Control of seizures by ketogenic diet-induced modulation of metabolic pathways

被引:25
|
作者
Clanton, Ryan M. [1 ,2 ,3 ]
Wu, Guoyao [4 ,5 ]
Akabani, Gamal [1 ,2 ,6 ]
Aramayo, Rodolfo [3 ]
机构
[1] Texas A&M Univ, Dept Nucl Engn, College Stn, TX 77843 USA
[2] Texas A&M Univ, Syst Radiobiol Lab, Texas A&M Inst Preclin Studies, 800 Raymond Stotzer Pkwy, College Stn, TX 77843 USA
[3] Texas A&M Univ, Dept Biol, Room 412A,Bldg BSBW, College Stn, TX 77843 USA
[4] Texas A&M Univ, Dept Anim Sci, College Stn, TX 77843 USA
[5] Texas A&M Univ, Dept Med Physiol, College Stn, TX 77843 USA
[6] Texas A&M Univ, Dept Vet Integrat Biosci, College Stn, TX 77843 USA
关键词
Epilepsy; Ketogenic diet; Hypom yelination; Malate-aspartate shuttle; Ketone bodies; Mitochondrial disorders; Short chain fatty acids; Medium chain fatty acids; Monocarboxylic acid transporters; HYDROPEROXIDE GLUTATHIONE-PEROXIDASE; MITOCHONDRIAL UNCOUPLING PROTEIN; KETONE-BODIES; LACTIC-ACID; MONOCARBOXYLATE TRANSPORTER; NEUROTROPHIC FACTOR; GLUCOSE-UTILIZATION; ENERGY-METABOLISM; BRAIN METABOLISM; AMINO-ACIDS;
D O I
10.1007/s00726-016-2336-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Epilepsy is too complex to be considered as a disease; it is more of a syndrome, characterized by seizures, which can be caused by a diverse array of afflictions. As such, drug interventions that target a single biological pathway will only help the specific individuals where that drug's mechanism of action is relevant to their disorder. Most likely, this will not alleviate all forms of epilepsy nor the potential biological pathways causing the seizures, such as glucose/amino acid transport, mitochondrial dysfunction, or neuronal myelination. Considering our current inability to test every individual effectively for the true causes of their epilepsy and the alarming number of misdiagnoses observed, we propose the use of the ketogenic diet (KD) as an effective and efficient preliminary/long-term treatment. The KD mimics fasting by altering substrate metabolism from carbohydrates to fatty acids and ketone bodies (KBs). Here, we underscore the need to understand the underlying cellular mechanisms governing the KD's modulation of various forms of epilepsy and how a diverse array of metabolites including soluble fibers, specific fatty acids, and functional amino acids (e.g., leucine, d-serine, glycine, arginine metabolites, and N-acetyl-cysteine) may potentially enhance the KD's ability to treat and reverse, not mask, these neurological disorders that lead to epilepsy.
引用
收藏
页码:1 / 20
页数:20
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