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N-甲基-D-天冬氨酸(NMDA)受体拮抗剂D-2-氨基-5-磷酰戊酸(D-APV)可抑制正常吗啡在大鼠海马切片中产生的兴奋性活动。

NMDA receptor antagonist D-APV depresses excitatory activity produced by normorphine in rat hippocampal slices.

作者信息

Swearengen E, Chavkin C

出版信息

Neurosci Lett. 1987 Jul 9;78(1):80-4. doi: 10.1016/0304-3940(87)90565-9.

Abstract

Both pentylenetetrazole and normorphine increased CA1 pyramidal cell sensitivity to afferent stimulation and caused the appearance of synchronous afterpotentials (secondary spikes). D-2-Amino-5-phosphonovalerate (D-APV) attenuated secondary spikes induced by both drugs, but had no effect on the change in excitability of the primary population spike. These results suggest that both opiates and GABA receptor antagonists are able to unmask NMDA receptors in the in vitro rat hippocampus slice preparation.

摘要

戊四氮和去甲吗啡均可增加CA1锥体细胞对传入刺激的敏感性,并导致同步后电位(继发性锋电位)的出现。D-2-氨基-5-磷酸戊酸(D-APV)可减弱这两种药物诱导的继发性锋电位,但对初级群体锋电位的兴奋性变化无影响。这些结果表明,阿片类药物和GABA受体拮抗剂均可在体外大鼠海马脑片制备中使NMDA受体暴露。

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