Decreased adenylate cyclase activity and expression of G(sα) in human myocardium after orthotopic cardiac transplantation

E. Loh, J. V. Barnett, A. M. Feldman, G. S. Couper, D. E. Vatner, W. S. Colucci, J. B. Galper

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

We studied several aspects of guanine nucleotide stimulated adenylate cyclase function in patients after orthotopic cardiac transplantation. In 28 patients, adenylate cyclase activity was measured in endomyocardial biopsy samples obtained just before and at monthly intervals after cardiac transplantation. In biopsies obtained ≥6 months after transplantation, basal adenylate cyclase activity was decreased by 67% (n=12; P<.05), GTPγS- stimulated adenylate cyclase activity was decreased by 78% (n=12; P<.05), Mn+2+ forskolin-stimulated adenylate cyclase activity was decreased by 80% (n=8; P<.05), and Mn+2-stimulated adenylate cyclase activity (a measure of activity of the catalytic subunit of adenylate cyclase) was decreased by 83% (n=8, P<.05). Western blot analysis demonstrated that 6 months after cardiac transplantation, the level of G(sα) protein was decreased by 61 ± 12% (n=8; P<.001). There was no change in the level of G(iα) as assessed by pertussis toxin-catalyzed ADP-ribosylation (n=4; P=NS). With the use of the quantitative polymerase chain reaction, a 50±10% (n=6; P<.001) reduction in the steady-state level of G(sα) mRNA was observed. There was no change in the level of mRNA for G(i-3α). Thus, after orthotopic cardiac transplantation in humans, guanine nucleotide-stimulated adenylate cyclase activity is decreased in parallel with decreased levels of G(sα) protein and mRNA.

Original languageEnglish (US)
Pages (from-to)852-860
Number of pages9
JournalCirculation research
Volume76
Issue number5
DOIs
StatePublished - 1995

All Science Journal Classification (ASJC) codes

  • Physiology
  • Cardiology and Cardiovascular Medicine

Keywords

  • adenylate cyclase
  • cardiac transplantation
  • guanine nucleotide regulatory proteins

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