睡茄根提取物对 Sprague Dawley 大鼠的急性和亚慢性口服 GLP 毒性。

Q2 Pharmacology, Toxicology and Pharmaceutics Drug metabolism and personalized therapy Pub Date : 2024-10-02 DOI:10.1515/dmdi-2024-0056
Pralhad Wangikar, Pradhnya Chaudhari, Eshita Sharma, Chhaya Godse, Ashit Vora, Sujit Nair
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引用次数: 0

摘要

目的睡茄(WS)是一种珍贵的药用植物,被用于治疗多种疾病。WS 的药用特性归因于其存在的次生代谢物,而这些次生代谢物在草药保健品行业中需求量很大。尽管 WS 的治疗效果众所周知,但仍有必要对 WS 植物在大鼠身上的临床前毒性进行评估,并进一步探索其在人类各种疾病治疗中的潜在应用。现有研究根据 OECD-423 和 -408 准则以及 GLP 合规性,分别对 Sprague Dawley(SD)大鼠(雄性和雌性)口服 WS 根提取物 14 天和 90 天的急性和亚慢性毒性进行了评估:在急性毒性试验中,给雌雄大鼠口服 2,000 毫克/千克的剂量。在亚慢性毒性试验中,给动物重复口服 250、500、1,000 毫克/千克剂量的 WS 根提取物,持续 90 天,再加上 14 天的恢复期。此外,还观察了另外两组动物(每组 5 只动物),分别在 90 天内服用载体和 1,000 毫克/千克的 WS 根提取物:结果:在急性毒性方面,结果显示 WS 根提取物对 SD 大鼠的半数致死剂量高于 2,000 毫克/千克。在亚慢性毒性方面,给大鼠口服 90 天提取物未显示出明显的毒性变化。血液和血清化学指标均在正常范围内。最后的尸体解剖没有发现大体或组织病理学结果:结论:WS 根提取物的无观测不良效应水平(NOAEL)为 1,000 毫克/千克体重,在此剂量下对大鼠使用是安全的。
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Acute and sub-chronic oral GLP toxicity of Withania somnifera root extract in Sprague Dawley rats.

Objectives: Withania somnifera (WS) is a valuable medicinal plant that has been used against several ailments. The medicinal properties of WS are ascribed to existence of secondary metabolites which are in great demand in herbal nutraceutical industry. Despite well-known therapeutic effects of WS, it is necessary to assess preclinical toxicity of WS plant on rats and further explore its potential application against treatment of various disorders in humans. The existing study assessed oral acute and sub-chronic toxicities of WS root extract in Sprague Dawley (SD) rats (male and female) for 14 and 90 days, respectively under OECD-423 and -408 guidelines as well as GLP compliance.

Methods: In acute toxicity, rats of either sex were orally fed a dose of 2,000 mg/kg. In sub-chronic toxicity, animals were orally administered repeated doses of WS root extract at 250, 500, 1,000 mg/kg for 90 days with an additional 14-day recovery period. Two more groups (n=5 animals each) receiving vehicle and 1,000 mg/kg of WS root extract for 90 days were also observed.

Results: In acute toxicity, the results revealed that LD50 of WS root extract in SD rats was higher than 2,000 mg/kg. In sub-chronic toxicity, oral administration of extract for 90 days showed no significant toxicological changes in rats. Haematological and serum chemistry markers were found within normal range. Terminal necropsy showed no gross or histopathological outcomes.

Conclusions: The no-observed-adverse-effect level (NOAEL) of WS root extract was 1,000 mg/kg body weight, and safe to use at this dose in rats.

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来源期刊
Drug metabolism and personalized therapy
Drug metabolism and personalized therapy Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
2.30
自引率
0.00%
发文量
35
期刊介绍: Drug Metabolism and Personalized Therapy (DMPT) is a peer-reviewed journal, and is abstracted/indexed in relevant major Abstracting Services. It provides up-to-date research articles, reviews and opinion papers in the wide field of drug metabolism research, covering established, new and potential drugs, environmentally toxic chemicals, the mechanisms by which drugs may interact with each other and with biological systems, and the pharmacological and toxicological consequences of these interactions and drug metabolism and excretion. Topics: drug metabolizing enzymes, pharmacogenetics and pharmacogenomics, biochemical pharmacology, molecular pathology, clinical pharmacology, pharmacokinetics and drug-drug interactions, immunopharmacology, neuropsychopharmacology.
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