Triheptanoin-A medium chain triglyceride with odd chain fatty acids: A new anaplerotic anticonvulsant treatment?

被引:50
作者
Borges, Karin [1 ]
Sonnewald, Ursula [2 ]
机构
[1] Univ Queensland, Sch Biomed Sci, Dept Pharmacol, St Lucia, Qld, Australia
[2] Norwegian Univ Sci & Technol, NTNU, Dept Neurosci, N-7034 Trondheim, Norway
关键词
Diet; Anaplerosis; Energy metabolism; Epilepsy; KETOGENIC DIET; PYRUVATE-CARBOXYLASE; ENTERAL METABOLISM; PROPIONIC ACIDEMIA; PRIMARY CULTURES; PARTIAL EPILEPSY; SEIZURE MODELS; RATS; THERAPY; PILOCARPINE;
D O I
10.1016/j.eplepsyres.2011.05.023
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
The triglyceride of heptanoate (C7 fatty acid), triheptanoin, is a tasteless oil used to treat rare metabolic disorders in USA and France. Heptanoate is metabolized by beta-oxidation to provide propionyl-CoA, which after carboxylation can produce succinyl-CoA, resulting in anaplerosis - the refilling of the tricarboxylic acid cycle. Heptanoate is also metabolized by the liver to the C5 ketones, beta-ketopentanoate and/or beta-hydroxypentanoate, which are released into the blood and thought to enter the brain via monocarboxylate transporters. Oral triheptanoin has recently been discovered to be reproducibly anticonvulsant in acute and chronic mouse seizures models. However, current knowledge on alterations of brain metabolism after triheptanoin administration and anaplerosis via propionyl-CoA carboxylation in the brain is limited. This review outlines triheptanoin's unique anticonvulsant profile and its clinical potential for the treatment of medically refractory epilepsy. Anaplerosis as a therapeutic approach for the treatment of epilepsy is discussed. More research is needed to elucidate the anticonvulsant mechanism of triheptanoin and to reveal its clinical potential for the treatment of epilepsy and other disorders of the brain. (c) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:239 / 244
页数:6
相关论文
共 56 条
[1]
Limbic structures show altered glial-neuronal metabolism in the chronic phase of kainate induced epilepsy [J].
Alvestad, Silje ;
Hammer, Janniche ;
Eyjolfsson, Elvar ;
Qu, Hong ;
Ottersen, Ole Petter ;
Sonnewald, Ursula .
NEUROCHEMICAL RESEARCH, 2008, 33 (02) :257-266
[2]
Metabolic fate of isoleucine in a rat model of hepatic encephalopathy and in cultured neural cells exposed to ammonia [J].
Bak, Lasse K. ;
Iversen, Peter ;
Sorensen, Michael ;
Keiding, Susanne ;
Vilstrup, Hendrik ;
Ott, Peter ;
Waagepetersen, Helle S. ;
Schousboe, Arne .
METABOLIC BRAIN DISEASE, 2009, 24 (01) :135-145
[3]
EVIDENCE FOR CATABOLIC PATHWAY OF PROPIONATE METABOLISM IN CNS: EXPRESSION PATTERN OF METHYLMALONYL-CoA MUTASE AND PROPIONYL-CoA CARBOXYLASE ALPHA-SUBUNIT IN DEVELOPING AND ADULT RAT BRAIN [J].
Ballhausen, D. ;
Mittaz, L. ;
Boulat, O. ;
Bonafe, L. ;
Braissant, O. .
NEUROSCIENCE, 2009, 164 (02) :578-587
[4]
Pharmacological characterization of the 6 Hz psychomotor seizure model of partial epilepsy [J].
Barton, ME ;
Klein, BD ;
Wolf, HH ;
White, HS .
EPILEPSY RESEARCH, 2001, 47 (03) :217-227
[5]
Assessment of seizure susceptibility in pilocarpine epileptic and nonepileptic Wistar rats and of seizure reinduction with pentylenetetrazole and electroshock models [J].
Blanco, Miriam Marcela ;
dos Santos, Jair Guilherme, Jr. ;
Perez-Mendes, Patricia ;
Kohek, Silvia R. B. ;
Cavarsan, Clarissa Fantin ;
Hummel, Michele ;
Albuquerque, Cristovao ;
Mello, Luiz E. .
EPILEPSIA, 2009, 50 (04) :824-831
[6]
Mouse models: The ketogenic diet and polyunsaturated fatty acids [J].
Borges, Karin .
EPILEPSIA, 2008, 49 :64-66
[7]
Mitochondrial biogenesis in the anticonvulsant mechanism of the ketogenic diet [J].
Bough, Kristopher J. ;
Wetherington, Jonathon ;
Hassel, Bjornar ;
Pare, Jean Francois ;
Gawryluk, Jeremy W. ;
Greene, James G. ;
Shaw, Renee ;
Smith, Yoland ;
Geiger, Jonathan D. ;
Dingledine, Raymond J. .
ANNALS OF NEUROLOGY, 2006, 60 (02) :223-235
[8]
Effects of the novel antiepileptic drug lacosamide on the development of amygdala kindling in rats [J].
Brandt, Claudia ;
Heile, Anna ;
Potschka, Heidrun ;
Stoehr, Thomas ;
Loescher, Wolfgang .
EPILEPSIA, 2006, 47 (11) :1803-1809
[9]
Anaplerotic molecules: Current and future [J].
Brunengraber, Henri ;
Roe, Charles R. .
JOURNAL OF INHERITED METABOLIC DISEASE, 2006, 29 (2-3) :327-331
[10]
CESAR M, 1995, J NEUROCHEM, V64, P2312