Volume 2, Issue 5 , Pages 318-325, September 2008
Oxytocin revisited: It is also a cardiovascular hormone
Abstract
Oxytocin (OT), traditionally associated with reproductive functions, was revisited recently, which revealed several new functions of the hormone in cardiovascular regulation. To support this contention, we have demonstrated the presence and synthesis of OT receptors in all heart compartments and the vasculature. The functionality of these receptors has been established by the ability of OT to induce atrial natriuretic peptide and nitric oxide (NO) release from the perfused heart and atrial slices. OT's cardiovascular actions include natriuresis, blood pressure reduction, negative inotropic and chronotropic effects, parasympathetic neuromodulation, as well as vasodilatation triggered by the NO pathway that is also involved in endothelial cell growth and anti-inflammatory activity. In addition, we have reported the abundance of the OT system in the early developing heart and OT's capacity to generate cardiomyocytes from mouse embryonic stem cells. The most potent inducer of cardiac differentiation, OT-Gly-Lys-Arg, is an extended form of OT that is abundantly expressed in the fetal heart. Therefore, in pathological conditions, OT plays an anti-inflammatory and cardioprotective role, improving vascular and metabolic functions; it has potential for therapeutic use.
Keywords: Nitric oxide, natriuretic peptides, heart, cardiomyogenesis
To access this article, please choose from the options below
This work was supported by the Canadian Institute of Health Research (CIHR, MOP-53217) and the Canadian Heart and Stroke Foundation (CHSF, NET Program) as Grants to Drs. Gutkowska and Jankowski. Lecture presented In Memoriam to Professor S.M. McCann at the International Symposium on Vasoactive Peptides, Ouro Preto, Brazil, February 14 to 16, 2008.
Conflict of interest: none.
PII: S1933-1711(08)00049-1
doi:10.1016/j.jash.2008.04.004
© 2008 American Society of Hypertension. Published by Elsevier Inc. All rights reserved.
Volume 2, Issue 5 , Pages 318-325, September 2008
