绿茶(Camellia sinensis)改善高活性抗逆转录病毒治疗诱导的非酒精性脂肪肝

Dr.Tesaka Wondimnew, S. Genet, N. Gnanasekaran
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引用次数: 1

摘要

背景:高效抗逆转录病毒治疗(HAART)显著提高了hiv感染患者的预期寿命。然而,HAART的使用已被确定有不良事件,包括非酒精性脂肪性肝病(NAFLD)。目的:探讨绿茶(Camellia sinensis)氢甲醇醇提取物(GTE)对高活性抗逆转录病毒治疗诱导的白化Wistar大鼠NAFLD的保护作用。方法:选取体重比较的成年大鼠30只,随机分为5组,每组6只。组1为对照组,组2给予HAART治疗并作为阴性对照,组3、组4、组5分别给予HAART治疗和GTE 100、200、400 mg/kg,疗程60 d。实验结束后,禁食颈椎脱位过夜,穿刺取血。分离血清,进行肝功能检查。从大鼠身上切除肝脏,进行组织病理学研究和脂质分析。结果:hart治疗大鼠血清TGL、总胆固醇、ALT、AST水平升高,肝脏TGL、TBARS水平升高,TAC水平降低。GTE的改善潜力呈剂量依赖性,最高剂量400mg/kg更有效地改善HAART影响的参数接近正常对照。结论:HAART诱导NAFLD的这种后果可能是由于线粒体ROS氧化应激导致肝细胞氧化损伤增加。这可能会发展为肝脏炎症和NAFLD的发展。GTE对NAFLD和氧化应激的作用可能是由于其抗氧化活性和清除HAART诱导的活性氧。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Green Tea (Camellia sinensis) Ameliorate Non-alcoholic Fatty Liver Disease Induced by Highly Active Antiretroviral Therapy
Background: Highly Active Antiretroviral Therapy (HAART) has significantly enhanced the life expectancy of HIV-infected patients. However, utilization of HAART has been identified with adverse events including nonalcoholic fatty liver disease (NAFLD). Objectives: The Objective of this experiment was to explore the conceivable protective effect of green tea (Camellia sinensis) hydro-methonolic extract (GTE) on highly active antiretroviral therapy-induced NAFLD in albino Wistar rats. Methods: Thirty adult rats of comparative weights were chosen and divided into 5 groups of six rats each. Group-1 was a control group, Group II was given HAART and served as negative control, Groups III, IV and V were given HAART and 100, 200 and 400 mg/kg of GTE, respectively for sixty days. At the end of experiment day, the rats were fasted overnight sacrificed by cervical dislocation and blood was taken via cardiac puncture. Serum was separated and liver function test was assessed. Liver were excised from the rats, histopathological studies and lipid profiles were also investigated. Results: Elevated levels of serum TGL, total cholesterol, ALT, AST and liver TGL, TBARS and decreased levels of TAC was seen in HARRT treated rats. The amelioration potential of GTE was observed in a dose-dependent manner, the highest dose 400mg/kg more potently ameliorated HAART affected parameters near to the normal control. Conclusion: This consequence of HAART induced NAFLD may be due to oxidative stress by mitochondrial ROS that leads to increased hepatocellular oxidative damage. This may progress to hepatic inflammation and the development of NAFLD. The effect of GTE against NAFLD and oxidative stress might be due to its antioxidant activity and scavenging of reactive oxygen species induced by HAART.
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