CENTRAL MUSCARINIC M(2) CHOLINOCEPTORS INVOLVED IN CHOLINERGIC HYPERTENSION


OZKUTLU U., ONAT F. , ASLAN A., OKTAY S.

EUROPEAN JOURNAL OF PHARMACOLOGY, vol.250, no.3, pp.349-354, 1993 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 250 Issue: 3
  • Publication Date: 1993
  • Doi Number: 10.1016/0014-2999(93)90020-i
  • Title of Journal : EUROPEAN JOURNAL OF PHARMACOLOGY
  • Page Numbers: pp.349-354

Abstract

Cholinomimetic agents increase blood pressure and heart rate via central muscarinic cholinoceptors in various species. It was reported that i.c.v. injection of the muscarinic M(1) and M(3) cholinoceptor selective antagonist, 4-DAMP (4-diphenylacetoxy-N-methyl-piperidine methiodide), inhibited the presser response to physostigmine, while the M, selective antagonist, pirenzepine, was ineffective. In the present study, the involvement of muscarinic M, cholinoceptors in central cholinergic hypertension and tachycardia was investigated. Physostigmine (10-80 mu g/kg i.v.), a cholinesterase inhibitor, and oxotremorine (20-40 mu g/kg i.v.), a direct muscarinic cholinoceptor agonist, caused a dose-dependent increase in blood pressure. Additionally, physostigmine induced dose-dependent tachycardiac responses. I.c.v. administration of the muscarinic M(2) cholinoceptor antagonists, AF-DX 116 and methoctramine, inhibited both physostigmine (60 mu g/kg) and oxotremorine (20 mu g/kg)-induced presser responses at their lower doses used in this study (100 nmol/rat and 10 nmol/rat, respectively). These findings indicate the partial involvement of postsynaptic muscarinic M, cholinoceptors. The higher doses of the antagonists (AF-DX 116 300 nmol/rat and methoctramine 30 nmol/rat) potentiated the blood pressure increase due to physostigmine but did not affect that due to oxotremorine. The physostigmine-induced tachycardiac responses were influenced similarly by these antagonists. These results suggest the presence and tonic influence of presynaptic inhibitory muscarinic M, cholinoceptors.