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硝苯地平和BAYK 8644对大鼠海马神经元腺苷反应的抑制作用。

Inhibition of adenosine responses of rat hippocampal neurones by nifedipine and BAYK 8644.

作者信息

Bartrup J T, Stone T W

机构信息

Department of Pharmacology, University of Glasgow, U.K.

出版信息

Brain Res. 1990 Aug 20;525(2):315-8. doi: 10.1016/0006-8993(90)90881-b.

Abstract

The application of adenosine to hippocampal slices caused a suppression of evoked population spikes in the CA1 region. This effect was enhanced by nifedipine and BAYK 8644 in control slices but was reduced by these dihydropyridines in the presence of dipyridamole. Several analogues of adenosine which are not substrates for the uptake system also depressed the population spikes in the CA1 region but these responses were inhibited by nifedipine and BAYK 8644. Other dihydropyridines including nimodipine and nitrendipine did not affect sensitivity to adenosine or its analogues. It is concluded that some agonist and antagonist dihydropyridines can inhibit adenosine uptake and thus potentiate its effects but can also antagonise receptor activation. Structural features of nifedipine and BAYK 8644 may be specific for a population of dihydropyridine receptors closely linked functionally with the adenosine receptor.

摘要

将腺苷应用于海马切片会导致CA1区诱发群体峰电位受到抑制。在对照切片中,硝苯地平和BAYK 8644可增强这种效应,但在双嘧达莫存在的情况下,这些二氢吡啶会使其减弱。几种不是摄取系统底物的腺苷类似物也会抑制CA1区的群体峰电位,但这些反应会被硝苯地平和BAYK 8644抑制。包括尼莫地平和尼群地平在内的其他二氢吡啶对腺苷或其类似物的敏感性没有影响。得出的结论是,一些激动剂和拮抗剂二氢吡啶可以抑制腺苷摄取,从而增强其作用,但也可以拮抗受体激活。硝苯地平和BAYK 8644的结构特征可能对与腺苷受体在功能上紧密相连的一群二氢吡啶受体具有特异性。

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