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The human temporal cortex: characterization of neurons expressing nitric oxide synthase, neuropeptides and calcium-binding proteins, and their glutamate receptor subunit profiles.

机译:人类颞叶皮质:表达一氧化氮合酶,神经肽和钙结合蛋白的神经元的特征及其谷氨酸受体亚单位谱。

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Immunocytochemical techniques were used to examine the distribution of neurons immunoreactive (-ir) for nitric oxide synthase (nNOS), somatostatin (SOM), neuropeptide Y (NPY), parvalbumin (PV), calbindin (CB) and calretinin (CR), in the inferotemporal gyrus (Brodmann's area 21) of the human neocortex. Neurons that colocalized either nNOS or SOM with PV, CB or CR were also identified by double-labeling techniques. Furthermore, glutamate receptor subunit profiles (GluR1, GluR2/3, GluR2/4, GluR5/6/7 and NMDAR1) were also determined for these cells. The number and distribution of cells containing nNOS, SOM, NPY, PV, CB or CR differed for each antigen. In addition, distinct subpopulations of neurons displayed different degrees of colocalization of these antigens depending on which antigens were compared. Moreover, cells that contained nNOS, SOM, NPY, PV, CB or CR expressed different receptor subunit profiles. These results show that specific subpopulations of neurochemically identified nonpyramidal cells may be activated via different receptor subtypes. As these different subpopulations of cells project to specific regions of pyramidal cells, facilitation of subsets of these cells via different receptor subunits may activate different inhibitory circuits. Thus, various distinct, but overlapping, inhibitory circuits may act in concert in the modulation of normal cortical function, plasticity and disease.
机译:免疫细胞化学技术用于检查一氧化氮合酶(nNOS),生长抑素(SOM),神经肽Y(NPY),小白蛋白(PV),钙结合蛋白(CB)和钙黄蛋白(CR)的免疫反应性(-ir)神经元的分布人类新皮层的颞下回(布罗德曼氏区21)。通过双标记技术还鉴定了nNOS或SOM与PV,CB或CR共定位的神经元。此外,还确定了这些细胞的谷氨酸受体亚单位谱(GluR1,GluR2 / 3,GluR2 / 4,GluR5 / 6/7和NMDAR1)。对于每种抗原,包含nNOS,SOM,NPY,PV,CB或CR的细胞数量和分布都不同。另外,取决于所比较的抗原,神经元的不同亚群显示这些抗原的共定位程度不同。此外,包含nNOS,SOM,NPY,PV,CB或CR的细胞表达不同的受体亚单位谱。这些结果表明,神经化学鉴定的非锥体细胞的特定亚群可以通过不同的受体亚型激活。当这些不同的细胞亚群投射到锥体细胞的特定区域时,通过不同的受体亚基促进这些细胞的亚群可能会激活不同的抑制回路。因此,各种不同的但重叠的抑制回路可以在正常皮质功能,可塑性和疾病的调节中协同作用。

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