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从水蓑衣中提取的标准化植物化学成分在斯普拉格-道利大鼠中的安全性评估。

Safety evaluation of a standardized phytochemical composition extracted from Bacopa monnieri in Sprague--Dawley rats.

作者信息

Joshua Allan J, Damodaran A, Deshmukh N S, Goudar K S, Amit A

机构信息

Natural Remedies Pvt. Ltd., 5B, Veerasandra Industrial Area, Bangalore 560 100, India.

出版信息

Food Chem Toxicol. 2007 Oct;45(10):1928-37. doi: 10.1016/j.fct.2007.04.010. Epub 2007 Apr 27.

Abstract

BacoMind is an enriched phytochemical composition derived from Bacopa monnieri, a common medicinal plant having multiple uses in the traditional system of medicine and particularly used as a memory enhancing agent for centuries. The plant and its extracts have been evaluated for anti-inflammatory, cardio tonic, sedative and neuro-muscular blocking activities. In view of the extensive use of this plant, BacoMind , standardized to bioactive compounds was evaluated in a series of toxicity studies, to confirm the safety of its usage. BacoMind , on single oral administration had a median lethal dose of 2,400 mg/kg in Sprague-Dawley rats. In a 14 day repeated dose oral toxicity study in rats, except for mild lowering in body weight gain in male rats, it was found to be tolerated well up to the dose of 500 mg/kg. A subchronic oral toxicity study for 90 days in rats at the dose levels of 85, 210 and 500 mg/kg did not reveal any evidence of toxicity with respect to clinical signs, neurological examination, food consumption, body weight gain, haematological and blood biochemistry parameters. The absolute and relative organ weight of vital organs did not differ significantly from that of the control. Necropsy and histopathological examination, did not reveal any remarkable and treatment related changes. A no-observed adverse effect level of 500 mg/kg body weight was established in rats.

摘要

BacoMind是一种从水蕹菜中提取的富含植物化学成分的物质,水蕹菜是一种常见的药用植物,在传统医学体系中有多种用途,尤其几个世纪以来一直被用作记忆增强剂。该植物及其提取物已被评估具有抗炎、强心、镇静和神经肌肉阻断活性。鉴于这种植物的广泛应用,对标准化为生物活性化合物的BacoMind进行了一系列毒性研究,以确认其使用的安全性。BacoMind单次口服给药时,在斯普拉格-道利大鼠中的半数致死剂量为2400毫克/千克。在大鼠进行的为期14天的重复给药口服毒性研究中,除雄性大鼠体重增加略有降低外,发现其在高达500毫克/千克的剂量下耐受性良好。在大鼠中进行的为期90天、剂量水平为85、210和500毫克/千克的亚慢性口服毒性研究未显示出任何关于临床体征、神经学检查、食物消耗、体重增加、血液学和血液生化参数的毒性证据。重要器官的绝对和相对器官重量与对照组相比没有显著差异。尸检和组织病理学检查未发现任何明显的与治疗相关的变化。在大鼠中确定了无观察到不良反应水平为500毫克/千克体重。

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