Glucocorticoids modulate human brown adipose tissue thermogenesis in vivo

Metabolism. 2017 May:70:125-132. doi: 10.1016/j.metabol.2017.01.024. Epub 2017 Jan 19.

Abstract

Introduction: Brown adipose tissue (BAT) is a thermogenic organ with substantial metabolic capacity and has important roles in the maintenance of body weight and metabolism. Regulation of BAT is primarily mediated through the β-adrenoceptor (β-AR) pathway. The in vivo endocrine regulation of this pathway in humans is unknown. The objective of our study was to assess the in vivo BAT temperature responses to acute glucocorticoid administration.

Methods: We studied 8 healthy male volunteers, not pre-selected for BAT presence or activity and without prior BAT cold-activation, on two occasions, following an infusion with hydrocortisone (0.2mg.kg-1.min-1 for 14h) and saline, respectively. Infusions were given in a randomized double-blind order. They underwent assessment of supraclavicular BAT temperature using infrared thermography following a mixed meal, and during β-AR stimulation with isoprenaline (25ng.kg fat-free mass-1.min-1 for 60min) in the fasting state.

Results: During hydrocortisone infusion, BAT temperature increased both under fasting basal conditions and during β-AR stimulation. We observed a BAT temperature threshold, which was not exceeded despite maximal β-AR activation. We conclude that BAT thermogenesis is present in humans under near-normal conditions. Glucocorticoids modulate BAT function, representing important physiological endocrine regulation of body temperature at times of acute stress.

Keywords: Beta adrenoceptor; Brown adipose tissue; Glucocorticoids; Humans; Infrared thermography.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adipose Tissue, Brown / physiology*
  • Adolescent
  • Adult
  • Animals
  • Body Temperature / drug effects
  • Double-Blind Method
  • Glucocorticoids / administration & dosage*
  • Glucocorticoids / physiology
  • Humans
  • Isoproterenol / pharmacology
  • Male
  • Receptors, Adrenergic, beta / drug effects
  • Receptors, Adrenergic, beta / metabolism
  • Thermogenesis / drug effects*
  • Thermography
  • Young Adult

Substances

  • Glucocorticoids
  • Receptors, Adrenergic, beta
  • Isoproterenol