z-logo
Premium
Adrenergic regulation of cardiac myocyte apoptosis
Author(s) -
Singh Krishna,
Xiao Lei,
Remondino Andrea,
Sawyer Douglas B.,
Colucci Wilson S.
Publication year - 2001
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.10024
Subject(s) - myocyte , cardiac myocyte , medicine , endocrinology , apoptosis , adrenergic receptor , biology , muscle hypertrophy , stimulation , signal transduction , microbiology and biotechnology , adrenergic , receptor , mapk/erk pathway , biochemistry
Abstract The direct effects of catecholamines on cardiac myocytes may contribute to both normal physiologic adaptation and pathologic remodeling, and may be associated with cellular hypertrophy, apoptosis, and alterations in contractile function. Norepinephrine (NE) signals via α‐ and β‐adrenergic receptors (AR) that are coupled to G‐proteins. Pharmacologic studies of cardiac myocytes in vitro demonstrate that stimulation of β 1 ‐AR induces apoptosis which is cAMP‐dependent and involves the voltage‐dependent calcium influx channel. In contrast, stimulation of β 2 ‐AR exerts an anti‐apoptotic effect which appears to be mediated by a pertussis toxin‐sensitive G protein. Stimulation of α 1 ‐AR causes myocyte hypertrophy and may exert an anti‐apoptotic action. In transgenic mice, myocardial overexpression of either β 1 ‐AR or Gαs is associated with myocyte apoptosis and the development of dilated cardiomyopathy. Myocardial overexpression of β 2 ‐AR at low levels results in improved cardiac function, whereas expression at high levels leads to dilated cardiomyopathy. Overexpression of wildtype α 1B ‐AR does not result in apoptosis, whereas overexpression of Gαq results in myocyte hypertrophy and/or apoptosis depending on the level of expression. Differential activation of the members of the mitogen‐activated protein kinase (MAPK) superfamily and production of reactive oxygen species appear to play a key role in mediating the actions of adrenergic pathways on myocyte apoptosis and hypertrophy. This review summarizes current knowledge about the molecular and cellular mechanisms involved in the regulation of cardiac myocyte apoptosis via stimulation of adrenergic receptors and their coupled effector pathways. © 2001 Wiley‐Liss, Inc.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here