Calorie restriction leads to greater Akt2 activity and glucose uptake by insulin-stimulated skeletal muscle from old rats

被引:20
作者
Wang, Haiyan [1 ,2 ]
Arias, Edward B. [1 ]
Cartee, Gregory D. [1 ,3 ,4 ]
机构
[1] Univ Michigan, Sch Kinesiol, Muscle Biol Lab, Ann Arbor, MI 48109 USA
[2] E China Normal Univ, Coll Phys Educ & Hlth, Shanghai 200062, Peoples R China
[3] Univ Michigan, Dept Mol & Integrat Physiol, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Inst Gerontol, Ann Arbor, MI 48109 USA
关键词
glucose transport; insulin signaling; insulin resistance; aging; GLUT4; TRANSLOCATION; FILAMIN-C; AS160; PHOSPHORYLATION; IN-VITRO; TRANSPORT; EXERCISE; SUBSTRATE; INCREASES; CONTRACTION; SENSITIVITY;
D O I
10.1152/ajpregu.00449.2015
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Skeletal muscle insulin resistance is associated with many common age-related diseases, but moderate calorie restriction (CR) can substantially elevate glucose uptake by insulin-stimulated skeletal muscle from both young and old rats. The current study evaluated the isolated epitrochlearis muscle from similar to 24.5-mo-old rats that were either fed ad libitum (AL) or subjected to CR (consuming similar to 65% of ad libitum, AL, intake beginning at similar to 22.5 mo old). Some muscles were also incubated with MK-2206, a potent and selective Akt inhibitor. The most important results were that in isolated muscles, CR vs. AL resulted in 1) greater insulin-stimulated glucose uptake 2) that was accompanied by significantly increased insulin-mediated activation of Akt2, as indicated by greater phosphorylation on both Thr(309) and Ser(474) along with greater Akt2 activity, 3) concomitant with enhanced phosphorylation of several Akt substrates, including an Akt substrate of 160 kDa on Thr(642) and Ser(588), filamin C on Ser(2213) and proline-rich Akt substrate of 40 kDa on Thr(246), but not TBC1D1 on Thr(596); and 4) each of the CR effects was eliminated by MK-2206. These data provide compelling new evidence linking greater Akt2 activation to the CR-induced elevation of insulin-stimulated glucose uptake by muscle from old animals.
引用
收藏
页码:R449 / R458
页数:10
相关论文
共 71 条
[1]   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
[2]   A high-affinity reversible protein stain for Western blots [J].
Antharavally, BS ;
Carter, B ;
Bell, PA ;
Mallia, AK .
ANALYTICAL BIOCHEMISTRY, 2004, 329 (02) :276-280
[3]   Comparison of short-term diet and exercise on insulin action in individuals with abnormal glucose tolerance [J].
Arciero, PJ ;
Vukovich, MD ;
Holloszy, JO ;
Racette, SB ;
Kohrt, WM .
JOURNAL OF APPLIED PHYSIOLOGY, 1999, 86 (06) :1930-1935
[4]   Short-term caloric restriction does not modify the in vivo insulin signaling pathway leading to Akt activation in skeletal muscle of ames dwarf (Prop1df/Prop1df) mice [J].
Argentino, DP ;
Muñoz, MC ;
Rocha, JS ;
Bartke, A ;
Turyn, D ;
Dominici, FP .
HORMONE AND METABOLIC RESEARCH, 2005, 37 (11) :672-679
[5]   Effects of long-term caloric restriction on early steps of the insulin-signaling system in mouse skeletal muscle [J].
Argentino, DP ;
Dominici, FP ;
Al-Regaiey, K ;
Bonkowski, MS ;
Bartke, A ;
Turyn, D .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2005, 60 (01) :28-34
[6]   Isoform-specific regulation of insulin-dependent glucose uptake by Akt/protein kinase B [J].
Bae, SS ;
Cho, H ;
Mu, J ;
Birnbaum, MJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (49) :49530-49536
[7]  
Boucher J., 2014, COLD SPRING HARBOR P, P6
[8]   siRNA-based gene silencing reveals specialized roles of IRS-1/Akt2 and IRS-2/Akt1 in glucose and lipid metabolism in human skeletal muscle [J].
Bouzakri, Karim ;
Zachrisson, Anna ;
Al-Khalili, Lubna ;
Zhang, Bei B. ;
Koistinen, Heikki A. ;
Krook, Anna ;
Zierath, Juleen R. .
CELL METABOLISM, 2006, 4 (01) :89-96
[9]   ADAPTATION OF MUSCLE GLUCOSE-TRANSPORT WITH CALORIC RESTRICTION IN ADULT, MIDDLE-AGED, AND OLD RATS [J].
CARTEE, GD ;
KIETZKE, EW ;
BRIGGSTUNG, C .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (05) :R1443-R1447
[10]   GROWTH-HORMONE REDUCES GLUCOSE-TRANSPORT BUT NOT GLUT-1 OR GLUT-4 IN ADULT AND OLD RATS [J].
CARTEE, GD ;
BOHN, EE .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1995, 268 (05) :E902-E909