首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Degeneration of dopaminergic neurons in the substantia nigra of zitter mutant rat and protection by chronic intake of Vitamin E.
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Degeneration of dopaminergic neurons in the substantia nigra of zitter mutant rat and protection by chronic intake of Vitamin E.

机译:突变型大鼠黑质中多巴胺能神经元的变性和长期摄入维生素E的保护作用。

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摘要

Dopaminergic cell death in the ventral and dorsal tiers of substantia nigra pars copmacta (SNc) and their prevention by anti-oxidant diet was immunohistochemically studied in the zitter mutant rats, which are characterized by abnormal metabolism of superoxide. Similar to previous reports, the number of SNc neurons in Nissl-stained section decreased with age. Tyrosine hydroxylase (TH) immunohistochemistry demonstrated that the dopaminergic neurons in the ventral tier of SNc degenerated early, whereas the dorsal tier gradually degenerated with age. Thus, the ventral tier dopaminergic neurons are affected first, but the dorsal tier neurons do become impact by the zi/zi mutation. Following 9-month period after weaning, zitter rats supplemented with 500 mg D,L-alpha-tocophenol (VE(+))/kg diet exhibited a significant increased of surviving TH-immunoreactive neurons in both the tiers of SNc as compared with the zi/zi rats with control and VE(-) diets. These results suggest that VE supplement may slow the dopaminergic cell loss in zitter mutant rat, and further support that degeneration of the dopaminergic neurons in this mutant rat is caused by oxidant stress. Thus, the zitter rat may represent a good model for studying the dopaminergic cell death by superoxide species.
机译:免疫组织化学研究了Zitter突变大鼠的黑质腹侧和背侧多巴胺能细胞死亡及其通过抗氧化饮食的预防,其特征在于超氧化物的异常代谢。与以前的报告类似,尼氏染色切片中的SNc神经元数量随着年龄的增长而减少。酪氨酸羟化酶(TH)免疫组织化学表明,SNc腹侧的多巴胺能神经元早期退化,而背侧随着年龄的增长逐渐退化。因此,腹层多巴胺能神经元首先受到影响,但是背层神经元的确受到zi / zi突变的影响。断奶后9个月后,补充了500 mg D,L-α-生育酚(VE(+))/ kg饮食的zitter大鼠与SNc相比,在SNc的两个阶段均表现出存活的TH免疫反应性神经元的显着增加。 zi / zi大鼠采用控制饮食和VE(-)饮食。这些结果表明VE补充剂可以减缓突变型大鼠中多巴胺能细胞的损失,并进一步支持该突变型大鼠中多巴胺能神经元的变性是由氧化应激引起的。因此,拉特鼠可能代表研究由超氧化物类引起的多巴胺能细胞死亡的良好模型。

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