BIMODAL REGULATION OF CYCLIC-AMP BY MUSCARINIC RECEPTORS - INVOLVEMENT OF MULTIPLE G-PROTEINS AND DIFFERENT FORMS OF ADENYLYL-CYCLASE

Citation
P. Onali et Mc. Olianas, BIMODAL REGULATION OF CYCLIC-AMP BY MUSCARINIC RECEPTORS - INVOLVEMENT OF MULTIPLE G-PROTEINS AND DIFFERENT FORMS OF ADENYLYL-CYCLASE, Life sciences, 56(11-12), 1995, pp. 973-980
Citations number
31
Categorie Soggetti
Biology,"Medicine, Research & Experimental","Pharmacology & Pharmacy
Journal title
ISSN journal
00243205
Volume
56
Issue
11-12
Year of publication
1995
Pages
973 - 980
Database
ISI
SICI code
0024-3205(1995)56:11-12<973:BROCBM>2.0.ZU;2-P
Abstract
In membranes of rat olfactory bulb, muscarinic receptor agonists stimu late basal adenylyl cyclase activity. This response is inhibited by a number of muscarinic receptor antagonists with a rank order of potency suggesting the involvement of the M(4) muscarinic receptor subtype. T he stimulatory effect does not require Ca2+ and occurs independently o f activation of phosphoinositide hydrolysis. Pretreatment with pertuss is toxin completely prevents the muscarinic stimulation of adenylyl cy clase, indicating the participation of G proteins of the Gi/Go family. Immunological impairment of the G protein, G(s), also reduces the mus carinic response, whereas concomitant activation of G(s)-coupled recep tors by CRH or VIP results in a synergistic stimulation of adenylyl cy clase activity. Although these data suggest a role for G(s), a body of evidence indicates that the muscarinic receptors do not interact dire ctly with this G protein. Moreover, the Ca2+/calmodulin (Ca2+/CaM)- an d forskolin-stimulated enzyme activities are inhibited by muscarinic r eceptor activation in a pertussis toxin -sensitive manner and with a p harmacological profile similar to that observed for the stimulatory re sponse. These data indicate that in rat olfactory bulb M(4) muscarinic receptors exert a bimodal control on cyclic AMP formation through a s equence of events that may involve activation of G(i)/G(o) proteins, s ynergistic interaction with G(s) and differential modulation of Ca2+/C aM-independent and -dependent forms of adenylyl cyclase.