花生四烯酸对硫乙酰胺所致大鼠肝肾损伤的改善作用。

IF 1.2 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Xenobiotica Pub Date : 2025-06-01 Epub Date: 2025-08-03 DOI:10.1080/00498254.2025.2535407
Siyu Xiang, Dong Kwon Yang, Jin-Shang Kim, Shang-Jin Kim
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引用次数: 0

摘要

1. 花生四烯酸(ArA)是一种必需的omega-6多不饱和脂肪酸,在各种生理过程和疾病条件下至关重要。然而,花生四烯酸对肝肾损害的影响尚不清楚。因此,本研究旨在探讨ArA对硫代乙酰胺(TAA)致大鼠肝肾损伤的有益作用,重点关注相关的血液学变化。六组,每组10只大鼠,分别为:对照组,30 mg/kg ArA处理组,20 mg/kg taa诱导肝损伤组,ArA(10、20和30 mg/kg)预处理肝损伤组。ArA预处理可改善taa处理大鼠肝、肾组织的病理损伤和肝功能障碍。TAA增加肝和肾损伤血清生物标志物,否则,ArA显著抑制这些参数水平的升高,并抑制代谢性酸中毒和脱水。此外,ArA能有效地保存taa诱导的肝损伤的蛋白质和胆固醇代谢。ArA抑制TAA引起离子失衡。值得注意的是,最高AA剂量(30 mg/kg)对taa诱导的肝、肾损伤的保护作用最强。本研究表明,ArA可有效减轻TAA引起的肝和肾损伤,表明其作为一种有前景的预防或治疗方法的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Arachidonic acid ameliorates the liver and kidney injuries induced by thioacetamide in rats.

Arachidonic acid (ArA) is an essential omega-6 polyunsaturated fatty acid is crucial in various physiological processes and disease conditions. Nevertheless, the effects of arachidonic acid on liver and kidney damage are not well understood. Therefore, this study aimed to explore the beneficial role of ArA on liver and kidney injuries caused by thioacetamide (TAA) in rats, focusing on the associated hematological changes.The six groups, each consisting of 10 rats, are as follows; Control, 30 mg/kg ArA-treated, 20 mg/kg TAA-induced liver injury, ArA (10, 20, and 30 mg/kg)-pre-treated liver injury groups.The pre-treatment of ArA ameliorated histopathological injuries of hepatic and kidney tissues and hepatic dysfunction in TAA-treated rats. TAA increased hepatic and kidney injury serum biomarkers, otherwise, ArA significantly suppressed increased levels of these parameters and inhibited metabolic acidosis and dehydration due to TAA treatment. Besides, ArA effectively preserved protein and cholesterol metabolism against TAA-induced hepatic injury. ArA suppressed TAA caused ionic imbalance. Notably, the highest AA dosage (30 mg/kg) provided the most protective effects against TAA-induced liver and kidney damage.This study demonstrated that ArA effectively reduces liver and kidney injuries caused by TAA, indicating its potential as a promising preventive or therapeutic approach.

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来源期刊
Xenobiotica
Xenobiotica 医学-毒理学
CiteScore
3.80
自引率
5.60%
发文量
96
审稿时长
2 months
期刊介绍: Xenobiotica covers seven main areas, including:General Xenobiochemistry, including in vitro studies concerned with the metabolism, disposition and excretion of drugs, and other xenobiotics, as well as the structure, function and regulation of associated enzymesClinical Pharmacokinetics and Metabolism, covering the pharmacokinetics and absorption, distribution, metabolism and excretion of drugs and other xenobiotics in manAnimal Pharmacokinetics and Metabolism, covering the pharmacokinetics, and absorption, distribution, metabolism and excretion of drugs and other xenobiotics in animalsPharmacogenetics, defined as the identification and functional characterisation of polymorphic genes that encode xenobiotic metabolising enzymes and transporters that may result in altered enzymatic, cellular and clinical responses to xenobioticsMolecular Toxicology, concerning the mechanisms of toxicity and the study of toxicology of xenobiotics at the molecular levelXenobiotic Transporters, concerned with all aspects of the carrier proteins involved in the movement of xenobiotics into and out of cells, and their impact on pharmacokinetic behaviour in animals and manTopics in Xenobiochemistry, in the form of reviews and commentaries are primarily intended to be a critical analysis of the issue, wherein the author offers opinions on the relevance of data or of a particular experimental approach or methodology
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