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衰老加速小鼠(SAM-P8)脑内儿茶酚胺能神经元的免疫细胞化学研究。

Immunocytochemical study of catecholaminergic neurons in the senescence-accelerated mouse (SAM-P8) brain.

作者信息

Karasawa N, Nagatsu I, Sakai K, Nagatsu T, Watanabe K, Onozuka M

机构信息

Department of Anatomy, School of Medicine, Fujita Health University, Aichi, Japan.

出版信息

J Neural Transm (Vienna). 1997;104(11-12):1267-75. doi: 10.1007/BF01294727.

Abstract

The catecholaminergic neurons of senescence-accelerated mice (SAM-P8) were analyzed by immunohistochemical microphotometry in terms of immunoreactivities to aromatic L-amino acid decarboxylase (AADC), dopamine (DA), or noradrenaline (NA). Accelerated senescence-resistant mice (SAM-R1) were used as control mice. The immunoreactivities to AADC, DA, and NA of the catecholaminergic neurons of the SAM-P8 mice were weaker than those of the SAM-R1 mice in all the brain regions. Immunoelectron microscopy revealed progressive degeneration of dopaminergic neurons and their terminal fibers in the substantia nigra as well as in noradrenergic neurons and their proximal dendrites in the locus coeruleus of the SAM-P8 mice. In contrast, there was no difference between the SAM-P8 and SAM-R1 mice in the distribution of AADC-only positive neurons (designated as D neurons in the rat brain by Jaeger et al.) nor in their immunoreactivities. These results may indicate that DA neurons in the substantia nigra and NA neurons in the locus coeruleus degenarate more rapidly during aging in SAM-P8 mice than in control SAM-R1 mice and that D neurons may function as a part of a compensatory system for the decreases in catecholaminergic neurons during aging.

摘要

采用免疫组织化学显微光度法,依据衰老加速小鼠(SAM-P8)的儿茶酚胺能神经元对芳香族L-氨基酸脱羧酶(AADC)、多巴胺(DA)或去甲肾上腺素(NA)的免疫反应性进行分析。将抗加速衰老小鼠(SAM-R1)用作对照小鼠。在所有脑区中,SAM-P8小鼠的儿茶酚胺能神经元对AADC、DA和NA的免疫反应性均弱于SAM-R1小鼠。免疫电子显微镜检查显示,SAM-P8小鼠黑质中的多巴胺能神经元及其终末纤维以及蓝斑中的去甲肾上腺素能神经元及其近端树突出现进行性退化。相比之下,SAM-P8小鼠和SAM-R1小鼠之间,仅AADC阳性神经元(在大鼠脑中被Jaeger等人称为D神经元)的分布及其免疫反应性并无差异。这些结果可能表明,与对照SAM-R1小鼠相比,SAM-P8小鼠衰老过程中黑质中的DA神经元和蓝斑中的NA神经元退化更快,并且D神经元可能作为衰老过程中儿茶酚胺能神经元减少的补偿系统的一部分发挥作用。

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