Suppr超能文献

成熟啤酒花提取物经热处理提取的遗传、急性和亚慢性毒性研究。

Genetic, acute and subchronic toxicity studies of matured hop extract produced by extraction from heat-treated hops.

机构信息

Research Laboratories for Health Science and Food Technologies, Kirin Co., Ltd.

Central Laboratories for Key Technologies, Kirin Co., Ltd.

出版信息

J Toxicol Sci. 2018;43(7):473-484. doi: 10.2131/jts.43.473.

Abstract

It has been demonstrated that successive ingestion of matured hop extract (MHE), produced by extraction from heat-treated hops, results in body fat reduction in animals and humans; however, preclinical safety studies have not been reported. In this study, we conducted in vitro and in vivo safety studies for MHE. Genotoxicity was evaluated using the Ames test, in vitro chromosomal aberration test, and in vivo micronucleus test. To assess acute safety, a single, oral administration of MHE to rats was monitored. Subchronic safety was assessed by repeated feeding with MHE for 90 days. The in vitro chromosomal aberration test was positive at 3,330 μg/mL and 5,000 μg/mL without metabolic activation. However, MHE did not induce any reverse mutation with or without metabolic activation in the Ames test, and no abnormalities were observed at a dose of 2,000 mg/kg body weight in the rat micronucleus test. In the acute and subchronic safety studies, no deaths or toxicological signs were recorded during the observation period. In addition, no changes in body weights, feed/water consumption, clinical signs, ophthalmoscopy, urinalysis, hematology, blood biochemistry, organ weights, or histopathology were observed after repeated administration of MHE. Therefore, the no-observed-adverse-effect-level (NOAEL) of MHE was considered to be over 3,484 and 4,022 mg/kg body weight/day in males and females, respectively. These results indicate that there is no safety concern for MHE in the present preclinical safety study.

摘要

已证实,连续摄入经热处理啤酒花提取而成的成熟啤酒花提取物(MHE)可减少动物和人体内的体脂肪;然而,目前尚未报道其临床前安全性研究。在这项研究中,我们对 MHE 进行了体外和体内安全性研究。使用 Ames 试验、体外染色体畸变试验和体内微核试验评估遗传毒性。为评估急性安全性,单次经口给予大鼠 MHE 后进行监测。通过重复给予 MHE 90 天来评估亚慢性安全性。未经代谢激活时,体外染色体畸变试验在 3,330 μg/mL 和 5,000 μg/mL 时呈阳性;然而,MHE 在 Ames 试验中无论是否有代谢激活均未引起任何回复突变,并且在大鼠微核试验中,在 2,000 mg/kg 体重的剂量下未观察到任何异常。在急性和亚慢性安全性研究中,在观察期间未记录到死亡或毒性体征。此外,在重复给予 MHE 后,体重、饲料/水消耗、临床体征、眼科学、尿液分析、血液学、血液生化学、器官重量或组织病理学均未发生变化。因此,雄性和雌性大鼠的 MHE 的未观察到不良效应水平(NOAEL)分别认为超过 3,484 和 4,022 mg/kg 体重/天。这些结果表明,在本临床前安全性研究中,MHE 不存在安全性问题。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验