1976
DOI: 10.1016/0005-2760(76)90083-7
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Studies on pulmonary surfactant

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1978
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Cited by 72 publications
(5 citation statements)
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“…In the present studies, brush-border membranes of dexamethasone-treated rats were also characterized by alterations in the composition of certain fatty acids in the PC fraction of their membrane phospholipids. Furthermore, in agreement with results of previous studies performed on the effects of corticosteroids on rabbit lung tissue (Rooney et al, 1976), concomitant with these lipid-compositional changes, the specific activities of lysophosphatidylcholine acyltransferase(s), with linoleoyl-CoA and arachidonic-CoA as acyl donors, were found to be increased by dexamethasone administration. It would therefore appear reasonable to suggest that dexamethasone-induced increases in these enzymic activities may, at least in part, be responsible for the fatty acid changes noted in the PC fraction of treated membranes.…”
Section: Discussionsupporting
confidence: 91%
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“…In the present studies, brush-border membranes of dexamethasone-treated rats were also characterized by alterations in the composition of certain fatty acids in the PC fraction of their membrane phospholipids. Furthermore, in agreement with results of previous studies performed on the effects of corticosteroids on rabbit lung tissue (Rooney et al, 1976), concomitant with these lipid-compositional changes, the specific activities of lysophosphatidylcholine acyltransferase(s), with linoleoyl-CoA and arachidonic-CoA as acyl donors, were found to be increased by dexamethasone administration. It would therefore appear reasonable to suggest that dexamethasone-induced increases in these enzymic activities may, at least in part, be responsible for the fatty acid changes noted in the PC fraction of treated membranes.…”
Section: Discussionsupporting
confidence: 91%
“…In agreement with results ofprevious studies performed on rabbit lung (Rooney et al, 1976), dexamethasone was also found to decrease the sphingomyelin/PC molar ratio of proximal-small-intestinal brush-border membranes by increasing the levels of PC in the treated membranes. Previous studies in rabbit (Rooney et al, 1976) and rat fetal lung (Post et al, 1986) demonstrated that glucocorticoid administration stimulated the activity of cholinephosphate cytidylyltransferase, but had no effect on the activities of pulmonary choline kinase and choline-phosphotransferase. Whether similar alterations in cholinephosphate cytidylyltransferase activity are responsible for the increases in PC seen in the brushborder membranes of treated animals in the present study must await further experiments.…”
Section: Discussionsupporting
confidence: 91%
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“…Studies of normal foetal lung development have shown that PG appears in amniotic fluid during the last weeks of pregnancy and increases in concentration in the fortnight before birth in particular [39]. The concentration of PG in LS can be increased by the administration of cortisol [40]. PG itself can be used as a treatment for RDS partly because it prevents alveolar epithelial apoptosis and profibrotic stimulation [41].…”
Section: Lung Surfactantmentioning
confidence: 99%
“…Antenatal induction of phosphatidylcholine synthesis in the lung of several animal species can be achieved by corticosteroid administration (Farrell & Zachman, 1973), and increased surfactant secretion into alveolar spaces in the foetal lung has been observed after thyrotropin-releasing hormone (Rooney et al, 1979) or cholinergic stimulation (Corbet et al, 1977). The acceleration of pulmonary maturation by corticosteroids, in part, is related to increased activity of cholinephosphotransferase (Farrell & Zachman, 1973), lysophosphatidylcholine acyltransferase (Rooney et al, 1976), and glycerophosphate phosphatidyltransferase (Rooney et al, 1975), and to increased incorporation of glucose into phosphatidylcholine (Gilden et al, 1977).…”
mentioning
confidence: 99%