Gamisoyo-san 的安全性评估:遗传毒性、急性毒性和对药物代谢酶的影响。

IF 2.1 4区 医学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Drug and Chemical Toxicology Pub Date : 2024-11-01 Epub Date: 2024-01-30 DOI:10.1080/01480545.2024.2308830
Seong Eun Jin, Mee-Young Lee, Hyekyung Ha, Hyeun-Kyoo Shin, Chang-Seob Seo
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引用次数: 0

摘要

Gamisoyo-san 是一种草药配方,被广泛用于治疗心理问题、更年期症状和痛经。然而,有关其安全性的信息不足。本研究旨在确认伽美索约山的基因毒性和急性毒性潜力。我们进行了一系列试验,包括使用五种细菌菌株进行细菌反向突变试验(艾姆斯试验)、使用中国仓鼠肺(CHL)细胞进行体外染色体畸变试验、小鼠体内微核试验以及人类细胞色素 P450(CYP450)和 UDP-葡萄糖醛酸转移酶(UGT)检测。在急性毒性研究中,给雄性和雌性大鼠口服 Gamisoyo-san 1000、2000 或 5000 毫克/千克,观察 14 天。使用重组杆菌体对人类 CYP450s 和 UGTs 的活性进行了评估。Gamisoyo-san 在五种细菌菌株、CHL 细胞或小鼠骨髓细胞中均未显示出遗传毒性迹象。急性毒性试验表明,大鼠服用伽米索苷的中位致死剂量(LD50)大于 5000 毫克/千克。Gamisoyo-san 可抑制 CYP1A2、CYP2C19 和 UGT1A1 的活性。总之,大鼠服用伽美索伊散的剂量达到 5000 毫克/千克时,可能不会产生严重的毒性事件或基因毒性影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Safety evaluation of Gamisoyo-san: genotoxicity, acute toxicity, and influence on drug-metabolizing enzymes.

Gamisoyo-san is an herbal formula widely used to treat psychological issues, menopausal symptoms, and dysmenorrhea. However, there is insufficient information on its safety profile. This study aimed to confirm the genotoxic and acute toxic potential of Gamisoyo-san. We performed a battery of tests, which included a bacterial reverse mutation test (Ames test) using five bacterial strains, an in vitro chromosomal aberration test using Chinese hamster lung (CHL) cells, an in vivo micronucleus test in mice, and human Cytochrome P450 (CYP450) and UDP-glucuronosyltransferase (UGT) assays. In the acute toxicity study, male and female rats were orally administered Gamisoyo-san 1000, 2000, or 5000 mg/kg and observed for 14 days. The activities of human CYP450s and UGTs were evaluated using recombinant baculosomes. Gamisoyo-san showed no signs of genotoxicity in the five bacterial strains, CHL cells, or mouse bone marrow cells. The acute toxicity test showed that the median lethal dose (LD50) of Gamisoyo-san was greater than 5000 mg/kg in rats. Gamisoyo-san inhibited the activities of CYP1A2, CYP2C19, and UGT1A1. In conclusion, Gamisoyo-san may not exert severe toxicological events or genotoxic effects at doses up to 5000 mg/kg in rats.

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来源期刊
Drug and Chemical Toxicology
Drug and Chemical Toxicology 医学-毒理学
CiteScore
6.00
自引率
3.80%
发文量
99
审稿时长
3 months
期刊介绍: Drug and Chemical Toxicology publishes full-length research papers, review articles and short communications that encompass a broad spectrum of toxicological data surrounding risk assessment and harmful exposure. Manuscripts are considered according to their relevance to the journal. Topics include both descriptive and mechanics research that illustrates the risk assessment implications of exposure to toxic agents. Examples of suitable topics include toxicological studies, which are structural examinations on the effects of dose, metabolism, and statistical or mechanism-based approaches to risk assessment. New findings and methods, along with safety evaluations, are also acceptable. Special issues may be reserved to publish symposium summaries, reviews in toxicology, and overviews of the practical interpretation and application of toxicological data.
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