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氧化应激在患有年龄相关性神经退行性变的SAMP10小鼠中的作用。

Involvement of oxidative stress in SAMP10 mice with age-related neurodegeneration.

作者信息

Wang Jun, Lei Hongtao, Hou Jincai, Liu Jianxun

机构信息

Institute of Basic Theory, China Academy of Chinese Medical Sciences, 16 Dong Zhi Men Nei Nan Xiao Jie, Beijing, 100700, China.

出版信息

Neurol Sci. 2015 May;36(5):743-50. doi: 10.1007/s10072-014-2029-5. Epub 2014 Dec 10.

Abstract

Age-related changes in the brain tissue are reflected in many aspects. We sought to determine the morphology, Nissl bodies, behavioral appearance and oxidative stress in the brain using SAMP10 mice, a substrain of the senescence-accelerated mouse. SAMP10 mice groups divided by different ages (3, 5, 8 and 14 months) were compared with those of control groups with the above corresponding ages. Cortical thickness, Nissl bodies, behavioral appearance and oxidative stress were evaluated through image software, thionine staining, step-down test and colorimetry, respectively. The weight and cortical thickness of the brain in SAMP10 mice significantly reduced from 8 months of age. The results showed that the number of Nissl bodies decreased or Nissl bodies shrank with dark staining in histology. The same result appeared in a step-down test. As the SAMP10 mice grew older, the oxidative stress-related markers superoxide dismutase decreased and malondialdehyde increased after 8 months. Glutathione peroxidase activities showed no age-related changes. The changes of brain morphology and productions of oxidative stress in the brain tissue might contribute to the behavioral abnormality. Deceleration of age-related production of oxidative stress might be expected to be a potent strategy for anti-aging interventions.

摘要

脑组织中与年龄相关的变化体现在多个方面。我们试图利用衰老加速小鼠的一个亚系SAMP10小鼠来确定大脑的形态、尼氏体、行为表现和氧化应激。将按不同年龄(3、5、8和14个月)划分的SAMP10小鼠组与上述相应年龄的对照组进行比较。分别通过图像软件、硫堇染色、跳台试验和比色法评估皮质厚度、尼氏体、行为表现和氧化应激。SAMP10小鼠大脑的重量和皮质厚度从8月龄起显著降低。结果显示,组织学上尼氏体数量减少或尼氏体萎缩且染色加深。跳台试验也出现了同样的结果。随着SAMP10小鼠年龄增长,8个月后与氧化应激相关的标志物超氧化物歧化酶减少,丙二醛增加。谷胱甘肽过氧化物酶活性未显示出与年龄相关的变化。脑组织中大脑形态的改变和氧化应激的产生可能导致行为异常。减缓与年龄相关的氧化应激产生有望成为抗衰老干预的有效策略。

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