Apparent absence of alpha-2 adrenergic receptors from hamster brown adipocytes

Life Sci. 1982 Apr 5;30(14):1185-92. doi: 10.1016/0024-3205(82)90661-0.

Abstract

The possible presence of alpha adrenergic control of lipolysis and cyclic AMP production in brown adipocytes of hamsters was studied in adipocytes isolated from interscapular, subscapular, cervical and axillary regions of normal male hamsters maintained at 25 degrees C. Lipolysis activated by either 3-isobutyl-l-methyl xanthine or isoproterenol was unaffected by the presence of the alpha adrenergic selective agonists clonidine and methoxamine. Similarly, accumulation of cyclic AMP in response to beta-receptor stimulation, alone or in combination with a methyl xanthine, was unaffected by clonidine or methoxamine. In contrast, both lipolysis and cyclic AMP accumulation in brown fat cells were effectively suppressed in the presence of nicotinic acid, prostaglandin E1 or N6-phenylisopropyl adenosine. Accumulation of cyclic AMP in response to the mixed agonist norepinephrine was not influenced when cells were exposed to the alpha adrenergic blocking drugs yohimbine or tolazoline. These observations suggest that alpha-2 adrenergic receptors which are present on hamster white fat cells and control production of cyclic AMP and lipolysis are absent from hamster brown adipocytes. On the other hand, brown fat cells of this species appear to respond to a number of other inhibitory compounds in a manner not markedly different from that of white adipocytes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adipose Tissue, Brown / metabolism*
  • Animals
  • Clonidine / pharmacology
  • Cricetinae
  • Cyclic AMP / metabolism*
  • Dose-Response Relationship, Drug
  • Isoproterenol / pharmacology
  • Lipolysis / drug effects*
  • Mesocricetus / metabolism
  • Methoxamine / pharmacology
  • Niacin
  • Nicotinic Acids / pharmacology
  • Phentolamine / pharmacology
  • Receptors, Adrenergic / metabolism*
  • Receptors, Adrenergic, alpha / metabolism*

Substances

  • Nicotinic Acids
  • Receptors, Adrenergic
  • Receptors, Adrenergic, alpha
  • Niacin
  • Cyclic AMP
  • Methoxamine
  • Isoproterenol
  • Clonidine
  • Phentolamine