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在培养的大鼠上丘神经元中,腺苷通过P2嘌呤受体而非腺苷受体激活钾通道。

Adenosine activates the potassium channel via a P2 purinoceptor but not via an adenosine receptor in cultured rat superior colliculus neurons.

作者信息

Ikeuchi Y, Nishizaki T, Mori M, Okada Y

机构信息

Department of Physiology, Kobe University School of Medicine, Japan.

出版信息

Neurosci Lett. 1995 Oct 6;198(3):205-8. doi: 10.1016/0304-3940(95)12000-t.

Abstract

The effect of adenosine on superior colliculus neurons was examined by whole-cell patch clamp recording. Adenosine elicited whole-cell potassium currents. A selective A1 or A2a adenosine receptor agonist induced no current and furthermore, adenosine-evoked currents were not inhibited by selective A1 or A2a adenosine receptor antagonists or a non-selective adenosine receptor (P1 purinoceptor) antagonist, indicating that the currents are not mediated by adenosine receptors. In contrast, P2 purinoceptor agonists, such as 2-methylthio ATP (2-MeSATP), ATP, ADP, and AMP, produced similar potassium currents, whereas alpha,beta-methylene ATP, beta,gamma-metylene ATP, or UTP had no response. The order of their potencies for the current amplitudes was 2-MeSATP > ADP > adenosine > ATP >> AMP and this order corresponds to that for the P2Y purinoceptor. These results, thus, suggest that adenosine exerts an inhibitory effect at the postsynaptic site by activating the potassium channel via a P2Y purinoceptor in superior colliculus neurons.

摘要

通过全细胞膜片钳记录研究了腺苷对上丘神经元的作用。腺苷诱发了全细胞钾电流。选择性A1或A2a腺苷受体激动剂未诱发电流,此外,腺苷诱发的电流不受选择性A1或A2a腺苷受体拮抗剂或非选择性腺苷受体(P1嘌呤受体)拮抗剂的抑制,这表明该电流不是由腺苷受体介导的。相反,P2嘌呤受体激动剂,如2-甲硫基ATP(2-MeSATP)、ATP、ADP和AMP,产生了类似的钾电流,而α,β-亚甲基ATP、β,γ-亚甲基ATP或UTP则无反应。它们对电流幅度的效力顺序为2-MeSATP > ADP > 腺苷 > ATP >> AMP,且该顺序与P2Y嘌呤受体的顺序一致。因此,这些结果表明,腺苷通过激活上丘神经元中的P2Y嘌呤受体的钾通道,在突触后位点发挥抑制作用。

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