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日本新生儿中人类红细胞NADH黄递酶变体的发生率及其活性与胎儿血红蛋白和F细胞的协同发育变化

Incidence of variants of human red cell NADH diaphorase in Japanese newborns and coordinate developmental changes of its activity with fetal hemoglobin and F cells.

作者信息

Shimizu K, Keino H, Mizutani A

出版信息

Biol Neonate. 1984;46(6):261-6. doi: 10.1159/000242075.

Abstract

615 human newborns were examined for detection of polymorphism of red cell NADH diaphorase by isoelectric focusing on polyacrylamide gels. Although the incidence of variant forms among Japanese is about 0.46%, no variants were encountered in newborns. Enzyme activity of red cell NADH diaphorase from newborns was less than half of that from adults. There were no differences in enzyme activity between premature and full-term newborns. Increase of enzyme activity during development after birth was admitted in parallel with decrease of fetal hemoglobin (Hb F) content and also with reduction of F cells (which produce only Hb F) number.

摘要

通过聚丙烯酰胺凝胶等电聚焦法对615例人类新生儿进行检查,以检测红细胞NADH黄递酶的多态性。尽管日本人群中变异型的发生率约为0.46%,但在新生儿中未发现变异型。新生儿红细胞NADH黄递酶的酶活性不到成年人的一半。早产儿和足月儿的酶活性没有差异。出生后发育过程中酶活性的增加与胎儿血红蛋白(Hb F)含量的降低以及F细胞(仅产生Hb F的细胞)数量的减少同时出现。

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