C. Soderman et al., EFFECT OF VASOACTIVE INTESTINAL POLYPEPTIDE (VIP) ON PULMONARY VENTILATION-PERFUSION RELATIONSHIPS AND CENTRAL HEMODYNAMICS IN HEALTHY-SUBJECTS, Clinical physiology, 13(6), 1993, pp. 677-685
Ventilation-perfusion relationships of the lung (VA/Q) and central hae
modynamics were studied in nine healthy subjects before and during 30
min of vasoactive intestinal polypeptide (VIP) infusion (20 ng kg.min-
1). During the infusion, arterial concentrations of VIP rose from 16.1
+/- 6.1 to 420 +/- 110 pmol l-1 and noradrenaline concentrations doub
led (P < 0.01). VA/Q distributions, determined by inert gas eliminatio
n technique, were significantly shifted to lower values for VA/Q with
slight increases in dispersions, but arterial oxygen tension remained
unchanged. Heart rate, stroke volume and cardiac output rose 27, 44 an
d 80% respectively (P < 0.01). Systematic arterial pressure stabilized
at a slightly lower level compared to basal (base line: 93 +/- 5 mmHg
, VIP: 88 +/- 6 mmHg, P < 0.05). Right atrial and pulmonary capillary
wedge pressures remained unchanged during VIP infusion, while pulmonar
y vascular resistance and systematic vascular resistance decreased sig
nificantly, by 25% (P < 0.03) and 53% (P < 0.01), respectively. It is
concluded that VIP causes: (1) alterations in ventilation-perfusion di
stributions, but generates no shunt and does not cause hypoxaemia duri
ng 30 min infusion, (2) reduction of pulmonary and systemic vascular r
esistances and afterload reduction of the left ventricle, (3) reflex s
ympathoadrenal stimulation with increasing heart rate and myocardial c
ontractility, and (4) a direct positive inotropic effect on the myocar
dium.