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由饮食诱导肥胖的雄性小鼠所生的雌性后代,其囊胚发育受损,卵巢、卵母细胞和卵丘细胞发生分子改变。

Female offspring sired by diet induced obese male mice display impaired blastocyst development with molecular alterations to their ovaries, oocytes and cumulus cells.

作者信息

Fullston Tod, Shehadeh Helana, Sandeman Lauren Y, Kang Wan Xian, Wu Linda L, Robker Rebecca L, McPherson Nicole O, Lane Michelle

机构信息

Discipline of Obstetrics and Gynaecology, School of Paediatrics and Reproductive Health, Robinson Research Institute, Level 3 Medical School South, The University of Adelaide, Adelaide, South Australia, 5005, Australia,

出版信息

J Assist Reprod Genet. 2015 May;32(5):725-35. doi: 10.1007/s10815-015-0470-x. Epub 2015 Apr 9.

Abstract

PURPOSE

To investigate the impacts that a paternal high fat diet (HFD) has on embryology, ovarian/cumulus cell gene expression and COC metabolism from female offspring, using a mouse model.

METHODS

Founder male mice were either fed a control diet (CD) or a HFD for 12 weeks. The HFD induced obesity but not diabetes, and founder males were then mated to normal weight CD fed female mice. Female offspring were maintained on a CD, super-ovulated, mated and the resultant zygotes were cultured to the blastocyst stage for embryo morphology, blastocyst cell number and apoptosis assessment. Ovaries and cumulus cells from offspring were collected for gene expression analysis of selected genes that maintain chromatin remodeling and endoplasmic reticulum (ER), metabolic and inflammatory homeostasis. Cumulus/oocyte complexes were also investigated for glucose uptake and lipid accumulation.

RESULTS

Female offspring sired by obese fathers produced embryos with delayed development and impaired quality, displayed increases in ovarian expression of Glut1, Glut3 and Glut4, and an increase in cumulus cell expression of Glut4. Interestingly their COCs did take up more glucose, but did accumulate more lipid.

CONCLUSIONS

A paternal HFD is associated with subfertility in female offspring despite the offspring being fed a CD and this subfertility is concomitant with ovarian/cumulus cell molecular alterations and increased lipid accumulation.

摘要

目的

使用小鼠模型研究父本高脂饮食(HFD)对雌性后代胚胎学、卵巢/卵丘细胞基因表达及卵丘-卵母细胞复合体(COC)代谢的影响。

方法

将奠基雄性小鼠分为两组,分别给予对照饮食(CD)或HFD,持续12周。HFD诱导小鼠肥胖但未诱发糖尿病,之后将奠基雄性小鼠与体重正常且喂食CD的雌性小鼠交配。雌性后代维持CD饮食,进行超数排卵、交配,所得受精卵培养至囊胚阶段,用于评估胚胎形态、囊胚细胞数量及细胞凋亡。收集后代的卵巢和卵丘细胞,对维持染色质重塑、内质网(ER)、代谢及炎症稳态的选定基因进行表达分析。同时研究卵丘/卵母细胞复合体的葡萄糖摄取和脂质积累情况。

结果

肥胖父本所生的雌性后代胚胎发育延迟且质量受损,卵巢中Glut1、Glut3和Glut4的表达增加,卵丘细胞中Glut4的表达也增加。有趣的是,它们的COC摄取了更多葡萄糖,但脂质积累也更多。

结论

尽管后代喂食CD,但父本HFD与雌性后代生育力低下有关,这种生育力低下与卵巢/卵丘细胞分子改变及脂质积累增加相伴。

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