Literature DB >> 7946893

The molecular basis of myocardial hypertrophy.

P L Puri1, G Natoli, M L Avantaggiati, C Balsano, P De Marzio, M Levrero.   

Abstract

Myocardial hypertrophy is an adaptive response of the heart to several pathological situations aimed at maintaining adequate cardiac contractile function. This process is characterized by complex qualitative and quantitative changes of both cardiomyocytes and nonmyocyte cardiac cells. The initial stimulus inducing these cellular responses is parietal stretch subsequent to either a pressure or volume overload. Many substances locally produced and acting in a paracrine-autocrine fashion are involved in the response to stretch by cardiac cells. The stretch, and, similarly, various growth factors (i.e. angiotensin II. endothelins, transforming growth factor beta, fibroblast growth factors), are able to modulate the expression of several protooncogenes in the cells of the myocardium, and these events are linked to the development of cardiac hypertrophy. Major goals of future research will include the detection of the molecular mechanisms enabling the cardiomyocyte, a terminally differentiated muscle cell, to respond to a mitogenic stimulus with hypertrophic rather than hyperplastic growth, as well as the identification of drugs able to block the evolution of hypertrophy to heart failure.

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Year:  1994        PMID: 7946893

Source DB:  PubMed          Journal:  Ann Ital Med Int        ISSN: 0393-9340


  3 in total

Review 1.  The heart: mostly postmitotic or mostly premitotic? Myocyte cell cycle, senescence, and quiescence.

Authors:  Sailay Siddiqi; Mark A Sussman
Journal:  Can J Cardiol       Date:  2014-08-23       Impact factor: 5.223

2.  The role of angiotensin II, endothelin-1 and transforming growth factor-beta as autocrine/paracrine mediators of stretch-induced cardiomyocyte hypertrophy.

Authors:  A J van Wamel; C Ruwhof; L E van der Valk-Kokshoom; P I Schrier; A van der Laarse
Journal:  Mol Cell Biochem       Date:  2001-02       Impact factor: 3.396

3.  Thyroid Hormone Increases TGF-beta1 in Cardiomyocytes Cultures Independently of Angiotensin II Type 1 and Type 2 Receptors.

Authors:  Gabriela Placoná Diniz; Marcela Sorelli Carneiro-Ramos; Maria Luiza Morais Barreto-Chaves
Journal:  Int J Endocrinol       Date:  2010-06-02       Impact factor: 3.257

  3 in total

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