槲皮素靶向RISC机制改善乙醇性肝损伤的作用

Lakshana D. Puttahanumantharayappa, Nirmala G. Sannappagowda, Varsha D. Shiragannanavar, Shreyas H. Karunakara, Prasanna K. Santhekadur
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引用次数: 0

摘要

背景:在过去的几十年里,酒精消费量的增加对人类健康产生了有害影响。酒精性脂肪性肝病(AFLD)正在成为一项重大的全球性挑战,因为目前批准的治疗AFLD的药物存在多种副作用。这扩大了天然化合物作为治疗药物的使用范围。作为治疗手段的营养保健品的最新进展揭示了像槲皮素这样的类黄酮。它是一种多种饮食来源的天然抗氧化剂,作为抗炎和抗癌剂的有益作用已被广泛研究。目的:在此框架下,本研究采用瑞士白化病小鼠模型和肝细胞系HepG2研究槲皮素对乙醇性肝损伤的治疗作用。方法:采用WST-1法观察槲皮素对细胞增殖的影响。测定乙醇对小鼠体重和肝重的影响,并采用h&e染色和TMS检测肝损伤。分析炎症基因(TNF-a、IL-6和il - 1b)和rna诱导沉默复合体(RISC)的重要单位SND1的mRNA表达水平。同时还测量了肝酶水平。结果:我们的实验结果显示,乙醇处理HepG2细胞增殖率较低,槲皮素处理后增殖率有所降低。在小鼠模型中,经乙醇处理后,体重明显减轻。相反,肝脏重量和酶活性显著升高。槲皮素处理后,上述效果均有所改善。免疫组织化学数据显示槲皮素治疗组肝组织炎症和纤维化特征有所改善。槲皮素治疗组炎症标志物的表达和SND1水平也有所下降。结论:槲皮素对乙醇处理的HepG2细胞株和乙醇诱导的小鼠肝损伤模型均有保护作用。在这里,我们通过靶向RISC机制阐明了槲皮素在酒精相关性肝病(ARLD)中的一种新的和可能的治疗作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ameliorating Effect Of Quercetin On Ethanol-Induced Liver Injury Via Targeting RISC Machinery
Background : Over the past few decades, increased alcohol consumption has had deleterious effects on human health. Alcoholic fatty liver disease (AFLD) is becoming a major global challenge, as the currently approved drugs for AFLDs are subject to several side effects. This has broadened the scope of the use of natural compounds as therapeutics. Recent advances in nutraceuticals as therapeutics have shed light on fl avonoids such as Quercetin. It is a natural antioxidant of multiple dietary origins and has been extensively studied for its bene fi cial role as an anti-in fl ammatory and anti-cancer agent. Objective : Based on this framework, in the proposed study, we investigated the therapeutic role of Quercetin in Ethanol-induced liver damage using the Swiss Albino mice model and the hepatic cell line HepG2. Methodology : WST-1 assay was performed to access the effect of Quercetin on cell proliferation. The impact of Ethanol on the body and liver weights of mice was measured, and liver injury was determined by H & E staining and TMS. The mRNA expression levels of in fl ammatory genes (TNF-a , IL-6, and IL-1 b ) and SND1, a signi fi cant unit of the RNA-induced silencing complex (RISC), were analyzed. The liver enzyme levels were also measured. Results : Our experimental results showed that HepG2 cells treated with ethanol had a lower proliferation rate, which was later mitigated by treatment with quercetin. In the mice model, a considerable reduction in body weight was detected after ethanol treatment. Conversely, there was a signi fi cant elevation in liver weight and enzyme activity. All of these effects were ameliorated by Quercetin treatment. Immunohistochemistry data revealed an improvement in the in fl ammation and fi brosis characteristics in liver tissues of the Quercetin-treated group. Decreased expression of in-fl ammatory markers and SND1 levels were also observed in the Quercetin-treated group. Conclusion : Based on our results it may be concluded that Quercetin demonstrated hepatoprotective activity in both ethanol-treated HepG2 cell line and ethanol-induced liver injury in mice model. Here, we elucidated a novel and possible therapeutic role of Quercetin in Alcohol-Related Liver Disease (ARLD) by targeting the RISC machinery.
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