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苗勒管抑制物质抑制胎鼠肺中双饱和磷脂酰胆碱的体外积聚。

Müllerian inhibiting substance depresses accumulation in vitro of disaturated phosphatidylcholine in fetal rat lung.

作者信息

Catlin E A, Manganaro T F, Donahoe P K

机构信息

Pediatric Surgical Research Laboratory, Massachusetts General Hospital, Boston 02114.

出版信息

Am J Obstet Gynecol. 1988 Nov;159(5):1299-303. doi: 10.1016/0002-9378(88)90467-x.

DOI:10.1016/0002-9378(88)90467-x
PMID:3189462
Abstract

Respiratory distress syndrome and associated pulmonary surfactant deficiency are more common in male neonates. Androgens have been shown to depress surfactant production. We tested the hypothesis that müllerian inhibiting substance, another fetal testicular product, might inhibit lung maturation measured as disaturated phosphatidylcholine accumulation. Initially, female fetal rat lungs were incubated with fetal testis or ovary or nanomolar concentrations of bovine müllerian inhibiting substance. Cultured lungs produced less disaturated phosphatidylcholine after incubation for 5 days with either testis (p = 0.012) or müllerian inhibiting substance than after coculture with ovary. In more comprehensive experiments, female lung fragments of 17.5 days' gestation, when incubated with nanomolar concentrations of bovine müllerian inhibiting substance or picomolar concentrations of human recombinant müllerian inhibiting substance, showed significant suppression of disaturated phosphatidylcholine accumulation (p less than 0.004) when compared with incubation with vehicle buffer. The suppression of surfactant accumulation produced in vitro by müllerian inhibiting substance, a potent male-specific fetal regressor, may be a factor in the increased susceptibility of male infants to respiratory distress syndrome.

摘要

呼吸窘迫综合征及相关的肺表面活性物质缺乏在男性新生儿中更为常见。雄激素已被证明会抑制表面活性物质的产生。我们检验了一种假说,即苗勒管抑制物质(另一种胎儿睾丸产物)可能会抑制以双饱和磷脂酰胆碱积累来衡量的肺成熟。最初,将雌性胎鼠肺与胎儿睾丸或卵巢或纳摩尔浓度的牛苗勒管抑制物质一起孵育。与卵巢共培养相比,用睾丸(p = 0.012)或苗勒管抑制物质孵育5天后,培养的肺产生的双饱和磷脂酰胆碱较少。在更全面的实验中,妊娠17.5天的雌性肺组织碎片,当与纳摩尔浓度的牛苗勒管抑制物质或皮摩尔浓度的人重组苗勒管抑制物质一起孵育时,与用赋形剂缓冲液孵育相比,双饱和磷脂酰胆碱的积累受到显著抑制(p < 0.004)。苗勒管抑制物质(一种强大的雄性特异性胎儿消退因子)在体外产生的对表面活性物质积累的抑制作用,可能是男婴对呼吸窘迫综合征易感性增加的一个因素。

相似文献

1
Müllerian inhibiting substance depresses accumulation in vitro of disaturated phosphatidylcholine in fetal rat lung.苗勒管抑制物质抑制胎鼠肺中双饱和磷脂酰胆碱的体外积聚。
Am J Obstet Gynecol. 1988 Nov;159(5):1299-303. doi: 10.1016/0002-9378(88)90467-x.
2
Sex-specific fetal lung development and müllerian inhibiting substance.性别特异性胎儿肺发育与苗勒管抑制物质
Am Rev Respir Dis. 1990 Feb;141(2):466-70. doi: 10.1164/ajrccm/141.2.466.
3
Müllerian inhibiting substance blocks epidermal growth factor receptor phosphorylation in fetal rat lung membranes.苗勒管抑制物质可阻断胎鼠肺膜中表皮生长因子受体的磷酸化。
Metabolism. 1991 Nov;40(11):1178-84. doi: 10.1016/0026-0495(91)90213-g.
4
Müllerian inhibiting substance inhibits branching morphogenesis and induces apoptosis in fetal rat lung.
Endocrinology. 1997 Feb;138(2):790-6. doi: 10.1210/endo.138.2.4906.
5
Müllerian inhibiting substance.
J Pathol. 1995 Jun;176(2):109-10. doi: 10.1002/path.1711760202.
6
Germ cell development in neonatal mouse testes in vitro requires müllerian inhibiting substance.新生小鼠睾丸生殖细胞的体外发育需要苗勒管抑制物质。
J Urol. 1993 Aug;150(2 Pt 2):613-6. doi: 10.1016/s0022-5347(17)35562-3.
7
Mullerian inhibiting substance binding and uptake.苗勒管抑制物质的结合与摄取
Dev Dyn. 1992 Apr;193(4):295-9. doi: 10.1002/aja.1001930402.
8
[Precocious production of müllerian inhibitor by the fetal rabbit testis].[胎兔睾丸过早产生苗勒管抑制物]
C R Seances Acad Sci III. 1982 Dec 6;295(12):701-5.
9
Cellular localization of müllerian inhibiting substance in the developing rat ovary.苗勒管抑制物质在发育中大鼠卵巢中的细胞定位。
Endocrinology. 1989 Feb;124(2):1000-6. doi: 10.1210/endo-124-2-1000.
10
Effect of human recombinant mullerian inhibiting substance on isolated epithelial and mesenchymal cells during mullerian duct regression in the rat.人重组苗勒管抑制物质对大鼠苗勒管退化过程中分离的上皮细胞和间充质细胞的影响。
Endocrinology. 1992 Sep;131(3):1481-8. doi: 10.1210/endo.131.3.1505479.

引用本文的文献

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Y It Matters-Sex Differences in Fetal Lung Development.Y 很重要——胎儿肺部发育的性别差异。
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