Defense Date
6-23-2010
Graduation Date
Summer 2010
Availability
Immediate Access
Submission Type
thesis
Degree Name
MS
Department
Biological Sciences
Committee Chair
John Pollock
Committee Member
Brady Porter
Committee Member
David Somers
Committee Member
Michael Jensen-Seaman
Keywords
CCI, DRG, QPCR, Rat, Splice Variant, TRPV1
Abstract
Transient Receptor Potential Vanilloid 1 (TRPV1) is ligand-gated ion channel that plays an important role in the pain signaling pathway. It is predominantly expressed by sensory neurons located in trigeminal ganglia or dorsal root ganglia (DRG). TRPV1 has been shown to play a crucial role in the generation and maintenance of inflammatory and neuropathic pain. The involvement of splice variants of TRPV1 in pain pathways is not well known. In this study, the mRNA expression of TRPV1 and 3 splice variants (TRPV1.b, TRPV1.β, and TRPV1.var) in DRG was measured following chronic constriction injury of the sciatic nerve in rats. This is the first study to isolate TRPV1.β in rat DRG. The expression of TRPV1 mRNA was elevated following peripheral nerve damage, but not TRPV1.b, TRPV1.var or TRPV1.β. These novel findings suggest that the expression of TRPV1 splice variants is not regulated by sciatic nerve injury.
Format
Language
English
Recommended Citation
Andersen, K. (2010). Exploration of TRPV1 Splice Variant Expression in Rat Dorsal Root Ganglia Following Sciatic Nerve Injury (Master's thesis, Duquesne University). Retrieved from https://dsc.duq.edu/etd/263