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. 2016 Jul 27:16:249.
doi: 10.1186/s12906-016-1236-4.

Acute and chronic toxicities of Bacopa monnieri extract in Sprague-Dawley rats

Affiliations

Acute and chronic toxicities of Bacopa monnieri extract in Sprague-Dawley rats

Seewaboon Sireeratawong et al. BMC Complement Altern Med. .

Abstract

Background: Bacopa monnieri is a medicinal plant which has long been used in Ayurvedic medicines to augment brain function and to improve memory. The purpose of our study was to identify and evaluate possible toxic effects of B. monnieri extract in rats by assessing hematological, biochemical, and histopathological parameters.

Methods: Acute oral toxicity of Bacopa monnieri extract was studied in female rats by giving a single orally administered dose at a level of 5,000 mg/kg. The rats were monitored for toxic signs for 14 days. In the chronic toxicity test, groups of both female and male rats were given daily oral doses of B. monnieri extract at dose levels of either 30, 60, 300 or 1,500 mg/kg for 270 days. The behavior and health of the animals was then monitored. At the end of the observation period, the body and organ weights of the rats in each group were measured. Blood was collected and necropsy was performed to evaluate their hematology, blood clinical chemistry, and microanatomy.

Results: The acute toxicity test found no significant differences between the experimental and the control group rats. In the chronic toxicity test, animal behavior and health of the experimental groups were normal, just as in the control rats. All values of other parameters assessed remained within the normal range.

Conclusion: A single oral administration of B. monnieri extract at the dose of 5,000 mg/kg did not cause any serious undesirable effects. B. monnieri extract at doses of 30, 60, 300 and 1,500 mg/kg given for 270 days did not produce any toxicity in rats.

Keywords: Acute toxicity; Bacopa monnieri; Chronic toxicity.

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Figures

Fig. 1
Fig. 1
Histopathology of the liver and kidney of rats in acute toxicity test at 40x magnification (haematoxylin-eosin stain)
Fig. 2
Fig. 2
Body weight of rats treated with B. monnieri in chronic toxicity. a Female. b Male. *Significantly different from control, p < 0.05
Fig. 3
Fig. 3
Histopathology of the liver and kidney of rats in chronic toxicity test at 40x magnification (haematoxylin-eosin stain)

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