Mechanisms underlying regulation of the expression and activities of the mammalian pyruvate dehydrogenase kinases
- PMID: 17132539
- DOI: 10.1080/13813450600935263
Mechanisms underlying regulation of the expression and activities of the mammalian pyruvate dehydrogenase kinases
Abstract
The mechanisms that control mammalian pyruvate dehydrogenase complex (PDC) activity include its phosphorylation (inactivation) by a family of pyruvate dehydrogenase kinases (PDKs 1 - 4). Here we review new developments in the regulation of the activities and expression of the PDKs, in particular PDK2 and PDK4, in relation to glucose and lipid homeostasis. This review describes recent advances relating to the acute and long-term modes of regulation of the PDKs, with particular emphasis on the regulatory roles of nuclear receptors including peroxisome proliferator-activated receptor (PPAR) alpha and Liver X receptor (LXR), PPAR gamma coactivator alpha (PGC-1alpha) and insulin, and the impact of changes in PDK activity and expression in glucose and lipid homeostasis. Since PDK4 may assist in lipid clearance when there is an imbalance between lipid delivery and oxidation, it may represent an attractive target for interventions aimed at rectifying abnormal lipid as well as glucose homeostasis in disease states.
Similar articles
-
Therapeutic potential of the mammalian pyruvate dehydrogenase kinases in the prevention of hyperglycaemia.Curr Drug Targets Immune Endocr Metabol Disord. 2002 Jul;2(2):151-65. Curr Drug Targets Immune Endocr Metabol Disord. 2002. PMID: 12476789 Review.
-
Selective modification of pyruvate dehydrogenase kinase isoform expression in rat pancreatic islets elicited by starvation and activation of peroxisome proliferator-activated receptor-alpha: implications for glucose-stimulated insulin secretion.Diabetes. 2001 Dec;50(12):2729-36. doi: 10.2337/diabetes.50.12.2729. Diabetes. 2001. PMID: 11723055
-
Investigation of potential mechanisms regulating protein expression of hepatic pyruvate dehydrogenase kinase isoforms 2 and 4 by fatty acids and thyroid hormone.Biochem J. 2003 Feb 1;369(Pt 3):687-95. doi: 10.1042/BJ20021509. Biochem J. 2003. PMID: 12435272 Free PMC article.
-
Estrogen-related receptors stimulate pyruvate dehydrogenase kinase isoform 4 gene expression.J Biol Chem. 2006 Dec 29;281(52):39897-906. doi: 10.1074/jbc.M608657200. Epub 2006 Nov 1. J Biol Chem. 2006. PMID: 17079227
-
Recent advances in mechanisms regulating glucose oxidation at the level of the pyruvate dehydrogenase complex by PDKs.Am J Physiol Endocrinol Metab. 2003 May;284(5):E855-62. doi: 10.1152/ajpendo.00526.2002. Am J Physiol Endocrinol Metab. 2003. PMID: 12676647 Review.
Cited by
-
Regulation of Glucose Metabolism by MuRF1 and Treatment of Myopathy in Diabetic Mice with Small Molecules Targeting MuRF1.Int J Mol Sci. 2021 Feb 23;22(4):2225. doi: 10.3390/ijms22042225. Int J Mol Sci. 2021. PMID: 33672385 Free PMC article.
-
Testosterone plus low-intensity physical training in late life improves functional performance, skeletal muscle mitochondrial biogenesis, and mitochondrial quality control in male mice.PLoS One. 2012;7(12):e51180. doi: 10.1371/journal.pone.0051180. Epub 2012 Dec 11. PLoS One. 2012. PMID: 23240002 Free PMC article.
-
Necrotic enteritis challenge regulates peroxisome proliferator-1 activated receptors signaling and β-oxidation pathways in broiler chickens.Anim Nutr. 2021 Mar;7(1):239-251. doi: 10.1016/j.aninu.2020.08.003. Epub 2020 Dec 17. Anim Nutr. 2021. PMID: 33997353 Free PMC article.
-
Assessment of growth and metabolism characteristics in offspring of dehydroepiandrosterone-induced polycystic ovary syndrome adults.Reproduction. 2016 Dec;152(6):705-714. doi: 10.1530/REP-16-0081. Reproduction. 2016. PMID: 27798284 Free PMC article.
-
Tissue-specific kinase expression and activity regulate flux through the pyruvate dehydrogenase complex.J Biol Chem. 2019 Jan 18;294(3):838-851. doi: 10.1074/jbc.RA118.006433. Epub 2018 Nov 27. J Biol Chem. 2019. PMID: 30482839 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources