EFFECTS OF IMIDAZOLE COMPOUNDS ON CATECHOLAMINE RELEASE IN ADRENAL CHROMAFFIN CELLS

1. Effects of imidazole compounds and guanabenz on the stimulus-evoked release of catecholamine (CA) were studied in cultured bovine adrenal chromaffin cells. 2. Clonidine, oxymetazoline, phentolamine, chlorpheniramine, and guanabenz inhibited acetylcholine (ACh)-evoked CA release in a dose-dependent manner, but not high K+-evoked release. 3. The inhibition by these compounds was not antagonized by nonimidazole and nonguanidine alpha-2-antagonists (yohimbine and phenoxybenzamine) but was significantly antagonized by tolazoline (imidazole alpha-2-antagonist) and cimetidine (imidazole H-2-antagonist). Moreover, tolazoline by itself augmented the ACh-evoked, but not the high K+-evoked, CA release. 4. Although chlorpheniramine and cimetidine are antagonists for H-1 and H-2 histaminergic receptors, the site of action for these compounds in our results seemed to differ from the histamine receptors. 5. These results suggest that the inhibitory action of imidazole compounds and guanabenz on ACh-evoked CA release in adrenal chromaffin cells is mediated through an imidazole receptor. Adrenal chromaffin cells may contain an endogenous clonidine-displacing substance (CDS) which has been found in adrenal gland and brain as an endogenous ligand for imidazole receptors. Thus, CDS may have a regulatory role in the stimulus-secretion coupling in these cells.