Improved insulin sensitivity with calorie restriction does not require reduced JNK1/2, p38, or ERK1/2 phosphorylation in skeletal muscle of 9-month-old rats

被引:10
作者
Sharma, Naveen [1 ]
Bhat, Abhijit D. [1 ]
Kassa, Anketse D. [1 ]
Xiao, Yuanyuan [1 ]
Arias, Edward B. [1 ]
Cartee, Gregory D. [1 ,2 ,3 ]
机构
[1] Univ Michigan, Sch Kinesiol, Muscle Biol Lab, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Mol & Integrat Physiol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Inst Gerontol, Ann Arbor, MI 48109 USA
关键词
mitogen-activated protein kinases; insulin signaling; insulin resistance; dietary restriction; oxidative stress; ACTIVATED PROTEIN-KINASE; BRIEF DIETARY RESTRICTION; AGE-RELATED DISEASES; GLUCOSE-TRANSPORT; MAP KINASE; ADRENOCORTICOTROPIC HORMONE; DIFFERENTIAL REGULATION; SIGNAL-TRANSDUCTION; FOOD RESTRICTION; OXIDATIVE STRESS;
D O I
10.1152/ajpregu.00372.2011
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Sharma N, Bhat AD, Kassa AD, Xiao Y, Arias EB, Cartee GD. Improved insulin sensitivity with calorie restriction does not require reduced JNK1/2, p38, or ERK1/2 phosphorylation in skeletal muscle of 9-month-old rats. Am J Physiol Regul Integr Comp Physiol 302: R126-R136, 2012. First published October 19, 2011; doi:10.1152/ajpregu.00372.2011.-Calorie restriction [CR; similar to 40% below ad libitum (AL) intake] improves the health of many species, including rats, by mechanisms that may be partly related to enhanced insulin sensitivity for glucose disposal by skeletal muscle. Excessive activation of several mitogen-activated protein kinases (MAPKs), including JNK1/2, p38, and ERK1/2 has been linked to insulin resistance. Although insulin can activate ERK1/2, this effect is not required for insulin-mediated glucose uptake. We hypothesized that skeletal muscle from male 9-mo-old Fischer 344/Brown Norway rats CR (35-40% beginning at 3 mo old) versus AL rats would have 1) attenuated activation of JNK1/2, p38, and ERK1/2 under basal conditions; and 2) no difference for insulin-induced ERK1/2 activation. In contrast to our hypothesis, there were significant CR-related increases in the phosphorylation of p38 (epitrochlearis, soleus, and gastrocnemius), JNK1 (epitrochlearis and soleus), and JNK2 (gastrocnemius). Consistent with our hypothesis, CR did not alter insulin-mediated ERK1/2 activation. The greater JNK1/2 and p38 phosphorylation with CR was not attributable to diet effects on muscle oxidative stress (assessed by protein carbonyls and 4-hydroxynonenal protein conjugates). In muscles from the same rats used for the present study, we previously reported a CR-related increase in insulin-mediated glucose uptake by the epitrochlearis and the soleus (Sharma N, Arias EB, Bhat AD, Sequea DA, Ho S, Croff KK, Sajan MP, Farese RV, Cartee GD. Am J Physiol Endocrinol Metab 300: E966-E978, 2011). The present results indicate that the improved insulin sensitivity with CR is not attributable to attenuated MAPK phosphorylation in skeletal muscle.
引用
收藏
页码:R126 / R136
页数:11
相关论文
共 74 条
[71]   Adiponectin increases fatty acid oxidation in skeletal muscle cells by sequential activation of AMP-activated protein kinase, p38 mitogen-activated protein kinase, and peroxisome proliferator-activated receptor α [J].
Yoon, Myeong Jin ;
Lee, Gha Young ;
Chung, Jun-Jae ;
Ahn, Young Ho ;
Hong, Seung Hwan ;
Kim, Jae Bum .
DIABETES, 2006, 55 (09) :2562-2570
[72]   Egr-1 decreases adipocyte insulin sensitivity by tilting PI3K/Akt and MAPK signal balance in mice [J].
Yu, Xiao ;
Shen, Ning ;
Zhang, Ming-Liang ;
Pan, Fei-Yan ;
Wang, Chen ;
Jia, Wei-Ping ;
Liu, Chang ;
Gao, Qian ;
Gao, Xiang ;
Xue, Bin ;
Li, Chao-Jun .
EMBO JOURNAL, 2011, 30 (18) :3754-3765
[73]   Impairment of cardiac insulin signaling in fructose-fed ovariectomized female Wistar rats [J].
Zakula, Zorica ;
Koricanac, Goran ;
Tepavcevic, Snezana ;
Stojiljkovic, Mojca ;
Milosavljevic, Tijana ;
Isenovic, Esma R. .
EUROPEAN JOURNAL OF NUTRITION, 2011, 50 (07) :543-551
[74]   Circulating adiponectin levels increase in rats on caloric restriction: the potential for insulin sensitization [J].
Zhu, M ;
Miura, J ;
Lu, LX ;
Bernier, M ;
DeCabo, R ;
Lane, MA ;
Roth, GS ;
Ingram, DK .
EXPERIMENTAL GERONTOLOGY, 2004, 39 (07) :1049-1059