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绿头苍蝇唾液腺上的5-羟色胺受体与3',5'-环磷酸腺苷或钙信号的产生相关联。

Separate 5-hydroxytryptamine receptors on the salivary gland of the blowfly are linked to the generation of either cyclic adenosine 3',5'-monophosphate or calcium signals.

作者信息

Berridge M J, Heslop J P

出版信息

Br J Pharmacol. 1981 Jul;73(3):729-38. doi: 10.1111/j.1476-5381.1981.tb16809.x.

DOI:10.1111/j.1476-5381.1981.tb16809.x
PMID:6265018
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2071686/
Abstract

1 5'-Hydroxytryptamine (5-HT) stimulates the formation of two separate second messengers in the salivary gland of the blowfly. Activation of adenylate cyclase raises adenosine 3',5'-monophosphate (cyclic AMP) whereas the hydrolysis of phosphatidylinositol (PI) is associated with an increase in calcium permeability. The possibility that these two signal pathways might be controlled by separate 5-HT receptors was studied by testing the specificity of 5-HT analogues and antagonists. 2 The parent compound 5-HT was found to stimulate both cyclic AMP formation and the related parameters of PI hydrolysis and calcium transport with similar dose-response relationships. 3 Certain analogues such as 4- and 5-fluoro-alpha-methyltryptamine were capable of raising cyclic AMP levels and stimulating fluid secretion but did not stimulate the hydrolysis of PI or the entry of calcium. 4 Other analogues, which had chloro or methyl substituents at the 5-position, were found to stimulate the hydrolysis of PI and the transport of calcium at much lower doses than those required to stimulate the formation of cyclic AMP. 5 Antagonists were also found to exert selective effects. Methysergide was a potent inhibitor of PI hydrolysis whereas cinanserin was far more selective in blocking the stimulatory effect of 5-HT on cyclic AMP formation. 6 It is concluded that 5-HT acts on two separate receptors, a 5-HT1 receptor acting through calcium and a 5-HT2 receptor which mediates its effects through cyclic AMP.

摘要

1 5-羟色胺(5-HT)刺激家蝇唾液腺中两种不同第二信使的形成。腺苷酸环化酶的激活会提高3',5'-环磷酸腺苷(环磷酸腺苷)水平,而磷脂酰肌醇(PI)的水解与钙通透性增加有关。通过测试5-HT类似物和拮抗剂的特异性,研究了这两条信号通路可能由不同5-HT受体控制的可能性。2 发现母体化合物5-HT能刺激环磷酸腺苷的形成以及PI水解和钙转运的相关参数,且具有相似的剂量反应关系。3 某些类似物,如4-氟和5-氟-α-甲基色胺,能够提高环磷酸腺苷水平并刺激液体分泌,但不刺激PI水解或钙内流。4 其他在5位有氯或甲基取代基的类似物,被发现以比刺激环磷酸腺苷形成所需剂量低得多的剂量刺激PI水解和钙转运。5 还发现拮抗剂发挥选择性作用。麦角新碱是PI水解的有效抑制剂,而辛那色林在阻断5-HT对环磷酸腺苷形成的刺激作用方面更具选择性。6 得出结论,5-HT作用于两种不同的受体,一种5-HT1受体通过钙起作用,一种5-HT2受体通过环磷酸腺苷介导其作用。

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