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Sir-2.1 调节“热量限制介导的”秀丽隐杆线虫神经退行性变的预防:对帕金森病的影响。

Sir-2.1 modulates 'calorie-restriction-mediated' prevention of neurodegeneration in Caenorhabditis elegans: implications for Parkinson's disease.

机构信息

Laboratory of Functional Genomics and Molecular Toxicology, Division of Toxicology, CSIR-Central Drug Research Institute, Lucknow 226 001, UP, India.

出版信息

Biochem Biophys Res Commun. 2011 Sep 23;413(2):306-10. doi: 10.1016/j.bbrc.2011.08.092. Epub 2011 Aug 26.

Abstract

The phenomenon of aging is known to modulate many disease conditions including neurodegenerative ailments like Parkinson's disease (PD) which is characterized by selective loss of dopaminergic neurons. Recent studies have reported on such effects, as calorie restriction, in modulating aging in living systems. We reason that PD, being an age-associated neurodegenerative disease might be modulated by interventions like calorie restriction. In the present study we employed the transgenic Caenorhabditis elegans model (P(dat-1)::GFP) expressing green fluorescence protein (GFP) specifically in eight dopaminergic (DA) neurons. Selective degeneration of dopaminergic neurons was induced by treatment of worms with 6-hydroxy dopamine (6-OHDA), a selective catecholaminergic neurotoxin, followed by studies on effect of calorie restriction on the neurodegeneration. Employing confocal microscopy of the dopaminergic neurons and HPLC analysis of dopamine levels in the nematodes, we found that calorie restriction has a preventive effect on dopaminergic neurodegeneration in the worm model. We further studied the role of sirtuin, sir-2.1, in modulating such an effect. Studies employing RNAi induced gene silencing of nematode sir-2.1, revealed that presence of Sir-2.1 is necessary for achieving the protective effect of calorie restriction on dopaminergic neurodegeneration. Our studies provide evidence that calorie restriction affords, an sir-2.1 mediated, protection against the dopaminergic neurodegeneration, that might have implications for neurodegenerative Parkinson's disease.

摘要

衰老现象被认为会调节许多疾病状况,包括神经退行性疾病,如帕金森病(PD),其特征是多巴胺能神经元的选择性丧失。最近的研究报告了这种影响,如热量限制,在调节生物系统的衰老方面。我们认为,作为一种与年龄相关的神经退行性疾病,PD 可能可以通过热量限制等干预措施来调节。在本研究中,我们使用了表达绿色荧光蛋白(GFP)的转基因秀丽隐杆线虫(P(dat-1)::GFP)模型,GFP 特异性地在 8 个多巴胺能(DA)神经元中表达。通过用 6-羟基多巴胺(6-OHDA)处理线虫,诱导多巴胺能神经元选择性退化,这是一种选择性儿茶酚胺神经毒素,然后研究热量限制对神经退行性变的影响。通过对多巴胺能神经元进行共聚焦显微镜观察和线虫中多巴胺水平的 HPLC 分析,我们发现热量限制对蠕虫模型中的多巴胺能神经退行性变具有预防作用。我们进一步研究了沉默信息调节因子 2.1(sir-2.1)在调节这种作用中的作用。通过 RNAi 诱导的线虫 sir-2.1 基因沉默研究表明,Sir-2.1 的存在对于实现热量限制对多巴胺能神经退行性变的保护作用是必要的。我们的研究提供了证据表明,热量限制提供了一种由 sir-2.1 介导的对多巴胺能神经退行性变的保护作用,这可能对神经退行性帕金森病有影响。

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