人参治疗酒精使用障碍的机制和风险综述。

IF 3 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Eli Frazer, Candi Zhao, Jacky Lee, Jonathan Shaw, Charles Lai, Peter Bota, Tina Allee
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引用次数: 0

摘要

酒精使用障碍(AUD)是一种广泛的、多方面的疾病,涉及促炎细胞因子的过度产生、氧化性肝损伤和大脑多巴胺能奖励回路的功能障碍。韩国红参(KRG)是一种从人参中提取的草药补充剂,已被证明具有治疗AUD的潜在功效,包括抗氧化、抗炎、神经保护和抗焦虑作用。这篇综述研究了KRG的活性成分、它们的药理作用,以及支持KRG在AUD背景下治疗潜力的证据,同时也评估了KRG的安全性、副作用和潜在的药物相互作用。KRG的主要生物活性成分人参皂苷似乎在调节酒精代谢酶、乙醇激活的炎症细胞因子级联反应和AUD破坏的神经系统(包括gaba能和多巴胺能途径)中发挥作用。来自动物模型和有限的小规模人体试验的证据表明,KRG可以通过这些途径缓解酒精戒断症状,增强认知能力并减轻焦虑。虽然食用一般是安全的,但一些病例报告和动物研究表明,KRG在高剂量和长时间服用时可能对弱势群体造成各种风险,包括肝毒性、心血管变化、情绪障碍和激素影响。此外,KRG的神经调节作用和对细胞色素P450酶的影响使其易于与几种药物相互作用,包括华法林、咪达唑仑、selegiline和5 -羟色胺能药物。总的来说,KRG有望作为管理AUD方面的补充,尽管目前的证据受到样本量小,关于人参皂苷机制细微差别的不一致报告以及少量人体试验的限制。需要进一步以人类为中心的研究来阐明其安全性、有效性和机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Review of the Mechanisms and Risks of Panax ginseng in the Treatment of Alcohol Use Disorder.

Alcohol use disorder (AUD) is a widespread, multifaceted disorder involving overproduction of pro-inflammatory cytokines, oxidative liver injury, and dysfunction of the brain's dopaminergic reward circuits. Korean red ginseng (KRG), an herbal supplement derived from Panax ginseng, has demonstrated qualities potentially useful to the treatment of AUD, including antioxidative, anti-inflammatory, neuroprotective, and anxiolytic effects. This review examines active constituents of KRG, their pharmacological actions, and evidence supporting KRG's therapeutic potential in the context of AUD, while also assessing its safety profile, adverse effects, and potential drug interactions. KRG's main bioactive constituents, ginsenosides, appear to have roles in modulating alcohol-metabolizing enzymes, ethanol-activated inflammatory cytokine cascades, and neurological systems disrupted by AUD, including GABAergic and dopaminergic pathways. Evidence from animal models and limited small-scale human trials suggests KRG may alleviate symptoms of alcohol withdrawal, enhance cognitive performance, and attenuate anxiety through these pathways. While generally safe for consumption, several case reports and animal studies have indicated KRG's potential to pose a variety of risks in vulnerable populations at high, prolonged doses, including hepatotoxicity, cardiovascular changes, mood disturbances, and hormonal effects. Furthermore, KRG's neuromodulating role and influence on cytochrome P450 enzymes make it liable to interact with several medications, including warfarin, midazolam, selegiline, and serotonergic agents. Overall, KRG shows promise as a complementary supplement in managing aspects of AUD, though current evidence is limited by low sample sizes, inconsistent reports regarding nuances of ginsenosides' mechanisms, and a low number of human trials. Further human-focused research is needed to elucidate its safety, efficacy, and mechanism.

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