Korea Institute of Oriental Medicine, 1672 Expo-ro, Yuseong-gu, Daejeon 34054, Republic of Korea.
Division of Nonclinical Studies, Korea Institute of Toxicology, P.O. Box 123, 19 Sinseongro, Yuseong-gu, Daejeon, 305-343, Republic of Korea.
J Ethnopharmacol. 2021 Aug 10;276:114122. doi: 10.1016/j.jep.2021.114122. Epub 2021 May 5.
Traditional herbal medicines have diverse efficacy and are increasingly used worldwide. However, some of these herbal medicines have toxicities or side effects, but the scientific understanding of traditional herbal medicine toxicity has not yet been established. Asiasari Radix et Rhizoma (ARE) is known as a herbal medicine used to relieve pain, and recent studies have shown that ARE has anticancer and antimelanogenesis efficacy.
Current study was conducted to assess the potential genotoxicity of an ethanolic extract of ARE.
The genotoxixity of ARE was confirmed by the bacterial reverse mutation assay (Ames test), a mammalian chromosomal aberration test, and a micronucleus test in vivo using ICR mice and comet assay using Sprague-Dawley rats.
ARE showed no genotoxicity in a micronucleus test up to 2000 mg/kg body weight in vivo. By contrast, the chromosomal aberration test showed that ARE induced an increase in the number of chromosomal aberrations after treatment for 6 h with a metabolic activation system and for 6 and 22 h without the metabolic activation system when compared with vehicle control. In the Ames test, all strains except TA1535, with or without a metabolic activation system, showed an increase in the number of revertant mutant colonies in the ARE-treated group. In comet assay, DNA damage was observed in the stomach when ARE was administered.
ARE potentially shows genotoxicity by inducing DNA damage.
传统草药具有多种功效,在全球范围内的应用日益广泛。然而,其中一些草药具有毒性或副作用,但对传统草药毒性的科学认识尚未建立。关白附(ARE)作为一种用于止痛的草药而闻名,最近的研究表明,ARE 具有抗癌和抗黑色素生成的功效。
本研究旨在评估 ARE 乙醇提取物的潜在遗传毒性。
通过细菌回复突变试验(Ames 试验)、哺乳动物染色体畸变试验和 ICR 小鼠体内微核试验以及 Sprague-Dawley 大鼠彗星试验,证实了 ARE 的遗传毒性。
在体内微核试验中,ARE 最高 2000mg/kg 体重时无遗传毒性。相比之下,染色体畸变试验表明,与对照组相比,在用代谢激活系统处理 6 小时后,以及在没有代谢激活系统的情况下处理 6 小时和 22 小时后,ARE 诱导染色体畸变数量增加。在 Ames 试验中,除 TA1535 菌株外,无论是否有代谢激活系统,经 ARE 处理的组中回复突变菌落数均增加。在彗星试验中,当给予 ARE 时,胃中观察到 DNA 损伤。
ARE 通过诱导 DNA 损伤可能表现出遗传毒性。