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Original Research Article


Inhibitory Effect of the root of Polygala tenuifolia on Bradykinin and COX 2-Mediated Pain and Inflammatory Activity

 

Jung Jin Oh and Sung-Jin Kim*

Department of Pharmacology and Toxicology, School of Dentistry, Kyung Hee University, Seoul 130-701, Republic of Korea

 

*For correspondence: Email: kimsj@khu.ac.kr; Tel: +82-2-961-0868; Fax: +82-2-957-5309.

 

Received: 17 July 2013                                                                          Revised accepted: 2 June 2013

Tropical Journal of Pharmaceutical Research, October 2013; 12(5): 755-759

http://dx.doi.org/10.4314/tjpr.v12i5.14   

Abstract

Purpose: To gain insight into the mechanisms of analgesic and anti-inflammatory activities of the root extract of Polygala tenuifolia.

Methods: Polygala tenuifolia was extracted with 70 % methanol and tested for analgesic and anti-inflammatory activities (0.1, 1, 10 and 100 mg/kg) using the following models: acetic acid-induced writhing, rat paw edema, bradykinin inhibtion with rat ileum, and prostaglandin assay.

Results: Administration of the Polygala tenuifolia extract at 100 mg/kg dose produced significant analgesic effect on acetic acid-induced writhing (97 % inhibition) but its effect in the tail-flick test was not significant (p < 0.05). In addition, the extract exerted significant anti-inflammatory effect in the rat paw edema model (8 to 33 % inhibition) at doses ranging from 0.1 - 100.0 mg/kg). A significant inhibitory action (53%) on the bradykinin-mediated contractions of rat ileum was also observed. Furthermore, the extract significantly (p < 0.05) inhibited the production of lipopolysaccharides-induced 6-keto-PGF1a by 28% in macrophage cultures.

Conclusion: These results provide evidence that the Polygala tenuifolia root extract exerts analgesic and anti-inflammatory effects via its significant inhibitory effect on acetic acid writhing test, bradykinin-mediated actions as well as on 6-keto-PGF1a induction.

Keywords: Polygalae radix, Bradylinin, Prostaglandin, COX-2, Inflammation, Analgesic

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