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哺乳期大量体重减轻会通过导致母猪卵巢细胞的线粒体功能障碍而损害卵泡发育,而补充丁酸盐可减轻这种损害。

Lactational high weight loss impairs follicular development by causing mitochondrial dysfunction of ovarian cells in sows and mitigated by butyrate supplement.

作者信息

Liu Kexiong, Zhang Luyao, Xu Xiaoling, Song Mengyao, Ding Haiquan, Xiao Linli, Wen Junhui, Zhou Chunmei, Bai Jiahua, Liu Yan

机构信息

Institute of Animal Husbandry and Veterinary Medicine, Beijing Academy of Agriculture and Forestry Sciences, Beijing 100097, China.

Key Laboratory of Adaptation and Evolution of Plateau Biota, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Qinghai 810008, China.

出版信息

J Adv Res. 2025 Jan 30. doi: 10.1016/j.jare.2025.01.050.

Abstract

INTRODUCTION

In modern sows, lactational high weight loss (HWL), caused by the large litter size and inadequate feed intake, has a negative effect on follicular development after weaning, resulting in poor reproductive performance in the subsequent parity. However, the underlying mechanism remains unclear.

OBJECTIVES

This research aimed to explore the mechanism that sows HWL during lactation damages follicular development and attempt to improve the reproductive function by treating with butyrate.

METHOD

Four multiparous sister sows were chosen to build a HWL model for lactating sows through feed restriction during the final week of a 21-day lactation. Spatially transcriptomics (ST) and tissue immunofluorescent staining were then utilized for the antral follicles in the ovarian surface to search for differentially expressed genes and proteins among different cell types. Subsequently, the mouse assay, including immunofluorescent staining, transmission electron microscopy, hormone detection and western blot, were conducted to verify the findings in sows and investigate the effect of butyrate on the follicular development in HWL mice.

RESULTS

Based on the transcriptomic analysis, differentially expressed genes in granulosa cells, theca cells, and ovarian stromal cells were examined. The findings revealed that HWL disturbs the mitochondrial electron transport chain and steroidogenesis in all three cell types by downregulating the expression of NDUFB3, SDHB, CYCS, COX8A and CYP19A1, as well as upregulating the expression of STAR, CYP11A1 and CYP17A1. Furthermore, results from mouse assays demonstrated that HWL causes apoptosis and alters sex hormone secretion by impairing mitochondrial function and disordering the expression of steroidogenesis key enzymes in ovarian cells, while these effects were partially mitigated by butyrate treatment.

CONCLUSION

The mitochondrial dysfunction and abnormal steroidogenesis induced by HWL during lactation in ovarian cells harm the follicular development of weaning sows, which could be alleviated by butyrate treatment.

摘要

引言

在现代母猪中,由于产仔数多和采食量不足导致的哺乳期高体重损失(HWL)对断奶后卵泡发育有负面影响,导致后续胎次的繁殖性能不佳。然而,其潜在机制仍不清楚。

目的

本研究旨在探讨母猪哺乳期HWL损害卵泡发育的机制,并尝试通过丁酸盐处理来改善生殖功能。

方法

选择4头经产的姐妹母猪,在21天哺乳期的最后一周通过限饲建立哺乳期母猪HWL模型。然后利用空间转录组学(ST)和组织免疫荧光染色对卵巢表面的窦卵泡进行研究,以寻找不同细胞类型之间差异表达的基因和蛋白质。随后,进行小鼠实验,包括免疫荧光染色、透射电子显微镜、激素检测和蛋白质免疫印迹,以验证母猪实验的结果,并研究丁酸盐对HWL小鼠卵泡发育的影响。

结果

基于转录组分析,检测了颗粒细胞、卵泡膜细胞和卵巢基质细胞中差异表达的基因。结果显示,HWL通过下调NDUFB3、SDHB、CYCS、COX8A和CYP19A1的表达,以及上调STAR、CYP11A1和CYP17A1的表达,扰乱所有三种细胞类型中的线粒体电子传递链和类固醇生成。此外,小鼠实验结果表明,HWL通过损害线粒体功能和扰乱卵巢细胞中类固醇生成关键酶的表达,导致细胞凋亡并改变性激素分泌,而丁酸盐处理可部分减轻这些影响。

结论

哺乳期HWL诱导的卵巢细胞线粒体功能障碍和类固醇生成异常损害了断奶母猪的卵泡发育,丁酸盐处理可缓解这种损害。

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