Channelpedia

PubMed 23596210


Referenced in Channelpedia wiki pages of: none

Automatically associated channels: TRP , TRPM , TRPM8 , TRPV , TRPV1



Title: TRPM8 activation attenuates inflammatory responses in mouse models of colitis.

Authors: Rithwik Ramachandran, Eric Hyun, Liena Zhao, Tamia K Lapointe, Kevin Chapman, Christina L Hirota, Subrata Ghosh, David D McKemy, Nathalie Vergnolle, Paul L Beck, Christophe Altier, Morley D Hollenberg

Journal, date & volume: Proc. Natl. Acad. Sci. U.S.A., 2013 Apr 30 , 110, 7476-81

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/23596210


Abstract
Transient Receptor Potential Melastatin-8 (TRPM8), a recently identified member of the transient receptor potential (TRP) family of ion channels, is activated by mild cooling and by chemical compounds such as the supercooling agent, icilin. Since cooling, possibly involving TRPM8 stimulation, diminishes injury-induced peripheral inflammation, we hypothesized that TRPM8 activation may also attenuate systemic inflammation. We thus studied the involvement of TRPM8 in regulating colonic inflammation using two mouse models of chemically induced colitis. TRPM8 expression, localized immunohistochemically in transgenic TRPM8(GFP) mouse colon, was up-regulated in both human- and murine-inflamed colon samples, as measured by real-time PCR. Wild-type mice (but not TRPM8-nulls) treated systemically with the TRPM8 agonist, icilin showed an attenuation of chemically induced colitis, as reflected by a decrease in macroscopic and microscopic damage scores, bowel thickness, and myeloperoxidase activity compared with untreated animals. Furthermore, icilin treatment reduced the 2,4,6-trinitrobenzenesulfonic acid-induced increase in levels of inflammatory cytokines and chemokines in the colon. In comparison with wild-type mice, Dextran Sodium Sulfate (DSS)-treated TRPM8 knockout mice showed elevated colonic levels of the inflammatory neuropeptide calcitonin-gene-related peptide, although inflammatory indices were equivalent for both groups. Further, TRPM8 activation by icilin blocked capsaicin-triggered calcitonin-gene-related peptide release from colon tissue ex vivo and blocked capsaicin-triggered calcium signaling in Transient Receptor Potential Vaniloid-1 (TRPV1) and TRPM8 transfected HEK cells. Our data document an anti-inflammatory role for TRPM8 activation, in part due to an inhibiton of neuropeptide release, pointing to a novel therapeutic target for colitis and other inflammatory diseases.