Mateo Z, Porter J T
Department of Biology, Pontifical Catholic University of Puerto Rico, Ponce, Puerto Rico 00717.
Department of Physiology, Pharmacology and Toxicology, Ponce School of Medicine, Ponce, Puerto Rico 00732.
Neuroscience. 2015 Apr 2;290:41-8. doi: 10.1016/j.neuroscience.2014.12.083. Epub 2015 Jan 13.
Previously, we demonstrated that group II metabotropic glutamate receptors (mGluRs) reduce glutamate release from thalamocortical synapses during early postnatal development (P7-11). To further examine the role of group II mGluRs in the modulation of somatosensory circuitry, we determined whether group II mGluRs continue to modulate thalamocortical synapses until adulthood and whether these receptors also modulate intra-cortical synapses in the barrel cortex. To address these issues, we examined the effect of the group II mGluR agonists on thalamocortical excitatory postsynaptic currents (EPSCs) and intra-barrel EPSCs in slices from animals of different ages (P7-53). We found that the depression of thalamocortical EPSCs by group II mGluRs rapidly declined after the second postnatal week. In contrast, adenosine continued to depress thalamocortical EPSCs via a presynaptic mechanism in young adult mice (P30-50). Activation of group II mGluRs also reduced intra-barrel EPSCs through a postsynaptic mechanism in young mice (P7-11). Similar to the thalamocortical synapses, the group II mGluR modulation of intra-barrel excitatory synapses declined with development. In young adult animals (P30-50), group II mGluR stimulation had little effect on intra-barrel EPSCs but did hyperpolarize the neurons. Together our results demonstrate that group II mGluRs modulate barrel cortex circuitry by presynaptic and postsynaptic mechanisms depending on the source of the synapse and that this modulation declines with development.
此前,我们证明II型代谢型谷氨酸受体(mGluRs)在出生后早期发育阶段(P7 - 11)可减少丘脑皮质突触处的谷氨酸释放。为进一步研究II型mGluRs在体感神经回路调节中的作用,我们确定II型mGluRs是否持续调节丘脑皮质突触直至成年,以及这些受体是否也调节桶状皮质内的皮质内突触。为解决这些问题,我们研究了II型mGluR激动剂对来自不同年龄(P7 - 53)动物脑片的丘脑皮质兴奋性突触后电流(EPSCs)和桶状皮质内EPSCs的影响。我们发现,出生后第二周后,II型mGluRs对丘脑皮质EPSCs的抑制作用迅速下降。相比之下,在年轻成年小鼠(P30 - 50)中,腺苷通过突触前机制持续抑制丘脑皮质EPSCs。在幼鼠(P7 - 11)中,II型mGluRs的激活还通过突触后机制减少了桶状皮质内EPSCs。与丘脑皮质突触类似,II型mGluRs对桶状皮质内兴奋性突触的调节作用随发育而下降。在年轻成年动物(P30 - 50)中,II型mGluR刺激对桶状皮质内EPSCs影响很小,但确实使神经元超极化。我们的结果共同表明,II型mGluRs根据突触来源通过突触前和突触后机制调节桶状皮质神经回路,且这种调节作用随发育而下降。