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睡茄(L.)Dunal 全植物提取物在 GLP 合规下的大鼠 28 天亚急性毒性评价中表现出可接受的非临床安全性。

Withania somnifera (L.) Dunal whole-plant extract demonstrates acceptable non-clinical safety in rat 28-day subacute toxicity evaluation under GLP-compliance.

机构信息

Drug Discovery and Development Division, Patanjali Research Institute, NH-58, Roorkee-Haridwar Road, Haridwar, Uttarakhand, 249 405, India.

Department of Allied and Applied Sciences, University of Patanjali, NH-58, Haridwar, Uttarakhand, 249405, India.

出版信息

Sci Rep. 2022 Jun 30;12(1):11047. doi: 10.1038/s41598-022-14944-x.

Abstract

Withania somnifera (L.) Dunal (Ashwagandha) is widely used in Ayurveda, Unani and Siddha systems of medicines due to its therapeutic application in numerous ailments. Traditionally, the medications prepared from the plant employ only its roots and based on the currently available scientific literature, their efficacy and safety is well established. Apart from the roots, the aerial parts also contain bioactive components and correspondingly certain marketed preparations also employ the leaves of the plant. Accordingly, Ministry of Ayush, Government of India has lately issued an advisory emphasizing the need for extensive efficacy and safety profiling of leaf-based products. Consequently, we have conducted the present GLP-driven study, in which the non-clinical safety of a hydromethanolic extract of the whole plant of Withania somnifera (WSWPE) has been assessed according to OECD guideline 407. In this study Sprague Dawley rats of either sex were orally administered with WSWPE for 28-consecutive days at the doses of 100, 300 and 1000 mg/kg/day. The study also included a satellite group of animals that received WSWPE for 28-days followed by a 14-days recovery period. Withania somnifera Whole Plant Extract was found to be safe up to the dose level of 1000 mg/kg/day as no toxicologically relevant findings could be detected.

摘要

睡茄(Withania somnifera(L.)Dunal)在阿育吠陀、顺势疗法和悉达医学体系中被广泛应用,因为它对许多疾病都有治疗作用。传统上,从植物中制备的药物仅使用其根,并且根据目前可用的科学文献,其疗效和安全性得到了很好的证实。除了根之外,地上部分也含有生物活性成分,相应地,某些市售制剂也使用植物的叶子。因此,印度政府的阿育吠陀部最近发布了一项咨询意见,强调需要对基于叶子的产品进行广泛的疗效和安全性评估。因此,我们进行了本项符合 GLP 原则的研究,根据 OECD 指南 407,评估了整个睡茄(Withania somnifera)植物的水-甲醇提取物(WSWPE)的非临床安全性。在这项研究中,雄性和雌性 Sprague Dawley 大鼠连续 28 天口服给予 WSWPE,剂量分别为 100、300 和 1000mg/kg/天。该研究还包括一组接受 WSWPE 治疗 28 天,然后进行 14 天恢复期的卫星组动物。在 1000mg/kg/天的剂量水平下,未发现与毒性相关的发现,因此可以认为睡茄全株提取物是安全的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7851/9246939/eb38426e5e55/41598_2022_14944_Fig1_HTML.jpg

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