Metabolomic and Lipidomic Analysis of the Heart of Peroxisome Proliferator-Activated Receptor-gamma Coactivator 1-beta Knock Out Mice on a High Fat Diet

被引:8
作者
McCombie, Gregor [1 ]
Medina-Gomez, Gema [2 ]
Lelliott, Christopher J. [3 ]
Vidal-Puig, Antonio [2 ]
Griffin, Julian L. [1 ,4 ]
机构
[1] Univ Cambridge, Dept Biochem, 80 Tennis Court Rd, Cambridge CB2 1GA, England
[2] Univ Cambridge, Addenbrookes Hosp, Inst Metab Sci, Metab Res Labs, Cambridge CB2 0QQ, England
[3] AstraZeneca R&D, CV GI iMED, Dept Biosci, S-43183 Molndal, Sweden
[4] Med Res Council Human Nutr Res, Elsie Widdowson Lab, Cambridge CB1 9NL, England
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会; 英国惠康基金;
关键词
metabolic syndrome; obesity; peroxisome proliferator activated receptors; peroxisome proliferator-activated receptor-gamma coactivator 1-beta; functional genomics;
D O I
10.3390/metabo2020366
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The peroxisome proliferator-activated receptor-gamma coactivators (PGC-1) are transcriptional coactivators with an important role in mitochondrial biogenesis and regulation of genes involved in the electron transport chain and oxidative phosphorylation in oxidative tissues including cardiac tissue. These coactivators are thought to play a key role in the development of obesity, type 2 diabetes and the metabolic syndrome. In this study we have used a combined metabolomic and lipidomic analysis of cardiac tissue from the PGC-1 beta null mouse to examine the effects of a high fat diet on this organ. Multivariate statistics readily separated tissue from PGC-1 beta null mice from their wild type controls either in gender specific models or in combined datasets. This was associated with an increase in creatine and a decrease in taurine in the null mouse, and an increase in myristic acid and a reduction in long chain polyunsaturated fatty acids for both genders. The most profound changes were detected by liquid chromatography mass spectrometry analysis of intact lipids with the tissue from the null mouse having a profound increase in a number of triglycerides. The metabolomic and lipodomic changes indicate PGC-1 beta has a profound influence on cardiac metabolism.
引用
收藏
页码:366 / 381
页数:16
相关论文
共 34 条
[1]   Altered metabolism causes cardiac dysfunction in perfused hearts from diabetic (db/db) mice [J].
Belke, DD ;
Larsen, TS ;
Gibbs, EM ;
Severson, DL .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2000, 279 (05) :E1104-E1113
[2]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[3]   Reduced cardiac efficiency and altered substrate metabolism precedes the onset of hyperglycemia and contractile dysfunction in two mouse models of insulin resistance and obesity [J].
Buchanan, J ;
Mazumder, PK ;
Hu, P ;
Chakrabarti, G ;
Roberts, MW ;
Yun, UJ ;
Cooksey, RC ;
Litwin, SE ;
Abel, ED .
ENDOCRINOLOGY, 2005, 146 (12) :5341-5349
[4]   Peroxisome proliferator activator receptor γ coactivator-1 expression is reduced in obesity -: Potential pathogenic role of saturated fatty acids and p38 mitogen-activated protein kinase activation [J].
Crunkhorn, Sarah ;
Dearie, Farrell ;
Mantzoros, Christos ;
Gami, Hiral ;
da Silva, Wagner S. ;
Espinoza, Daniel ;
Faucette, Ryan ;
Barry, Kristen ;
Bianco, Antonio C. ;
Patti, Mary Elizabeth .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (21) :15439-15450
[5]   Altered expression of nuclear hormone receptors and coactivators in mouse heart during the acute-phase response [J].
Feingold, K ;
Kim, MS ;
Shigenaga, J ;
Moser, A ;
Grunfeld, C .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2004, 286 (02) :E201-E207
[6]   Design of experiments:: an efficient strategy to identify factors influencing extraction and derivatization of Arabidopsis thaliana samples in metabolomic studies with gas chromatography/mass spectrometry [J].
Gullberg, J ;
Jonsson, P ;
Nordström, A ;
Sjöström, M ;
Moritz, T .
ANALYTICAL BIOCHEMISTRY, 2004, 331 (02) :283-295
[7]   Deletion of the metabolic transcriptional coactivator PGC1β induces cardiac arrhythmia [J].
Gurung, Iman S. ;
Medina-Gomez, Gema ;
Kis, Adrienn ;
Baker, Michael ;
Velagapudi, Vidya ;
Neogi, Sudeshna Guha ;
Campbell, Mark ;
Rodriguez-Cuenca, Sergio ;
Lelliott, Christopher ;
McFarlane, Ian ;
Oresic, Matej ;
Grace, Andrew A. ;
Vidal-Puig, Antonio ;
Huang, Christopher L. -H. .
CARDIOVASCULAR RESEARCH, 2011, 92 (01) :29-38
[8]   Inhibition of ceramide synthesis ameliorates glucocorticoid-, saturated-fat-, and obesity-induced insulin resistance [J].
Holland, William L. ;
Brozinick, Joseph T. ;
Wang, Li-Ping ;
Hawkins, Eric D. ;
Sargent, Katherine M. ;
Liu, Yanqi ;
Narra, Krishna ;
Hoehn, Kyle L. ;
Knotts, Trina A. ;
Siesky, Angela ;
Nelson, Don H. ;
Karathanasis, Sotirios K. ;
Fontenot, Greg K. ;
Birnbaum, Morris J. ;
Summers, Scott A. .
CELL METABOLISM, 2007, 5 (03) :167-179
[9]   Estrogen-related receptor α directs peroxisome proliferator-activated receptor at signaling in the transcriptional control of energy metabolism in cardiac and skeletal muscle [J].
Huss, JM ;
Torra, IP ;
Staels, B ;
Giguère, V ;
Kelly, DP .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (20) :9079-9091
[10]   Peroxisome proliferator-activated receptor coactivator-1α (PGC-1α) coactivates the cardiac-enriched nuclear receptors estrogen-related receptor-α and -γ -: Identification of novel leucine-rich interaction motif within PGC-1α [J].
Huss, JM ;
Kopp, RP ;
Kelly, DP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (43) :40265-40274