Calcitriol Reduces Hepatic Triglyceride Accumulation and Glucose Output Through Ca2+/CaMKKβ/AMPK Activation Under Insulin-Resistant Conditions in Type 2 Diabetes Mellitus

Curr Mol Med. 2016;16(8):747-758. doi: 10.2174/1566524016666160920111407.

Abstract

Objectives: The present study was designed to investigate the effects of calcitriol (the active hormonal metabolite of vitamin D) on hepatic metabolic abnormalities in type 2 diabetes.

Methods: Type 2 diabetic db/db mice were used to investigate the effects of calcitriol on hepatic and systemic metabolic disorders. HepG2 cells cultured in insulin-resistant conditions were used to examine the potential mechanisms for calcitriol-induced changes in hepatic lipid and glucose metabolism.

Results: 8-week calcitriol treatment ameliorated abnormal hepatic lipid and glucose production in db/db mice. In HepG2 cells under insulin-resistant condition, calcitriol increased cytosolic calcium concentration and induced 5'-AMP-activated protein kinase/acetyl-CoAcarboxylase (AMPK/ACC) phosphorylation via the Ca2+/calmodulin-dependent protein kinase kinase β (CaMKKβ) pathway, contributing to the reductions in hepatic triglyceride accumulation and glucose output. Calcitriol also induced AMPK/ACC phosphorylation in liver of db/db mice.

Conclusion: Our data indicate that calcitriol, at above-physiological serum concentrations, reduces hepatic triglyceride accumulation and glucose output, at least in part through activation of Ca2+/CaMKKβ/AMPK under insulin-resistant condition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases / metabolism*
  • Animals
  • Biomarkers
  • Calcitriol / pharmacology*
  • Calcium / metabolism*
  • Calcium-Calmodulin-Dependent Protein Kinase Kinase / metabolism*
  • Diabetes Mellitus, Type 2 / metabolism
  • Disease Models, Animal
  • Enzyme Activation
  • Glucose / metabolism*
  • Hep G2 Cells
  • Humans
  • Hyperglycemia / metabolism
  • Insulin / metabolism
  • Insulin Resistance*
  • Lipid Metabolism / drug effects
  • Liver / drug effects
  • Liver / metabolism*
  • Male
  • Mice
  • Phosphorylation
  • Triglycerides / metabolism*

Substances

  • Biomarkers
  • Insulin
  • Triglycerides
  • Calcium-Calmodulin-Dependent Protein Kinase Kinase
  • AMP-Activated Protein Kinases
  • Calcitriol
  • Glucose
  • Calcium