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Biomedical subjects

C T Jones

Publications and source records attributed to C T Jones.

At least 91 records · Page 5Linked to original sources
PubMed1985

Metabolic and cardiovascular effects on fetal sheep of sustained reduction of uterine blood flow.

The effects on the fetus and placenta of graded reductions of uterine blood flow to 30-90% of control have been studied in sheep at days 125-143 of pregnancy. Reduction of uterine flow to 70-90% of control had little effect upon fetal oxygenation or heart rate or blood pressure but elevated fetal plasma catecholamine concentration. Reduction of flow to 30-50% of control depressed fetal arterial and umbilical venous PO2 but had little effect upon oxygen consumption unless the umbilical venous value fell below about 14 mmHg when it was depressed by up to 30%. Placental oxygen consumption did not fall and was therefore maintained at the expense of the fetus. Fetal arterial pressure rose by 10-12 mmHg and heart rate fell by about 30 beats/min during the first 10-15 min then rose above its initial value. Plasma adrenaline and noradrenaline concentrations rose progressively at a rate which increased with greater degrees of asphyxia. When uterine blood flow was reduced below one-half of normal, net placental consumption of glucose fell and there was evidence of substantial provision of glucose and lactate from the fetus. Fetal production of lactate increased sharply and much of this appeared to be consumed by the placenta at a rate sufficient to account entirely for the deficit in net glucose consumption. The results are consistent with the hypothesis that the fetus senses even small changes in uterine blood flow that are alone insufficient to elicit significant blood gas changes. When the fall in uterine flow caused by arterial compression is relatively large, nutrient supply to the placenta is maintained at the expense of the fetus and as a result of fetal glucose and lactate production. The elevation of fetal arterial PCO2 appears to enhance fetal responses to hypoxia. The results are discussed in relation to the fetal responses to brief and prolonged reductions in uterine blood flow.

Animals↗
PubMed1985

Regional changes in catecholamine content of the pregnant uterus.

High-pressure liquid chromatography with electrochemical detection was used to identify and measure catecholamines in rat, rabbit, sheep, guinea-pig and human uteri and follow changes with pregnancy. Noradrenaline was consistently the major catecholamine and pregnancy caused a regionally specific fall in its concentration which, in rat, rabbit and guinea-pig, was associated with a decline in total content. Adrenaline was undetectable (less than 10 pmol/g myometrium) in all species and at all gestational ages studied. Dopamine and its metabolite 3,4-dihydroxyphenylacetic acid (DOPAC) were detected at high concentrations in guinea-pig and particularly sheep uterus. In guinea-pig uterus the dopamine/DOPAC ratio fell dramatically with pregnancy, suggesting that increased quantities of dopamine were released and catabolized. The dopamine/noradrenaline ratios suggested that dopamine is stored with noradrenaline in adrenergic neurones in guinea-pig myometrium and within an additional neuronal or cellular store(s) in sheep uterus.

3,4-Dihydroxyphenylacetic Acid↗
PubMed1985

Inhibitory effects on steroid production from isolated adrenal cells of rhesus monkey (Macaca mulatta) of pro-opiomelanocorticotrophic peptides.

Adrenal glands from Rhesus monkeys (Macaca mulatta) of 160 days gestation, newborn, 2 months-old infants or 6 months-old infants were excised and prepared, by a collagenase digestion, as a cell suspension. The cells were incubated with 10 pg/ml, 100 pg/ml or 1 ng/ml of a peptide of the ACTH/pro-opiomelanocortin 'family', 57K, 31K, 20K, alpha MSH, ovine-CLIP or gamma LPH either in the presence or absence of 166 pg/ml ACTH1-39. The production by cortisol and androstenedione was measured by radioimmunoassay. Using the steroid production by aliquots of the cell suspension with either no stimulating agent or ACTH1-39 alone as controls, the net influence of these different peptides on basal or ACTH1-39-stimulated production was observed. alpha MSH, ovine-CLIP and gamma LPH had no influence on either basal or stimulated cortisol or androstenedione production. Corticotrophic peptides of 57K, and 20K and pro-opiomelanocortin each had a steroidogenic activity alone, in all age groups. In the fetal and newborn monkeys' adrenal cells, peptides of 57K and 20K at 1 ng/ml had an inhibitory influence on ACTH1-39 stimulated cortisol and androstenedione production. The influence of the 20K peptide is partially inhibitory as the steroidogenic potential of this peptide is not additive with that of ACTH1-39. These results show that, as observed in other species, that the ACTH/pro-opiomelanocortin range of peptides are inhibitory to the action of ACTH1-39 in the developing adrenal.

Adrenal Glands↗
PubMed1985

Studies on experimental growth retardation in sheep. The effects of a small placenta in restricting transport to and growth of the fetus.

Fetal and placental growth rate in sheep has been manipulated by removal of endometrial caruncles prior to conception. This produced two groups of fetuses, one in which prenatal growth rate was similar to normal and a second group in which the fetuses were about half of the normal size. The mortality in the latter group was high, particularly after catheterisation, and there was evidence of early intra-uterine death and fetal reabsorption. Prior to 125 days the relationship between fetal and placental size was poor, but after 126 days a close correlation between the two was apparent. The small fetuses had comparably small placentas and in all cases there was a close relationship between fetal and placental weight. The experimental growth retardation was associated with hypoglycaemia, hypoxia and hypoinsulinaemia. Plasma T3, T4 and particularly prolactin were very low in the small fetuses whilst levels of cortisol and alanine were high. In contrast to the controls these fetuses showed little evidence of net glucose, alanine or lactate consumption. Infusion of 50% glucose into the pregnant ewe, sufficient to elevate maternal plasma glucose concentrations 2 to 3 fold, caused a comparable increase in the plasma concentrations of normal fetuses but only a 50% rise in the concentration in small fetuses. In contrast administration of 50% O2 to the ewes sufficient to cause a 2 to 3-fold increase in maternal PO2 caused only a small increase of arterial PO2 of normal fetuses but doubled that to normal levels in small fetuses. The results are discussed in relation to the effect of reduced placental size causing a fall in placental and transport and transport capacity and significance of this to the associated fetal growth retardation.

Age Factors↗
PubMed1984

ACTH control of steroid secretion from adrenal cells of the developing rhesus monkey (Macaca mulatta).

Cells from adrenal glands of 140-160 days foetal, neonatal and infant Rhesus monkeys (Macaca mulatta) were prepared, by collagenase digestion and incubated with 10 pg-16 ng/ml ACTH. The production of cortisol, androstenedione, corticosterone, progesterone and prostaglandins was measured. The cortisol production in the 140 day and 160 day foetuses and in the neonatal adrenal cells was comparable. It was 2-fold higher in adrenal cells of 6 month infant monkeys. In all the groups there was an increasing production of cortisol with increasing ACTH concentration, and a response to low physiological concentrations of ACTH. The androstenedione production was significantly greater in the 160 day foetuses than in either those of 140 days or of the neonate which demonstrated a poor response to increasing ACTH concentrations. It responded well to increasing ACTH in adrenal cells from 6 month infant monkeys. Corticosterone output was 1/10th of cortisol with only the 140 day foetuses showing an increase in production with increasing ACTH concentrations. The results demonstrate that cells of the primate foetal adrenal gland are not inherently unresponsive to ACTH stimulation as regards cortisol production, which per/micrograms DNA does not appear to change over the last 25 days before term.

Adrenal Cortex Hormones↗
PubMed1984

Studies on the growth of the fetal guinea pig. Changes in plasma hormone concentration during normal and abnormal growth.

The endocrine changes associated with fetal growth retardation caused by unilateral uterine artery ligation of guinea pigs at day 30 of pregnancy were studied. Plasma hormone levels in fetuses that, about 20 or 30 days later, were 35-50% of normal size were measured by radioimmunoassay. The small fetuses were severely hypoglycaemic and hypoinsulinaemic; both showing close correlation and relationship to the degree of growth retardation. Plasma thyroid and cortisol and concentrations were much lower than normal and that glucagon and androstenedione were much higher. Plasma growth hormone level appeared to be unaffected by growth retardation. The developmental changes in glucagon and thyroid hormone concentrations were consistent with a delay in the timing of prenatal events in growth-retarded fetuses. However the late cortisol rise, although somewhat blunted, still occurred at 58-60 in the small fetal guinea pigs.

Adrenocorticotropic Hormone↗
PubMed1984

A morphometric comparison of five axenic Giardia isolates.

The length and width of trophozoites from axenic cultures of 5 Giardia isolates were measured both live and after fixation and Giemsa staining. These isolates, as named on the basis of host source, are classified as G. lamblia (3 isolates), G. felis (1 isolate), and G. caviae (1 isolate). The size of live, unstained trophozoites from the 5 isolates, measured without regard to the presence or absence of median bodies, showed only occasional significant differences in length. Statistically significant differences in length and/or width were observed for all comparisons when stained preparations of the isolates were compared. These size differences occurred between isolates assigned to different species as well as among the 3 G. lamblia isolates. These data and previously reported isozyme studies of these isolates most appropriately led to a re-examination of the presently utilized criteria for Giardia speciation.

Animals↗
PubMed1984

Studies on the growth of the fetal guinea pig. The effects of ligation of the uterine artery on organ growth and development.

The effects of reduced maternal placental blood flow on the growth and development of the fetal guinea pig have been studied by unilateral ligation of the uterine artery at day 30 of pregnancy. Fetal guinea pigs were investigated about 20 or 30 days later. In about one-third of cases fetal death occurred, in another third fetuses less than 60% of normal weight were observed and in the remainder all fetuses were in the normal weight range. In the growth retarded fetuses prenatal growth occurred at about 50% of the rate in control. There was no postnatal 'catch up' as growth still remained lower than in controls. Restricted fetal growth affected particularly development of the visceral tissues in which case size declined in proportion to body weight. Brain and adrenal by comparison were less affected as their contribution to total body weight increased, but even so in the severely retarded fetuses the mass of both fell. The responses of the liver were in general consistent with a delay in the pattern of development. Thus DNA, RNA, protein and haematopoietic cell content changes occurred later than normal. In contrast an enhanced deposition of glycogen was apparent in the liver of the growth-retarded fetus. The results indicate some of the ways in which nutritional deprivation of the fetuses leads to reprogramming of growth and maturation of selected fetal tissues to allow non-essential changes to await more favourable times.

Animals↗
PubMed1983

The effect of alterations in placental blood flow on the growth of and nutrient supply to the fetal guinea-pig.

The distribution of the cardiac output and the maternal placental blood flow has been measured in guinea-pigs at days 49-51 of pregnancy using radioactively labelled microspheres. In some instances uterine blood flow was reduced chronically by ligating one uterine artery at day 30 of pregnancy. Between 3 and 4% of the cardiac output passed normally to placenta, and this could be reduced to less than 2% after uterine artery ligation. The result of the ligation was to reduce fetal and placental weight by up to 70%. Fetal and placental weight showed a close linear correlation in controls and in pregnancies with uterine artery ligation. However, when placental size was reduced below 60% of control, fetal weight was less affected by a reduction in placental weights than normal. Placental blood flow and placental size exhibited a close linear relationship over the whole range of values, but there was limiting placental weight which approached 1.3 g as placental blood flow approached zero. Thus a reduced placental size, particularly below about 50%, was associated with a proportionately greater reduction in maternal placental blood flow. Maternal placental blood flow or the percentage of maternal cardiac output to the placenta and fetal weight also showed a well-correlated linear relationship. However, when placental blood flow was below about 50% of control values further reduction had a less than normal effect upon fetal growth. Small fetuses were hypoglycaemic and hypoinsulinaemic and the degree of each was dependent upon the extent of the reduction in fetal weight and in maternal placental blood flow. In fetuses that were below about 40% of normal size, and in which placental blood was below about 30% of control, fetal weight was less sensitive to falls in blood glucose, which in turn was more sensitive than normal to a fall in maternal placental blood flow. The results indicate that over the range of 50-100% of normal fetal growth, maternal placental blood flow and probably nutrient supply to the fetus vary in parallel. Hence over this range fetal and placental growth rates are determined in part by placental blood flow. At placental blood flow rates and fetal growth rates below 40% of normal fetal growth is less dependent upon placental blood flow than usual, presumably because of a reduced dependence upon glucose metabolism for growth. This would appear to be essential, since as maternal placental blood flow is reduced to low values the placenta has to utilize an increasing proportion of the available glucose.

Animals↗
PubMed1983

Corticosteroid stimulation of phosphatidylcholine synthesis in cultured fetal rabbit lung: evidence for de novo protein synthesis mediated by glucocorticoid receptors.

To investigate further the mechanism whereby glucocorticoids accelerate the maturation of the pulmonary surfactant system, we studied both binding of glucocorticoids and their effect on phosphatidylcholine synthesis in organ cultures of fetal rabbit lung grown in serum-free medium. The greatest effect of dexamethasone (100 nM for 48 h) occurred at 24 days gestation when there was a 103% increase in the rate of choline incorporation into phosphatidylcholine and a 24% increase in the tissue content of disaturated phosphatidylcholine. Stimulation by corticosteroid was first observed after 12 h of exposure. Choline incorporation increased in a linear fashion for 36 h and then began to plateau; removal of the steroid after 24 h prevented any further increase in stimulation. The presence of other hormones in the culture medium was not a prerequisite for the corticosteroid action. Fetal sex had no influence on dexamethasone-induced phosphatidylcholine synthesis or on nuclear binding of dexamethasone. There was a striking similarity between the Kd values for specific nuclear binding of dexamethasone and cortisol (0.6 +/- 0.1 and 7.3 +/- 0.1 nM, respectively) and the concentrations for half-maximal stimulation of phosphatidylcholine synthesis (0.7 +/- 0.1 and 6.8 +/- 0.5 nM). The relative potencies of a number of steroids (100 nM) for both nuclear binding and stimulation of choline incorporation were the same: dexamethasone greater than cortisol greater than cortisone greater than corticosterone greater than dehydrocorticosterone, with no effect by progesterone, testosterone, or estradiol at this dose. Actinomycin D and cycloheximide blocked dexamethasone-induced phosphatidylcholine synthesis in a dose-dependent fashion. Actinomycin D had a marked effect if added at the initiation of hormone exposure, but little effect when added after 24 h, whereas cycloheximide was primarily effective between 24-48 h. These findings suggest that glucocorticoid stimulation of phosphatidylcholine synthesis in fetal lung is mediated by binding to specific receptors, with subsequent de novo synthesis of RNA and protein.

Animals↗
PubMed1983

Regulation of glycolytic flux in the heart of the fetal guinea pig.

Functional glycolytic capacity and its regulation have been studied in the fetal guinea-pig heart during O2 deprivation in situ and in the Langendorff perfused heart. Anaerobic glycolytic flux, at 2 mumol/min per g wet wt. was similar in the 48-50 and 60-65 days fetal and adult guinea-pig heart, despite lower fetal phosphofructokinase activity. During O2 deprivation in situ and in the perfused heart glucose was the major substrate, with glycogen making a smaller contribution. Glycolytic capacity became more tightly regulated during fetal heart development. Thus at 48-50 days glycolysis was increased during O2 deprivation by substrate supply, but at 60-65 days activation of phosphofructokinase was required also. Low malate/aspartate cycle activity in the fetal heart was suggested by the absence of an increase in malate and alanine at the expense of aspartate. The large proportion of aerobic glycolytic flux converted to lactate concurred with this. Because of the low O2 consumption and relatively high aerobic glycolytic flux, the proportion of glycolytically-derived ATP was 3-4 fold higher in the fetal than adult heart, and may explain its functional resistance to O2 deprivation.

Anaerobiosis↗
PubMed1983

Studies on experimental growth retardation in sheep. The effects of maternal hypoxaemia.

Intrauterine growth retardation in fetal sheep was caused by removal of endometrial caruncles prior to conception. Such fetuses are chronically hypoxaemic and to establish their ability to withstand additional episodes of hypoxia, the effects of administration of 9% O2 to the pregnant ewe was investigated. Fetuses were studied at 135-140 days. During maternal hypoxia the small fetuses showed a greater tendency to further hypoxaemia and acidaemia, but the differences compared with controls were not large. Whilst the initial response to hypoxaemia was a fall in heart rate in the small fetuses, unlike the controls, the heart rate returned to normal within 15 min. Metabolite responses to hypoxia in the small fetuses were less than normal and the changes in plasma insulin concentrations were uncommonly small. In contrast the plasma cortisol and ACTH responses to hypoxia were larger than normal in the small fetus. The results are discussed in relation to the altered physiological state of the growth-retarded fetal sheep.

Adrenocorticotropic Hormone↗
PubMed1983

The effects of adrenergic blockade on fetal response to hypoxia.

The actions of the adrenergic blocking agents propranolol and phentolamine upon the responses of 124-135 days fetal sheep to hypoxia induced by causing pregnant ewes to breathe 9% O2 and 3% CO2 in N2 have been studied. During hypoxia fetal heart rate fell and any tendency for this to return was prevented by propranolol and stimulated by phentolamine. The ability of the fetal heart rate to return during hypoxia appears to be related to the rise in plasma catecholamines. Hypoxia induced increases in plasma ACTH and cortisol and in plasma metabolites appear to have the same characteristics as those changes induced by catecholamine infusion; the former being largely an alpha-receptor effect and the latter being beta-receptor mediated. The results indicate but do not prove that many of the fetal responses to hypoxia could be caused by the rise in plasma catecholamines.

Adrenocorticotropic Hormone↗
PubMed1983

The effects of hypoxia on glucose turnover in the fetal sheep.

The origin of the hypoxia-induced rise in fetal blood glucose concentration in fetal sheep of 124-135 days was investigated. Hypoxia was induced in pregnant sheep and fetuses with chronically implanted vascular catheters by causing the ewes to breathe 9% O2 and 3% CO2 in N2 for 60 min. The rise in fetal plasma glucose caused by a 60% reduction in maternal PaO2 was associated with a 50% fall in plasma insulin concentration. The fall in insulin and rise in glucose was prevented by the alpha-adrenergic blocking agent phentolamine but not by the beta-antagonist propranolol. Turnover of glucose in the fetus under these conditions was measured with [6-3H] and [U-14C] glucose. Hypoxia reduced fetal glucose consumption despite the hyperglycaemia. After 30 min of hypoxia there was no evidence of fetal production of glucose but by 60 min substantial production was evident. The reduced fetal consumption and increased production of glucose was inhibited by phentolamine but not by propranolol. It is concluded that in the fetal sheep hypoxia induced hyperglycaemia is first caused by reduced consumption of glucose and thus fetal glycogen stores are not depleted. If the hypoxia persists fetal blood glucose is elevated further by fetal production of glucose.

Animals↗