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肉桂提取物(Cinnamomum cassia)在一般和遗传毒理学方面的体外和体内安全性研究。

In vitro and in vivo safety studies of cinnamon extract (Cinnamomum cassia) on general and genetic toxicology.

机构信息

Department of Biotechnology, The Catholic University of Korea, Bucheon, Republic of Korea.

Department of Experimental Animal Research, Biomedical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.

出版信息

Regul Toxicol Pharmacol. 2018 Jun;95:115-123. doi: 10.1016/j.yrtph.2018.02.017. Epub 2018 Mar 6.

DOI:10.1016/j.yrtph.2018.02.017
PMID:29501463
Abstract

Cinnamomum cassia has been widely used as a natural product to treat diseases in Asia due to its diverse pharmacological functions including anti-inflammatory, anti-oxidant, anti-microbial, anti-diabetic, and anti-tumor effects. Despite its ethnomedicinal benefits, little information regarding its toxicity is currently available. The aim of this study was to evaluate its potential long-term toxicity and genotoxicity in compliance with test guidelines of the Organization for Economic Cooperation and Development. A 13-week repeat-dose oral toxicity study revealed that body weights of rats were normal after receiving cinnamon extract at up to 2000 mg/kg. High-dose intake of cinnamon extract (2000 mg/kg) showed potential nephrotoxicity and hepatotoxicity to both males and females as evidenced by obvious increases of kidney/liver weight along with a small but statistically elevation of total cholesterol level. Overall findings from genetic toxicity testing battery including Ames test, in vitro mammalian cell micronucleus assay, and in vivo bone marrow micronucleus assay indicated that cinnamon extract was not mutagenic or clastogenic. In conclusion, cinnamon extract may possess potential nephrotoxicity and hepatotoxicity at dose higher than its recommended daily safe dose. Further study is needed to clarify the mechanism involved in its induction of liver and kidney injury.

摘要

肉桂已被广泛用作天然产物来治疗亚洲的疾病,因为它具有多种药理作用,包括抗炎、抗氧化、抗菌、抗糖尿病和抗肿瘤作用。尽管具有民族医学上的益处,但目前关于其毒性的信息很少。本研究旨在根据经济合作与发展组织的测试指南评估其潜在的长期毒性和遗传毒性。为期 13 周的重复剂量口服毒性研究表明,大鼠在接受高达 2000mg/kg 的肉桂提取物后体重正常。高剂量摄入肉桂提取物(2000mg/kg)对雄性和雌性均表现出潜在的肾毒性和肝毒性,这表现在肾脏/肝脏重量明显增加,以及总胆固醇水平略有但统计学上升高。包括 Ames 试验、体外哺乳动物细胞微核试验和体内骨髓微核试验在内的遗传毒性测试组合的总体结果表明,肉桂提取物没有致突变性或断裂作用。总之,肉桂提取物在高于其推荐的每日安全剂量时可能具有潜在的肾毒性和肝毒性。需要进一步的研究来阐明其诱导肝和肾损伤的机制。

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