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支配膈肌和背最长肌的大鼠运动神经元与年龄相关的三维形态学变化。

Age-related three-dimensional morphological changes in rat motoneurons innervating diaphragm and longissimus muscles.

作者信息

Miyata H, Suzuki T, Maruyama A, Wada N

机构信息

Department of Biological Sciences, Graduate School of Medicine, Yamaguchi University, Yamaguchi 753-8515, Japan.

出版信息

Anat Histol Embryol. 2008 Oct;37(5):394-9. doi: 10.1111/j.1439-0264.2008.00873.x. Epub 2008 Jul 15.

Abstract

We investigated age-related morphological changes of rat motoneurons innervating diaphragm muscle (DI-MN) and lumber longissimus muscle (LL-MN) in which quite different activation patterns exist. In young (2-4 months) and old (24-26 months) rats, the motoneurons innervating both muscles were labelled retrogradely by intramuscular injection of cholera toxin B subunit. After a 4-day survival, horizontal slices of the spinal cord were processed with immunohistochemical staining (first antibody to cholera toxin B subunit and second antibody with Cy3) and observed with a confocal microscope. Three-dimensional reconstruction of labelled motoneurons was performed to examine soma and dendrite morphology. As compared to the soma volume in young rats, significantly smaller values were found in old rats in both motoneurons and the degrees of decline were 16.1% in DI-MN and 20.3% in LL-MN. Significant decreases in the thickness of primary dendrites were also found in both motoneurons, and the degrees of decline were 17.5% in DI-MN and 22.3% in LL-MN. Smaller changes were found in DI-MN than in LL-MN, indicating the possibility that increased activation by central drives can attenuate age-related morphological changes of the motor system in the spinal cord.

摘要

我们研究了支配膈肌(DI-MN)和腰部最长肌(LL-MN)的大鼠运动神经元与年龄相关的形态变化,这两种肌肉存在截然不同的激活模式。在年轻(2 - 4个月)和年老(24 - 26个月)的大鼠中,通过肌肉内注射霍乱毒素B亚基对支配这两种肌肉的运动神经元进行逆行标记。在存活4天后,对脊髓水平切片进行免疫组织化学染色处理(用抗霍乱毒素B亚基的一抗和Cy3标记的二抗),并用共聚焦显微镜观察。对标记的运动神经元进行三维重建,以检查其胞体和树突形态。与年轻大鼠的胞体体积相比,年老大鼠的两种运动神经元胞体体积均显著减小,DI-MN的下降幅度为16.1%,LL-MN的下降幅度为20.3%。两种运动神经元的初级树突厚度也显著减小,DI-MN的下降幅度为17.5%,LL-MN的下降幅度为22.3%。DI-MN的变化小于LL-MN,这表明中枢驱动增加可能会减弱脊髓中运动系统与年龄相关的形态变化。

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