Stimulation of human omental adipose tissue lipolysis by growth hormone plus dexamethasone

Mol Cell Endocrinol. 2008 Nov 25;295(1-2):101-5. doi: 10.1016/j.mce.2008.05.014. Epub 2008 Jul 21.

Abstract

Growth hormone [GH] administration results in a reduction in adiposity of humans that is attributed to stimulation of lipolysis. We examined the effect of direct addition of human GH, in both the absence and presence of dexamethasone [Dex], as well as that of interferon beta on lipolysis by omental adipose tissue explants from obese women incubated for 48h in primary culture. There was a significant stimulation of lipolysis by GH in the presence of Dex but not by Dex or GH alone. There was also a significant further stimulation by GH in the presence of Dex of hormone-sensitive lipase, perilipin, lipoprotein lipase and beta1 adrenergic receptor mRNA. We conclude that the direct lipolytic effect of GH is accompanied by an increase in HSL mRNA in the presence of DEX, but GH also increased the mRNAs for other proteins that could explain all or part of its lipolytic action.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carrier Proteins
  • Dexamethasone / pharmacology*
  • Female
  • Glucocorticoids / pharmacology*
  • Human Growth Hormone / metabolism*
  • Humans
  • Interferon-beta / metabolism
  • Intra-Abdominal Fat / drug effects*
  • Intra-Abdominal Fat / enzymology
  • Intra-Abdominal Fat / metabolism
  • Lipase / genetics
  • Lipase / metabolism
  • Lipolysis / drug effects*
  • Obesity, Morbid / enzymology
  • Obesity, Morbid / metabolism*
  • Omentum
  • Perilipin-1
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism
  • RNA, Messenger / metabolism
  • Receptors, Adrenergic, beta-1 / genetics
  • Receptors, Adrenergic, beta-1 / metabolism
  • Sterol Esterase / genetics
  • Sterol Esterase / metabolism
  • Time Factors
  • Tissue Culture Techniques

Substances

  • Carrier Proteins
  • Glucocorticoids
  • Perilipin-1
  • Phosphoproteins
  • RNA, Messenger
  • Receptors, Adrenergic, beta-1
  • Human Growth Hormone
  • Interferon-beta
  • Dexamethasone
  • Sterol Esterase
  • Lipase
  • PNPLA2 protein, human