Sladeczek F, Momiyama A, Takahashi T
Department of Physiology, Kyoto University Faculty of Medicine, Japan.
Proc Biol Sci. 1993 Sep 22;253(1338):297-303. doi: 10.1098/rspb.1993.0117.
A family of metabotropic glutamate receptors (mGluRs) has been elucidated by molecular cloning. To study the possible modulatory role of mGluRs in synaptic transmission, we tested the effect of a mGluR agonist, (+/-)-1-aminocyclopentane-trans-1,3-dicarboxylic acid (trans-ACPD), on the excitatory post-synaptic currents (EPSCS) recorded from neurons in thin slices of rat visual cortex, by using the whole-cell patch-clamp method. We found that trans-ACPD markedly suppressed the evoked EPSCS without affecting the mean amplitude of spontaneous miniature EPSCS. This effect on the evoked EPSCS was blocked by a potassium channel blocker, 4-aminopyridine (4-AP) in a dose-dependent manner. We suggest that trans-ACPD presynaptically inhibits EPSCS by a mechanism involving the 4-AP-sensitive channels.
通过分子克隆已阐明了代谢型谷氨酸受体(mGluRs)家族。为研究mGluRs在突触传递中可能的调节作用,我们使用全细胞膜片钳方法,测试了mGluR激动剂(±)-1-氨基环戊烷-反式-1,3-二羧酸(反式-ACPD)对大鼠视皮层薄片神经元记录的兴奋性突触后电流(EPSCs)的影响。我们发现反式-ACPD显著抑制诱发的EPSCs,而不影响自发微小EPSCs的平均幅度。这种对诱发EPSCs的作用被钾通道阻滞剂4-氨基吡啶(4-AP)以剂量依赖性方式阻断。我们认为反式-ACPD通过涉及4-AP敏感通道的机制在突触前抑制EPSCs。