Developmental changes in adenylyl cyclase and GTP binding proteins in brown fat

Am J Physiol. 1991 Aug;261(2 Pt 2):R403-11. doi: 10.1152/ajpregu.1991.261.2.R403.

Abstract

During the perinatal period, norepinephrine (NE)-stimulated adenylyl cyclase activity increased in interscapular brown adipose tissue (IBAT) membranes and then declined to adult levels by 23 days postpartum. The developmental patterns of NE- and NaF-stimulated activities were identical, indicating that the developmental increase in transmitter-stimulated activity resulted from the increased interaction of alpha-subunit of guanine nucleotide-binding stimulatory protein of adenylyl cyclase (Gs alpha) with the catalytic subunit (C). This increased Gs alpha-C interaction was the result of an increase in Gs alpha specific activity, as assessed in cyc- reconstitution assays, as well as an increased C activity, as assessed by forskolin-Mn(2+)-stimulated adenylyl cyclase activity. Although adenylyl cyclase activity increased during the perinatal period, total Gs alpha levels significantly declined because of the loss of the small-molecular-mass form of Gs alpha. Thus the ratio of large to small form of Gs alpha increased threefold and might have contributed to the perinatal increase in activity. Gi alpha-like proteins, as assessed by pertussis toxin-catalyzed [32P]ADP ribosylation, declined dramatically after birth. However, this loss of Gi alpha did not contribute to developmental changes in adenylyl cyclase activity because pertussis toxin treatment failed to alter NE-stimulated activity. In contrast to G alpha subunits, there were no changes in membrane levels of G beta subunits.

Publication types

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

MeSH terms

  • Adenylyl Cyclases / metabolism*
  • Adipose Tissue, Brown / metabolism*
  • Animals
  • Animals, Newborn / growth & development
  • Animals, Newborn / metabolism*
  • Dose-Response Relationship, Drug
  • Embryonic and Fetal Development*
  • Fetus / metabolism*
  • Fetus / physiology
  • GTP-Binding Proteins / metabolism*
  • Immunochemistry
  • Isomerism
  • Isoproterenol / pharmacology
  • Lymphoma / metabolism
  • Norepinephrine / pharmacology
  • Osmolar Concentration
  • Rats
  • Tumor Cells, Cultured

Substances

  • GTP-Binding Proteins
  • Adenylyl Cyclases
  • Isoproterenol
  • Norepinephrine