Title : Pharmacology of vanilloids at recombinant and endogenous rat vanilloid receptors.

Pub. Date : 2003 Jan 1

PMID : 12473388






4 Functional Relationships(s)
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1 This study compared the actions of members of five different chemical classes of vanilloid agonists at the recombinant rat vanilloid VR1 receptor expressed in HEK293 cells, and at endogenous vanilloid receptors on dorsal root ganglion cells and sensory nerves in the rat isolated mesenteric arterial bed. Capsaicin transient receptor potential cation channel, subfamily V, member 1 Rattus norvegicus
2 In VR1-HEK293 cells and dorsal root ganglion neurones, Ca(2+) responses were induced by resiniferatoxin>capsaicin=olvanil>PPAHV; all four were full agonists. Capsaicin transient receptor potential cation channel, subfamily V, member 1 Rattus norvegicus
3 Olvanil had a Hill coefficient of approximately 1 whilst capsaicin, resiniferatoxin and PPAHV had Hill coefficients of approximately 2 in VR1-HEK293 cells. Capsaicin transient receptor potential cation channel, subfamily V, member 1 Rattus norvegicus
4 These data show that resiniferatoxin, capsaicin, olvanil and PPAHV, but not scutigeral and isovelleral, are agonists at recombinant rat VR1 receptors and endogenous vanilloid receptors on dorsal root ganglion neurones and in the rat mesenteric arterial bed. Capsaicin transient receptor potential cation channel, subfamily V, member 1 Rattus norvegicus