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腺苷A2A受体介导的去甲肾上腺素释放促进作用涉及蛋白激酶C激活以及大鼠输精管中突触前抑制性受体介导效应的减弱。

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.

作者信息

Queiroz Glória, Talaia Carlos, Gonçalves Jorge

机构信息

Laboratório de Farmacologia, Faculdade de Farmácia, Universidade do Porto, Porto, Portugal.

出版信息

J Neurochem. 2003 May;85(3):740-8. doi: 10.1046/j.1471-4159.2003.01715.x.

Abstract

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.

摘要

在大鼠输精管的附睾部分,由腺苷A2A受体介导的去甲肾上腺素释放促进作用,而非由β2 -肾上腺素能受体介导或通过直接激活腺苷酸环化酶介导的促进作用,会因α2 -肾上腺素能受体阻断而减弱,并因同时阻断α2 -肾上腺素能受体、腺苷A1和P2Y受体而消除。腺苷A2A受体介导的促进作用不受蛋白激酶A、蛋白激酶G或钙调蛋白激酶II抑制剂的影响,但会因白屈菜红碱或双吲哚马来酰亚胺XI抑制蛋白激酶C而被阻止。用佛波酯12 -肉豆蔻酸13 -乙酸酯激活蛋白激酶C会导致去甲肾上腺素释放促进,这种促进作用会被双吲哚马来酰亚胺XI消除,并被α2 -肾上腺素能受体、腺苷A1和P2Y受体拮抗剂减弱。腺苷A2A受体的激活减弱了由突触前抑制性受体介导的去甲肾上腺素释放抑制作用。这种效应可被佛波酯12 -肉豆蔻酸13 -乙酸酯模拟,并被双吲哚马来酰亚胺XI阻止。结论是,腺苷A2A受体通过一种机制促进去甲肾上腺素释放,该机制涉及蛋白激酶C介导的对由突触前抑制性受体(即α2 -肾上腺素能受体、腺苷A1和P2Y受体)介导的效应的减弱。

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