Cold acclimation induces physiological cardiac hypertrophy and increases assimilation of triacylglycerol metabolism through lipoprotein lipase

Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids

Volumn 1781, Issue 10, 2008, Pages 618-626

  Cheng, Y ^a   Hauton, D ^a  

^a UNIVERSITY OF BIRMINGHAM   (United Kingdom)

Author keywords

AMPK; Cardiac hypertrophy; Triacylglycerol; Very low density lipoprotein receptor

Indexed keywords

ADENOSINE PHOSPHATE; DOBUTAMINE; DOPAMINE; HEPARIN; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE KINASE; LIPID; LIPID EMULSION; LIPOPROTEIN LIPASE; OLEIC ACID; SARCOPLASMIC RETICULUM CALCIUM TRANSPORTING ADENOSINE TRIPHOSPHATASE; TRIACYLGLYCEROL; VERY LOW DENSITY LIPOPROTEIN; VERY LOW DENSITY LIPOPROTEIN RECEPTOR;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BLOOD PRESSURE; COLD ACCLIMATIZATION; CONTROL GROUP; CONTROLLED STUDY; DIASTOLIC BLOOD PRESSURE; ENERGY METABOLISM; ENZYME PHOSPHORYLATION; FATTY ACID OXIDATION; HEART LEFT VENTRICLE; HEART MUSCLE CONTRACTILITY; HEART PERFORMANCE; HEART PERFUSION; HEART RATE; HEART VENTRICLE ENDDIASTOLIC PRESSURE; HEART VENTRICLE HYPERTROPHY; HEART VENTRICLE OVERLOAD; HEART VENTRICLE PRESSURE; ISOLATED HEART; LIPID METABOLISM; LIPID STORAGE; MALE; MEAN ARTERIAL PRESSURE; NONHUMAN; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FOLDING; PROTEIN PHOSPHORYLATION; RAT; TEMPERATURE ACCLIMATIZATION; VASCULAR ENDOTHELIUM; WESTERN BLOTTING;

ACCLIMATIZATION; AMP-ACTIVATED PROTEIN KINASES; ANIMALS; BLOOD PRESSURE; BODY WEIGHT; CARDIOMEGALY; CARNITINE O-PALMITOYLTRANSFERASE; CHOLESTEROL ESTERS; COLD TEMPERATURE; DIGLYCERIDES; DOBUTAMINE; FAT EMULSIONS, INTRAVENOUS; HEART; LIPOPROTEIN LIPASE; MALE; MYOCARDIUM; OLEIC ACID; ORGAN SIZE; OXIDATION-REDUCTION; PERFUSION; RATS; RATS, WISTAR; RECEPTORS, LDL; SARCOPLASMIC RETICULUM CALCIUM-TRANSPORTING ATPASES; TRIGLYCERIDES;

RATTUS;

EID: 52049127012     PISSN: 13881981     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbalip.2008.07.006     Document Type: Article

References (60)

1. Lopaschuk G.D., Belke D.D., Gamble J., Itoi T., and Schonekess B.O. Regulation of fatty acid oxidation in the mammalian heart in health and disease. Biochim. Biophys. Acta 1213 (1994) 263-267
2. Hauton D., Bennett M.J., and Evans R.D. Utilisation of triacylglycerol and non-esterified fatty acid by the working rat heart: myocardial lipid substrate preference. Biochim. Biophys. Acta 1533 (2001) 99-109
3. Augustus A.S., Kako Y., Yagyu H., and Goldberg I.J. Routes of FA delivery to cardiac muscle: modulation of lipoprotein lipolysis alters uptake of TG-derived FA. Am. J. Physiol. 284 (2003) E331-E339
4. O'Brien K.D., Ferguson M., Gordon D., Deeb S.S., and Chait A. Lipoprotein lipase is produced by cardiac myocytes rather than interstitial cells in human myocardium. Arterioscler. Thromb. 14 (1994) 1445-1451
5. Sambandam N., Abrahani M.A., St Pierre E., Al-Atar O., Cam M.C., and Rodrigues B. Localisation of lipoprotein lipase in the diabetic heart: regulation by acute changes in insulin. Arterioscler. Thromb. Vasc. Biol. 19 (1999) 1526-1534
6. Goudriaan J.R., Espirito-Santo S.M., Voshol P.J., Teusink B., van Dijk K.W., van Vlijmen B.J., Romijn J.A., Havekes L.M., and Rensen P.C. The VLDL receptor plays a major role in chylomicron metabolism by enhancing LPL-mediated triglyceride hydrolysis. J. Lip. Res. 45 (2004) 1475-1481
7. Niu Y.G., Hauton D., and Evans R.D. Utilisation of triacylglycerol-rich lipoproteins by the working rat heart: routes of uptake and metabolic fates. J. Physiol. 558 (2004) 225-237
8. Obunike J.C., Lutz E.P., Li Z., Paka L., Katopodis T., Strickalnd D.K., Kozarsky K.F., Pillarisetti S., and Goldberg I.J. Transcytosis of lipoprotein lipase across cultured endothelial cells requires both heparan sulphate proteoglycans and the very low density lipoprotein receptor. J. Biol. Chem. 276 (2001) 8934-8941
9. Zenimaru Y., Takahashi S., Takahashi M., Yamada K., Iwasaki T., Hattori H., Imagawa M., Ueno M., Suzuki J., and Miyamori I. Glucose deprivation accelerates VLDL receptor-mediated TG-rich lipoprotein uptake by AMPK activation in skeletal muscle cells. Biochem. Biophys. Res. Comm. 368 (2008) 716-722
10. An D., Kewalramani G., Qi D., Pulinilkunnil T., Ghosh S., Abrahani A., Wambolt R., Allard M., Innis S.M., and Rodrigues B. B-agonist stimulation produces changes in cardiac AMPK and coronary lumen LPL only during increased workload. Am J. Physiol. 288 (2005) E246-E253
11. Kudo N., Gillespie J.G., Kung L., Witters L.A., Schulz R., Clanachan A.S., and Lopaschuk G.D. Characterisation of %'AMP-activated protein kinase activity in the heart and its role in inhibiting acetyl-CoA carboxylase during reperfusion following ischemia. Biochim. Biophys. Acta 1301 (1996) 67-75
12. Atkinson L.L., Kozak R., Kelly S.E., Onay-Besikci A., Russell J.C., and Lopaschuk G.D. Potential mechanisms and consequences of cardiac triacylglycerol accumulation in insulin-resistant rats. Am. J. Physiol. 284 (2003) E923-E930
13. Deveci D., and Egginton S. Differing mechanisms of cold-induced changes in capillary supply in m. tibialis anterior of rats and hamsters. J. Exp. Biol 205 (2002) 829-840
14. Hauton D., Richards S.B., and Egginton S. The role of the liver in lipid metabolism during cold acclimation in non-hibernator rodents. Comp. Physiol. Biochem. Part B 144 (2006) 372-381
15. Li G., Xiao Y., Estrella J.L., Ducsay C.A., Gilbert R.D., and Zhang L. Effect of fetal hypoxia on heart susceptibility to ischemia and reperfusion injury in adult rat. J. Soc. Gynecol. Invest. 10 (2003) 265-274
16. Xu Y., Williams S.J., O'Brien D., and Davidge S.T. Hypoxia or nutrient restriction during pregnancy in rats leads to progressive cardiac remodelling and impairs postischemic recovery in adult male offspring. FASEB J. 20 (2006) E536-E545
17. Nilsson-Ehle P., and Schotz M.C. A stable, radioactive substrate emulsion for assay of lipoprotein lipase. J. Lip. Res. 17 (1976) 536-541
18. Herpin P., Vincent A., Fillaut M., Bonito B.P., and Hocquette J.F. Mitochondrial and peroxisomal fatty acid oxidation capacities increase in the skeletal muscles of young pigs during early postnatal development but are not affected by cold stress. Reprod. Nutr. Dev. 93 (2003) 155-166
19. Eghbali M., Deva R., Alioua A., Minosyan T.Y., Ruan H., Wang Y., Toro L., and Stefani E. Molecular and functional signature of heart hypertrophy during pregnancy. Circ. Res. 96 (2005) 1208-1216
20. Naylor L.H., George K., O'Driscoll G., and Green D.J. The athlete's heart: a contemporary appraisal of the 'Morganroth hypothesis'. Sports Med. 38 (2008) 69-90
21. Roukoyatkina N.I., Shefer S.I., Rifkind J., Ajmani R., and Talan M.I. Cold acclimation-induced increase of systolic blood pressure in rats is associated with volume expansion. Am. J. Hypertens. 12 (1999) 54-62
22. Heroux O., and St Pierre J. Effect of cold acclimation on vascularisation of ears, heart, liver and muscles of white rats. Am. J. Physiology. 188 (1956) 163-168
23. Kayar S.R., and Banchero N. Volume overload hypertrophy elicited by cold and its effects on myocardial capillarity. Respir. Physiol. 59 (1985) 1-14
24. Konhilas J.P., Widegren U., Allen D.L., Paul A.C., Cleary A., and Leinwand L.A. Loaded wheel running and muscle adaptation in the mouse. Am. J. Physiol. 289 (2005) H455-H465
25. Lopez-Luna P., Olea J., and Herrera E. Effect of starvation on lipoprotein lipase activity in different tissues during gestation in the rat. Biochim. Biophys. Acta 1215 (1994) 275-279
26. Foster D.O., and Frydman M.L. Tissue distribution of cold-induced thermogenesis in conscious warm- or cold-acclimated rats reevaluated from changes in tissue blood flow: the dominant role of brown adipose tissue in the replacement of shivering by nonshivering thermogenesis. Can. J. Physiol. Pharmacol. 57 (1979) 257-270
27. Tan L.B., Benjamin I.J., and Clark W.A. Beta adrenergic desensitisation may serve a cardioprotective role. Cardiovasc. Res. 26 (1992) 608-614
28. Matthews J.M., Falckh P.H., Molenaar P., and Summers R.J. Chronic (-)-isoprenaline infusion down-regulates beta 1- and beta 2-adrenoceptors but does not transregulate muscarinic cholinoceptors in rat heart. Naunyn Schmiedebergs Arch. Pharmacol. 353 (1996) 213-225
29. Depocas F., and Behrens W.A. Levels of noradrenaline in plasma during thermogenesis induced by cold-exposure or by noradrenaline infusion in warm- and cold-acclimated rats. Experientia Suppl. 32 (1978) 135-146
30. Ishii K., Kuwahara M., Tsubone H., and Sugano S. The telemetric monitoring of heart rate, locomotor activity and body temperature in mice and voles (Microtus arvalis) during ambient temperature changes. Lab. Animal 30 (1996) 7-12
31. Chambers J.B., Williams T.D., Nakamura A., Henderson R.P., Overton J.M., and Rashotte M.E. Cardiovascular and metabolic responses to hypertensive and normotensive rats to one week of cold exposure. Am. J. Physiol. 279 (2000) 1486-1494
32. Begin-Heick N., and Heick H.M. Increased lipoprotein lipase activity of skeletal muscle in cold-acclimated rats. Can. J. Biochem. 55 (1977) 1241-1243
33. Bertin R., Goubern M., and Portet R. Effects of diets and cold acclimation on lipoprotein lipase activity and cyclic nucleotide levels in some tissues of rats. Experientia Suppl. 32 (1978) 185-190
34. Ong J.M., Simsolo R.B., Saghizadeh M., Goers J.W., and Kern P.A. Effects of exercise training and feeding on lipoprotein lipase gene expression in adipose tissue, heart, and skeletal muscle of the rat. Metabolism 44 (1995) 1596-1605
35. Lopez-Luna P., Olea J., and Herrera E. Effect of starvation on lipoprotein lipase activity in different tissues during gestation in the rat. Biochim. Biophys. Acta 1215 (1994) 275-279
36. Sato T., Liang K., and Vaziri N.D. Down-regulation of lipoprotein lipase and VLDL receptor in rats with focal glomerulosclerosis. Kid. Int. 67 (2002) 157-162
37. Jia L., Takahashi M., Morimoto H., Takahashi S., Izawa A., Ise H., Iwasaki T., Hattori H., Wu K.J., and Ikeda U. Changes in cardiac lipid metabolism during sepsis: the essential role of very-low-density lipoprotein receptors. Cardiovasc. Res. 69 (2006) 545-555
38. Bennett M.J., Hauton D., Hole D.G., and Evans R.D. Utilisation of very low density lipoprotein by the rat heart: the effect of endotoxin. Am. J. Physiol. 278 (2000) E802-E810
39. Qi D., Kuo K.H., Abrahani A., An D., Qi Y., Heung J., Kewalramani G., Pulinilkunnil T., Ghosh S., Innis S.M., and Rodrigues B. Acute intralipid infusion reduces cardiac luminal lipoprotein lipase but recruits additional enzyme from cardiomyocytes. Cardiovasc. Res. 72 (2006) 124-133
40. Gonzalez A.A., Kumar R., Mulligan J.D., Davis A.J., Weindruch R., and Saupe K.W. Metabolic adaptations to fasting and chronic caloric restriction in heart, muscle and liver do not include changes to AMPK activity. Am. J. Physiol. 287 (2004) E1032-E1037
41. Ruge T., Bergo M., Hultin M., Olivecrona G., and Olivecrona T. Nutritional regulation of binding sites for lipoprotein lipase. Am. J. Physiol 278 (2000) E211-E218
42. Allard M., Parsons H.L., Saeedi R., Wambolt R.B., and Brownsey R. AMPK and metabolic adaptation by the heart to pressure-overload. Am. J. Physiol. 292 (2007) 140-148
43. Liu G.Q., and Olivecrona T. Pulse-chase study on lipoprotein lipase in perfused guinea pig heart. Am. J. Physiol. 261 (1991) H2044-H2050
44. el Alaoui-Talibi Z., Landormy S., Loireau A., and Moravec J. Fatty acid oxidation and mechanical performance of volume-overloaded rat hearts. A. J. Physiol. 262 (1992) H1068-H1074
45. Saeedi R., Parsons H.L., Wambolt R.B., Paulson K., Sharma V., Dyck J.R.B., Brownsey R.W., and Allard M.F. Metabolic actions of metformin in the heart can occur by AMPK-independent mechanisms. Am. J. Physiol. (2008) 10.1152/ajpheart.00873.2007
46. de Jong H., Neal A.C., Coleman R.A., and Lewin T.A. Ontogeny of mRNA expression and activity of long-chain acyl-CoA synthetase (ASCL) isoforms in Mus muscles heart. Biochim. Biophys. Acta 1771 (2007) 75-82
47. Hammond L.E., Gallagher P.A., Wang S., Hiller S., Kluckman K.D., Posey-Marcos E.L., Maeda N., and Coleman R.A. Mitochondrial glycerol-3-phosphate acyltransferase-deficient mice have reduced weight and liver triacylglycerol content and altered glycerolipid fatty acid composition. Mol. Cell. Biol. 22 (2002) 8204-8214
48. Darnley A.C., Carpenter C.A., and Saggerson E.D. Changes in activities of some enzymes of glycerolipid synthesis in brown adipose tissue of cold-acclimated rats. Biochem. J. 253 (1988) 351-355
49. Listenberger L.L., Han X., Lewis S.E., Cases S., Farese Jr. R.V., Ory D.S., and Schaffer J.E. Triglyceride accumulation protects against fatty acid-induced lipotoxicity. Proc. Natl. Acad. Sci. USA 100 (2003) 3077-3082
50. Saddik M., and Lopaschuk G.D. Myocardial triglyceride turnover and contribution to energy utilisation in isolated working rat hearts. J. Biol. Chem. 266 (1991) 8162-8170
51. Oliveira H.C., Hirata M.H., Redgrave T.G., and Maranhao R.C. Competition between chylomicrons and their remnants for plasma removal: a study with artificial emulsions models of chylomicrons. Biochim. Biophys. Acta 958 (1998) 211-217
52. Hirata H.M., Oliveira H.C., Quintao E.C., Redgrave T.G., and Maranhao R.C. The effects of Triton WR-1339, protamine sulphate and heparin on the plasma removal of emulsion models of chylomicrons and remnants in rats. Biochim. Biophys. Acta 917 (1987) 344-346
53. Martins I.J., Mortimer B.C., Miller J., and Redgrave T.G. Effects of particle size and number on the plasma clearance of chylomicrons and remnants. J. Lipid Res. 37 (1996) 2696-2705
54. Pillutla P., Hwang Y.C., Augustus A., Yokoyama M., Yagyu H., Johnston T.P., Kaneko M., Ramasamy R., and Goldberg I.J. Perfusion of hearts with triglyceride-rich particles reproduces the metabolic abnormalities in lipotoxic cardiomyopathy. Am. J. Physiol. 288 (2005) E1229-E1235
55. Yamakawa H., Imamura T., Matsuo T., Onitsuka H., Tsumori Y., Kato J., Kitamura K., Koiwaya Y., and Eto T. Diastolic wall stress and ANGII in cardiac hypertrophy and gene expression induced by volume overload. Am. J. Physiol. 279 (2000) H2939-H2946
56. Doolittle M.H., Ben-Zeev O., Elovson J., Martin D., and Kirchgessner T.G. The response of lipoprotein lipase to feeding and fasting. Evidence for posttranslational regulation. J. Biol. Chem. 265 (1990) 4570-4577
57. Yu X., Bugess S.C., Ge H., Wong K.K., Nassem R.H., Garry D.J., Sherry A.D., Mallory C.R., Berger J.P., and Li C. Inhibition of cardiac lipoprotein utilisation by transgenic overexpression of Angptl4 in the heart. Proc. Nat. Acad. Sci. 102 (2005) 1767-1772
58. Sukonina V., Lookene A., Olivecrona T., and Olivecrona G. Angiopoietin-like protein 4 converts lipoprotein lipase to inactive monomers and modulates lipase activity in adipose tissue. Proc. Nat. Acad. Sci. 103 (2006) 17450-17455
59. G. Wu, L. Zhang, J. Gupta, G. Olivecrona, T. Olivecrona. A transcription-dependent mechanism, akin to that in adipose tissue, modulates lipoprotein lipase activity in rat heart. Am. J. Physiol. 293 (207) E908-E925.
60. Sharma S., Adrogue J.V., Golfman L., Uray I., Lemm J., Youker K., Noon G.P., Frazier O.H., and Taegtmeyer H. Intramyocardial lipid accumulation in the failing human heart resembles the lipotoxic rat heart. FASEB J. 18 (2004) 1692-1700