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首页> 外文期刊>Neurochemical Research >Apoptotic Mode of Cell Death in Substantia Nigra Following Intranigral Infusion of the Parkinsonian Neurotoxin, MPP+ in Sprague-Dawley Rats: Cellular, Molecular and Ultrastructural Evidences
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Apoptotic Mode of Cell Death in Substantia Nigra Following Intranigral Infusion of the Parkinsonian Neurotoxin, MPP+ in Sprague-Dawley Rats: Cellular, Molecular and Ultrastructural Evidences

机译:经鼻输注帕金森氏神经毒素MPP + 在Sprague-Dawley大鼠中的黑质细胞凋亡的细胞死亡模式:细胞,分子和超微结构的证据。

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摘要

The potent parkinsonian neurotoxin 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP) is known to cause dopaminergic neurodegeneration in nigrostriatal system. In the present study we investigated the nuclear morphology of cells in the substantia nigra pars compacta (SNpc) region of rats following unilateral intranigral infusion of the active metabolite, 1-methyl-4-phenyl pyridinium ion (MPP+), which resulted in a dose-dependent and prolonged dopamine depletion in the ipsilateral striatum. There appeared a substantial loss of tyrosine hydroxylase immunoreactive neurons in the SNpc that received the neurotoxin. Specific nuclear staining with Hoechst 33342 or acridine orange revealed bright pyknotic, shrunken, distorted nuclei and condensed chromatin with perinuclear nucleolus respectively following visualization with the former and latter dyes in the ipsilateral SNpc, as compared to the round, intact nuclei and centrally positioned nucleolus in the contralateral side. Ultrastructural details of the nucleus under transmission electron microscope confirmed distorted nuclear organization with shrunken or condensed nuclei and disrupted nuclear membrane. These features are typical of nucleus undergoing apoptosis, and suggest that MPP+ causes dopaminergic neuronal death through an apoptotic mode. Typical laddering pattern of genomic DNA isolated from the ipsilateral SN in agarose gel electrophoresis conclusively established apoptosis following intranigral administration of MPP+ in rats.
机译:已知有效的帕金森氏神经毒素1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)在黑质纹状体系统中引起多巴胺能神经变性。在本研究中,我们调查了大鼠单侧鼻内注入活性代谢物1-甲基-4-苯基吡啶鎓离子(MPP + )后黑质致密部(SNpc)区细胞的核形态。导致同侧纹状体的剂量依赖性和长期多巴胺耗竭。在接受神经毒素的SNpc中出现酪氨酸羟化酶免疫反应性神经元的大量损失。用Hoechst 33342或a啶橙进行的特定核染色显示,同侧SNpc中的前一种和后一种染料显色后,分别具有明亮的致密性,萎缩的,扭曲的核和浓缩的染色质以及核周围的核仁,与圆形,完整的核和居中定位的核仁相比,对侧。透射电子显微镜下核的超微结构细节证实核组织扭曲,核收缩或凝缩,核膜破裂。这些特征是细胞核发生凋亡的典型特征,提示MPP +通过凋亡模式引起多巴胺能神经元死亡。在大鼠腹腔注射MPP + 后,琼脂糖凝胶电泳分离自同侧SN的基因组DNA的典型梯形模式最终确定了细胞凋亡。

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