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Adrenergic agents, but not triiodo-L-thyronine induce c-fos and c-myc expression in the rat heart.

AbstractWe have examined the expression of two nuclear-acting oncogenes, c-fos and c-myc in the rat heart following administration of hormones implicated in the development of cardiac hypertrophy. A single injection of norepinephrine (2.5 micrograms/kg to 2.5 mg/kg) led to transient increases in the levels of both c-fos and c-myc mRNA. The response was sequential: elevated levels of c-fos mRNA were first observed 15 min after treatment and peaked at 1 h whilst c-myc mRNA levels increased 30 min after treatment and peaked at 2 h. The response of both cellular oncogenes to norepinephrine was reduced significantly by alpha blockade but beta blockade was less effective. Administration of triiodo-L-thyronine (0.25 mg/kg), a level known to promote cardiac hypertrophy, did not produce elevated levels of c-fos or c-myc mRNA. In an initial study, it was possible to demonstrate induction of c-fos and c-myc in rat hearts perfused in vitro with medium containing 2 x 10(-7) M norepinephrine. These results provide support for the notion that c-fos and c-myc expression may play a transducing role in the development of adrenergic-mediated, but not thyroid hormone-mediated cardiac hypertrophy.
AuthorsR D Hannan, A K West (Affiliation: Department of Biochemistry, University of Tasmania, Australia.)
JournalBasic research in cardiology (Basic Res Cardiol) 1991 Mar-Apr Vol. 86 Issue 2 Pg. 154-64 ISSN: 0300-8428 GERMANY
PMID1908674 (Publication Type: In Vitro, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-myc
  • RNA, Messenger
  • Sympathomimetics
  • Triiodothyronine
Topics
  • Animals
  • Blotting, Northern
  • Gene Expression
  • Heart (drug effects)
  • Male
  • Myocardium (metabolism)
  • Perfusion
  • Proto-Oncogene Proteins (biosynthesis, genetics)
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-myc (biosynthesis, genetics)
  • Proto-Oncogenes
  • RNA, Messenger (biosynthesis)
  • Rats
  • Rats, Inbred Strains
  • Sympathomimetics (pharmacology)
  • Triiodothyronine (pharmacology)