| Literature DB >> 29501463 |
Jun-Won Yun1, Ji-Ran You2, Yun-Soon Kim2, Seung-Hyun Kim2, Eun-Young Cho2, Jung-Hee Yoon2, Euna Kwon2, Ja-June Jang3, Jin-Sung Park4, Hyoung-Chin Kim5, Jeong-Hwan Che6, Byeong-Cheol Kang7.
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.Entities:
Keywords: Cinnamomum cassia; Cinnamon; Genotoxicity; Subchronic; Toxicity
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Year: 2018 PMID: 29501463 DOI: 10.1016/j.yrtph.2018.02.017
Source DB: PubMed Journal: Regul Toxicol Pharmacol ISSN: 0273-2300 Impact factor: 3.271