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Age-related changes in the rat hippocampus.

机译:大鼠海马中与年龄相关的变化。

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摘要

The human brain is uniquely powerful in its cognitive abilities, yet the hippocampal and neocortical circuits that mediate these complex functions are highly vulnerable during aging. In this study, we analyzed age-related changes in the rat hippocampus by studying newborn (1 month), middle-aged (12 months), and older (24 months) male and female Sprague-Dawley rats. We evaluated neuronal dystrophy, neuron scattering, and granulovacuolar degeneration in the hippocampal area using light microscopy, according to age and gender. We detected significant neuronal dystrophy in the CA1, CA2, and CA3 areas in male rats, and in the CA1, CA3, and CA4 areas in female rats. Degenerative changes, indicated by neuron scattering, were observed in the CA1, CA2, and CA3 areas of male and the CA2 and CA4 areas of female rats. Changes in all areas of the hippocampus were observed with increasing age; these changes included neuronal dystrophy and neuron scattering and did not differ significantly between male and female rats.
机译:人脑在认知能力方面具有独特的强大功能,但是在衰老过程中,介导这些复杂功能的海马和新皮层回路非常脆弱。在这项研究中,我们通过研究新生(1个月),中年(12个月)和年龄较大(24个月)的雄性和雌性Sprague-Dawley大鼠,分析了大鼠海马中与年龄相关的变化。根据年龄和性别,我们使用光学显微镜评估了海马区的神经元营养不良,神经元散射和颗粒性肺泡炎。我们在雄性大鼠的CA1,CA2和CA3区域以及雌性大鼠的CA1,CA3和CA4区域检测到明显的神经营养不良。在雄性大鼠的CA1,CA2和CA3区域以及雌性大鼠的CA2和CA4区域中观察到了神经元散射所指示的变性变化。随着年龄的增长,观察到海马各区域的变化。这些变化包括神经元营养不良和神经元散射,并且在雌雄大鼠之间没有显着差异。

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