Exercise and type 2 diabetes: molecular mechanisms regulating glucose uptake in skeletal muscle

被引:224
作者
Stanford, Kristin I. [1 ]
Goodyear, Laurie J. [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sect Integrat Physiol & Metab, Joslin Diabet Ctr,Dept Med,Med Sch, Boston, MA 02215 USA
基金
美国国家卫生研究院;
关键词
exercise; type; 2; diabetes; ACTIVATED PROTEIN-KINASE; INSULIN-STIMULATED PHOSPHORYLATION; LIFE-STYLE INTERVENTION; AS160; PHOSPHORYLATION; GLUT4; TRANSLOCATION; 3-KINASE ACTIVITY; AKT SUBSTRATE; CONTRACTION; TRANSPORT; AMPK;
D O I
10.1152/advan.00080.2014
中图分类号
G40 [教育学];
学科分类号
040101 ; 120403 ;
摘要
Exercise is a well-established tool to prevent and combat type 2 diabetes. Exercise improves whole body metabolic health in people with type 2 diabetes, and adaptations to skeletal muscle are essential for this improvement. An acute bout of exercise increases skeletal muscle glucose uptake, while chronic exercise training improves mitochondrial function, increases mitochondrial biogenesis, and increases the expression of glucose transporter proteins and numerous metabolic genes. This review focuses on the molecular mechanisms that mediate the effects of exercise to increase glucose uptake in skeletal muscle.
引用
收藏
页码:308 / 314
页数:7
相关论文
共 87 条
[1]   AMPKα2 deficiency uncovers time dependency in the regulation of contraction-induced palmitate and glucose uptake in mouse muscle [J].
Abbott, Marcia J. ;
Bogachus, Lindsey D. ;
Turcotte, Lorraine P. .
JOURNAL OF APPLIED PHYSIOLOGY, 2011, 111 (01) :125-134
[2]   TBC1D1 Regulates Insulin- and Contraction-Induced Glucose Transport in Mouse Skeletal Muscle [J].
An, Ding ;
Toyoda, Taro ;
Taylor, Eric B. ;
Yu, Haiyan ;
Fujii, Nobuharu ;
Hirshman, Michael F. ;
Goodyear, Laurie J. .
DIABETES, 2010, 59 (06) :1358-1365
[3]   The selectivity of protein kinase inhibitors: a further update [J].
Bain, Jenny ;
Plater, Lorna ;
Elliott, Matt ;
Shpiro, Natalia ;
Hastie, C. James ;
Mclauchlan, Hilary ;
Klevernic, Iva ;
Arthur, J. Simon C. ;
Alessi, Dario R. ;
Cohen, Philip .
BIOCHEMICAL JOURNAL, 2007, 408 :297-315
[4]  
Billington CJ, 2000, ARCH INTERN MED, V160, P898, DOI 10.1001/archinte.160.7.898
[5]   TRANSMEMBRANE GLUCOSE-TRANSPORT IN SKELETAL-MUSCLE OF PATIENTS WITH NON-INSULIN-DEPENDENT DIABETES [J].
BONADONNA, RC ;
DELPRATO, S ;
SACCOMANI, MP ;
BONORA, E ;
GULLI, G ;
FERRANNINI, E ;
BIER, D ;
COBELLI, C ;
DEFRONZO, RA .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (01) :486-494
[6]   Increased phosphorylation of Akt substrate of 160 kDa (AS160) in rat skeletal muscle in response to insulin or contractile activity [J].
Bruss, MD ;
Arias, EB ;
Lienhard, GE ;
Cartee, GD .
DIABETES, 2005, 54 (01) :41-50
[7]   Splanchnic and leg substrate exchange after ingestion of a natural mixed meal in humans [J].
Capaldo, B ;
Gastaldelli, A ;
Antoniello, S ;
Auletta, M ;
Pardo, F ;
Ciociaro, D ;
Guida, R ;
Ferrannini, E ;
Saccà, L .
DIABETES, 1999, 48 (05) :958-966
[8]   Exercise and Insulin: Convergence or Divergence at AS160 and TBC1D1? [J].
Cartee, Gregory D. ;
Funai, Katsuhiko .
EXERCISE AND SPORT SCIENCES REVIEWS, 2009, 37 (04) :188-195
[9]  
Centers for Disease Control and Prevention (CDC), 2004, MMWR Morb Mortal Wkly Rep, V53, P1066
[10]   Inhibition of GLUT4 translocation by Tbc1d1, a Rab GTPase-activating protein abundant in skeletal muscle, is partially relieved by AMP-activated protein kinase activation [J].
Chavez, Jose A. ;
Roach, William G. ;
Keller, Susanna R. ;
Lane, William S. ;
Lienhard, Gustav E. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (14) :9187-9195