首页> 外文期刊>European Journal of Pharmacology: An International Journal >Ryanodine receptor modulation by diadenosine polyphosphates in synaptosomal and microsomal preparations of rat brain.
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Ryanodine receptor modulation by diadenosine polyphosphates in synaptosomal and microsomal preparations of rat brain.

机译:腺苷多磷酸对鼠脑突触体和微粒体制剂中Ryanodine受体的调节作用。

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摘要

Diadenosine polyphosphates (Ap(n)As) are transmitter-like substances that act intracellularly via unclear mechanisms. Here we tested hypotheses that diadenosine tetraphosphate (Ap(4)A) modulates ryanodine binding in microsomal and synaptosomal fractions of rat brain, and that Ap(4)A affects modulation of ryanodine binding by divalent cations and caffeine. Using [3H]ryanodine-binding assays, we showed that Ap(4)A produced significant and concentration-dependent increases in [3H]ryanodine binding in microsomes and these actions were reduced by Mg(2+) and potentiated by caffeine. In synaptosomal subfractions, effects of Ap(4)A on [3H]ryanodine binding were most profound in subfractions enriched in synaptic vesicle-associated protein synaptophysin. These results suggest that Ap(n)As and ryanodine receptors are well placed to modulate Ca(2+)-dependent synaptic processes.
机译:腺苷多磷酸(Ap(n)As)是类似递质的物质,通过不清楚的机制在细胞内起作用。在这里,我们测试了以下假设:四磷酸二氢腺苷(Ap(4)A)调节大鼠脑的微粒体和突触体部分中的ryanodine结合,而Ap(4)A影响二价阳离子和咖啡因对ryanodine结合的调节。使用[3H] ryanodine结合测定,我们表明Ap(4)A产生微粒体中[3H] ryanodine结合的显着且浓度依赖性的增加,这些作用被Mg(2+)减少并被咖啡因增强。在突触体亚组中,Ap(4)A对[3H] ryanodine结合的影响在富含突触小泡相关蛋白突触素的亚组中最为明显。这些结果表明,Ap(n)As和ryanodine受体处于很好的位置,以调节Ca(2+)依赖的突触过程。

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