Dietary Methionine Restriction in Mice Elicits an Adaptive Cardiovascular Response to Hyperhomocysteinemia

被引:55
作者
Ables, Gene P. [1 ]
Ouattara, Amadou [1 ]
Hampton, Thomas G. [2 ]
Cooke, Diana [1 ]
Perodin, Frantz [1 ]
Augie, Ines [1 ]
Orentreich, David S. [1 ]
机构
[1] Orentreich Fdn Adv Sci Inc, Cold Spring On Hudson, NY 10516 USA
[2] Mouse Specif Inc, Quincy, MA USA
关键词
LIFE-SPAN; INTRACELLULAR CALCIUM; HOMOCYSTEINE; DEFICIENT; ATHEROSCLEROSIS; SUPPLEMENTATION; ADIPONECTIN; DYSFUNCTION; EXPRESSION; PROTECTS;
D O I
10.1038/srep08886
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Dietary methionine restriction (MR) in rodents increased lifespan despite higher heart-to-body weight ratio (w/w) and hyperhomocysteinemia, which are symptoms associated with increased risk for cardiovascular disease. We investigated this paradoxical effect of MR on cardiac function using young, old, and apolipoprotein E-deficient (ApoE-KO) mice. Indeed, MR animals exhibited higher heart-to-body weight ratio (w/w) and hyperhomocysteinemia with a molecular pattern consistent with cardiac stress while maintaining the integrity of cardiac structure. Baseline cardiac function, which was measured by non-invasive electrocardiography (ECG), showed that young MR mice had prolonged QRS intervals compared with control-fed (CF) mice, whereas old and ApoE-KO mice showed similar results for both groups. Following beta-adrenergic challenge, responses of MR mice were either similar or attenuated compared with CF mice. Cardiac contractility, which was measured by isolated heart retrograde perfusion, was similar in both groups of old mice. Finally, the MR diet induced secretion of cardioprotective hormones, adiponectin and fibroblast growth factor 21 (FGF21), in MR mice with concomitant alterations in cardiac metabolic molecular signatures. Our findings demonstrate that MR diet does not alter cardiac function in mice despite the presence of hyperhomocysteinemia because of the adaptive responses of increased adiponectin and FGF21 levels.
引用
收藏
页数:10
相关论文
共 58 条
[31]   Homocysteine lowering and cardiovascular disease risk: Lost in translation [J].
Marcus, Jeremy ;
Sarnak, Mark J. ;
Menon, Vandana .
CANADIAN JOURNAL OF CARDIOLOGY, 2007, 23 (09) :707-710
[32]   Homocysteine-lowering interventions for preventing cardiovascular events [J].
Marti-Carvajal, Arturo J. ;
Sola, Ivan ;
Lathyris, Dimitrios ;
Karakitsiou, Despoina-Elvira ;
Simancas-Racines, Daniel .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2013, (01)
[33]  
MCCULLY KS, 1969, AM J PATHOL, V56, P111
[34]   Methionine-deficient diet extends mouse lifespan, slows immune and lens aging, alters glucose, T4, IGF-I and insulin levels, and increases hepatocyte MIF levels and stress resistance [J].
Miller, RA ;
Buehner, G ;
Chang, Y ;
Harper, JM ;
Sigler, R ;
Smith-Wheelock, M .
AGING CELL, 2005, 4 (03) :119-125
[35]   Homocyst(e)ine and coronary artery disease - Clinical evidence and genetic and metabolic background [J].
Moghadasian, MH ;
McManus, BM ;
Frohlich, JJ .
ARCHIVES OF INTERNAL MEDICINE, 1997, 157 (20) :2299-2308
[36]   PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes [J].
Mootha, VK ;
Lindgren, CM ;
Eriksson, KF ;
Subramanian, A ;
Sihag, S ;
Lehar, J ;
Puigserver, P ;
Carlsson, E ;
Ridderstråle, M ;
Laurila, E ;
Houstis, N ;
Daly, MJ ;
Patterson, N ;
Mesirov, JP ;
Golub, TR ;
Tamayo, P ;
Spiegelman, B ;
Lander, ES ;
Hirschhorn, JN ;
Altshuler, D ;
Groop, LC .
NATURE GENETICS, 2003, 34 (03) :267-273
[37]  
ORENTREICH N, 1993, J NUTR, V123, P269
[38]   Cardiac dysfunction caused by myocardium-specific expression of a mutant thyroid hormone receptor [J].
Pazos-Moura, C ;
Abel, ED ;
Boers, ME ;
Moura, E ;
Hampton, TG ;
Wang, JF ;
Morgan, JP ;
Wondisford, FE .
CIRCULATION RESEARCH, 2000, 86 (06) :700-706
[39]   Genomic and Metabolic Responses to Methionine-Restricted and Methionine-Restricted, Cysteine-Supplemented Diets in Fischer 344 Rat Inguinal Adipose Tissue, Liver and Quadriceps Muscle [J].
Perrone, Carmen E. ;
Mattocks, Dwight A. L. ;
Plummer, Jason D. ;
Chittur, Sridar V. ;
Mohney, Rob ;
Vignola, Katie ;
Orentreich, David S. ;
Orentreich, Norman .
JOURNAL OF NUTRIGENETICS AND NUTRIGENOMICS, 2012, 5 (03) :132-157
[40]   Fibroblast growth factor 21 protects against cardiac hypertrophy in mice [J].
Planavila, A. ;
Redondo, I. ;
Hondares, E. ;
Vinciguerra, M. ;
Munts, C. ;
Iglesias, R. ;
Gabrielli, L. A. ;
Sitges, M. ;
Giralt, M. ;
van Bilsen, M. ;
Villarroya, F. .
NATURE COMMUNICATIONS, 2013, 4