Inhibitory effects of clonidine and dopamine on adenylate cyclase of rabbit ciliary processes
作者:
ČepelfkJindřich,
HynieSixtus,
期刊:
Current Eye Research
(Taylor Available online 1990)
卷期:
Volume 9,
issue 2
页码: 111-120
ISSN:0271-3683
年代: 1990
DOI:10.3109/02713689008995197
出版商: Taylor&Francis
数据来源: Taylor
摘要:
The inhibitory effects of theα2-adren-ergic agonist clonidine and that or dopamine were studied on the adenylate cyclase activity in homogenates of ciliary processes.Clonidine inhibited in a dose-dependent manner basal adenylate cyclase activity as well as that stimulated by isoproterenol or forskolin. However, the adenylate cyclase activity stimulated by isoproterenol was sensitive to at least one order lower inhibitory concentrations of clonidine than basal or forskolin-stimulated adeny-ate cyclase. Dopamine inhibited adenylate cyclase stimulated by isoproterenol considerably less potently than clonidine. The slope of the dopamine dose-response curve was, however, similar to that of the dose -response curve of clonidine. The inhibitory effects of clonidine and dopamine were antagonized by anα2-adrenergic antagonist, yohlmbine, in a manner suggesting a competitive nature of this interaction. On the contrary, the inhibitory effects of neither clonidine nor dopamine were prevented by anα1-adrenergic antagonist, prazosin. In addition, the effect of dopamine was not antagonized by the D2-antagonist, tiapride. Taken together, tnese results strongly indicate that both clonidine and dopamine exert their inhibitory effects by the stimulation ofα2-adrener-gic receptors. Accordingly, they provide experimental evidence that both basal and drug-stimulated adenylate cyclase activity of ciliary processes can be inhibited via stimulation ofα2-adrenergic receptors.The substantially higher sensitivity of isoproterenol-stimulated than basal or forskolin stimulated adenylate cyclase toα2-adrenergic inhibition seems to be a unique feature of this enzyme of ciliary processes. It is suggested that this may reflect an involvement ofα2-adrenergic receptors in the physiological feedback mechanism preventing the over-stimulation of adenylate cyclase of ciliary processes
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