Kaviyarasan Shobana, Chung Sia Edmund Lee, Retinasamy Thaarvena, Arulsamy Alina, Shaikh Mohd Farooq
Clinical School Johor Bahru, Jeffrey Cheah School of Medicine and Health Sciences, Monash University Malaysia, Johor, Malaysia.
Neuropharmacology Research Laboratory, Jeffrey Cheah School of Medicine and Health Sciences, Monash University Malaysia, Selangor, Malaysia.
Front Aging Neurosci. 2022 Oct 14;14:1015837. doi: 10.3389/fnagi.2022.1015837. eCollection 2022.
The gut taxonomical profile is one of the contributory factors in maintaining homeostasis within the central nervous system (CNS). Of late, the efficacy of diet as a target of treatment, and how various dietary interventions may modulate gut microbiota differently have been an area of focus in research. The role of ketogenic diet (KD) in particular has been well-established in other diseases like intractable epilepsy due to its postulated effects on gut microbiome modulation, resulting in neuronal stability and prevention of epileptogenesis. Therefore, this systematic review aimed to critically evaluate the current available literature investigating the interplay between the three distinct entities: ketogenic diet, neurodegeneration, and gut microbiota, which may serve as a focus guide for future neurodegenerative diseases (ND) therapeutic research. A comprehensive literature search was performed on three databases; PubMed, Scopus, and Ovid Medline. A total of 12 articles were selected for critical appraisal, after subjecting to the inclusion and exclusion criteria in this study. The selected articles revealed that the hopes of KD as a treatment modality for ND are being ventured into as these individuals are said to acquire gut dysbiosis, primarily through increased colonization of phyla and . Although positive effects including restoration of healthy gut microbes such as sp., improvement in cognitive functioning and decline in neuro-inflammatory markers were noted, this systematic review also depicted conflicting results such as decrease in alpha and beta species diversity as well as diminution of healthy gut commensals such as . In addition, positive neuromodulation were also observed, notably an increase in cerebral blood perfusion to ventromedial hippocampal region increased expression of eNOS and clearance of amyloid-beta proteins across the blood-brain-barrier expression of p-glycoprotein. Neuroprotective mechanisms of ketogenic diet also included downregulation of mTOR expression, to prevention acceleration of pathological diseases such as Alzheimer's. Thus due to this conflicting/contrasting results demonstrated by ketogenic diet, such as a decline in gut species richness, diminution in beneficial microbes and decline cognition unless delivered in an intermittent fasting pattern, further studies may still be required before prior recommendation of a ketogenic diet therapeutic regime in ND patients.
肠道分类学特征是维持中枢神经系统(CNS)内稳态的促成因素之一。近来,饮食作为治疗靶点的功效以及各种饮食干预如何不同地调节肠道微生物群一直是研究的重点领域。生酮饮食(KD)的作用尤其在其他疾病如难治性癫痫中已得到充分证实,因为其对肠道微生物群调节的假定作用,导致神经元稳定性并预防癫痫发生。因此,本系统评价旨在严格评估当前关于研究三个不同实体之间相互作用的现有文献:生酮饮食、神经退行性变和肠道微生物群,这可为未来神经退行性疾病(ND)治疗研究提供重点指导。对三个数据库进行了全面的文献检索:PubMed、Scopus和Ovid Medline。在符合本研究的纳入和排除标准后,共选择了12篇文章进行严格评估。所选文章表明,KD作为ND治疗方式的希望正在被探索,因为据说这些个体主要通过门 和 菌的定植增加而出现肠道菌群失调。尽管注意到了一些积极影响,包括恢复健康的肠道微生物如 菌属、改善认知功能和神经炎症标志物下降,但本系统评价也描述了相互矛盾的结果,如α和β物种多样性降低以及健康肠道共生菌如 菌减少。此外,还观察到了积极的神经调节作用,特别是向腹内侧海马区的脑血流灌注增加、血脑屏障上eNOS表达增加和β淀粉样蛋白清除增加、P糖蛋白表达增加。生酮饮食的神经保护机制还包括mTOR表达下调,以预防阿尔茨海默病等病理性疾病的加速发展。因此,由于生酮饮食显示出这种相互矛盾/对比的结果,如肠道物种丰富度下降、有益微生物减少和认知能力下降,除非采用间歇性禁食模式,否则在向ND患者推荐生酮饮食治疗方案之前可能仍需要进一步研究。