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对表没食子儿茶素没食子酸酯进行的重复给药研究表明,其具有剂量和给药途径依赖性肝毒性,并伴有血脂异常。

Repeated dose studies with pure Epigallocatechin-3-gallate demonstrated dose and route dependant hepatotoxicity with associated dyslipidemia.

作者信息

Ramachandran Balaji, Jayavelu Subramani, Murhekar Kanchan, Rajkumar Thangarajan

机构信息

Department of Molecular Oncology, Cancer Institute (W.I.A), No. 38, Sardar Patel Road, Adyar, 600 036 Chennai, India.

Department of Oncopathology, Cancer Institute (W.I.A), No. 38, Sardar Patel Road, Adyar, 600 036 Chennai, India.

出版信息

Toxicol Rep. 2016 Mar 5;3:336-345. doi: 10.1016/j.toxrep.2016.03.001. eCollection 2016.

Abstract

EGCG (Epigallocatechin-3-gallate) is the major active principle catechin found in green tea. Skepticism regarding the safety of consuming EGCG is gaining attention, despite the fact that it is widely being touted for its potential health benefits, including anti-cancer properties. The lack of scientific data on safe dose levels of pure EGCG is of concern, while EGCG has been commonly studied as a component of GTE (Green tea extract) and not as a single active constituent. This study has been carried out to estimate the maximum tolerated non-toxic dose of pure EGCG and to identify the treatment related risk factors. In a fourteen day consecutive treatment, two different administration modalities were compared, offering an improved [i.p (intraperitoneal)] and limited [p.o (oral)] bioavailability. A trend of dose and route dependant hepatotoxicity was observed particularly with i.p treatment and EGCG increased serum lipid profile in parallel to hepatotoxicity. Fourteen day tolerable dose of EGCG was established as 21.1 mg/kg for i.p and 67.8 mg/kg for p.o. We also observed that, EGCG induced effects by both treatment routes are reversible, subsequent to an observation period for further fourteen days after cessation of treatment. It was demonstrated that the severity of EGCG induced toxicity appears to be a function of dose, route of administration and period of treatment.

摘要

表没食子儿茶素没食子酸酯(EGCG)是绿茶中发现的主要活性成分儿茶素。尽管EGCG因其潜在的健康益处(包括抗癌特性)而被广泛推崇,但对其食用安全性的怀疑正日益受到关注。缺乏关于纯EGCG安全剂量水平的科学数据令人担忧,因为EGCG通常作为绿茶提取物(GTE)的一个成分进行研究,而非单一活性成分。本研究旨在估计纯EGCG的最大耐受无毒剂量,并确定与治疗相关的风险因素。在连续十四天的治疗中,比较了两种不同的给药方式,即具有更高生物利用度的腹腔注射(i.p)和生物利用度有限的口服(p.o)。观察到了剂量和给药途径依赖性肝毒性趋势,尤其是腹腔注射治疗时,并且EGCG在导致肝毒性的同时使血清脂质水平升高。确定EGCG的十四天耐受剂量腹腔注射为21.1毫克/千克,口服为67.8毫克/千克。我们还观察到,在治疗停止后的另外十四天观察期后,两种治疗途径引起的EGCG效应都是可逆的。结果表明,EGCG诱导的毒性严重程度似乎是剂量、给药途径和治疗时间的函数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b47c/5615837/657d4ca98845/gr1.jpg

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