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L. 叶通过在酒精处理的肝细胞和小鼠中表现出抗氧化和抗炎作用来抑制酒精性肝病。

L. leaves Suppress Alcohol-Related Liver Disease by Exhibiting Antioxidant and Anti-Inflammatory Effects in Alcohol-Treated Hepatocytes and Mice.

机构信息

Department of Food Innovation and Health, Kyung Hee University, Gyeonggi, Korea.

Department of Medical Nutrition, Kyung Hee University, Yongin, Republic of Korea.

出版信息

J Med Food. 2024 Nov;27(11):1080-1091. doi: 10.1089/jmf.2024.k.0111. Epub 2024 Aug 30.

DOI:10.1089/jmf.2024.k.0111
PMID:39212582
Abstract

Excessive and prolonged alcohol consumption can lead to a serious health condition known as alcohol-related liver disease (ARLD). This ailment represents a significant worldwide health challenge, affecting populations across various demographics. ARLD has a multifactorial pathogenesis involving oxidative stress, inflammation, dysregulated lipid metabolism, and apoptosis. In this study, we investigated the hepatoprotective effects of L. leaf water extract (LLE) against ARLD in alcohol-treated hepatocytes and mice. LLE exhibited antioxidant and anti-inflammatory properties by enhancing antioxidant enzyme activities and suppressing proinflammatory cytokines and CYP2E1 expression in ethanol-treated hepatocytes. Moreover, LLE mitigated lipogenesis by modulating the expression of lipogenic factors in ethanol-treated hepatocytes. , LLE administration attenuated liver injury, oxidative stress, inflammation, and lipid accumulation induced by alcohol consumption in mice. Additionally, LLE suppressed apoptosis signaling pathways implicated in alcohol-induced hepatocyte apoptosis. These findings suggest that LLE functions as a multifaceted therapeutic agent for ARLD by modulating multiple cellular mechanisms, including the reduction of oxidative damage, mitigation of inflammatory responses, alleviation of lipid-mediated toxicity, and regulation of programmed cell death pathways.

摘要

过量和长期饮酒会导致一种严重的健康问题,称为酒精相关性肝病(ARLD)。这种疾病是一个全球性的重大健康挑战,影响着不同人群。ARLD 的发病机制涉及氧化应激、炎症、脂质代谢失调和细胞凋亡等多种因素。在这项研究中,我们研究了 L. 叶水提取物(LLE)对酒精处理的肝细胞和小鼠的 ARLD 的保护作用。LLE 通过增强抗氧化酶活性和抑制乙醇处理的肝细胞中促炎细胞因子和 CYP2E1 的表达,表现出抗氧化和抗炎特性。此外,LLE 通过调节乙醇处理的肝细胞中脂肪生成因子的表达来减轻脂肪生成。LLE 给药可减轻小鼠饮酒引起的肝损伤、氧化应激、炎症和脂质积累。此外,LLE 抑制了与酒精诱导的肝细胞凋亡相关的凋亡信号通路。这些发现表明,LLE 通过调节多种细胞机制,包括减少氧化损伤、减轻炎症反应、缓解脂质介导的毒性以及调节程序性细胞死亡途径,作为 ARLD 的多效治疗剂发挥作用。

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