Beneficial effects of combinatorial micronutrition on body fat and atherosclerosis in mice

被引:4
作者
El Kochairi, Ilhem [1 ]
Montagner, Alexandra [1 ,2 ]
Rando, Gianpaolo [1 ]
Lohmann, Christine [3 ,4 ,5 ]
Matter, Christian M. [3 ,4 ,5 ]
Wahli, Walter [1 ]
机构
[1] Univ Lausanne, Ctr Integrat Genom, Natl Res Ctr Frontiers Genet, CH-1015 Lausanne, Switzerland
[2] INRA ToxAlim Integrat Toxicol & Metab, F-31027 Toulouse, France
[3] Univ Zurich, Inst Physiol, Zurich, Switzerland
[4] Univ Zurich Hosp, Ctr Cardiovasc, CH-8091 Zurich, Switzerland
[5] Univ Zurich, Zurich Ctr Integrat Human Physiol ZIHP, CH-8057 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
Atherosclerosis; Lipids; PPAR alpha; Nutrition; Prevention; CARDIOVASCULAR-DISEASE; ADIPOSE-TISSUE; ACID OXIDATION; PPAR-ALPHA; LEAN RATS; METABOLISM; INFLAMMATION; EXPRESSION; OBESITY; INDIVIDUALS;
D O I
10.1093/cvr/cvr146
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims More than two billion people worldwide are deficient in key micronutrients. Single micronutrients have been used at high doses to prevent and treat dietary insufficiencies. Yet the impact of combinations of micronutrients in small doses aiming to improve lipid disorders and the corresponding metabolic pathways remains incompletely understood. Thus, we investigated whether a combination of micronutrients would reduce fat accumulation and atherosclerosis in mice. Methods and results Lipoprotein receptor-null mice fed with an original combination of micronutrients incorporated into the daily chow showed reduced weight gain, body fat, plasma triglycerides, and increased oxygen consumption. These effects were achieved through enhanced lipid utilization and reduced lipid accumulation in metabolic organs and were mediated, in part, by the nuclear receptor PPAR alpha. Moreover, the micronutrients partially prevented atherogenesis when administered early in life to apolipoprotein E-null mice. When the micronutrient treatment was started before conception, the anti-atherosclerotic effect was stronger in the progeny. This finding correlated with decreased post-prandial tri-glyceridaemia and vascular inflammation, two major atherogenic factors. Conclusion Our data indicate beneficial effects of a combination of micronutritients on body weight gain, hypertriglyceridaemia, liver steatosis, and atherosclerosis in mice, and thus our findings suggest a novel cost-effective combinatorial micro-nutrient-based strategy worthy of being tested in humans.
引用
收藏
页码:732 / 741
页数:10
相关论文
共 38 条
[1]   The relationships between post-prandial lipaemia, endothelial function and oxidative stress in healthy individuals and patients with type 2 diabetes [J].
Anderson, RA ;
Evans, ML ;
Ellis, GR ;
Graham, J ;
Morris, K ;
Jackson, SK ;
Lewis, MJ ;
Rees, A ;
Frenneaux, MP .
ATHEROSCLEROSIS, 2001, 154 (02) :475-483
[2]   FETAL NUTRITION AND CARDIOVASCULAR-DISEASE IN ADULT LIFE [J].
BARKER, DJP ;
GLUCKMAN, PD ;
GODFREY, KM ;
HARDING, JE ;
OWENS, JA ;
ROBINSON, JS .
LANCET, 1993, 341 (8850) :938-941
[3]   Adipose tissue, inflammation, and cardiovascular disease [J].
Berg, AH ;
Scherer, PE .
CIRCULATION RESEARCH, 2005, 96 (09) :939-949
[4]   TRAFFICKING OF DIETARY-FAT IN LEAN RATS [J].
BESSESEN, DH ;
RUPP, CL ;
ECKEL, RH .
OBESITY RESEARCH, 1995, 3 (02) :191-203
[5]   Trafficking of dietary oleic, linolenic, and stearic acids in fasted or fed lean rats [J].
Bessesen, DH ;
Vensor, SH ;
Jackman, MR .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2000, 278 (06) :E1124-E1132
[6]  
BOURGEOISLUGAND MFY, 2009, Patent No. 2009050580
[7]   Paternally Induced Transgenerational Environmental Reprogramming of Metabolic Gene Expression in Mammals [J].
Carone, Benjamin R. ;
Fauquier, Lucas ;
Habib, Naomi ;
Shea, Jeremy M. ;
Hart, Caroline E. ;
Li, Ruowang ;
Bock, Christoph ;
Li, Chengjian ;
Gu, Hongcang ;
Zamore, Phillip D. ;
Meissner, Alexander ;
Weng, Zhiping ;
Hofmann, Hans A. ;
Friedman, Nir ;
Rando, Oliver J. .
CELL, 2010, 143 (07) :1084-1096
[8]   Fat oxidation during whole body exercise appears to be a good example of regulation by the interaction of physiological systems [J].
Coyle, Edward F. .
JOURNAL OF PHYSIOLOGY-LONDON, 2007, 581 (03) :886-886
[9]   Endothelin-1 and atherosclerosis: potential complications associated with endothelin-receptor blockade [J].
Dashwood, MR ;
Tsui, JCS .
ATHEROSCLEROSIS, 2002, 160 (02) :297-304
[10]   PPARα and dyslipidemia [J].
Duval, Caroline ;
Muller, Michael ;
Kersten, Sander .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2007, 1771 (08) :961-971