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生酮饮食可增加琥珀酸脱氢酶(SDH)的活性,并恢复老年大鼠小脑浦肯野细胞中与年龄相关的 SDH 阳性线粒体数量密度的减少。

A ketogenic diet increases succinic dehydrogenase (SDH) activity and recovers age-related decrease in numeric density of SDH-positive mitochondria in cerebellar Purkinje cells of late-adult rats.

机构信息

Neurobiology of Aging Laboratory, INRCA, Via Birarelli 8, 60121 Ancona, Italy.

出版信息

Micron. 2010 Feb;41(2):143-8. doi: 10.1016/j.micron.2009.08.010. Epub 2009 Oct 8.

Abstract

Ketogenic diets (KDs) have been applied in the therapy of paediatric epilepsy for nearly a century. Recently, beneficial results have also been reported on metabolic disorders and neurodegeneration, designating aged individuals as possible recipients. However, KDs efficacy decrease after the suckling period, and very little is known about their impact on the aging brain. In the present study, the effect on the neuronal energetic supply of a KD containing 20% of medium chain triglycerides (MCT) was investigated in Purkinje cells of the cerebellar vermis of late-adult (19-month-old) rats. The animals were fed with the KD for 8 weeks, and succinic dehydrogenase (SDH) activity was cytochemically determined. The following parameters of SDH-positive mitochondria were evaluated by the use of a computer-assisted image analysis system connected to a transmission electron microscope: numeric density (Nv), average volume (V), volume density (Vv), and cytochemical precipitate area/mitochondrial area (R). Young, age-matched, and old animals fed with a standard chow were used as controls. We found significantly higher Nv in MCT-KD-fed rats vs. all the control groups, in young vs. late-adult and old controls, and in late-adult vs. old controls. V and Vv showed no significant differences among the groups. R was significantly higher in MCT-KD-fed rats vs. all the control animals, and in old vs. young and late-adult controls. Present data indicate that the ketogenic treatment counteracted age-related decrease in numeric density of SDH-positive mitochondria, and enhanced their metabolic efficiency. Given the central role of mitochondrial impairment in age-related physio-pathological changes of the brain, these findings may represent a starting point to examine novel potentialities for KDs.

摘要

生酮饮食(KDs)在儿科癫痫的治疗中已经应用了近一个世纪。最近,关于代谢紊乱和神经退行性变的有益结果也有报道,将老年个体指定为可能的接受者。然而,KDs 的疗效在哺乳期后会下降,并且对于它们对衰老大脑的影响知之甚少。在本研究中,研究了含有 20%中链甘油三酯(MCT)的 KD 对小脑蚓部浦肯野细胞的神经元能量供应的影响。动物用 KD 喂养 8 周,并通过细胞化学测定琥珀酸脱氢酶(SDH)活性。使用连接到透射电子显微镜的计算机辅助图像分析系统评估 SDH 阳性线粒体的以下参数:数值密度(Nv)、平均体积(V)、体积密度(Vv)和细胞化学沉淀物面积/线粒体面积(R)。年轻、年龄匹配和用标准饲料喂养的老年动物作为对照。我们发现,与所有对照组相比,MCT-KD 喂养的大鼠的 Nv 显著更高,与年轻组相比,MCT-KD 喂养的大鼠的 Nv 更高,与老年组相比,MCT-KD 喂养的大鼠的 Nv 更高。V 和 Vv 各组之间无显著差异。与所有对照动物相比,MCT-KD 喂养的大鼠的 R 显著更高,与年轻组和老年组相比,MCT-KD 喂养的大鼠的 R 更高。目前的数据表明,生酮治疗可以对抗与年龄相关的 SDH 阳性线粒体数量密度的下降,并提高其代谢效率。鉴于线粒体损伤在与年龄相关的大脑生理病理变化中的核心作用,这些发现可能为研究 KDs 的新潜力提供了一个起点。

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