酰胺通过氧化应激、炎症、DNA损伤、自噬、线粒体功能障碍和肾细胞和肝细胞形态学改变等不同的分子机制对肾脏和肝脏产生有害作用,引起肾毒性和肝毒性。本文综述了各种动物和细胞研究,证明了aa引起的肾毒性和肝毒性。最后,文章强调了各种药物干预对丙烯酰胺引起的肝毒性和肾毒性的潜在保护分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Toxicology Reports
Toxicology Reports Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
7.60
自引率
0.00%
发文量
228
审稿时长
11 weeks
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