Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2007-4-30
pubmed:abstractText
The transient receptor potential channel of melastatin type 8 (TRPM8), which is gated by low (<25 degrees C) temperature and chemical compounds, is regulated by protein kinase C-mediated phosphorylation in a way opposite to that observed with the transient receptor potential channel of vanilloid type 1 (TRPV1), i.e. by being desensitized and not sensitized. As TRPV1 is sensitized also by protein kinase A (PKA)-mediated phosphorylation, we investigated the effect of two activators of the PKA pathway, 8-Br-cAMP and forskolin, on the activity of menthol and icilin at TRPM8 in HEK-293 cells stably overexpressing the channel (TRPM8-HEK-293 cells). We also studied the effect on TRPM8 of: (1) a series of compounds previously shown to activate or antagonize TRPV1, and (2) co-stimulation of transiently co-expressed cannabinoid CB(1) receptors. Both 8-Br-cAMP (100 microM) and forskolin (10 microM) right-shifted the dose-response curves for the TRPM8-mediated effect of icilin and menthol on intracellular Ca(2+). The inhibitory effects of 8-Br-cAMP and forskolin were attenuated by the selective PKA inhibitor Rp-cAMP-S. Stimulation of human CB(1) receptors transiently co-expressed in TRPM8-HEK-293 cells also inhibited TRPM8 response to icilin. Finally, some TRPV1 agonists and antagonists, but not iodinated antagonists, antagonized icilin- and much less so menthol-, induced TRPM8 activation. Importantly, the endovanilloids/endocannabinoids, anandamide and NADA, also antagonized TRPM8 at submicromolar concentrations. Although these findings need to be confirmed by experiments directly measuring TRPM8 activity in natively TRPM8-expressing cells, they support the notion that the same regulatory events have opposing actions on TRPM8 and TRPV1 receptors and identify anandamide and NADA as the first potential endogenous functional antagonists of TRPM8 channels.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/8-Bromo Cyclic Adenosine..., http://linkedlifedata.com/resource/pubmed/chemical/Arachidonic Acids, http://linkedlifedata.com/resource/pubmed/chemical/Benzaldehydes, http://linkedlifedata.com/resource/pubmed/chemical/Cyclic AMP, http://linkedlifedata.com/resource/pubmed/chemical/Cyclic AMP-Dependent Protein Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Endocannabinoids, http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors, http://linkedlifedata.com/resource/pubmed/chemical/Forskolin, http://linkedlifedata.com/resource/pubmed/chemical/Menthol, http://linkedlifedata.com/resource/pubmed/chemical/Polyunsaturated Alkamides, http://linkedlifedata.com/resource/pubmed/chemical/Pyrimidinones, http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Cannabinoid, CB1, http://linkedlifedata.com/resource/pubmed/chemical/TRPM Cation Channels, http://linkedlifedata.com/resource/pubmed/chemical/TRPM8 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/anandamide, http://linkedlifedata.com/resource/pubmed/chemical/arachidonyl dopamine, http://linkedlifedata.com/resource/pubmed/chemical/icilin, http://linkedlifedata.com/resource/pubmed/chemical/vanillin
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0014-4827
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
313
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1911-20
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:17428469-8-Bromo Cyclic Adenosine Monophosphate, pubmed-meshheading:17428469-Arachidonic Acids, pubmed-meshheading:17428469-Benzaldehydes, pubmed-meshheading:17428469-Cell Line, pubmed-meshheading:17428469-Cell Membrane, pubmed-meshheading:17428469-Cyclic AMP, pubmed-meshheading:17428469-Cyclic AMP-Dependent Protein Kinases, pubmed-meshheading:17428469-Dopamine, pubmed-meshheading:17428469-Dose-Response Relationship, Drug, pubmed-meshheading:17428469-Drug Interactions, pubmed-meshheading:17428469-Endocannabinoids, pubmed-meshheading:17428469-Enzyme Inhibitors, pubmed-meshheading:17428469-Forskolin, pubmed-meshheading:17428469-Humans, pubmed-meshheading:17428469-Ion Channel Gating, pubmed-meshheading:17428469-Menthol, pubmed-meshheading:17428469-Polyunsaturated Alkamides, pubmed-meshheading:17428469-Pyrimidinones, pubmed-meshheading:17428469-Receptor, Cannabinoid, CB1, pubmed-meshheading:17428469-Signal Transduction, pubmed-meshheading:17428469-TRPM Cation Channels, pubmed-meshheading:17428469-Transfection
pubmed:year
2007
pubmed:articleTitle
Regulation of transient receptor potential channels of melastatin type 8 (TRPM8): effect of cAMP, cannabinoid CB(1) receptors and endovanilloids.
pubmed:affiliation
Endocannabinoid Research Group, Institute of Cybernetics, National Research Council, Via Campi Flegrei 34, Comprensorio Olivetti, 80078 Pozzuoli, Naples, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't