Summary
MATERIALS AND METHODSBaseline plasma osmolality (pOsm) and plasma arginiie vasopressin (pAVP) were measured in chronically catheterized fetal sheep. Mean baseline pAVP in fetuses from 101-120 days was 1.9 + 0.46 pU/ml (mean * SEM) with a pOsm of 293 rt 1.8 mOsm/kg. In fetuses of 121-141 days of gestation, mean pAVP was significantly lower, 0.77 0.19 pU/ml (P < 0.05), with a similar pOsm (293 2 1.9 mOsm/kg). The logarithmic baseline pAVP values were linearly correlated with pOsm for both groups. Hypertonic saline infusion resulted in a similar increase in the log pAVP corrected for the rise in pOsm in the 101-120-day fetuses and in 121-141-day fetuses. The slope of this response was similar to that of the steady state relationship. The data indicates that the fetal osmoreceptor system for control of arginine vasopressin secretion is fully functional in the last trimester of pregnancy.
SpeculationThe fetal hypothalamic posterior pituitary system appears to show a relatively heightened response to increases in plasma osmolality during the last trimester of gestation. This may reflect the heightened hypothalamic activity postulated to explain the high circulating growth hormone levels at this time. The higher baseline plasma vasopressin levels in the younger fetuses would support this view. Alternatively, the augmented responsiveness may represent an adaptive response to the immaturity of the fetal kidney with respect to free water clearance or an adaptive response to some extrarenal function of the hormone on salt and water homeostasis in utero.Vasopressin secretion is regulated by two systems of r e c e p tors: the osmoreceptors located in or near the supraoptic nuclei in the hypothalamus and a series of volume receptors, including left atrial stretch receptors and carotid sinus and aortic arch baroreceptors. Available information suggests that the newborn is capable of secreting vasopressin at birth and that both the osmoreceptor and volume control systems are functional (3-6). Data regarding fetal vasopressin physiology, however, are meager. Vasopressin has been identified in the human fetal pituitary at 10-12 weeks of gestation (9, 12) and in the fetal pituitary of other mammalian species, including the guinea pig, sheep, and seal, during the last half of gestation (1,2,10,12,14). In addition, in the sheep and monkey, significant concentrations of circulating vasopressin have been detectable in fetal blood during the last half of gestation (1, 1 l ) , and increases in circulating levels have been evoked either by osmolar or volume (hemorrhage) stimuli (1, 11). However, little is known about the sensitivity and relative responsiveness of the fetal osmoreceptor control system. The present studies were designed to provide this information.
5Pregnant Columbia or Columbia-Suffolk ewes were obtained from a local source and the gestational age based on the induced ovulation technique (7). The animals were maintained in the vivarium and fasted 4 8 hr before surgery. The pregnant ewes were anesthetized using a m...