O. Mizuno et al., Effects of therapeutic doses of human atrial natriuretic peptide on load and myocardial performance in patients with congestive heart failure, AM J CARD, 88(8), 2001, pp. 863-866
Citations number
28
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
The benefits of atrial natriuretic peptide (ANP) in patients with congestiv
e heart failure (CHF) have been demonstrated. However, the myocardial actio
ns of ANP remain unclear. Using relatively load-insensitive left ventricula
r pressure-volume analysis, the myocardial and load-altering actions of ANP
in patients with moderate CHF were studied. After obtaining steady-state d
ata using micromanometers and conductance catheters, ANP was infused in 9 p
atients with CHF at 0.01 and 0.1 mug/kg/ min for 30 minutes, respectively.
Hemodynamic variables, plasma ANP, and cyclic quanosine monophosphate (cGMP
) levels were determined before and 30 minutes after each ANP infusion. ANP
at 0.01 mug/kg/ min increased plasma ANP and cGMP levels from 73 +/- 34 to
139 +/- 34 pg/ml and from 4 +/- 1 to 8 +/- 2 pmol/ml, respectively. ANP in
fusion caused a significant decrease in end-systolic pressure without any c
hanges in heart rate. End-diastolic pressure was significantly decreased bu
t there was no significant change in left ventricular end-diastolic volume.
The time constant for isovolumetric relaxation was decreased. ANP infusion
at 0.1 mug/kg/min caused further decreases in end-systolic pressure, end-d
iastolic pressure and volume, and the time constant for isovolumetric relax
ation (p <0.05) without any changes in heart rate. The slope of the end-sys
tolic pressure-volume relation was increased from 1.3 +/- 0.2 to 1.6 +/- 0.
3 mm Hg/ml (p <0.05), indicating increased contractility. Plasma ANP and cG
MP levels were increased to 422 +/- 44 pg/ml and 16 +/- 3 pmol/ml, respecti
vely. Thus, ANP infusion increased cGMP generation, decreased afterload and
preload, and improved left ventricular systolic and diastolic function. (C
) 2001 by Excerpta Medica, Inc.