1980
DOI: 10.1016/0002-9378(80)90244-6
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Copper and ceruloplasmin activity in human amniotic fluid

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Cited by 13 publications
(4 citation statements)
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“…The data of Fleming and Gitlin (40) suggest that the fetal (and newborn) lung may also contribute ceruloplasmin to the blood plasma of the rat. In humans, the fetal circulation contains ceruloplasmin already well before birth (42,43), and there are traces of it in amniotic fluid (61,62), as we have now also shown for the rat. These various findings confirm the importance of ceruloplasmin in copper transport, not just for the normal mammalian adult, but also for the pregnant adult and the developing fetus, as it prepares for birth.…”
Section: Discussionmentioning
confidence: 56%
“…The data of Fleming and Gitlin (40) suggest that the fetal (and newborn) lung may also contribute ceruloplasmin to the blood plasma of the rat. In humans, the fetal circulation contains ceruloplasmin already well before birth (42,43), and there are traces of it in amniotic fluid (61,62), as we have now also shown for the rat. These various findings confirm the importance of ceruloplasmin in copper transport, not just for the normal mammalian adult, but also for the pregnant adult and the developing fetus, as it prepares for birth.…”
Section: Discussionmentioning
confidence: 56%
“…These, in turn, may be related to increases in the levels of copper-binding and zinc-binding proteins, such as ceruloplasmnin, superoxide dismutase, and metallothionein [31][32][33][34]. The amniotic fluid levels of these acute-phase reactants tend to increase during late pregnancy in response to increased oxidative stress, with the increases being particularly pronounced in obstetric disorders [35][36][37].…”
Section: Discussionmentioning
confidence: 99%
“…The protein content of amniotic fluid reduced towards term. Ceruloplasmin demonstrated a major rise during 20–38 weeks of gestation, with a later decrease after 38 weeks [ 47 , 48 ]. Anagnostopoulos and co-workers reported that ceruloplasmin, alpha-1-antitrypsin, and zinc-alpha-2-glycoprotein are upregulated in specimens from pregnancies with Klinefelter syndrome fetuses, and were downregulated against proteins identified in specimens from normal fetuses [ 49 ].…”
Section: Discussionmentioning
confidence: 99%