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神经系统中双腺苷多磷酸的P2嘌呤能受体

P2 purinergic receptors for diadenosine polyphosphates in the nervous system.

作者信息

Pintor J, Miras-Portugal M T

机构信息

E. U. Optica, Madrid, Spain.

出版信息

Gen Pharmacol. 1995 Mar;26(2):229-35. doi: 10.1016/0306-3623(94)00182-m.

Abstract
  1. The actions of diadenosine polyphosphates, diadenosine tetraphosphate (Ap4A), diadenosine pentaphosphate (Ap5A) and diadenosine hexaphosphate (Ap6A) in the nervous system have been reviewed. 2. In the peripheral nervous system, diadenosine polyphosphates bind to P2-purinergic receptors such as the P2Y in chromaffin cells and Torpedo synaptosomes, P2X in vas deferens and urinary bladder and also Torpedo synaptosomes and P2U in endothelial chromaffin cells. 3. In the central nervous system ApnA compounds can act through P2X-purinoceptors opening cation channels in nodose ganglion neurones. Diadenosine polyphosphates bind to a P2d-purinergic receptor in rat brain synaptic terminals and hippocampus, linked to protein kinase C (PKC) activation. 4. P4-purinoceptors are specific receptors for diadenosine polyphosphates, coupled to the Ca2+ influx, in the central synapses. This purinoceptor is not activated by ATP and synthetic analogs. The P4-purinoceptor could act as a positive modulator of the synaptic transmission, giving even more importance to diadenosine polyphosphates as neurotransmitters.
摘要
  1. 已对双腺苷多磷酸、四磷酸双腺苷(Ap4A)、五磷酸双腺苷(Ap5A)和六磷酸双腺苷(Ap6A)在神经系统中的作用进行了综述。2. 在周围神经系统中,双腺苷多磷酸与P2-嘌呤能受体结合,如嗜铬细胞和电鳐突触体中的P2Y、输精管和膀胱中的P2X以及电鳐突触体和内皮嗜铬细胞中的P2U。3. 在中枢神经系统中,ApnA化合物可通过P2X-嘌呤受体作用于结状神经节神经元,打开阳离子通道。双腺苷多磷酸与大鼠脑突触终末和海马中的P2d-嘌呤能受体结合,与蛋白激酶C(PKC)激活相关。4. P4-嘌呤受体是双腺苷多磷酸的特异性受体,在中枢突触中与Ca2+内流偶联。该嘌呤受体不会被ATP和合成类似物激活。P4-嘌呤受体可作为突触传递的正性调节剂,使双腺苷多磷酸作为神经递质的重要性进一步提高。

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