Insulin resistance: cross-talk between adipose tissue and skeletal muscle, through free fatty acids, liver X receptor, and peroxisome proliferator-activated receptor-α signaling
- PMID: 25436738
- DOI: 10.1515/hmbci-2013-0019
Insulin resistance: cross-talk between adipose tissue and skeletal muscle, through free fatty acids, liver X receptor, and peroxisome proliferator-activated receptor-α signaling
Abstract
Skeletal muscle and adipose tissue play a major role in the regulation of whole-body glucose homeostasis. Much of the coordinated regulation of whole-body glucose homeostasis results from the regulation of lipid storage and release by adipose tissue and efficient switching between glucose oxidation and fatty acid oxidation in skeletal muscle. A control point for these biochemical actions center around the regulation of the insulin responsive glucose transporter, GLUT4. This review examines the regulation of GLUT4 in adipose tissue and skeletal muscle, in the context of the steroid nuclear hormone receptor signaling.
Similar articles
-
Adipose tissue compensates for defect of phosphatidylinositol 3'-kinase induced in liver and muscle by dietary fish oil in fed rats.Am J Physiol Endocrinol Metab. 2006 Jan;290(1):E78-E86. doi: 10.1152/ajpendo.00200.2005. Am J Physiol Endocrinol Metab. 2006. PMID: 16339925
-
Blockade of interleukin 6 signalling ameliorates systemic insulin resistance through upregulation of glucose uptake in skeletal muscle and improves hepatic steatosis in high-fat diet fed mice.Liver Int. 2015 Feb;35(2):550-61. doi: 10.1111/liv.12645. Epub 2014 Aug 12. Liver Int. 2015. PMID: 25066281
-
Activation of liver X receptor improves glucose tolerance through coordinate regulation of glucose metabolism in liver and adipose tissue.Proc Natl Acad Sci U S A. 2003 Apr 29;100(9):5419-24. doi: 10.1073/pnas.0830671100. Epub 2003 Apr 15. Proc Natl Acad Sci U S A. 2003. PMID: 12697904 Free PMC article.
-
PPARgamma-mediated insulin sensitization: the importance of fat versus muscle.Am J Physiol Endocrinol Metab. 2005 Feb;288(2):E287-91. doi: 10.1152/ajpendo.00440.2004. Am J Physiol Endocrinol Metab. 2005. PMID: 15637349 Review.
-
Role of nuclear receptors in the modulation of insulin secretion in lipid-induced insulin resistance.Biochem Soc Trans. 2008 Oct;36(Pt 5):891-900. doi: 10.1042/BST0360891. Biochem Soc Trans. 2008. PMID: 18793157 Review.
Cited by
-
Characterization of Metabolic Parameters in Responders and Nonresponders Treated with Canagliflozin Monotherapy in Drug-naive Subjects with Type 2 Diabetes.Indian J Endocrinol Metab. 2018 Mar-Apr;22(2):185-190. doi: 10.4103/ijem.IJEM_578_17. Indian J Endocrinol Metab. 2018. PMID: 29911028 Free PMC article.
-
Two Glucose-Lowering Mechanisms of Canagliflozin Depending on Body Weight Changes in Drug-Naïve Subjects with Type 2 Diabetes.Drugs R D. 2018 Dec;18(4):309-315. doi: 10.1007/s40268-018-0250-z. Drugs R D. 2018. PMID: 30324549 Free PMC article. Clinical Trial.
-
Berberis integerrima ameliorates insulin resistance in high- fructose-fed insulin-resistant rats.Iran J Basic Med Sci. 2017 Oct;20(10):1093-1101. doi: 10.22038/IJBMS.2017.9409. Iran J Basic Med Sci. 2017. PMID: 29147484 Free PMC article.
-
Efficacy of Sitagliptin on Nonalcoholic Fatty Liver Disease in High-fat-diet-fed Diabetic Mice.Curr Med Sci. 2022 Jun;42(3):513-519. doi: 10.1007/s11596-022-2573-9. Epub 2022 Apr 22. Curr Med Sci. 2022. PMID: 35451807
-
Inter-Tissue Gene Co-Expression Networks between Metabolically Healthy and Unhealthy Obese Individuals.PLoS One. 2016 Dec 1;11(12):e0167519. doi: 10.1371/journal.pone.0167519. eCollection 2016. PLoS One. 2016. PMID: 27907186 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources