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组胺H2受体拮抗剂在大鼠大脑皮层中的特异性

On the specificity of histamine H2-receptor antagonists in the rat cerebral cortex.

作者信息

Phillis J W, Kostopoulos G K, Odutola A

出版信息

Can J Physiol Pharmacol. 1975 Dec;53(6):1205-9. doi: 10.1139/y75-169.

Abstract

The effects of iontophoretically applied histamine H2-receptor antagonists and their antagonism of various amines, acetylcholine (ACh), and adenosine 5'-monophosphate (5'-AMP) were studied on spontaneously active rat cerebral cortical neurons. Metiamide selectively blocked the depressant actions of histamine. Burimamide, in amounts necessary for histamine antagonism, also antagonized the depressant effects of noradrenaline, dopamine, and 5-hydroxytryptamine. Neither antagonist affected 5'-AMP-induced depressions, but both reduced or blocked the excitatory actions of ACh. It is concluded that metiamide may be useful as a reliable antagonist of H2 receptors on cerebral cortical neurons.

摘要

研究了离子电渗法应用组胺H2受体拮抗剂及其对各种胺类、乙酰胆碱(ACh)和5'-单磷酸腺苷(5'-AMP)的拮抗作用对自发活动的大鼠大脑皮层神经元的影响。甲硫米特选择性地阻断组胺的抑制作用。在拮抗组胺所需的剂量下,布立马胺也拮抗去甲肾上腺素、多巴胺和5-羟色胺的抑制作用。两种拮抗剂均不影响5'-AMP诱导的抑制,但均降低或阻断了ACh的兴奋作用。得出结论,甲硫米特可能作为大脑皮层神经元上H2受体的可靠拮抗剂有用。

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