Literature DB >> 1336712

Increase in functional activity rather than in amount of Gi-alpha in failing human heart with dilated cardiomyopathy.

L X Fu1, Q M Liang, F Waagstein, J Hoebeke, C Sylvén, E Jansson, P Sotonyi, A Hjalmarson.   

Abstract

OBJECTIVE: The aim was to investigate whether or not increased pertussis toxin catalysed ADP ribosylation correlates with increased amount of Gi-alpha in failing human heart.
DESIGN: Antisera raised against unique synthetic peptides corresponding to alpha subunits of Gs and Gi 1-3 were used in immunoblotting and ELISA to determine amounts of various G proteins. Adenylyl cyclase activity, beta adrenoceptors, and muscarinic receptors were then measured in cardiomyopathic hearts (n = 6) obtained at transplant in order to study whether or not an altered expression of G proteins has relevance to the integrity and function of the receptor--adenylyl cyclase system. Six non-failing control hearts were also studied.
RESULTS: No significant differences in the peptide equivalent amounts of either Gs or Gi were found in the failing human heart as compared to the non-failing heart. However, functional activity of Gi was shown to increase significantly since there was a decrease in basal (57%), isoprenaline stimulated (60%), and guanyliminodiphosphate stimulated (52%) adenylyl cyclase activity. In contrast the density of beta adrenoceptors was markedly decreased (51%) in failing human heart in comparison to non-failing hearts. Neither the density nor the affinity of muscarinic receptors changed in the failing human heart.
CONCLUSION: These results suggest that in the failing human heart, there is an increase in functional activity rather than in amount of Gi, and an important part of functional expression of Gi-alpha may be regulated at the post-translational level.

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Year:  1992        PMID: 1336712     DOI: 10.1093/cvr/26.10.950

Source DB:  PubMed          Journal:  Cardiovasc Res        ISSN: 0008-6363            Impact factor:   10.787


  5 in total

Review 1.  Functional M3 muscarinic acetylcholine receptors in mammalian hearts.

Authors:  Zhiguo Wang; Hong Shi; Huizhen Wang
Journal:  Br J Pharmacol       Date:  2004-05-17       Impact factor: 8.739

2.  Conditional expression of a Gi-coupled receptor causes ventricular conduction delay and a lethal cardiomyopathy.

Authors:  C H Redfern; M Y Degtyarev; A T Kwa; N Salomonis; N Cotte; T Nanevicz; N Fidelman; K Desai; K Vranizan; E K Lee; P Coward; N Shah; J A Warrington; G I Fishman; D Bernstein; A J Baker; B R Conklin
Journal:  Proc Natl Acad Sci U S A       Date:  2000-04-25       Impact factor: 11.205

3.  Effects of theophylline and dibutyryl-cAMP on adenosine receptors and heart rate in cultured cardiocytes.

Authors:  D el-Ani; K A Jacobson; A Shainberg
Journal:  J Basic Clin Physiol Pharmacol       Date:  1996

4.  Expression of a Gi-coupled receptor in the heart causes impaired Ca2+ handling, myofilament injury, and dilated cardiomyopathy.

Authors:  Diana T McCloskey; Sally Turcato; Guan-Ying Wang; Lynne Turnbull; Bo-Qing Zhu; Thomas Bambino; Anita P Nguyen; David H Lovett; Robert A Nissenson; Joel S Karliner; Anthony J Baker
Journal:  Am J Physiol Heart Circ Physiol       Date:  2007-10-26       Impact factor: 4.733

Review 5.  β-adrenergic receptor responsiveness in aging heart and clinical implications.

Authors:  Nicola Ferrara; Klara Komici; Graziamaria Corbi; Gennaro Pagano; Giuseppe Furgi; Carlo Rengo; Grazia D Femminella; Dario Leosco; Domenico Bonaduce
Journal:  Front Physiol       Date:  2014-01-09       Impact factor: 4.566

  5 in total

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