D.A. Nixon
Imperial College London
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Featured researches published by D.A. Nixon.
Neonatology | 1974
Pauline Alexander; H.G. Britton; Mary L. Forsling; D.A. Nixon; J.G. Ratcliffe
Fetal haemorrhage in exteriorized fetuses of 90 to 143 days conceptual age caused marked increases in fetal plasma ACTH and AVP with maximal values for ACTH at about 40% blood loss and maximal values
Neonatology | 1983
V. Rubio; C.B. Tan; W.H.H. † Andrews; D.A. Nixon; D.P. Alexander; H.G. Button
Ammonium ions added in large quantity disappear rapidly from the reservoir of the sheep placenta perfused in situ through the umbilical vessels. Ammonium ions are removed from the reservoir of perfused sheep fetal livers of 108-141 days of conceptual age at a rate of at least 1 mumol/min/g liver. The majority appears as urea. There is little or no change in glutamine concentration. Hepatic carbamoylphosphate synthetase I, ornithine transcarbamylase, argininosuccinate synthetase, argininosuccinase and arginase are present, even at 97 days of conceptual age, in adequate amounts to account for the observed urea production. With the exception of arginase, all levels rise with fetal age. The levels in the maternal liver are comparable with those at 106 days of conceptual age. Arginase is high in the younger fetuses, falls progressively with fetal age and is very low in the mother. It is concluded that (a) the perfused placenta is permeable to ammonia and the placenta may be able to clear ammonia from the fetal circulation at a rate comparable with that of fetal liver; (b) the fetal liver converts ammonia to urea at a rate comparable with the urea production of the fetus; (c) there is virtually no glutamine production by the fetal liver; (d) adequate amounts of the enzymes of urea synthesis are present even in the immature fetal liver to account for the total urea production of the fetus, and (e) the anomalously low arginase level in the maternal liver may conserve maternal arginine, and the high levels in the younger fetuses may be related to fetal polyamine production from maternally derived arginine.
Neonatology | 1973
D.P. Alexander; H.G. Britton; D.A. Nixon; J.G. Ratcliffe; David Redstone
Plasma from six chronically catheterised sheep fetuses of 113–126 days conceptual age showed high levels of corticotrophin at all ages with somewhat higher values towards term. Plasma cortisol was not clearly related to corticotrophin in individual samples but was highly correlated in the pooled data. Short bouts of hypoxia (5–10 min 10% O2 in N2 to the mother) produced no significant change in either corticotrophin or cortisol although small transient changes in PO2 and lactate occurred. The high levels of corticotrophin suggest that the possibility of stress in the chronically catheterised preparation must be considered.
Neonatology | 1973
Pauline Alexander; R. Assan; H.G. Britton; D.A. Nixon
The permeability of the placenta to glucagon was studied in sheep of gestational ages of 99–143 days. Administration of large doses of glucagon to the mother was associated with little or no change in
Neonatology | 1973
D.P. Alexander; H.G. Britton; N.M. Cohen; D.A. Nixon; R.A. Parker
The effect on plasma insulin of elevating plasma glucose levels was studied in exteriorized sheep fetuses of 68 to 142 days conceptual age and in 2 lambs, 1 and 7 days old. Fetuses of less than 110 da
Neonatology | 1978
Enid Fenton; K.G. Britton; D.A. Nixon
In situ placental perfusion has been used to study the role of the sheep placenta in fetal citrate metabolism. The perfusate citrate concentrations rose steadily to values higher than in fetal plasma. This rise was not influenced by intravenous administration of citrate to the ewe. Concentration and electropotential gradients indicate that transplacental passage is unlikely and the rise is probably due to placental synthesis. However, the quantity of citrate supplied to the fetus was calculated to be small compared with the fetal metabolic rate. Comparison with the guinea pig shows close similarity in fetal plasma concentrations and the amount of citrate formed per unit weight of fetus.
Neonatology | 1976
Enid Fenton; H.G. Britton; D.A. Nixon
The role of the guinea pig placenta in fetal citrate metabolism has been studied by perfusing the placenta in situ. The initial citrate concentrations in the perfusate plasma were lower than in the maternal plasma but rose progressively until, in some cases, they exceeded those in the mother. The rise was uninfluenced by intravenous administration of citrate to the mother. Citrate therefore does not enter the perfusate by simple diffusion from the maternal compartment. It may be synthesised within the placenta. From the rate of accumulation of citrate in the perfusate, the supply to the fetus was calculated to be small compared to the fetal metabolic rate. Citrate added to the perfusate became distributed in a space similar to the extracellular space and no change occurred in maternal citrate concentrations. Thus, the placenta does not appear to metabolise citrate or allow transport to the mother.
Neonatology | 1974
Enid Fenton; D.A. Nixon
The mean concentration of citric acid in male and non-pregnant female adult guinea pig plasma was 0.308 ± 0.042 mM. Pregnant females with fetuses of 49–69 days gestational age had mean maternal and fetal plasma concentrations of 0.440 ± 0.011 and 0.217 ± 0.053 mM, respectively. Maternal and fetal values were not correlated. Neonates up to 96 h old had plasma citrate values similar to those in the fetus. The citrate concentration of the amniotic fluid was lower than that in fetal plasma and showed a negative correlation with conceptual age (p
Neonatology | 1972
Pauline Alexander; Mary L. Forsling; Marion J. Martin; D.A. Nixon; J.G. Ratcliffe; David Redstone; D. Tunbridge
Neonatology | 1969
Pauline Alexander; H.G. Britton; N.M. Cohen; D.A. Nixon