Regulation of Skeletal Muscle Physiology and Metabolism by Peroxisome Proliferator-Activated Receptor δ

被引:162
作者
Ehrenborg, Ewa [2 ]
Krook, Anna [1 ]
机构
[1] Karolinska Inst, Dept Physiol & Pharmacol, Integrat Physiol Grp, SE-17177 Stockholm, Sweden
[2] Karolinska Univ Hosp, Karolinska Inst, Ctr Mol Med, Dept Med,Atherosclerosis Res Unit, Stockholm, Sweden
基金
英国医学研究理事会;
关键词
FATTY-ACID OXIDATION; SINGLE NUCLEOTIDE POLYMORPHISMS; IMPAIRED GLUCOSE-TOLERANCE; MESSENGER-RNA EXPRESSION; LIGAND-BINDING DOMAIN; PPAR-DELTA; GENE-EXPRESSION; FIBER-TYPE; INSULIN-RESISTANCE; LIPID-METABOLISM;
D O I
10.1124/pr.109.001560
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Agonists directed against the alpha and gamma isoforms of the peroxisome proliferator-activated receptors (PPARs) have become important for the respective treatment of hypertriglyceridemia and insulin resistance associated with metabolic disease. PPAR delta is the least well characterized of the three PPAR isoforms. Skeletal muscle insulin resistance is a primary risk factor for the development of type 2 diabetes. There is increasing evidence that PPAR delta is an important regulator of skeletal muscle metabolism, in particular, muscle lipid oxidation, highlighting the potential utility of this isoform as a drug target. In addition, PPAR delta seems to be a key regulator of skeletal muscle fiber type and a possible mediator of the adaptations noted in skeletal muscle in response to exercise. In this review we summarize the current status regarding the regulation, and the metabolic effects, of PPAR delta in skeletal muscle.
引用
收藏
页码:373 / 393
页数:21
相关论文
共 201 条
[1]   Diverging regulation of pyruvate dehydrogenase kinase isoform gene expression in cultured human muscle cells [J].
Abbot, EL ;
McCormack, JG ;
Reynet, C ;
Hassall, DG ;
Buchan, KW ;
Yeaman, SJ .
FEBS JOURNAL, 2005, 272 (12) :3004-3014
[2]  
Abbott BD, 2009, REPROD TOXICOL, V75, P72
[3]   Association of peroxisome proliferator-activated receptor delta+294T/C with body mass index and interaction with peroxisome proliferator-activated receptor alpha L162V [J].
Aberle, J. ;
Hopfer, I. ;
Beil, F. U. ;
Seedorf, U. .
INTERNATIONAL JOURNAL OF OBESITY, 2006, 30 (12) :1709-1713
[4]  
Aberle Jens, 2006, Int J Med Sci, V3, P108
[5]   Diabetic dyslipidaemia [J].
Adiels, Martin ;
Olofsson, Sven-Olof ;
Taskinen, Marja-Riitta ;
Boren, Jan .
CURRENT OPINION IN LIPIDOLOGY, 2006, 17 (03) :238-246
[6]   Peroxisome proliferator-activated receptor β/δ regulates very low density lipoprotein production and catabolism in mice on a Western diet [J].
Akiyama, TE ;
Lambert, G ;
Nicol, CJ ;
Matsusue, K ;
Peters, JM ;
Brewer, HB ;
Gonzalez, FJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (20) :20874-20881
[7]   Single nucleotide polymorphisms of PPARD in combination with the Gly482Ser substitution of PGC-1A and the Pro12Ala substitution of PPARG2 predict the conversion from impaired glucose tolerance to type 2 diabetes -: The STOP-NIDDM trial [J].
Andrulionyte, Laura ;
Peltola, Paula ;
Chiasson, Jean-Louis ;
Laakso, Markku .
DIABETES, 2006, 55 (07) :2148-2152
[8]  
[Anonymous], LANCET
[9]   Tissue distribution and quantification of the expression of mRNAs of peroxisome proliferator-activated receptors and liver X receptor-alpha in humans - No alteration in adipose tissue of obese and NIDDM patients [J].
Auboeuf, D ;
Rieusset, J ;
Fajas, L ;
Vallier, P ;
Frering, V ;
Riou, JP ;
Staels, P ;
Auwerx, J ;
Laville, M ;
Vidal, H .
DIABETES, 1997, 46 (08) :1319-1327
[10]  
Auwerx J, 1999, CELL, V97, P161