T₃-induced liver AMP-activated protein kinase signaling: redox dependency and upregulation of downstream targets

World J Gastroenterol. 2014 Dec 14;20(46):17416-25. doi: 10.3748/wjg.v20.i46.17416.

Abstract

Aim: To investigate the redox dependency and promotion of downstream targets in thyroid hormone (T3)-induced AMP-activated protein kinase (AMPK) signaling as cellular energy sensor to limit metabolic stresses in the liver.

Methods: Fed male Sprague-Dawley rats were given a single ip dose of 0.1 mg T3/kg or T3 vehicle (NaOH 0.1 N; controls) and studied at 8 or 24 h after treatment. Separate groups of animals received 500 mg N-acetylcysteine (NAC)/kg or saline ip 30 min prior T3. Measurements included plasma and liver 8-isoprostane and serum β-hydroxybutyrate levels (ELISA), hepatic levels of mRNAs (qPCR), proteins (Western blot), and phosphorylated AMPK (ELISA).

Results: T3 upregulates AMPK signaling, including the upstream kinases Ca(2+)-calmodulin-dependent protein kinase kinase-β and transforming growth factor-β-activated kinase-1, with T3-induced reactive oxygen species having a causal role due to its suppression by pretreatment with the antioxidant NAC. Accordingly, AMPK targets acetyl-CoA carboxylase and cyclic AMP response element binding protein are phosphorylated, with the concomitant carnitine palmitoyltransferase-1α (CPT-1α) activation and higher expression of peroxisome proliferator-activated receptor-γ co-activator-1α and that of the fatty acid oxidation (FAO)-related enzymes CPT-1α, acyl-CoA oxidase 1, and acyl-CoA thioesterase 2. Under these conditions, T3 induced a significant increase in the serum levels of β-hydroxybutyrate, a surrogate marker for hepatic FAO.

Conclusion: T3 administration activates liver AMPK signaling in a redox-dependent manner, leading to FAO enhancement as evidenced by the consequent ketogenic response, which may constitute a key molecular mechanism regulating energy dynamics to support T3 preconditioning against ischemia-reperfusion injury.

Keywords: AMP-activated protein kinase; Fatty acid oxidation; Liver; N-acetylcysteine; Thyroid hormone.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3-Hydroxybutyric Acid / blood
  • AMP-Activated Protein Kinases / genetics
  • AMP-Activated Protein Kinases / metabolism*
  • Animals
  • Antioxidants / pharmacology
  • Dinoprost / analogs & derivatives
  • Dinoprost / metabolism
  • Enzyme Activation
  • Fatty Acids / metabolism*
  • Gene Expression Regulation, Enzymologic
  • Injections, Intraperitoneal
  • Liver / drug effects*
  • Liver / enzymology
  • Male
  • Oxidation-Reduction
  • Phosphorylation
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction
  • Time Factors
  • Triiodothyronine / administration & dosage
  • Triiodothyronine / pharmacology*

Substances

  • Antioxidants
  • Fatty Acids
  • RNA, Messenger
  • Triiodothyronine
  • 8-epi-prostaglandin F2alpha
  • Dinoprost
  • AMP-Activated Protein Kinases
  • 3-Hydroxybutyric Acid