Suppr超能文献

人胎盘15-羟基前列腺素脱氢酶活性受胎儿基因控制。

Human placental 15-hydroxy-prostaglandin dehydrogenase activity is under fetal genetic control.

作者信息

Erwich J J, Keirse M J

机构信息

Department of Obstetrics, Leiden University Hospital, The Netherlands.

出版信息

Prostaglandins. 1988 Jan;35(1):123-31. doi: 10.1016/0090-6980(88)90280-8.

Abstract

Placental 15-hydroxy-prostaglandin dehydrogenase (PGDH type I) was measured in 33 placentae obtained from 1 trizygotic, 7 dizygotic and 8 monozygotic pregnancies. PGDH activity ranged from 0.33 to 4.62 nmol PGF2 alpha metabolized per mg placental protein per min, which was within the range observed in singleton pregnancies. Expressing PGDH activity per mg DNA, offered no advantage over expressing it per mg total protein. PGDH activity differed significantly between the placentae of 6 of the 9 genetically non-identical placental pairs. The placentae of genetically identical twins, on the other hand, showed no difference in PGDH activity between the pairs. The data indicate that the genetic constitution of the fetus determines placental PGDH activity. They also provide us with the first evidence that the variation in prostaglandin catabolizing capacity of the human placenta is not entirely dictated by the maternal endocrine environment, but is under fetal control.

摘要

对取自1例三卵性、7例二卵性和8例单卵性妊娠的33个胎盘进行了胎盘15-羟基前列腺素脱氢酶(I型PGDH)测定。PGDH活性范围为每分钟每毫克胎盘蛋白代谢0.33至4.62 nmol前列腺素F2α,这在单胎妊娠所观察到的范围内。以每毫克DNA表示PGDH活性,与以每毫克总蛋白表示相比并无优势。在9对基因不同的胎盘中,有6对胎盘的PGDH活性存在显著差异。另一方面,同卵双胞胎的胎盘在PGDH活性上并无差异。数据表明胎儿的基因构成决定胎盘PGDH活性。它们还为我们提供了首个证据,即人类胎盘前列腺素分解代谢能力的变化并非完全由母体内分泌环境决定,而是受胎儿控制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验