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


Autoria(s): Matiello, Renata ; Fukui, Rosa T; Silva, Maria ER; Rocha, Dalva M; Wajchenberg, Bernardo L; Azhar, Salman ; Santos, Rosa F
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

26/08/2013

26/08/2013

01/04/2010

Resumo

Abstract Background The beneficial actions of exercise training on lipid, glucose and energy metabolism and insulin sensitivity appear to be in part mediated by PGC-1α. 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-1α 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-1α 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-1α 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-1α protein content in either soleus muscle or liver tissue. These results indicate that exercise training selectively up regulates the PGC-1α protein expression in high-oxidative fast skeletal muscle type such as plantaris muscle. Conclusion These data suggest that PGC-1α most likely plays a restricted role in exercise-mediated improvements in insulin resistance (sensitivity) and lowering of circulating FFA levels.

This work was supported by a grant from Foundation for Research Support of Sao Paulo State, Brazil (FAPESP n° 06/549908; 07/566028) (RS) and Office of Research and Development, Medical Service, Department of Veterans Affairs (SA), and grants from the National Institutes of Health (HL033881 and HL092473) (SA).

This work was supported by a grant from Foundation for Research Support of Sao Paulo State, Brazil (FAPESP n° 06/54990-8; 07/56602-8) (RS) and Office of Research and Development, Medical Service, Department of Veterans Affairs (SA), and grants from the National Institutes of Health (HL033881 and HL092473) (SA).

Identificador

Nutrition & Metabolism. 2010 Apr 30;7(1):36

1743-7075

http://www.producao.usp.br/handle/BDPI/33083

10.1186/1743-7075-7-36

http://www.nutritionandmetabolism.com/content/7/1/36

Idioma(s)

eng

Relação

Nutrition & Metabolism

Direitos

openAccess

Matiello et al; licensee BioMed Central Ltd. - This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Tipo

article

original article