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FMRF酰胺可提高软体动物心脏的腺苷酸环化酶活性和环磷酸腺苷水平。

FMRFamide increases the adenylate cyclase activity and cylic AMP level of molluscan heart.

作者信息

Higgins W J, Price D A, Greenberg M J

出版信息

Eur J Pharmacol. 1978 Apr 15;48(4):425-30. doi: 10.1016/0014-2999(78)90170-x.

Abstract

FMRFamide (phenylalanyl-methionyl-arginyl-phenylalanine amide) is a cardioexcitatory peptide recently isolated and identified in molluscan ganglia. Both FMRFamide and 5-hydroxytryptamine (5HT), the cardioexcitatory neurotransmitter in molluscs, were tested on the ventricle of the bivalve Mercenaria mercenaria. Both agents increased myocardial contractility, the intracellular cyclic AMP concentration of intact hearts and the adenylate cyclase activity of a myocardial membrane fraction. FMRFamide was 5--10 times more potent than 5HT. All of the effects of 5HT, and none of those of FMRFamide, were blocked by methysergide, a specific 5HT antagonist.

摘要

FMRF酰胺(苯丙氨酰-甲硫氨酰-精氨酰-苯丙氨酸酰胺)是一种最近在软体动物神经节中分离并鉴定出的心脏兴奋肽。FMRF酰胺和5-羟色胺(5HT),即软体动物中的心脏兴奋神经递质,都在双壳贝类硬壳蛤的心室上进行了测试。这两种物质都增加了心肌收缩力、完整心脏的细胞内环磷酸腺苷(cAMP)浓度以及心肌膜部分的腺苷酸环化酶活性。FMRF酰胺的效力比5HT强5至10倍。5HT的所有作用都被特异性5HT拮抗剂麦角新碱阻断,而FMRF酰胺的作用则没有被阻断。

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