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 |
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Main Authors: | , |
Format: | Journal Article |
Language: | English |
Published: |
Amsterdam
Elsevier B.V
30-09-2011
Elsevier |
Subjects: | |
Online Access: | Get full text |
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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. |
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Bibliography: | http://dx.doi.org/10.1016/j.ejphar.2011.06.017 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0014-2999 1879-0712 |
DOI: | 10.1016/j.ejphar.2011.06.017 |