Interscapular brown adipose tissue metabolic reprogramming during cold acclimation: Interplay of HIF-1α and AMPKα

Biochim Biophys Acta. 2011 Dec;1810(12):1252-61. doi: 10.1016/j.bbagen.2011.09.007. Epub 2011 Sep 16.

Abstract

Background: Brown adipose tissue thermogenic program includes complex molecular and structural changes. However, energetic aspects of this process are poorly depicted.

Methods: We investigated time-dependent reprogramming of interscapular brown adipose tissue (IBAT) energy metabolism during cold-acclimation, as well as the effects of nitric oxide (()NO) on those changes. Rats were exposed to cold (4±1°C) for periods of 1, 3, 7, 12, 21, and 45days, and divided into three groups: control, treated with L-arginine, and treated with N(ω)-nitro-L-arginine methyl ester (L-NAME).

Results: In the early phase of cold-acclimation (up to 7days), the protein levels of all metabolic parameters and oxidative phosphorylation components were below the control. However, metabolic parameters and respiratory chain components entered a new homeostatic level in the late phase of cold-acclimation. These changes were accompanied with increased protein levels of phospho-AMP-dependent protein kinase-α (phospho-AMPKα) on the first day of cold-acclimation, and hypoxia-inducible factor-1α (HIF-1α) throughout early cold-acclimation. L-arginine positively affected protein expression of enzymes involved in glucose metabolism and β-oxidation of fatty acids in the early phase of cold-acclimation, and oxidative phosphorylation components throughout cold-acclimation. In contrast, L-NAME had the opposite effects.

Conclusion: Results suggest that IBAT structural remodeling is followed by energy metabolism reprogramming, which control might be orchestrated by the action of AMPKα and HIF-1α. Data also indicated the involvement of L-arginine-()NO in the regulation of IBAT metabolism.

General significance: Results obtained in this study might be of great importance for elucidating regulatory pathways governing energy metabolism in both physiological and pathophysiological states.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases / metabolism*
  • Adaptation, Physiological*
  • Adipose Tissue, Brown / metabolism*
  • Animals
  • Blotting, Western
  • Citric Acid Cycle
  • Cold Temperature*
  • Electron Transport
  • Electrophoresis, Polyacrylamide Gel
  • Glucose / metabolism
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism*
  • Male
  • Microscopy, Electron
  • Oxidative Phosphorylation
  • Rats

Substances

  • Hif1a protein, rat
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • AMP-Activated Protein Kinases
  • PRKAA1 protein, human
  • Glucose