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正性肌力药和负性肌力药作用的细胞机制研究。

Studies on the cellular mechanisms of action of positive and negative inotropic agents.

作者信息

Watanabe A M, Green F, Ahmad Z

机构信息

Department of Medicine, Indiana University School of Medicine.

出版信息

Basic Res Cardiol. 1989;84 Suppl 1:19-22. doi: 10.1007/BF02650343.

DOI:10.1007/BF02650343
PMID:2554872
Abstract

We have reviewed the mechanism by which drugs that elevate cyclic AMP level modify myocardial contractility. We have presented preliminary evidence about the mechanism by which muscarinic agonists antagonize the effects of these drugs. Finally, we suggest that the protein phosphorylation experiments, particularly if done in dispersed myocytes, could be an efficient and cost-effective method of screening drugs which may act by elevating intracellular levels of cyclic AMP.

摘要

我们已经回顾了提高环磷酸腺苷(cAMP)水平的药物改变心肌收缩力的机制。我们已经给出了关于毒蕈碱激动剂拮抗这些药物作用机制的初步证据。最后,我们认为蛋白质磷酸化实验,特别是在分离的心肌细胞中进行的实验,可能是一种高效且经济有效的筛选药物的方法,这些药物可能通过提高细胞内环磷酸腺苷水平起作用。

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1
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Basic Res Cardiol. 1989;84 Suppl 1:19-22. doi: 10.1007/BF02650343.
2
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引用本文的文献

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本文引用的文献

1
beta-Adrenergic stimulation of phospholamban phosphorylation and Ca2+-ATPase activity in guinea pig ventricles.豚鼠心室中β-肾上腺素能刺激对受磷蛋白磷酸化和Ca2+-ATP酶活性的影响
J Biol Chem. 1983 Jan 10;258(1):464-71.
2
Phosphorylation of phospholamban in intact myocardium. Role of Ca2+-calmodulin-dependent mechanisms.
J Biol Chem. 1985 Apr 10;260(7):4516-25.
3
Adenosine inhibits the positive inotropic effect of 3-isobutyl-1-methylxanthine in papillary muscles without effect on cyclic AMP or cyclic GMP.腺苷可抑制3-异丁基-1-甲基黄嘌呤对乳头肌的正性肌力作用,而对环磷酸腺苷(cAMP)或环磷酸鸟苷(cGMP)无影响。
Br J Pharmacol. 1988 Apr;93(4):729-38. doi: 10.1111/j.1476-5381.1988.tb11456.x.
4
Phosphodiesterase-inhibiting properties of newer inotropic agents.新型正性肌力药物的磷酸二酯酶抑制特性。
Circulation. 1986 Mar;73(3 Pt 2):III99-108.
5
Muscarinic cholinergic inhibition of beta-adrenergic stimulation of phospholamban phosphorylation and Ca2+ transport in guinea pig ventricles.毒蕈碱胆碱能对豚鼠心室中β-肾上腺素能刺激的受磷蛋白磷酸化和Ca2+转运的抑制作用。
J Biol Chem. 1985 Oct 25;260(24):13122-9.
6
Muscarinic cholinergic receptor modulation of beta-adrenergic receptor affinity for catecholamines.
J Biol Chem. 1978 Jul 25;253(14):4833-6.