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Intravascular catheterization of the uterine and umbilical vessels, which was first developed for use chronically in ruminants (Meschia, Cotter, Breathnach & Barron, 1965) has been used in the present acute experiments on pregnant sows (75 to 110 days' gestation). The animals were anaesthetized with sodium pentobarbitone. Vinyl catheters, filled with heparin-saline, were placed in the maternal aorta, vena cava and the uterine veins of each horn. Similar catheters were also inserted into the umbilical artery and vein through placental branches without exposure of either the cord or foetus. The P o2 , P co2 and pH of both the foetal and maternal blood were recorded during each experiment which from the induction of anaesthesia to the final sample usually lasted 5–6 h. In some animals uterine and umbilical blood flows were estimated by the diffusion—equilibrium method of Crenshaw, Huckabee, Curet, Mann & Barron (1968).
Plasma samples were separated immediately and
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Insulin secretion and the factors influencing β-cell function were investigated in the chronically catheterized fetal foal and mare during the second half of gestation. The response of the fetal β cells to exogenous glucose was also examined. The mean concentration of insulin in the fetal foal was 7·5 ± 0·5 (s.e.m.) μu./ml (n = 20) which was significantly less than the corresponding maternal value of 49·0 ± 5·0μu./ml (n = 20, P<0·01). The insulin concentration in non-pregnant horses was 24·5 ± 1·5 μu./ml (n = 5) which was significantly less than the value in the pregnant animals (P<0·01). However, there was no significant difference in the mean glucose concentration between the groups of adult animals.
The insulin concentration was related to the endogenous glucose level in both adult and fetal horses. Wide variation in the maternal insulin concentration was observed above a glucose concentration of about 5·0 mmol/l. The mean concentration of insulin in pregnant mares decreased with increasing gestational age while the mean glucose concentration remained unaltered throughout the second half of gestation. There was no change in the basal concentrations of insulin or glucose in the fetus with gestational age although the fetal β-cell response to exogenous glucose appeared to increase with increasing fetal age after 270 days of gestation (term 330 days). There was a significant arterio-venous difference in the concentration of insulin across the gravid uterus in the mare when the arterial insulin level was greater than 30 μu./ml. Below this value, there was no consistent uptake of insulin by the uterus. The observations are discussed in relation to the regulation of insulin release in utero and the effects of pregnancy on maternal β-cell function.
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Abstract
Continuous infusion of cortisol into adrenalectomized fetal sheep during the last 72 h of gestation (term=145 ± 2 days) produced a significant (P<0·05) rise in fetal serum tri-iodothyronine (T3) mean ± s.e.m. concentrations from 398 ± 65 to 1340 ± 238 ng/l. A concurrent decrease in plasma thyroxine (T4) levels was observed in three out of four animals. No significant changes in the concentrations of either hormone were noted prior to the start of cortisol infusion. The plasma concentrations of cortisol, T3 and T4 at term were similar to those in untreated full-term lambs. Adrenalectomized fetuses not given cortisol infusions still had low levels of T3 at term, with no increase being observed. The results suggest that cortisol plays an important role in the increase of fetal plasma T3 observed towards the end of gestation. This is probably achieved by the stimulation of the monodeiodination of T4 to T3 in the peripheral tissues.
Journal of Endocrinology (1994) 140, 79–83
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SUMMARY
The concentrations of 13,14-dihydro-15-oxo-prostaglandin F (PGFM), the stable metabolite of prostaglandin F, were measured in the plasma of catheterized mares and foetuses and non-catheterized thoroughbred mares and ponies during the last months of gestation. The plasma concentration of PGFM increased gradually towards term in all groups of animals. During the operation for insertion of catheters, maternal and foetal concentrations of PGFM were high, but the values fell to basal levels 24–48 h after the operation. It was found that preoperative starvation (24 h) led to a rise in the concentration oef PGFM in th maternal plasma. The raised concentrations of PGFM during the operation were associated with low progestogen and high oestrogen concentrations in umbilical venous plasma. The subsequent survival period of the catheterized foal was inversely related to the maximum concentration of PGFM attained during the operation.
Changes in the plasma concentration of PGFM were studied during normal parturition in thoroughbred mares, during oxytocin-induced delivery in non-catheterized ponies and during premature delivery or abortion in the catheterized animals. The greatest increase in the concentration of PGFM was seen in the thoroughbred animals during second-stage labour; oxytocin also resulted in a very rapid rise in the level of PGFM, which remained high until delivery. In the catheterized animals, the birth of live foetuses was associated with a rise in the concentration of PGFM in both foetal and maternal plasma during the last 2 h before delivery. Less consistent changes were found during abortion.