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首页> 外文期刊>Hippocampus >High affinity group III mGluRs regulate mossy fiber input to CA3 interneurons.
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High affinity group III mGluRs regulate mossy fiber input to CA3 interneurons.

机译:高亲和力的III类mGluRs调节生苔纤维输入到CA3中间神经元。

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Stratum lacunosum-moleculare interneurons (L-Mi) in hippocampal area CA3 target the apical dendrite of pyramidal cells providing feedforward inhibition. Here we report that selective activation of group III metabotropic glutamate receptors (mGluRs) 4/8 with L(+)-2-amino-4-phosphnobytyric acid (L-AP4; 10 muM) decreased the probability of glutamate release from the mossy fiber (MF) terminals synapsing onto L-Mi. Consistent with this interpretation, application of L-AP4 in the presence of 3 mM strontium decreased the frequency of asynchronous MF EPSCs in L-Mi. Furthermore, the dose response curve showed that L-AP4 at 400 muM produced no further decrease in MF EPSC amplitude compared with 20 muM L-AP4, indicating the lack of mGluRs 7 at these MF terminals. We also found that one mechanism of mGluRs 4/8-mediated inhibition of release is linked to N-type voltage gated calcium channels at MF terminals. Application of the group III mGluR antagonist MSOP (100 muM) demonstrated that mGluRs 4/8 are neither tonically active nor activated by low and moderate frequencies of activity. However, trains of stimuli to the MF at 20 and 40 Hz delivered during the application of MSOP revealed a relief of inhibition of transmitter release and an increase in the overall probability of action potential firing in the postsynaptic L-Mi. Interestingly, the time to first action potential was significantly shorter in the presence of MSOP, indicating that mGluR 4/8 activation delays L-Mi firing in response to MF activity. Taken together, our data demonstrate that the timing and probability of action potentials in L-Mi evoked by MF synaptic input is regulated by the activation of presynaptic high affinity group III mGluRs.
机译:海马CA3区的层状乳酸分子中间神经元(L-Mi)靶向锥体细胞的顶端树突,从而提供前馈抑制作用。在这里我们报告说,选择性激活第三组代谢型谷氨酸受体(mGluRs)4/8与L(+)-2-氨基-4-膦酸(L-AP4; 10μM)降低了从苔藓纤维中释放谷氨酸的可能性(MF)终端突触到L-Mi上。与该解释一致,在3 mM锶存在下应用L-AP4降低了L-Mi中异步MF EPSC的频率。此外,剂量响应曲线表明,与20μML-AP4相比,400μM的L-AP4不会进一步降低MF EPSC幅度,表明在这些MF末端缺少mGluRs 7。我们还发现,mGluRs 4/8介导的释放抑制的一种机制与MF末端的N型电压门控钙通道有关。 III组mGluR拮抗剂MSOP(100μM)的应用表明,mGluR 4/8既不具有音调活性,也没有被中低频率的频率激活。但是,在应用MSOP期间以20和40 Hz的频率对MF发出的刺激序列显示出抑制递质释放的释放以及突触后L-Mi动作电位激发的总体可能性增加。有趣的是,在MSOP存在下,首次动作时间的时间明显缩短,表明mGluR 4/8激活延迟了对MF活性的L-Mi激发。两者合计,我们的数据表明,MF突触输入诱发的L-Mi动作电位的时机和概率受突触前高亲和力组III mGluRs的激活调节。

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