Streamlining fluid pathways lessens flow energy dissipation: relevance to atriocavopulmonary connections.

Flow energy dissipation reduces cardiac efficiency, particularly in the Fontan-modified, single-ventricle heart. To provide insight into flow energetics relevant to Fontan-type anatomy, a simple, analytical description of fluid motion was employed. Mechanical energy balance and the force-momentum relationship were used to describe theoretical pressure changes and flow energy losses.

Pressure loss from flow energy dissipation: relevance to Fontan-type modifications.

Pressure loss from flow energy dissipation may impair cardiac performance when a heart with a single ventricle must support the circulation. Therefore, the goal of this study was to use a simple description of fluid motion to provide insight into flow energetics relevant to Fontan-type procedures. Our findings indicate that when either the cross-sectional area or the axial direction of flow changes "abruptly," disturbances are set up within the fluid that lead to dissipation of available energy.

Mechanical and metabolic characterization of ischemic contracture in the neonatal pig heart.

Isolated, paced, isovolumetrically beating piglet hearts (n = 37) underwent retrograde aortic perfusion with a crystalloid solution during three periods: 1) baseline (coronary perfusion pressure 60 mm Hg), 2) ischemia (coronary flow 10% of baseline for approximately 80 min), and 3) reperfusion (perfusion pressure returned to baseline). In one group of hearts, glycolysis (using 3H2O formation from [3H]glucose) was assessed. During baseline, peak systolic pressure (PSP) was 101.

Vasoactive intestinal peptide: electrophysiologic activity in the newborn heart.

We performed intracardiac electrophysiologic studies of the effects of vasoactive intestinal peptide (VIP, 0.125 micrograms/kg/min) on sinus and atrioventricular (AV) nodal function, intracardiac conduction, and myocardial refractoriness in two groups of neonatal dogs (aged 6-16 d). Group I consisted of eight neonates in whom VIP was administered after bilateral vagotomy and beta-blockade with propranolol.

Pituitary adenylate cyclase activating polypeptide: a neuropeptide with potent inotropic and coronary vasodilatory effects in neonatal pig hearts.

Cardiac effects of the neuropeptide pituitary adenylate cyclase activating polypeptide (PACAP) have not previously been reported. We investigated the influence of PACAP, vasoactive intestinal polypeptide (68% homology with PACAP) and the beta-adrenergic receptor agonist isoproterenol on contractile function and coronary vascular tone in isolated piglet hearts (1 to 5 d of age). Paced (180 beats/min) isovolumically beating hearts underwent retrograde aortic perfusion at constant coronary flow (approximately 3 mL.