Pharamacological characterization of excitaory synaptic potentials in rat basolateral amygdaloid neurons

Po‐Wu ‐W Gean, Fang‐Chia ‐C Chang

研究成果: Article同行評審

40 引文 斯高帕斯(Scopus)

摘要

The pharmacological properties of synaptic responses in rat basolateral amygdaloid (BLA) neurons were studied using intracellular recording techniques. Three distinct types of synaptic potential were evoked by stimulation of the adjacent ventral endopyriform nucleus: (1) a fast excitatory postsynaptic potential (f‐EPSP);(2) a late EPSP (1‐EPSP) following the f‐EPSP; and (3) a multiphasic hyperpolarization following the initial depolarizing potential. Superfusion of 6‐cyano‐7‐nitroquinoxaline‐2, 3‐dione (CNQX), a selective non‐N‐methyl‐D‐aspartate (non‐NMDA) receptor antagonist, blocked the f‐EPSP in a concentration‐dependent manner. The ED50 for this effect was around 4 m̈M. In the presence of CNQX, however, a small depolarizing potential remained. This residual depolarizing component was markedly enhanced on removing Mg++ from the perfusing medium and could subsequently be abolished by DL‐2‐amino‐5‐ phosphonovaleate (DL‐APV, 50 m̈M) indicating its mediation via NMDA receptor‐coupled ionophore. The l‐EPSP was reversibly blocked by DL‐APV. These results suggest that the pyriform cortex‐amygdala pathway is mediated through excitatory amino acids acting on non‐NMDA as well as NMDA receptors located on the BLA neurons.

原文English
頁(從 - 到)1-9
頁數9
期刊Synapse
11
發行號1
DOIs
出版狀態Published - 1992 五月

All Science Journal Classification (ASJC) codes

  • Cellular and Molecular Neuroscience

指紋 深入研究「Pharamacological characterization of excitaory synaptic potentials in rat basolateral amygdaloid neurons」主題。共同形成了獨特的指紋。

引用此