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对黄斑突变小鼠小脑皮质线粒体酶的组织化学研究,该小鼠为门克斯卷发疾病模型。

Histochemical study of mitochondrial enzymes in cerebellar cortex of macular mutant mouse, a model of Menkes kinky hair disease.

作者信息

Kumode M, Yamano T, Shimada M

机构信息

Department of Pediatrics, Shiga University of Medical Science, Japan.

出版信息

Acta Neuropathol. 1994;87(3):313-6. doi: 10.1007/BF00296748.

Abstract

The cerebellar Purkinje cells in the hemizygote of the macular mutant mouse contain numerous abnormal mitochondria which show a marked decrease in cytochrome c oxidase activity. Using histochemical methods we studied the activity of other mitochondrial enzymes, such as NADH diaphorase and succinic dehydrogenase, in the cerebellar cortex of this mutant mouse. Such activities were markedly increased in the Purkinje cells, especially in the soma and stem dendrite, from 10 days after birth in the hemizygote as compared with findings in normal littermates. These results were considered to be due to an increased number of abnormal mitochondria.

摘要

黄斑突变小鼠半合子中的小脑浦肯野细胞含有大量异常线粒体,这些线粒体的细胞色素c氧化酶活性显著降低。我们使用组织化学方法研究了这种突变小鼠小脑皮质中其他线粒体酶的活性,如NADH黄递酶和琥珀酸脱氢酶。与正常同窝小鼠相比,半合子小鼠出生后10天起,浦肯野细胞中的这些酶活性显著增加,尤其是在胞体和主树突中。这些结果被认为是由于异常线粒体数量增加所致。

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