1994
DOI: 10.1016/0143-4004(94)90017-5
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Endothelial nitric oxide synthase in the human placenta: Regional distribution and proposed regulatory role at the feto-maternal interface☆

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Cited by 120 publications
(60 citation statements)
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“…4A, B) immunostaining was observed mainly in syncytiotrophoblast cells and endothelial cells. Myatt et al [14,16,17], Conrad et al [15] and Buttery et al [13] reported that eNOS expression was observed in trophoblast cells in the human placenta. These findings are relevant to our present results.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…4A, B) immunostaining was observed mainly in syncytiotrophoblast cells and endothelial cells. Myatt et al [14,16,17], Conrad et al [15] and Buttery et al [13] reported that eNOS expression was observed in trophoblast cells in the human placenta. These findings are relevant to our present results.…”
Section: Discussionmentioning
confidence: 99%
“…Three isoforms of NOS have been identified to date, two of which are constitutively expressed as neuronal NOS (nNOS) and endothelial NOS (eNOS) requiring calcium/ calmodulin for their activity, whereas inducible NOS (iNOS) is calcium/calmodulin independent [11,12]. Biochemical experiments demonstrated the presence of eNOS in the feto-placental vasculature or dissected placental villous tissue [13][14][15][16]. However, some investigators have also provided evidence for calcium/calmodulin-independent iNOS activity in placental tissues [15,[17][18][19], although other researchers reported that iNOS mRNA expression was not detected in normal human placental tissues by RT-PCR analysis [20,21].…”
mentioning
confidence: 99%
“…Using the perfused placental cotyledon preparation, Myatt, Brewer & Brockman (1991) have shown that infusion of an inhibitor of the enzyme nitric oxide synthase (NOS) leads to an increase in perfusion pressure. The constitutive calcium-dependent endothelial isoform of NOS (eNOS) has also been identified by immunohistochemical techniques to be present in placental vessels (Myatt, Brockman, Eis & Pollock, 1993;Buttery, McCarthy, Springall, Sullivan, Elder & Polak, 1994) and, perhaps surprisingly, to show strong staining in the syncytiotrophoblast. In our laboratory we have used an isolated artery preparation to show the in vitro release of NO by small fetoplacental arteries.…”
Section: Clinical and Experimental Evaluation Of Placental Blood Flowmentioning
confidence: 99%
“…Most studies hitherto have used immunohistochemical or histochemical techniques to examine the distribution of NOS in the normal umbilical cord and placenta (Springall et al, 1992;Myatt et al, 1993a;Buttery et al, 1994b), however, these methods are only semiquantitative and demonstration of NADPH-diaphorase activity is not specific for NOS. In situ hybridization has also been employed to identify eNOS mRNA in placental sections (Conrad et al, 1993b), but due to the need to measure, as well as localize, NOS in tissues from normal, PE and IUGR complicated pregnancies, we have sought an alternative quantitative method.…”
Section: Introductionmentioning
confidence: 99%