Ontogeny of cardiac β-adrenoceptor desensitization mechanisms: Agonist treatment enhances receptor/G-protein transduction rather than eliciting uncoupling

J. L. Zeiders, F. J. Seidler, G. Iaccarino, W. J. Koch, T. A. Slotkin

Research output: Contribution to journalArticle

43 Citations (Scopus)

Abstract

In the fetus and neonate, β-adrenoceptor stimulation fails to produce physiological desensitization. The current study explores the mechanisms underlying the response pattern in neonatal rats. Homologous cardiac β-adrenergic desensitization caused by isoproterenol treatment in vivo was demonstrable in adult rats by the immediate (2 h) and specific loss of the ability of isoproterenol, but not glucagon, to stimulate adenylyl cyclase in vitro. Homologous desensitization was absent when the same treatment was given to neonates. By 12 h post-treatment, the adults showed heterologous desensitization (loss of the response to glucagon), an effect which was once again absent in the immature rats. The absence of desensitization in neonates did not reflect a deficiency in the activity or subcellular distribution of βARK1, the enzyme that initiates the phosphorylation and consequent desensitization of β-adrenoceptors. On the other hand, neonates showed relatively poor receptor-G(S) transduction as assessed by the GTP-induced shift in receptor ligand binding. Repeated isoproterenol treatment of adult rats led to uncoupling of receptor-G-protein transduction but the same treatment in neonates enhanced transduction. Furthermore, neonatal sympathectomy with 6-OHDA interfered with the ontogenetic rise in β-adrenoceptor-G(S) interactions. These results indicate that the maintenance of agonist responses in the face of neonatal adrenergic stimulation does not reflect simply an absence of the ability to elicit homologous or heterologous desensitization but rather represents an active regulatory mechanism in which neural input exerts a positive trophic role at the level of G-protein function.

Original languageEnglish
Pages (from-to)413-423
Number of pages11
JournalJournal of Molecular and Cellular Cardiology
Volume31
Issue number2
DOIs
Publication statusPublished - Feb 1999

Fingerprint

GTP-Binding Proteins
Adrenergic Receptors
Isoproterenol
Glucagon
Adrenergic Agents
Sympathectomy
Oxidopamine
Guanosine Triphosphate
Adenylyl Cyclases
Fetus
Maintenance
Phosphorylation
Ligands
Enzymes

Keywords

  • β-Adrenoceptor
  • Adenylyl cyclase
  • Desensitization
  • Development of cardiac β-adrenoceptors and adenylyl cyclase
  • Heart, development of β-adrenoceptor signaling
  • Isoproterenol, effects on β-adrenoceptors and adenylyl cyclase

ASJC Scopus subject areas

  • Molecular Biology
  • Cardiology and Cardiovascular Medicine

Cite this

Ontogeny of cardiac β-adrenoceptor desensitization mechanisms : Agonist treatment enhances receptor/G-protein transduction rather than eliciting uncoupling. / Zeiders, J. L.; Seidler, F. J.; Iaccarino, G.; Koch, W. J.; Slotkin, T. A.

In: Journal of Molecular and Cellular Cardiology, Vol. 31, No. 2, 02.1999, p. 413-423.

Research output: Contribution to journalArticle

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