Gough Sarah M, Casella Alicia, Ortega Kristen Jasmin, Hackam Abigail S
Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL, United States.
Front Nutr. 2021 Nov 23;8:782657. doi: 10.3389/fnut.2021.782657. eCollection 2021.
The ketogenic diet (KD) is a high-fat low-carbohydrate diet that has been used for decades as a non-pharmacologic approach to treat metabolic disorders and refractory pediatric epilepsy. In recent years, enthusiasm for the KD has increased in the scientific community due to evidence that the diet reduces pathology and improves various outcome measures in animal models of neurodegenerative disorders, including multiple sclerosis, stroke, glaucoma, spinal cord injury, retinal degenerations, Parkinson's disease and Alzheimer's disease. Clinical trials also suggest that the KD improved quality of life in patients with multiple sclerosis and Alzheimer's disease. Furthermore, the major ketone bodies BHB and ACA have potential neuroprotective properties and are now known to have direct effects on specific inflammatory proteins, transcription factors, reactive oxygen species, mitochondria, epigenetic modifications and the composition of the gut microbiome. Neuroprotective benefits of the KD are likely due to a combination of these cellular processes and other potential mechanisms that are yet to be confirmed experimentally. This review provides a comprehensive summary of current evidence for the effectiveness of the KD in humans and preclinical models of various neurological disorders, describes molecular mechanisms that may contribute to its beneficial effects, and highlights key controversies and current gaps in knowledge.
生酮饮食(KD)是一种高脂肪低碳水化合物饮食,数十年来一直被用作治疗代谢紊乱和难治性小儿癫痫的非药物方法。近年来,科学界对生酮饮食的热情有所增加,因为有证据表明,这种饮食可减轻神经退行性疾病动物模型(包括多发性硬化症、中风、青光眼、脊髓损伤、视网膜变性、帕金森病和阿尔茨海默病)的病理状况并改善各种结果指标。临床试验还表明,生酮饮食改善了多发性硬化症和阿尔茨海默病患者的生活质量。此外,主要酮体β-羟基丁酸(BHB)和乙酰乙酸(ACA)具有潜在的神经保护特性,现在已知它们对特定的炎症蛋白、转录因子、活性氧、线粒体、表观遗传修饰和肠道微生物群的组成有直接影响。生酮饮食的神经保护益处可能归因于这些细胞过程与其他尚未经实验证实的潜在机制的共同作用。本综述全面总结了目前关于生酮饮食在人类以及各种神经系统疾病临床前模型中的有效性的证据,描述了可能促成其有益作用的分子机制,并突出了关键争议和当前的知识空白。