Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/198770
Type: Artigo de periódico
Title: Increased Spontaneous Activity And Reduced Inotropic Response To Catecholamines In Ventricular Myocytes From Footshock-stressed Rats.
Author: Penna, Larissa B
Bassani, Rosana A
Abstract: Exposure to stressors has been shown to change atrial responsiveness to catecholamines, but it is not clear yet how it affects the ventricular myocardium, which plays a major role in the catecholamine-stimulated increase in cardiac output. Adult male rats were submitted to restraint (RST) or footshock (FS) sessions for 3 days. Reactivity to agonists of the beta-adrenergic pathway was analyzed in left ventricular myocytes isolated from stressed and control rats (CTR). Whereas no significant changes were detected after RST, enhancement of catecholamine-induced spontaneous activity, accompanied by decrease in inotropic maximal response, was observed in myocytes from FS rats. Changes were reversed by beta(1)-, but not by alpha(1)-or beta(2)-adrenoceptor (AR) blockade. Similar alterations were seen in response to forskolin. However, responsiveness to 3-isobutyl-1-methylxanthine and CaCl(2) was comparable in control and FS groups. A significant negative correlation was observed between the maximally stimulated spontaneous activity rate and contraction amplitude. Results indicate that: (a) enhanced automatism during adrenergic stimulation of myocytes from FS rats is mediated by beta(1)-ARs and seems to involve post-receptor mechanisms, probably decreased cAMP degradation; (b) the exaggerated spontaneous activity, which may contribute to generation of catecholaminergic arrhythmias, might limit the development of the inotropic response.
Subject: 1-methyl-3-isobutylxanthine
Adrenergic Agents
Animals
Calcium
Dose-response Relationship, Drug
Electroshock
Isoproterenol
Male
Muscle Contraction
Myocardium
Myocytes, Cardiac
Norepinephrine
Phosphodiesterase Inhibitors
Prazosin
Random Allocation
Rats
Rats, Wistar
Receptors, Adrenergic, Alpha-1
Receptors, Adrenergic, Beta-1
Receptors, Adrenergic, Beta-2
Regression Analysis
Stress, Physiological
Rights: fechado
Identifier DOI: 10.3109/10253890902951778
Address: http://www.ncbi.nlm.nih.gov/pubmed/19697264
Date Issue: 2010
Appears in Collections:Unicamp - Artigos e Outros Documentos

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