BETA-ADRENERGIC REGULATION OF CYCLIC-GMP IN RAT PINEALOCYTES

被引:10
作者
SUGDEN, D
机构
[1] Biomedical Sciences Division, King's College London, London, W8 7AH, Campden Hill Road, Kensington
关键词
D O I
10.1016/0006-291X(90)92101-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Stimulation of rat pinealocyte cyclic GMP by β-adrenergic agonists (in the presence of prazosin to block α1-adrenoceptors) showed an identical potency order (isoproterenol> epinephrine = norepinephrine>> salbutamol> terbutaline) to the stimulation of pinealocyte cyclic AMP. The increase in cyclic AMP and cyclic GMP produced by norepinephrine was inhibited by various subtype-selective β-adrenergic antagonists with the same potency order (propranolol> atenolol = ICI 118,551>> practolol). These results indicate that pinealocytes have a single β-adrenoceptor, of the β1-subtype. Activation of this β1-adrenoceptor mediates adrenergic stimulation of not only cyclic AMP but also cyclic GMP. © 1990.
引用
收藏
页码:835 / 841
页数:7
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