脂肪肝
氧化应激
谷胱甘肽
脂肪性肝炎
医学
肝功能
酒精性肝病
内科学
丙氨酸转氨酶
肝功能检查
天冬氨酸转氨酶
胃肠病学
药理学
生物信息学
疾病
肝硬化
生物
生物化学
碱性磷酸酶
酶
作者
M. Hong Nguyen,Andrew Lian,Frederick T. Guilford,Vishwanath Venketaraman
出处
期刊:Biomedicines
[Multidisciplinary Digital Publishing Institute]
日期:2025-03-06
卷期号:13 (3): 644-644
被引量:13
标识
DOI:10.3390/biomedicines13030644
摘要
Non-alcoholic fatty liver disease (NAFLD) is a global cause of liver dysfunction. This spectrum of hepatic disorders can progress to severe conditions, such as non-alcoholic steatohepatitis (NASH) and cirrhosis, due to oxidative stress and sustained cellular injury. With limited pharmacological options, glutathione (GSH), a key antioxidant, has shown promising potential in reducing oxidative stress, maintaining redox balance, and improving liver function. This literature review examines studies from 2014-2024 exploring GSH therapy in NAFLD patients. Eligible studies assessed GSH as the primary intervention for NAFLD in human subjects, reporting outcomes such as liver function or oxidative stress markers. Randomized clinical trials (RCTs) were eligible, while combination therapy studies were included if GSH's effect could be isolated. Exclusions applied to non-NAFLD studies, animal/in vitro models, and non-GSH antioxidant interventions. Analysis of three studies (totaling 109 participants) demonstrated consistent improvements in alanine transaminase (ALT) levels and reductions in oxidative stress markers like 8-hydroxy-2-deoxyguanosine (8-OHdG). However, small sample sizes and inconsistent protocols limit generalizability. Further large-scale RCTs are required to confirm GSH's efficacy, determine optimal dosing, and assess long-term effects. This literature review highlights GSH's potential as a novel NAFLD therapeutic strategy while emphasizing the need for further studies to refine its clinical application.
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