Proteinase-activated receptor-2 and hyperalgesia: A novel pain pathway

Using a combined pharmacological and gene-deletion approach, we have deline ated a novel mechanism of neurokinin-1 (NK-1) receptor-dependent hyperalges ia induced by proteinase-activated receptor-2 (PAR2), a G-protein-coupled r eceptor expressed on nociceptive primary afferent neurons. Injections into the paw of sub-inflammatory doses of PAR2 agonists in rats and mice induced a prolonged thermal and mechanical hyperalgesia and elevated spinal Fos pr otein expression. This hyperalgesia was markedly diminished or absent in mi ce lacking the NK-1 receptor, preprotachykinin-A or PAR2 genes, or in rats treated with a centrally acting cyclooxygenase inhibitor or treated by spin al cord injection of NK-1 antagonists. Here we identify a previously unreco gnized nociceptive pathway with important therapeutic implications, and our results point to a direct role for proteinases and their receptors in pain transmission.