Sebastião A M, Ribeiro J A
Laboratory of Pharmacology, Gulbenkian Institute of Science, Oeiras, Portugal.
Neurosci Lett. 1992 Apr 13;138(1):41-4. doi: 10.1016/0304-3940(92)90467-l.
The A2 adenosine receptor agonist, CGS 21680 in nanomolar concentrations, reversibly increased in a concentration-dependent manner the amplitude of orthodromically-evoked population spikes recorded from the CA1 pyramidal cell layer of rat hippocampal slices. The adenosine receptor antagonist, 3,7-dimethyl-l-propargylxanthine (DMPX, 10 microM), which has selectivity for A2 adenosine receptors, prevented this excitatory effect of CGS 21680. These results suggest that A2 adenosine receptors are present in the rat hippocampus and that activation of these receptors enhance hippocampal excitability.
A2 型腺苷受体激动剂 CGS 21680 在纳摩尔浓度下,能以浓度依赖的方式可逆地增加从大鼠海马切片 CA1 锥体细胞层记录到的顺向诱发群体峰电位的幅度。对 A2 型腺苷受体具有选择性的腺苷受体拮抗剂 3,7-二甲基-1-丙炔基黄嘌呤(DMPX,10 μM)可阻止 CGS 21680 的这种兴奋作用。这些结果表明 A2 型腺苷受体存在于大鼠海马中,并且这些受体的激活可增强海马的兴奋性。