Cardiac and skeletal muscle fatty acid transport and transporters and triacylglycerol and fatty acid oxidation in lean and Zucker diabetic fatty rats

被引:46
|
作者
Bonen, Arend [1 ]
Holloway, Graham P. [1 ]
Tandon, Narendra N. [2 ]
Han, Xiao-Xia [1 ]
McFarlan, Jay [1 ]
Glatz, Jan F. C. [3 ]
Luiken, Joost J. F. P. [3 ]
机构
[1] Univ Guelph, Dept Human Hlth & Nutr Sci, Guelph, ON N1G 2W1, Canada
[2] Otsuka Maryland Med Labs, Thrombosis Res Lab, Rockville, MD USA
[3] Maastricht Univ, Dept Mol Genet, Maastricht, Netherlands
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
plasma membrane-associated fatty acid-binding protein; FAT/CD36; GLUT4; mitochondria; giant vesicles; MITOCHONDRIAL ASPARTATE-AMINOTRANSFERASE; INSULIN-RESISTANCE; FAT/CD36; CONTENT; CELLULAR REDISTRIBUTION; PALMITATE OXIDATION; MEMBRANE-TRANSPORT; LIPID-ACCUMULATION; BINDING PROTEIN; ZDF DRT; OBESE;
D O I
10.1152/ajpregu.90820.2008
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Bonen A, Holloway GP, Tandon NN, Han X, McFarlan J, Glatz JF, Luiken JJ. Cardiac and skeletal muscle fatty acid transport and transporters and triacylglycerol and fatty acid oxidation in lean and Zucker diabetic fatty rats. Am J Physiol Regul Integr Comp Physiol 297: R1202-R1212, 2009. First published August 12, 2009; doi:10.1152/ajpregu.90820.2008.-We examined fatty acid transporters, transport, and metabolism in hearts and red and white muscles of lean and insulin-resistant (week 6) and type 2 diabetic (week 24) Zucker diabetic fatty (ZDF) rats. Cardiac fatty acid transport was similar in lean and ZDF hearts at week 6 but was reduced at week 24 (-40%) in lean but not ZDF hearts. Red muscle of ZDF rats exhibited an early susceptibility to upregulation (+66%) of fatty acid transport at week 6 that was increased by 50% in lean and ZDF rats at week 24 but remained 44% greater in red muscle of ZDF rats. In white muscle, no differences were observed in fatty acid transport between groups or from week 6 to week 24. In all tissues (heart and red and white muscle), FAT/CD36 protein and plasmalemmal content paralleled the changes in fatty acid transport. Triacylglycerol content in red and white muscles, but not heart, in lean and ZDF rats correlated with fatty acid transport (r = 0.91) and sarcolemmal FAT/CD36 (r = 0.98). Red and white muscle fatty acid oxidation by isolated mitochondria was not impaired in ZDF rats but was reduced by 18-24% in red muscle of lean rats at week 24. Thus, in red, but not white, muscle of insulin-resistant and type 2 diabetic animals, a marked upregulation in fatty acid transport and intramuscular triacylglycerol was associated with increased levels of FAT/CD36 expression and plasmalemmal content. In heart, greater rates of fatty acid transport and FAT/CD36 in ZDF rats (week 24) were attributable to the inhibition of age-related reductions in these parameters. However, intramuscular triacylglycerol did not accumulate in hearts of ZDF rats. Thus insulin resistance and type 2 diabetes are accompanied by tissue-specific differences in FAT/CD36 and fatty acid transport and metabolism. Upregulation of fatty acid transport increased red muscle, but not cardiac, triacylglycerol accumulation. White muscle lipid metabolism dysregulation was not observed.
引用
收藏
页码:R1202 / R1212
页数:11
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