We studied the involvement of deep cortical layer neurons in processing callosal information in the rat. We observed with electron microscopy that both parvalbumin (PV)-labeled profiles and unlabeled dendritic spines of deep cortical layer neurons receive synapses from the contralateral hemisphere. Stimulation of callosal fibers elicited monosynaptic excitatory postsynaptic currents in both layer VI pyramidal neurons and gamma-aminobutyric acidergic (GABAergic) interneurons immunopositive for the vesicular GABA transporter and PV. Pyramidal cells had intrinsic electrophysiological properties and synaptic responses with slow kinetics and a robust N-metyhl-D-aspartate (NMDA) component. In contrast, GABAergic interneurons had intrinsic membrane properties and synaptic responses with faster kinetics and a less pronounced NMDA component. Consistent with these results, the temporal integration of callosal input was effective over a significantly longer time window in pyramidal neurons compared with GABAergic interneurons. Interestingly, callosal stimulation did not evoke feedforward inhibition in all GABAergic interneurons and in the majority of pyramidal neurons tested. Furthermore, retrogradely labeled layer VI pyramidal neurons of the contralateral cortex responded monosynaptically to callosal stimulation, suggesting interconnectivity between callosally projecting neurons. The data show that pyramidal neurons and GABAergic interneurons of deep cortical layers receive interhemispheric information directly and have properties supporting their distinct roles.

译文

我们研究了深皮质层神经元在处理大鼠call骨信息中的参与。我们用电子显微镜观察到,浅白蛋白 (PV) 标记的轮廓和深皮质层神经元的未标记的树突棘均从对侧半球接收突触。Call骨纤维的刺激在VI层锥体神经元和 γ-氨基丁酸 (GABA能) 中间神经元中均引起单突触兴奋性突触后电流,对囊泡GABA转运蛋白和PV免疫呈阳性。锥体细胞具有内在的电生理特性和突触反应,动力学缓慢,并且具有强大的N-metyhl-D-天冬氨酸 (NMDA) 成分。相反,gaba能中间神经元具有内在的膜特性和突触反应,其动力学更快,NMDA成分不那么明显。与这些结果一致,与gaba能中间神经元相比,在锥体神经元中,call骨输入的时间整合在明显更长的时间窗口内有效。有趣的是,在所有gaba能中间神经元和大多数测试的锥体神经元中,call刺激并未引起前馈抑制。此外,对侧皮层的逆行标记的第VI层锥体神经元对call骨刺激单突触反应,表明call骨投射神经元之间的相互连接。数据表明,皮层深层的锥体神经元和gaba能中间神经元直接接收半球间信息,并具有支持其独特作用的特性。

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