Desensitization of β-adrenoceptors following repeated injections of 2-substituted 4-phenylquinolines
- 1 September 1987
- journal article
- research article
- Published by Oxford University Press (OUP) in Journal of Pharmacy and Pharmacology
- Vol. 39 (9) , 746-747
- https://doi.org/10.1111/j.2042-7158.1987.tb06984.x
Abstract
The chronic effects of five 2-substituted 4-phenylquinoline derivatives on the sensitivity of the noradrenergic cyclic AMP-generating system in the rat brain cortex have been determined, and compared with those of the typical and atypical antidepressants imipramine and trazodone, respectively. Acute treatment (single i.p. dose of 20 mg kg−1) and sub-chronic treatment (20 mg kg−1 daily for 10 days) induced no significant desensitization of the β-adrenoceptors. However, chronic treatment (20 mg kg−1 daily for 3 weeks) significantly decreased the isoprenaline-induced increase in cyclic AMP, suggesting desensitization. This effect, coupled with previous findings, points to a potential role of these compounds as antidepressants.Keywords
This publication has 4 references indexed in Scilit:
- Antihistamine, anticholinergic and cardiovascular effects of 2-substituted-4-phenylquinoline derivativesLife Sciences, 1986
- Design, synthesis and pharmacological activities of 2-substituted 4-phenylquinolines as potential antidepressant drugsJournal of Medicinal Chemistry, 1985
- Tricyclic antidepressant drug action correlates with its tissue levels in anterior neocortexNeuropharmacology, 1982
- Action of various antidepressant treatments reduces reactivity of noradrenergic cyclic AMP-generating system in limbic forebrainNature, 1975