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一种稳定的腺苷类似物对海马切片中去甲肾上腺素释放的抑制作用。

Inhibition of noradrenaline release from hippocampal slices by a stable adenosine analogue.

作者信息

Fredholm B B, Jonzon B, Lindgren E

出版信息

Acta Physiol Scand Suppl. 1983;515:7-10.

PMID:6578673
Abstract

Electrical field stimulation elicits a calcium-dependent release of 3H-NA from rat hippocampal slices. The release is inhibited by the alpha 2-agonist clonidine and enhanced by the alpha 2-antagonist yohimbine. The stable adenosine analogue N6-L-phenylisopropyl-adenosine (L-PIA) caused a dose-dependent inhibition of 3H-NA overflow. The effect of L-PIA was antagonized by the adenosine receptor antagonist 8-phenyl-theophylline, which caused a slight, but significant increase in overflow per se. The results suggest that there are functionally important presynaptic adenosine receptors on nor-adrenergic nerve terminals in the rat hippocampus.

摘要

电场刺激可引发大鼠海马切片中3H-去甲肾上腺素(3H-NA)的钙依赖性释放。该释放受到α2-激动剂可乐定的抑制,并被α2-拮抗剂育亨宾增强。稳定的腺苷类似物N6-L-苯异丙基腺苷(L-PIA)引起3H-NA释放的剂量依赖性抑制。L-PIA的作用被腺苷受体拮抗剂8-苯基茶碱拮抗,后者本身会导致释放略有但显著增加。结果表明,大鼠海马中去甲肾上腺素能神经末梢上存在功能重要的突触前腺苷受体。

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