Clinical Applications of Ketogenic Diet-Induced Ketosis in Neurodegenerative and Metabolism-Related Pathologies

R. Pilla
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引用次数: 5

Abstract

: Metabolic-based therapies such as nutritional ketosis have been proven effective for seizure disorders and various acute and chronic neurological pathologies. In a healthy brain, glucose is the primary metabolic fuel for cells. However, neurodegenerative disorders, such as Alzheimer’s disease (AD), Parkinson’s disease (PD), seizure disorders, and traumatic brain injury (TBI) are associated with impaired glucose transport and metabolism and with mitochondrial dysfunction leading to energy deficit. Therapeutic ketosis can be considered as a form of metabolic therapy by providing alternative energy substrates. In addition, ketosis leads to metabolic adaptations that improve brain metabolism, restore mitochondrial ATP production, decrease reactive oxygen species production, reduce inflammation, and increase the activity of neurotrophic factors. Moreover, the synaptic activity between neurons is also stabilized through the increase of Szent-Györgyi–Krebs cycle intermediates, antioxidant effects, increased GABA-to-glutamate ratio, and activation of ATP-sensitive potassium channels.
生酮饮食诱导的酮症在神经退行性和代谢相关病理中的临床应用
以代谢为基础的疗法,如营养酮症,已被证明对癫痫和各种急慢性神经系统疾病有效。在健康的大脑中,葡萄糖是细胞的主要代谢燃料。然而,神经退行性疾病,如阿尔茨海默病(AD)、帕金森病(PD)、癫痫发作性疾病和创伤性脑损伤(TBI)与葡萄糖转运和代谢受损以及导致能量不足的线粒体功能障碍有关。治疗性酮症可以被认为是一种形式的代谢治疗提供替代的能量底物。此外,酮症导致代谢适应,改善脑代谢,恢复线粒体ATP的产生,减少活性氧的产生,减少炎症,增加神经营养因子的活性。此外,神经元之间的突触活性也通过Szent-Györgyi-Krebs循环中间体的增加、抗氧化作用、GABA-to-glutamate比例的增加和atp敏感钾通道的激活而稳定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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