Exploring the potential of telmisartan in chronic constriction injury-induced neuropathic pain in rats

The present study was designed to investigate the potential of telmisartan, an angiotensin AT 1 receptor, in chronic constriction injury-induced neuropathic pain in rats. Four loose ligatures were placed around the sciatic nerve to induce chronic constriction injury and neuropathic pain. Acetone dro...

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Published in:European journal of pharmacology Vol. 667; no. 1; pp. 215 - 221
Main Authors: Jaggi, Amteshwar Singh, Singh, Nirmal
Format: Journal Article
Language:English
Published: Amsterdam Elsevier B.V 30-09-2011
Elsevier
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Summary:The present study was designed to investigate the potential of telmisartan, an angiotensin AT 1 receptor, in chronic constriction injury-induced neuropathic pain in rats. Four loose ligatures were placed around the sciatic nerve to induce chronic constriction injury and neuropathic pain. Acetone drop, pin-prick, hot plate and paint brush tests were performed to assess cold allodynia; mechanical and heat hyperalgesia; and dynamic mechanical allodynia, respectively along with assessment of spontaneous pain and postural index in terms of foot deformity. The levels of TNF-α were measured in the sciatic nerve as an index of inflammation. Chronic constriction injury was associated with development of cold allodynia; mechanical and heat hyperalgesia; dynamic mechanical allodynia; and spontaneous pain and foot deformity along with rise in the levels of TNF-α. Telmisartan (1, 2, 5 mg/kg, p.o.) was administered for 14 days in chronic constriction injury subjected rats. Administration of telmisartan (2, 5 mg/kg) significantly attenuated chronic constriction injury-induced pain related behavior, foot deformity and rise in TNF-α level. It may be concluded that telmisartan has a potential in attenuating neuropathic pain behavior in chronic constriction injury model which may possibly be attributed to its anti-inflammatory properties.
Bibliography:http://dx.doi.org/10.1016/j.ejphar.2011.06.017
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ISSN:0014-2999
1879-0712
DOI:10.1016/j.ejphar.2011.06.017