Ketogenic diet versus ketoacidosis: what determines the influence of ketone bodies on neurons?

被引:42
作者
Fedorovich, Sergei V. [1 ]
Voronina, Polina P. [1 ]
Waseem, Tatyana V. [2 ]
机构
[1] Inst Biophys & Cell Engn, Minsk, BELARUS
[2] Univ Oxford, Dept Pharmacol, Oxford, England
关键词
beta-hydroxybutirate; epilepsy; diabetes mellitus; alcoholism; metabolism; hydroxyl-carboxylic acid receptor; epigenetics; acidosis; BETA-HYDROXYBUTYRATE; MITOCHONDRIA; METABOLITES;
D O I
10.4103/1673-5374.241442
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Glucose is the main energy substrate for neurons, however, at certain conditions, e.g. in starvation, these cells could also use ketone bodies. This approach is used in clinical conditions as the ketogenic diet. The ketogenic diet is actually a biochemical model of fasting. It includes replacing carbohydrates by fats in daily meal. Synthesis of ketone bodies beta-hydroxubutirate, acetoacetate and acetone begins once glycogen stores have depleted in the liver. The ketogenic diet can be used to treat clinical conditions, primarily epilepsy. The mechanism of neuroprotective action of ketogenic diet is not very clear. It is shown that ketone bodies influence neurons at three different levels, namely, metabolic, signaling and epigenetic levels. Ketone bodies are not always neuroprotective. Sometimes they can be toxic for the brain. Ketoacidosis which is a very dangerous complication of diabetes mellitus or alcoholism can be taken as an example. The exact mechanism of how neuroprotective properties of ketone bodies reverse to neurotoxic is yet to be established.
引用
收藏
页码:2060 / 2063
页数:4
相关论文
共 24 条
[1]   β-Hydroxybutyrate in the Brain: One Molecule, Multiple Mechanisms [J].
Achanta, Lavanya B. ;
Rae, Caroline D. .
NEUROCHEMICAL RESEARCH, 2017, 42 (01) :35-49
[2]   PLASMA ACID-BASE PATTERNS IN DIABETIC-KETOACIDOSIS [J].
ADROGUE, HJ ;
WILSON, H ;
BOYD, AE ;
SUKI, WN ;
EKNOYAN, G .
NEW ENGLAND JOURNAL OF MEDICINE, 1982, 307 (26) :1603-1610
[3]   G protein-coupled receptors for energy metabolites as new therapeutic targets [J].
Blad, Clara C. ;
Tang, Cong ;
Offermanns, Stefan .
NATURE REVIEWS DRUG DISCOVERY, 2012, 11 (08) :603-619
[4]   Metabolic regulation of synaptic activity [J].
Fedorovich, Sergei, V ;
Waseem, Tatyana, V .
REVIEWS IN THE NEUROSCIENCES, 2018, 29 (08) :825-835
[5]   Ketogenic diets, mitochondria, and neurological diseases [J].
Gano, Lindsey B. ;
Patel, Manisha ;
Rho, Jong M. .
JOURNAL OF LIPID RESEARCH, 2014, 55 (11) :2211-2228
[6]   The anticonvulsant activity of acetone, the major ketone body in the ketogenic diet, is not dependent on its metabolites acetol, 1,2-propanediol, methylglyoxal, or pyruvic acid [J].
Gasior, Maciej ;
French, Amy ;
Joy, Michelle T. ;
Tang, Rebecca S. ;
Hartman, Adam L. ;
Rogawski, Michael A. .
EPILEPSIA, 2007, 48 (04) :793-800
[7]   Bioenergetic regulation of microglia [J].
Ghosh, Soumitra ;
Castillo, Erika ;
Frias, Elma S. ;
Swanson, Raymond A. .
GLIA, 2018, 66 (06) :1200-1212
[8]   Energy substrate availability as a determinant of neuronal resting potential, GABA signaling and spontaneous network activity in the neonatal cortex in vitro [J].
Holmgren, Carl D. ;
Mukhtarov, Marat ;
Malkov, Anton E. ;
Popova, Irina Y. ;
Bregestovski, Piotr ;
Zilberter, Yuri .
JOURNAL OF NEUROCHEMISTRY, 2010, 112 (04) :900-912
[9]   β-Hydroxybutyrate supports synaptic vesicle cycling but reduces endocytosis and exocytosis in rat brain synaptosomes [J].
Hrynevich, Sviatlana V. ;
Waseem, Tatyana V. ;
Hebert, Audrey ;
Pellerin, Luc ;
Fedorovich, Sergei V. .
NEUROCHEMISTRY INTERNATIONAL, 2016, 93 :73-81
[10]   β-hydroxybutyrate fuels synaptic function during development -: Histological and physiological evidence in rat hippocampal slices [J].
Izumi, Y ;
Ishii, K ;
Katsuki, H ;
Benz, AM ;
Zorumski, CF .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (05) :1121-1132