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葡萄籽提取物通过调节I相解毒途径预防毒死蜱诱导的大鼠肝脏毒性。

Grape seed extract prevents chlorpyrifos-induced toxicity in rat liver through the modulation of phase I detoxification pathway.

作者信息

Ghrir Slim, Ben Abbes Wassim, Chourabi Adam, Abid Ghassen, Jallouli Selim, Elkahoui Salem, Limam Ferid, Aouani Ezzedine, Charradi Kamel

机构信息

Laboratory of Bioactive Substances, Center of Biotechnology of Borj-Cedria, BP 901, 2050, Hammam-Lif, Tunisia.

Laboratory of Legumes and Sustainable Agrosystems, Center of Biotechnology of Borj-Cedria, BP 901, Hammam-Lif 2050, Tunisia.

出版信息

Environ Sci Pollut Res Int. 2024 Mar;31(12):18566-18578. doi: 10.1007/s11356-024-32201-8. Epub 2024 Feb 13.

Abstract

Chlorpyrifos (CPF) poisoning is a public health problem for which there is not currently any effective prophylaxis. In this study, we investigated the protective effect of grape seed extract (GSE) against CPF-induced hepatotoxicity. Rats were daily treated either with CPF (2 mg/kg) or CPF and GSE (20 mg/kg) for 1 week, sacrificed, and their livers dissected for biochemical, molecular, and histopathological analyses. CPF generated liver dysfunction by altering carbohydrate, lipid, amino acid, ammonia and urea metabolism, and provoked mitochondrial impairment through disturbing tricarboxylic acid (TCA) cycle, oxidative phosphorylation (OXPHOS), and mitochondrial viability. CPF also induced cholinergic excitotoxicity along with oxidative stress and histopathological alterations. Interestingly, treatment with GSE prevented all the detrimental effects of CPF through the regulation of cytochrome P450 (CYP450) gene expression. Molecular docking analysis indicated that GSE-containing polyphenols acted as epigenetic modulators through inhibiting DNA (cytosine-5)-methyltransferase 1 (DNMT1), thus favoring the CYP2C6 detoxification pathway. Thereby, GSE might be a promising strategy in the protection of the liver against CPF toxicity.

摘要

毒死蜱(CPF)中毒是一个公共卫生问题,目前尚无有效的预防措施。在本研究中,我们调查了葡萄籽提取物(GSE)对CPF诱导的肝毒性的保护作用。大鼠每天用CPF(2毫克/千克)或CPF与GSE(20毫克/千克)处理1周,然后处死,解剖其肝脏进行生化、分子和组织病理学分析。CPF通过改变碳水化合物、脂质、氨基酸、氨和尿素代谢导致肝功能障碍,并通过干扰三羧酸(TCA)循环、氧化磷酸化(OXPHOS)和线粒体活力引发线粒体损伤。CPF还诱导胆碱能兴奋性毒性以及氧化应激和组织病理学改变。有趣的是,GSE处理通过调节细胞色素P450(CYP450)基因表达预防了CPF的所有有害影响。分子对接分析表明,含GSE的多酚通过抑制DNA(胞嘧啶-5)-甲基转移酶1(DNMT1)作为表观遗传调节剂,从而有利于CYP2C6解毒途径。因此,GSE可能是保护肝脏免受CPF毒性的一种有前景的策略。

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