Abstract

We have shown previously in dogs with right heart failure that the reduction of myocardial β-adrenoceptor density occurs only in the failing right ventricle, while cardiac inotropic responses to β-adrenergic stimulation are reduced in both the right and left ventricles. The purpose of the present study was to determine whether a post-receptor defect in the guanine nucleotide-binding regulatory proteins (G-proteins) existed which would explain, at least in part, the adrenergic subsensitivity in both ventricles of the heart failure dogs. Using both immunoblotting technique and the bacterial toxin-mediated ADP ribosylation assays, we found that the stimulatory G-protein (G s) was reduced in both ventricles of the heart failure dogs. In contrast, there were no changes in the inhibitory G-protein (G i). In addition, receptor subtype analysis showed that only β 1-adrenoceptors were reduced in the failing right ventricle of the heart failure animals. This study demonstrated that the reduction of β-adrenoceptors in right heart failure was chamber-specific whereas the reduction of G s was non-selective, occurring in both ventricles of right heart failure dogs. The findings further suggest that the reduction of G s probably was caused by systemic neurohormonal activation, independent of local ventricular stress.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.