24-HOUR PATTERN OF ATRIAL-NATRIURETIC-PEPTIDE IN HEART-TRANSPLANTATION - EVIDENCE FOR LACK OF CIRCADIAN-RHYTHM - TEMPORAL INTERRELATIONSHIPS WITH PLASMA-RENIN ACTIVITY, ALDOSTERONE AND CORTISOL

Citation
P. Cugini et al., 24-HOUR PATTERN OF ATRIAL-NATRIURETIC-PEPTIDE IN HEART-TRANSPLANTATION - EVIDENCE FOR LACK OF CIRCADIAN-RHYTHM - TEMPORAL INTERRELATIONSHIPS WITH PLASMA-RENIN ACTIVITY, ALDOSTERONE AND CORTISOL, International journal of cardiology, 42(1), 1993, pp. 7-14
Citations number
59
Categorie Soggetti
Cardiac & Cardiovascular System
ISSN journal
01675273
Volume
42
Issue
1
Year of publication
1993
Pages
7 - 14
Database
ISI
SICI code
0167-5273(1993)42:1<7:2POAIH>2.0.ZU;2-M
Abstract
We have investigated the circadian rhythm of plasma atrial natriuretic peptide in 13 stable output heart transplanted patients, all without evidence of histological rejection and cardiac impairment, following a ntirejection therapy with Cyclosporine, Azathioprine and Prednisone. T he 24-h pattern of plasma renin activity, plasma aldosterone and plasm a cortisol has been studied as well. All the investigated variables we re assayed six times over the 24-h span. The circadian time-qualified data were analyzed by ANOVA and Cosinor method. The 24-h mean levels o f atrial natriuretic peptide, plasma renin activity and plasma aldoste rone are significantly increased, while the concentrations of plasma c ortisol are reduced in the heart transplanted recipients. ANOVA detect ed a significant within-day variability of all these humoral variables only in healthy subjects. A statistically significant circadian rhyth m was validated by Cosinor procedure for all the investigated molecule s in healthy subjects but not in heart transplanted patients. In our o pinion, the increase of atrial natriuretic peptide is a counterregulat ory mechanism aimed to compensate the cyclosporine-mediated activation of the renin-angiotensin-aldosterone system. The disappearance of the plasma renin activity, aldosterone and atrial natriuretic peptide cir cadian rhythm can be ascribed to the constant activation of the renin- angiotensin-aldosterone system. The hypocortisolism is due, in our opi nion, both to glucocorticoid therapy and increase of plasma ANP concen tration.