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Metabotropic glutamate receptors modulate feedback inhibition in a developmentally regulated manner in rat dentate gyrus

机译:代谢型谷氨酸受体以发育调控的方式调节大鼠齿状回中的反馈抑制

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摘要

We investigated group II metabotropic glutamate receptor (mGluR) modulation of glutamatergic input onto hilar-border interneurones and its regulation of feedback inhibition in the dentate gyrus. Selective activation of group II mGluRs with (2S,2′R,3′R)-2-(2′,3′-dicarboxycyclopropyl)glycine (DCG-IV) depressed mossy fibre (MF)-evoked excitatory drive to these interneurones with significantly greater depression in juvenile than adult rats. During 20 Hz MF stimulus trains, EPSCs became depressed. Depression during the early, but not later part of the train was significantly greater in juvenile than adult rats and was blocked by the mGluR antagonist (2S)-2-amino-2-[(1S,2S)-2-carboxycycloprop-1-yl]-3-(xanth-9-yl) propanoic acid (). In dentate granule cells from juvenile rats polysynaptic feedback IPSCs, but not monosynaptic IPSCs, were strongly suppressed by DCG-IV. DCG-IV also suppressed feedback inhibition of perforant path-evoked population spikes. In contrast, in adult animals DCG-IV did not significantly depress feedback inhibition. During 20 Hz stimulus trains in juvenile animals the summation of polysynaptic, but not monosynaptic IPSCs was suppressed by synaptically activated group II mGluRs. Blockade of these mGluRs with significantly increased the area and duration of the summated IPSC, causing greater feedback inhibition of granule cell firing. In contrast, in adult animals did not alter feedback inhibition following the stimulus train. These findings indicate that group II mGluRs modulate excitatory drive to interneurones in a developmentally regulated manner and thereby modulate feedback inhibition in the dentate gyrus.
机译:我们研究了II组代谢谷氨酸受体(mGluR)的谷氨酸输入到肺门边界interneurones的调制及其对齿状回的反馈抑制的调节。用(2S,2'R,3'R)-2-(2',3'-二羧基环丙基)甘氨酸(DCG-IV)抑制的苔藓纤维(MF)诱发的驱使驱使II型mGluRs选择性活化与成年大鼠相比,少年的抑郁症明显更大。在20 Hz MF刺激训练期间,EPSC变得沮丧。幼年时期火车的早期但不是后期抑郁比成年大鼠大得多,并且被mGluR拮抗剂(2S)-2-氨基-2-[(1S,2S)-2-羧基环丙-1- yl] -3-(黄嘌呤-9-基)丙酸()。在来自幼年大鼠的齿状颗粒细胞中,DCG-IV强烈抑制了多突触反馈IPSC,而不是单突触IPSC。 DCG-IV还抑制了通径诱发的群体峰值的反馈抑制。相反,在成年动物中,DCG-IV并未显着抑制反馈抑制。在幼稚动物的20 Hz刺激训练期间,被突触激活的II型mGluRs抑制了多突触,而不是单突触IPSC的总和。这些mGluR的阻滞显着增加了IPSC汇总的面积和持续时间,从而导致了对颗粒细胞射击的更大反馈抑制。相反,成年动物在刺激训练后没有改变反馈抑制。这些发现表明,II类mGluRs以发育调节的方式调节对中间神经元的兴奋性驱动,从而调节齿状回中的反馈抑制。

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