Inactivation of PKCtheta leads to increased susceptibility to obesity and dietary insulin resistance in mice
- PMID: 16896164
- DOI: 10.1152/ajpendo.00178.2006
Inactivation of PKCtheta leads to increased susceptibility to obesity and dietary insulin resistance in mice
Abstract
In this study, we investigated the metabolic phenotype of PKCtheta knockout mice (C57BL/6J) on chow diet and high-fat diet (HFD). The knockout (KO) mice are normal in growth and reproduction. On the chow diet, body weight and food intake were not changed in the KO mice; however, body fat content was increased with a corresponding decrease in body lean mass. Energy expenditure and spontaneous physical activity were decreased in the KO mice. On HFD, energy expenditure and physical activity remained low in the KO mice. The body weight and fat content were increased rapidly in the KO mice. At 8 wk on HFD, severe insulin resistance was detected in the KO mice with hyperinsulinemic euglycemic clamp and insulin tolerance test. Insulin action in both hepatic and peripheral tissues was reduced in the KO mice. Plamsa free fatty acid was increased, and expression of adiponectin in the adipose tissue was decreased, in the KO mice on HFD. This study suggests that loss of PKCtheta reduces energy expenditure and increases the risk of dietary obesity and insulin resistance in mice.
Similar articles
-
PKC-theta knockout mice are protected from fat-induced insulin resistance.J Clin Invest. 2004 Sep;114(6):823-7. doi: 10.1172/JCI22230. J Clin Invest. 2004. PMID: 15372106 Free PMC article.
-
Peroxisome proliferator-activated receptor-alpha deficiency does not alter insulin sensitivity in mice maintained on regular or high-fat diet: hyperinsulinemic-euglycemic clamp studies.Endocrinology. 2004 Apr;145(4):1662-7. doi: 10.1210/en.2003-1015. Epub 2003 Dec 11. Endocrinology. 2004. PMID: 14670996
-
TNFα gene knockout differentially affects lipid deposition in liver and skeletal muscle of high-fat-diet mice.J Nutr Biochem. 2012 Dec;23(12):1685-93. doi: 10.1016/j.jnutbio.2011.12.001. Epub 2012 Mar 29. J Nutr Biochem. 2012. PMID: 22464148
-
CTRP3 deficiency reduces liver size and alters IL-6 and TGFβ levels in obese mice.Am J Physiol Endocrinol Metab. 2016 Mar 1;310(5):E332-45. doi: 10.1152/ajpendo.00248.2015. Epub 2015 Dec 15. Am J Physiol Endocrinol Metab. 2016. PMID: 26670485 Free PMC article.
-
Deficiency of the tumor promoter gene wip1 induces insulin resistance.Mol Endocrinol. 2015 Jan;29(1):28-39. doi: 10.1210/me.2014-1136. Mol Endocrinol. 2015. PMID: 25379953 Free PMC article.
Cited by
-
Protein kinase C function in muscle, liver, and beta-cells and its therapeutic implications for type 2 diabetes.Diabetes. 2008 Jul;57(7):1774-83. doi: 10.2337/db07-1769. Diabetes. 2008. PMID: 18586909 Free PMC article. Review. No abstract available.
-
Inactivation of NF-kappaB p50 leads to insulin sensitization in liver through post-translational inhibition of p70S6K.J Biol Chem. 2009 Jul 3;284(27):18368-76. doi: 10.1074/jbc.M109.007260. Epub 2009 May 11. J Biol Chem. 2009. PMID: 19433583 Free PMC article.
-
Protein kinase Cθ is required for cardiomyocyte survival and cardiac remodeling.Cell Death Dis. 2010 May 27;1(5):e45. doi: 10.1038/cddis.2010.24. Cell Death Dis. 2010. PMID: 21364651 Free PMC article.
-
Intracellular ATP in balance of pro- and anti-inflammatory cytokines in adipose tissue with and without tissue expansion.Int J Obes (Lond). 2017 Apr;41(4):645-651. doi: 10.1038/ijo.2017.3. Epub 2017 Feb 7. Int J Obes (Lond). 2017. PMID: 28074058 Free PMC article.
-
Mechanisms for insulin resistance: common threads and missing links.Cell. 2012 Mar 2;148(5):852-71. doi: 10.1016/j.cell.2012.02.017. Cell. 2012. PMID: 22385956 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases
Research Materials