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Original Research Article


Preliminary Phytochemical Screening, Acute Oral Toxicity and Anticonvulsant Activity of the Berries of Solanum nigrum Linn

 

Hoang Le Son1* and Phan Thi Hai Yen1

1School of Biotechnology, International University – Vietnam National University, Ho Chi Minh City, Vietnam

 

*For correspondence: Email: hlson@hcmiu.edu.vn; Tel: +84 908 311518; Fax: +84 8 37244271

 

Received: 15 November 2013                                          Revised accepted: 9 April 2014

Tropical Journal of Pharmaceutical Research, June 2014; 13(6): 907-912

http://dx.doi.org/10.4314/tjpr.v13i6.12   

Abstract

 

Purpose: To investigate the preliminary phytochemical properties, acute oral toxicity and anticonvulsant activity of the berries of Solanum nigrum Linn (S. nigrum)

Methods: Phytochemicals from the ethanol berry extract were screened by standard methods. Acute oral toxicity study was conducted as per Organisation for Economic Co-operation and Development (OECD) 425 guidelines while anticonvulsant activity was evaluated against pentylenetetrazole (PTZ)-induced seizure in mice. The effect of the extract at dose levels of 50, 100, 200 and 300 mg/kg body weight was evaluated in an experimental mice model, using phenobarbital as positive control (100 mg/kg p.o).

Results: Phytochemical screening revealed that the berries of S. nigrum contain carbohydrates, flavonoids, saponins, tannins, alkaloids, phenols and steroids. The oral median lethal dose of the extract was 3129 mg/kg body weight. The extract significantly delayed the latency of convulsion (p ˂ 0.05) in PTZ-induced seizure mice in at the dose of 300 mg/kg p.o. The extract also reduced the frequency of convulsion and provided up to 100 % protection (300 mg/kg p.o) against death.

Conclusion: The results obtained in this study suggest that the ethanol berry extract of Solanum nigrum is safe and possesses anticonvulsant activity in PTZ-induced seizure in mice.

 

Keywords: Solanum nigrum, Phytochemical, Anticonvulsant, Pentylenetetrazole, Lethal dose, Acute toxicity

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