Metabolic crosstalk between choline/1-carbon metabolism and energy homeostasis

被引:93
作者
Zeisel, Steven H. [1 ]
机构
[1] Univ N Carolina Chapel Hill, Inst Nutr Res, Kannapolis, NC USA
基金
美国国家卫生研究院;
关键词
betaine; choline; insulin sensitivity; obesity; phosphatidylcholine; PHOSPHATIDYLETHANOLAMINE N-METHYLTRANSFERASE; HOMOCYSTEINE S-METHYLTRANSFERASE; NONALCOHOLIC FATTY LIVER; CHOLINE-DEFICIENT DIET; NEURAL-TUBE DEFECTS; INSULIN-RESISTANCE; PPAR-ALPHA; DNA METHYLATION; BETAINE SUPPLEMENTATION; CARCASS CHARACTERISTICS;
D O I
10.1515/cclm-2012-0518
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
There are multiple identified mechanisms involved in energy metabolism, insulin resistance and adiposity, but there are here-to-fore unsuspected metabolic factors that also influence these processes. Studies in animal models suggest important links between choline/1-carbon metabolism and energy homeostasis. Rodents fed choline deficient diets become hypermetabolic. Mice with deletions in one of several different genes of choline metabolism have phenotypes that include increased metabolic rate, decreased body fat/lean mass ratio, increased insulin sensitivity, decreased ATP production by mitochondria, or decreased weight gain on a high fat diet. In addition, farmers have recognized that the addition of a metabolite of choline (betaine) to cattle and swine feed reduces body fat/lean mass ratio. Choline dietary intake in humans varies over a >three-fold range, and genetic variation exists that modifies individual requirements for this nutrient. Although there are some epidemiologic studies in humans suggesting a link between choline/1-carbon metabolism and energy metabolism, there have been no controlled studies in humans that were specifically designed to examine this relationship.
引用
收藏
页码:467 / 475
页数:9
相关论文
共 91 条
[1]   Folate intake and the MTHFR C677T genotype influence choline status in young Mexican American women [J].
Abratte, Christian M. ;
Wang, Wei ;
Li, Rui ;
Moriarty, David J. ;
Caudilla, Marie A. .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2008, 19 (03) :158-165
[2]   The metabolic syndrome - a new worldwide definition [J].
Alberti, KGMM ;
Zimmet, P ;
Shaw, J .
LANCET, 2005, 366 (9491) :1059-1062
[3]   A RAT-BRAIN CYTOSOLIC N-METHYLTRANSFERASE(S) ACTIVITY CONVERTING PHOSPHORYLETHANOLAMINE INTO PHOSPHORYLCHOLINE [J].
ANDRIAMAMPANDRY, C ;
MASSARELLI, R ;
FREYSZ, L ;
KANFER, JN .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 171 (02) :758-763
[4]  
[Anonymous], 1998, Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline, P390
[5]   Usual choline and betaine dietary intake and incident coronary heart disease: The Atherosclerosis Risk in Communities (ARIC) Study [J].
Bidulescu A. ;
Chambless L.E. ;
Siega-Riz A.M. ;
Zeisel S.H. ;
Heiss G. .
BMC Cardiovascular Disorders, 7 (1)
[6]   Repeatability and measurement error in the assessment of choline and betaine dietary intake: the Atherosclerosis Risk in Communities (ARIC) Study [J].
Bidulescu, Aurelian ;
Chambless, Lloyd E. ;
Siega-Riz, Anna Maria ;
Zeisel, Steven H. ;
Heiss, Gerardo .
NUTRITION JOURNAL, 2009, 8
[7]   A High-Fat Diet Elicits Differential Responses in Genes Coordinating Oxidative Metabolism in Skeletal Muscle of Lean and Obese Individuals [J].
Boyle, K. E. ;
Canham, J. P. ;
Consitt, L. A. ;
Zheng, D. ;
Koves, T. R. ;
Gavin, T. P. ;
Holbert, D. ;
Neufer, P. D. ;
Ilkayeva, O. ;
Muoio, D. M. ;
Houmard, J. A. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2011, 96 (03) :775-781
[8]   Molecular mediators of hepatic steatosis and liver injury [J].
Browning, JD ;
Horton, JD .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (02) :147-152
[9]   Choline deficiency causes reversible hepatic abnormalities in patients receiving parenteral nutrition: Proof of a human choline requirement: A placebo-controlled trial [J].
Buchman, AL ;
Ament, ME ;
Sohel, M ;
Dubin, M ;
Jenden, DJ ;
Roch, M ;
Pownall, H ;
Farley, W ;
Awal, M ;
Ahn, C .
JOURNAL OF PARENTERAL AND ENTERAL NUTRITION, 2001, 25 (05) :260-268
[10]   Identification of a Physiologically Relevant Endogenous Ligand for PPARα in Liver [J].
Chakravarthy, Manu V. ;
Lodhi, Irfan J. ;
Yin, Li ;
Malapaka, Raghu R. V. ;
Xu, H. Eric ;
Turk, John ;
Semenkovich, Clay F. .
CELL, 2009, 138 (03) :476-488