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胎儿生长受限与幼年豚鼠后代卵巢卵泡数量减少和卵泡生长受损有关。

Fetal Growth Restriction Is Associated With Decreased Number of Ovarian Follicles and Impaired Follicle Growth in Young Adult Guinea Pig Offspring.

机构信息

Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Canada.

Department of Obstetrics and Gynecology, University of Western Ontario, London, Ontario, Canada.

出版信息

Reprod Sci. 2019 Dec;26(12):1557-1567. doi: 10.1177/1933719119828041. Epub 2019 Feb 11.

Abstract

BACKGROUND

The mechanisms mediating the impacts of fetal growth restriction (FGR) on follicular development are commonly studied in mouse/rat models, where ovarian development occurs largely during the early postnatal period. These models have shown that FGR is associated with premature follicle loss, early pubertal onset, and accelerated ovarian aging. Whether the same occurs in precocious species is unknown.

OBJECTIVE

Since guinea pig follicle development occurs in utero in a manner consistent with human ovarian development, we sought to determine whether FGR had similar impacts on guinea pig ovarian development.

METHODS

Dunkin-Hartley guinea pig dams were randomized to receive a control (CON) or a nutrient-restricted diet (FGR) prior to conception until weaning. Offspring ovaries were collected at prepubertal (postnatal day [P] 25) and young adult (P110) time points.

RESULTS

Prepubertal offspring exposed to FGR showed little differences in ovarian transcript levels and follicle counts. Young adult FGR offspring, however, showed reductions in the number of transitioning, primary, and antral follicles, as well as corpora lutea. This loss in follicles was associated with reduced insulin-like growth factor receptor and growth differentiation factor-9 messenger RNA levels in FGR P110 offspring compared to CON.

CONCLUSION

We demonstrate that FGR in guinea pigs is accompanied by perturbations in signaling pathways essential for proper follicle growth and manifests as reductions in growing follicles in offspring, but these changes do not manifest until postpuberty. These data support the fact that accelerated reproductive maturation/aging is a conserved phenotype that is associated with in utero nutritional adversity.

摘要

背景

胎儿生长受限(FGR)对卵泡发育影响的机制通常在小鼠/大鼠模型中进行研究,其中卵巢发育主要发生在出生后的早期阶段。这些模型表明,FGR 与卵泡过早丢失、青春期提前和卵巢衰老加速有关。在早熟物种中是否会发生同样的情况尚不清楚。

目的

由于豚鼠卵泡发育与人类卵巢发育方式一致,因此我们试图确定 FGR 是否对豚鼠卵巢发育有类似的影响。

方法

在受孕前,将 Dunkin-Hartley 豚鼠母鼠随机分为对照组(CON)或营养受限组(FGR),直至断奶。在青春期前(出生后第 25 天 [P])和成年早期(P110)收集后代的卵巢。

结果

暴露于 FGR 的青春期前后代的卵巢转录水平和卵泡计数差异不大。然而,年轻的成年 FGR 后代的过渡性、原发性和腔前卵泡以及黄体数量减少。与 CON 相比,FGR P110 后代的胰岛素样生长因子受体和生长分化因子 9 信使 RNA 水平降低,导致卵泡丢失。

结论

我们证明,豚鼠的 FGR 伴随着对卵泡生长至关重要的信号通路的干扰,并表现为后代生长卵泡减少,但这些变化直到青春期后才表现出来。这些数据支持这样一个事实,即加速的生殖成熟/衰老是一种与宫内营养逆境相关的保守表型。

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