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菊科植物地上部分乙醇提取物对大鼠的急性和亚急性毒性评估。

Assessment of the acute and sub-acute toxicity of the ethanolic extract of the aerial parts of (Asteraceae) in rats.

作者信息

Hsu Pang-Kuei, Tsai Yueh-Ting, Lin Yu-Cheng, Kuan Chen-Meng

机构信息

Greenyn Biotechnology Co., Ltd., Taichung City, 42881, Taiwan.

Testing Center, Super Laboratory Inc., New Taipei City, 24890, Taiwan.

出版信息

Toxicol Rep. 2021 Dec 16;9:58-63. doi: 10.1016/j.toxrep.2021.12.005. eCollection 2022.

Abstract

This pioneering study was to assess the acute and sub-acute toxicity of the ethanolic extract of the aerial parts of (Asteraceae) in rats. is a common vegetable and herb for treating inflammation-related syndromes in Taiwan. Pharmacological studies have unveiled that the extracts of have potential to become hepatoprotective, anti-inflammatory, or anti-cancer agents. The toxicological effects of the aerial parts of in rodents are still elusive. For the acute toxicity study, rats were administrated with a single dose of 5,000 mg/kg body weight (BW) and observed for 14 days in accordance with the Organization for Economic Cooperation and Development (OECD) guideline No. 420. For the sub-acute toxicity study, animals were orally treated with daily doses of 0, 416.7, 833.3, and 1,666.7 mg/kg BW for 28 days based on the OECD guideline No. 407. The toxicity of the repeated dose was observed with anthropometric, hematological, and biochemical parameters as well as histology. The mortality and critical pathological and biochemical abnormalities were not observed in the acute and/or sub-acute toxicity studies. The oral median lethal dose (LD) of the extract was greater than 5000 mg/kg BW. The no-observed-adverse-effect-level (NOAEL) in male and female rats was greater than 1,666.7 mg/kg BW. As such, the extract of the aerial parts of is considered a non-toxic substance.

摘要

这项开创性研究旨在评估菊科植物地上部分乙醇提取物对大鼠的急性和亚急性毒性。该菊科植物是台湾一种用于治疗炎症相关综合征的常见蔬菜和草药。药理学研究表明,该植物提取物有潜力成为保肝、抗炎或抗癌药物。该菊科植物地上部分在啮齿动物中的毒理学效应仍不明确。在急性毒性研究中,按照经济合作与发展组织(OECD)第420号指南,给大鼠单次灌胃5000毫克/千克体重,并观察14天。在亚急性毒性研究中,根据OECD第407号指南,给动物每日口服0、416.7、833.3和1666.7毫克/千克体重的剂量,持续28天。通过人体测量、血液学和生化参数以及组织学观察重复给药的毒性。在急性和/或亚急性毒性研究中未观察到死亡以及严重的病理和生化异常。该提取物的口服半数致死剂量(LD)大于5000毫克/千克体重。雄性和雌性大鼠的未观察到有害作用水平(NOAEL)大于1666.7毫克/千克体重。因此,该菊科植物地上部分的提取物被认为是一种无毒物质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b142/8717411/ac714c33a97d/ga1.jpg

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