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Topic: Research - CGRP inhibitors (Read 328 times) |
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floridian
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Very interesting article on how COX2 inhibitors reduce CGRP. This isn't directly a study on clusters, but it could be relevant to us as many researchers believe that CGRP is a linch-pin in the cluster headache pain mechanism. This ties in with previous threads on Vioxx/Celebrex and also with threads on diet (several plant compounds are COX2 inhibitors) and TMJ (injury increases CGRP).
Quote:J Orofac Pain. 2002 Fall;16(4):312-6.
Attenuation of pro-inflammatory neuropeptide levels produced by a cyclooxygenase-2 inhibitor in an animal model of chronic temporomandibular joint inflammation.
Hutchins B, Patel H, Spears R.
Department of Biomedical Sciences, Texas A&M University System Health Science Center, Baylor College of Dentistry, Dallas, Texas 75246, USA. bhutchins@tambcd.edu
AIMS: To study the neurogenic effects of a cyclooxygenase-2 (COX-2) inhibitor, rofecoxib, in an animal model of persistent inflammation. METHODS: Arthritis was induced within the temporomandibular joint (TMJ) by placing complete Freund's adjuvant (CFA) within the superior joint space of the TMJ in adult male rats. The CFA animals were divided into 2 groups, with 1 group given the COX-2 inhibitor, rofecoxib, on days 21 through 28. Tissues were taken from experimental and control animals 4 weeks post-injection and analyzed by radioimmunoassay. The inflammatory-related neuropeptide, immunoreactive calcitonin gene-related peptide (CGRPi), was assayed from both the TMJ tissues and the trigeminal brain stem subnucleus caudalis. RESULTS: CGRPi content was significantly increased in TMJ tissues within the untreated CFA group (72%) and was found to be effectively no different between the CFA/COX-2 group and controls. Trigeminal brain stem subnucleus caudalis CGRPi levels were not different between the groups. CONCLUSION: These results suggest that use of an inhibitor selective for the inducible form of cyclooxygenase enzyme, COX-2, may significantly attenuate the neurogenic component in an inflammatory TMJ animal model.
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