Referenced in: none

Automatically associated channels: TRP , TRPV , TRPV1

Title: Colonic inflammation up-regulates voltage-gated sodium channels in bladder sensory neurons via activation of peripheral transient potential vanilloid 1 receptors.

Authors: Q Lei, A P Malykhina

Journal, date & volume: , 2012 Mar 15 , ,

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/22420642

Abstract
Primary sensory neurons express several types of ion channels including transient receptor potential vanilloid 1 (TRPV1) and voltage-gated Na(+) channels. Our previous studies showed an increased excitability of bladder primary sensory and spinal neurons triggered by inflammation in the distal colon as a result of pelvic organ cross-sensitization. The goal of this work was to determine the effects of TRPV1 receptor activation by potent agonists and/or colonic inflammation on voltage-gated Na(+) channels expressed in bladder sensory neurons.Sprague-Dawley rats were treated with intracolonic saline (control), resiniferatoxin (RTX, 10(-7 ) mol L(-1)), TNBS (colonic irritant) or double treatment (RTX followed by TNBS).TNBS-induced colitis increased the amplitude of total Na(+) current by two-fold and of tetrodotoxin resistant (TTX-R) Na(+) current by 78% (P ≤ 0.05 to control) in lumbosacral bladder neurons during acute phase (3 days post-TNBS). Instillation of RTX in the distal colon caused an enhancement in the amplitude of total Na(+) current at -20 mV from -112.1 ± 18.7 pA/pF (control) to -183.6 ± 27.8 pA/pF (3 days post-RTX, P ≤ 0.05) without changes in TTX resistant component. The amplitude of net Na(+) current was also increased by 119% at day 3 in the group with double treatment (RTX followed by TNBS, P ≤ 0.05 to control) which was significantly higher than in either group with a single treatment.These results provide evidence that colonic inflammation activates TRPV1 receptors at the peripheral sensory terminals leading to an up-regulation of voltage gated Na(+) channels on the cell soma of bladder sensory neurons. This mechanism may underlie the occurrence of peripheral cross-sensitization in the pelvis and functional chronic pelvic pain.