抑制性神经递质受体在人黑质多巴胺能神经元上的定位。

H J Waldvogel, K Baer, R L M Faull
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引用次数: 7

摘要

黑质致密部(SNc)主要由多巴胺能染色神经元组成,并有少量非染色神经元分散在这些神经元群中。这些不同类型的神经元拥有GABAA、GABAB和甘氨酸受体。snc -色素沉着的多巴胺能神经元具有突触后GABAA受体(GABAAR),其亚基结构含有alpha3和gamma2亚基,少量色素沉着的神经元含有alpha1 beta2,3 gamma2亚基。由R1和R2亚基和甘氨酸受体组成的GABAB受体也定位于色素神经元上。相比之下,位于SNc的非色素(主要是小白蛋白阳性神经元)在形态和神经化学上与黑质网状部(SNr)神经元相似,对小白蛋白和GABAARs表现出免疫反应性,这些GABAARs含有对alpha1、alpha3、beta2、3和gamma2亚基以及GABAB R1和R2亚基和甘氨酸受体的免疫反应性。因此,SNc的这两种神经元类型,无论是色素多巴胺能神经元还是非色素小白蛋白阳性神经元,都具有相似的GABAB和甘氨酸受体组合,但主要区别在于其膜上GABAARs的亚基组成。不同类型的gabaar表明,这些神经元类型的gabaar能输入通过具有不同药理和生理特征的gabaar运作,而这些细胞类型的GABABR和甘氨酸受体可能具有相似的特性。
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The localization of inhibitory neurotransmitter receptors on dopaminergic neurons of the human substantia nigra.

The substantia nigra pars compacta (SNc) is comprised mainly of dopaminergic pigmented neurons arranged in groups, with a small population of nonpigmented neurons scattered among these groups. These different types of neurons possess GABAA, GABAB, and glycine receptors. The SNc-pigmented dopaminergic neurons have postsynaptic GABAA receptors (GABAAR) with a subunit configuration containing alpha3 and gamma2 subunits, with a small population of pigmented neurons containing alpha1 beta2,3 gamma2 subunits. GABAB receptors comprised of R1 and R2 subunits and glycine receptors are also localized on pigmented neurons. In contrast, nonpigmented (mainly parvalbumin positive neurons) located in the SNc are morphologically and neurochemically similar to substantia nigra pars reticulata (SNr) neurons by showing immunoreactivity for parvalbumin and GABAARs containing immunoreactivity for alpha1, alpha3, beta2,3, and gamma2 subunits as well as GABAB R1 and R2 subunits and glycine receptors. Thus, these two neuronal types of the SNc, either pigmented dopaminergic neurons or nonpigmented parvalbumin positive neurons, have similar GABAB and glycine receptor combinations, but differ mainly in the subunit composition of the GABAARs located on their membranes. The different types of GABAARs suggest that GABAergic inputs to these neuronal types operate through GABAARs with different pharmacological and physiological profiles, whereas GABABR and glycine receptors of these cell types are likely to have similar properties.

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