首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Adenosine A2A receptor-mediated facilitation of noradrenaline release involves protein kinase C activation and attenuation of presynaptic inhibitory receptor-mediated effects in the rat vas deferens.
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Adenosine A2A receptor-mediated facilitation of noradrenaline release involves protein kinase C activation and attenuation of presynaptic inhibitory receptor-mediated effects in the rat vas deferens.

机译:腺苷A2A受体介导的去甲肾上腺素释放的促进作用涉及蛋白激酶C的激活和大鼠输精管中突触前抑制性受体介导的作用的减弱。

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In the epididymal portion of rat vas deferens, facilitation of noradrenaline release mediated by adenosine A2A receptors, but not that mediated by beta2-adrenoceptors or by direct activation of adenylyl cyclase, was attenuated by blockade of alpha2-adrenoceptors and abolished by simultaneous blockade of alpha2-adrenoceptors, adenosine A1 and P2Y receptors. The adenosine A2A receptor-mediated facilitation was not changed by inhibitors of protein kinase A, protein kinase G or calmodulin kinase II but was prevented by inhibition of protein kinase C with chelerythrine or bisindolylmaleimide XI. Activation of protein kinase C with phorbol 12-myristate 13-acetate caused a facilitation of noradrenaline release that was abolished by bisindolylmaleimide XI and reduced by antagonists of alpha2-adrenoceptors, adenosine A1 and P2Y receptors. Activation of adenosine A2A receptors attenuated the inhibition of noradrenaline release mediated by the presynaptic inhibitory receptors. This effect was mimicked by phorbol 12-myristate 13-acetate and prevented by bisindolylmaleimide XI. It is concluded that adenosine A2A receptors facilitate noradrenaline release by a mechanism that involves a protein kinase C-mediated attenuation of effects mediated by presynaptic inhibitory receptors, namely alpha2-adrenoceptors, adenosine A1 and P2Y receptors.
机译:在大鼠输精管的附睾部分,通过α2-肾上腺素受体的阻滞减弱了由腺苷A2A受体介导的去甲肾上腺素释放的促进,但不是由β2-肾上腺素受体或腺苷酸环化酶直接介导的去甲肾上腺素的释放,而被同时阻断α2所消除。 -肾上腺素受体,腺苷A1和P2Y受体。腺苷A2A受体介导的促进作用没有被蛋白激酶A,蛋白激酶G或钙调蛋白激酶II的抑制剂改变,但被白屈菜红碱或双吲哚基马来酰亚胺XI抑制蛋白激酶C阻止了。佛波醇12-肉豆蔻酸酯13-乙酸酯激活蛋白激酶C导致去甲肾上腺素释放的促进,被二辛多基马来酰亚胺XI消除,并被α2-肾上腺素受体,腺苷A1和P2Y受体的拮抗剂减少。腺苷A2A受体的激活减弱了突触前抑制受体介导的去甲肾上腺素释放的抑制作用。佛波醇12-肉豆蔻酸酯13-乙酸酯可模仿此作用,而双辛基基马来酰亚胺XI则可防止这种作用。结论是,腺苷A2A受体通过一种机制促进去甲肾上腺素的释放,该机制涉及蛋白激酶C介导的突触前抑制受体(α2-肾上腺素受体,腺苷A1和P2Y受体)介导的作用减弱。

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