Up-regulation of uncoupling proteins by beta-adrenergic stimulation in L6 myotubes

FEBS Lett. 2001 Apr 13;494(3):175-80. doi: 10.1016/s0014-5793(01)02341-9.

Abstract

Catecholamine-induced and beta-adrenergic receptor (beta-AR)-mediated thermogenesis in skeletal muscle is a significant component of whole-body energy expenditure. Skeletal muscle expresses uncoupling protein (UCP) 2 and UCP3, which can dissipate the transmitochondrial electrochemical gradient and thereby may be involved in regulation of energy metabolism. We investigated the effects of beta-AR stimulation on UCP2 and UCP3 expression in L6 myotubes. Stimulation of the cells with epinephrine increased the UCP3 mRNA level transiently at 6 h, and also the UCP2 mRNA level at 6-24 h. The stimulatory effects of epinephrine were also observed in the presence of carbacyclin and 9-cis retinoic acid, and mimicked by isoproterenol and salbutamol (beta2-AR agonists), but abolished by propranolol and ICI-118,551 (beta2-AR antagonists). Pharmacological and mRNA analyses revealed the existence of beta2-AR, but not beta1- and beta3-ARs, in L6 myotubes. These results suggested that catecholamines up-regulate UCP2 and UCP3 expression through direct action on the beta2-AR in skeletal muscle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Agonists / pharmacology*
  • Adrenergic beta-Antagonists / pharmacology
  • Albuterol / pharmacology
  • Alitretinoin
  • Animals
  • Carrier Proteins / genetics*
  • Cell Line
  • Cyclic AMP / metabolism
  • Energy Metabolism
  • Epinephrine / pharmacology
  • Epoprostenol / analogs & derivatives
  • Epoprostenol / pharmacology
  • Ion Channels
  • Isoproterenol / pharmacology
  • Membrane Transport Proteins*
  • Mitochondrial Proteins*
  • Muscle, Skeletal / cytology
  • Muscle, Skeletal / drug effects*
  • Muscle, Skeletal / metabolism
  • Propanolamines / pharmacology
  • Propranolol / pharmacology
  • Proteins / genetics*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Receptors, Adrenergic, beta / genetics
  • Receptors, Adrenergic, beta / metabolism*
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Receptors, Retinoic Acid / metabolism
  • Retinoid X Receptors
  • Time Factors
  • Transcription Factors / metabolism
  • Tretinoin / pharmacology
  • Uncoupling Protein 2
  • Uncoupling Protein 3
  • Up-Regulation / drug effects*

Substances

  • Adrenergic beta-Agonists
  • Adrenergic beta-Antagonists
  • Carrier Proteins
  • Ion Channels
  • Membrane Transport Proteins
  • Mitochondrial Proteins
  • Propanolamines
  • Proteins
  • RNA, Messenger
  • Receptors, Adrenergic, beta
  • Receptors, Cytoplasmic and Nuclear
  • Receptors, Retinoic Acid
  • Retinoid X Receptors
  • Transcription Factors
  • Ucp2 protein, rat
  • Ucp3 protein, rat
  • Uncoupling Protein 2
  • Uncoupling Protein 3
  • Alitretinoin
  • ICI 118551
  • Tretinoin
  • carboprostacyclin
  • Propranolol
  • Epoprostenol
  • Cyclic AMP
  • Isoproterenol
  • Albuterol
  • Epinephrine