Differential regulation of PGC-1α expression in rat liver and skeletal muscle in response to voluntary running

被引:16
作者
Matiello, Renata [2 ]
Fukui, Rosa T. [2 ]
Silva, Maria E. R. [2 ]
Rocha, Dalva M. [2 ]
Wajchenberg, Bernardo L. [2 ]
Azhar, Salman [1 ,3 ]
Santos, Rosa F. [2 ]
机构
[1] VA Palo Alto Hlth Care Syst, Educ & Clin Ctr, Palo Alto, CA 94304 USA
[2] Univ Sao Paulo, Sch Med, Hosp Clin, Div Endocrinol & Metab,Lab Med Invest,LIM 18, BR-01246903 Sao Paulo, Brazil
[3] Stanford Univ, Stanford, CA 94305 USA
基金
美国国家卫生研究院; 巴西圣保罗研究基金会;
关键词
TRIGLYCERIDE TRANSFER PROTEIN; INSULIN-RESISTANCE; LIPID-METABOLISM; HEPATIC GLUCONEOGENESIS; EXERCISE PERFORMANCE; ENERGY-METABOLISM; KINASE-ACTIVITY; PGC-1; PATHOGENESIS; GLUCOSE;
D O I
10.1186/1743-7075-7-36
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: The beneficial actions of exercise training on lipid, glucose and energy metabolism and insulin sensitivity appear to be in part mediated by PGC-1 alpha. Previous studies have shown that spontaneously exercised rats show at rest enhanced responsiveness to exogenous insulin, lower plasma insulin levels and increased skeletal muscle insulin sensitivity. This study was initiated to examine the functional interaction between exercise-induced modulation of skeletal muscle and liver PGC-1 alpha protein expression, whole body insulin sensitivity, and circulating FFA levels as a measure of whole body fatty acid (lipid) metabolism. Methods: Two groups of male Wistar rats (2 Mo of age, 188.82 +/- 2.77 g BW) were used in this study. One group consisted of control rats placed in standard laboratory cages. Exercising rats were housed individually in cages equipped with running wheels and allowed to run at their own pace for 5 weeks. At the end of exercise training, insulin sensitivity was evaluated by comparing steady-state plasma glucose (SSPG) concentrations at constant plasma insulin levels attained during the continuous infusion of glucose and insulin to each experimental group. Subsequently, soleus and plantaris muscle and liver samples were collected and quantified for PGC-1 alpha protein expression by Western blotting. Collected blood samples were analyzed for glucose, insulin and FFA concentrations. Results: Rats housed in the exercise wheel cages demonstrated almost linear increases in running activity with advancing time reaching to maximum value around 4 weeks. On an average, the rats ran a mean (Mean +/- SE) of 4.102 +/- 0.747 km/day and consumed significantly more food as compared to sedentary controls (P < 0.001) in order to meet their increased caloric requirement. Mean plasma insulin (P < 0.001) and FFA (P < 0.006) concentrations were lower in the exercise-trained rats as compared to sedentary controls. Mean steady state plasma insulin (SSPI) and glucose (SSPG) concentrations were not significantly different in sedentary control rats as compared to exercise-trained animals. Plantaris PGC-1 alpha protein expression increased significantly from a 1.11 +/- 0.12 in the sedentary rats to 1.74 +/- 0.09 in exercising rats (P < 0.001). However, exercise had no effect on PGC-1 alpha protein content in either soleus muscle or liver tissue. These results indicate that exercise training selectively up regulates the PGC-1 alpha protein expression in high-oxidative fast skeletal muscle type such as plantaris muscle. Conclusion: These data suggest that PGC-1 alpha most likely plays a restricted role in exercise-mediated improvements in insulin resistance (sensitivity) and lowering of circulating FFA levels.
引用
收藏
页数:8
相关论文
共 70 条
  • [1] Exercise stimulates Pgc-1α transcription in skeletal muscle through activation of the p38 MAPK pathway
    Akimoto, T
    Pohnert, SC
    Li, P
    Zhang, M
    Gumbs, C
    Rosenberg, PB
    Williams, RS
    Yan, Z
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (20) : 19587 - 19593
  • [2] CHARACTERIZATION OF INSULIN-RECEPTOR KINASE-ACTIVITY AND AUTOPHOSPHORYLATION IN DIFFERENT SKELETAL-MUSCLE TYPES
    AZHAR, S
    BUTTE, JC
    SANTOS, RF
    MONDON, CE
    REAVEN, GM
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (01): : E1 - E7
  • [3] PPARα:: its role in the human metabolic syndrome
    Azhar, Salman
    Kelley, Glen
    [J]. FUTURE LIPIDOLOGY, 2007, 2 (01): : 31 - 53
  • [4] Adaptations of skeletal muscle to exercise: rapid increase in the transcriptional coactivator PGC-1
    Baar, K
    Wende, AR
    Jones, TE
    Marison, M
    Nolte, LA
    Chen, M
    Kelly, DP
    Holloszy, JO
    [J]. FASEB JOURNAL, 2002, 16 (14) : 1879 - 1886
  • [5] PGC-1α- mediated regulation of gene expression and metabolism: implications for nutrition and exercise prescriptions
    Benton, Carley R.
    Wright, David C.
    Bonen, Arend
    [J]. APPLIED PHYSIOLOGY NUTRITION AND METABOLISM, 2008, 33 (05) : 843 - 862
  • [6] BOBYLEVAGUARRIERO V, 1986, ARCH BIOCHEM BIOPHYS, V245, P470, DOI 10.1016/0003-9861(86)90239-0
  • [7] Lipid metabolism, exercise and insulin action
    Bonen, Arend
    Dohm, G. Lynis
    van Loon, Luc J. C.
    [J]. ESSAYS IN BIOCHEMISTRY, VOL 42: THE BIOCHEMICAL BASIS OF THE HEALTH EFFECTS OF EXERCISE, 2006, 42 : 47 - 59
  • [8] PGC-1α-induced improvements in skeletal muscle metabolism and insulin sensitivity
    Bonen, Arend
    [J]. APPLIED PHYSIOLOGY NUTRITION AND METABOLISM, 2009, 34 (03) : 307 - 314
  • [9] Tricarboxylic acid cycle intermediate pool size - Functional importance for oxidative metabolism in exercising human skeletal muscle
    Bowtell, Joanna L.
    Marwood, Simon
    Bruce, Mark
    Constantin-Teodosiu, Dumitru
    Greenhaff, Paul L.
    [J]. SPORTS MEDICINE, 2007, 37 (12) : 1071 - 1088
  • [10] Diminished hepatic gluconeogenesis via defects in tricarboxylic acid cycle flux in peroxisome proliferator-activated receptor γ coactivator-1α (PGC-1α)-deficient mice
    Burgess, Shawn C.
    Leone, Teresa C.
    Wende, Adam R.
    Croce, Michelle A.
    Chen, Zhouji
    Sherry, A. Dean
    Malloy, Craig R.
    Finck, Brian N.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (28) : 19000 - 19008