Combination of a Rapidly Penetrating Agonist and a Slowly Penetrating Antagonist Affords Agonist Action of Limited Duration at the Cellular Level
10.4062/biomolther.2019.013
- Author:
Larry V PEARCE
1
;
Jihyae ANN
;
Peter M BLUMBERG
;
Jeewoo LEE
Author Information
1. Laboratory of Cancer Biology and Genetics, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892-4255, USA. burrows@fred.net
- Publication Type:Original Article
- Keywords:
TRPV1;
Capsaicin;
Resiniferatoxin;
Vanilloid;
Pain;
Pharmacodynamics
- MeSH:
Capsaicin;
Ligands;
Nociception
- From:Biomolecules & Therapeutics
2019;27(5):435-441
- CountryRepublic of Korea
- Language:English
-
Abstract:
The capsaicin receptor TRPV1 (transient receptor potential vanilloid 1) has been an object of intense interest for pharmacological development on account of its critical role in nociception. In the course of structure activity analysis, it has become apparent that TRPV1 ligands may vary dramatically in the rates at which they interact with TRPV1, presumably reflecting differences in their abilities to penetrate into the cell. Using a fast penetrating agonist together with an excess of a slower penetrating antagonist, we find that we can induce an agonist response of limited duration and, moreover, the duration of the agonist response remains largely independent of the absolute dose of agonist, as long as the ratio of antagonist to agonist is held constant. This general approach for limiting agonist duration under conditions in which absolute agonist dose is variable should have more general applicability.
