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白藜芦醇可提高小鼠卵母细胞对排卵后老化的抵抗力。

Resveratrol increases resistance of mouse oocytes to postovulatory aging .

作者信息

Liang Qiu-Xia, Lin Yi-Hua, Zhang Chun-Hui, Sun Hong-Mei, Zhou Liang, Schatten Heide, Sun Qing-Yuan, Qian Wei-Ping

机构信息

Department of Reproductive Medicine, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, China.

State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.

出版信息

Aging (Albany NY). 2018 Jul 23;10(7):1586-1596. doi: 10.18632/aging.101494.


DOI:10.18632/aging.101494
PMID:30036861
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6075442/
Abstract

After ovulation, metaphase II oocytes undergo a time-dependent deterioration or , which is referred to as postovulatory oocyte aging, a process during which a series of deleterious molecular and cellular changes occur. In this study, we found that short-term injection of resveratrol (3,5,4'-trihydroxystilbene) effectively ameliorated oxidative stress-induced damage in postovulatory oocyte aging of middle-aged mice . Resveratrol induced changes that delayed the aging-induced oocyte deterioration including the elevated expression of the anti-aging molecule Sirtuin 1 (SIRT1); it reduced intracellular reactive oxygen species (ROS) level, and improved mitochondria function. In addition, these beneficial changes may also help to prevent apoptosis. Taken together, our data suggest that resveratrol can effectively protect against postovulatory oocyte aging primarily by preventing ROS production.

摘要

排卵后,中期II期卵母细胞会经历随时间推移的退化,这被称为排卵后卵母细胞老化,在此过程中会发生一系列有害的分子和细胞变化。在本研究中,我们发现短期注射白藜芦醇(3,5,4'-三羟基茋)可有效改善中年小鼠排卵后卵母细胞老化过程中氧化应激诱导的损伤。白藜芦醇诱导的变化延缓了老化诱导的卵母细胞退化,包括抗衰老分子沉默调节蛋白1(SIRT1)表达升高;降低了细胞内活性氧(ROS)水平,并改善了线粒体功能。此外,这些有益变化可能还有助于防止细胞凋亡。综上所述,我们的数据表明白藜芦醇主要通过阻止ROS产生来有效保护卵母细胞免受排卵后老化的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e585/6075442/b66bd3585247/aging-10-101494-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e585/6075442/9810c5279370/aging-10-101494-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e585/6075442/f2e46cd8a27e/aging-10-101494-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e585/6075442/e9dce875212e/aging-10-101494-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e585/6075442/e074fa9b9746/aging-10-101494-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e585/6075442/f64c3f0f34cb/aging-10-101494-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e585/6075442/b66bd3585247/aging-10-101494-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e585/6075442/9810c5279370/aging-10-101494-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e585/6075442/f2e46cd8a27e/aging-10-101494-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e585/6075442/e9dce875212e/aging-10-101494-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e585/6075442/e074fa9b9746/aging-10-101494-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e585/6075442/f64c3f0f34cb/aging-10-101494-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e585/6075442/b66bd3585247/aging-10-101494-g006.jpg

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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
Resveratrol aggravated H2O2-induced the HK-2 cell damage by inhibiting AKT phosphorylation.

PLoS One. 2025-7-31

[2]
Molecular Mechanisms Behind Organ-Related Aging and Regulatory Effects of Natural Therapeutics.

Cell Biochem Biophys. 2025-6-17

[3]
Identification of GDP as a small inhibitory molecule in HepG2 cells by non‑targeted metabolomics analysis.

Oncol Lett. 2025-2-11

[4]
Impact of psychological stress on ovarian function: Insights, mechanisms and intervention strategies (Review).

Int J Mol Med. 2025-2

[5]
Resveratrol and Female Fertility: A Systematic Review.

Int J Mol Sci. 2024-11-28

[6]
RNA m6A methylation regulatory mechanism of resveratrol in premature senescence cells.

Food Sci Nutr. 2024-9-30

[7]
Comprehensive atlas of mitochondrial distribution and dynamics during oocyte maturation in mouse models.

Biomark Res. 2024-10-16

[8]
Telomeres and SIRT1 as Biomarkers of Gamete Oxidative Stress, Fertility, and Potential IVF Outcome.

Int J Mol Sci. 2024-8-8

[9]
[Research Progress in the Role of Mitochondrial Dysfunction in Endometriosis-Associated Infertility].

Sichuan Da Xue Xue Bao Yi Xue Ban. 2024-5-20

[10]
Chemical reversion of age-related oocyte dysfunction fails to enhance embryo development in a bovine model of postovulatory aging.

J Assist Reprod Genet. 2024-8

本文引用的文献

[1]
Sonic hedgehog signaling mediates resveratrol to improve maturation of pig oocytes in vitro and subsequent preimplantation embryo development.

J Cell Physiol. 2018-1-5

[2]
Resveratrol attenuates high glucose-induced endothelial cell apoptosis via mediation of store-operated calcium entry.

Mol Cell Biochem. 2017-9-18

[3]
Postnatal resveratrol supplementation improves cardiovascular function in male and female intrauterine growth restricted offspring.

Physiol Rep. 2017-1

[4]
Low dose resveratrol ameliorates mitochondrial respiratory dysfunction and enhances cellular reprogramming.

Mitochondrion. 2017-5

[5]
Resveratrol and capsaicin used together as food complements reduce tumor growth and rescue full efficiency of low dose gemcitabine in a pancreatic cancer model.

Cancer Lett. 2017-1-13

[6]
Protective effects of resveratrol against mancozeb induced apoptosis damage in mouse oocytes.

Oncotarget. 2017-1-24

[7]
Resveratrol Improves Cognitive Impairment by Regulating Apoptosis and Synaptic Plasticity in Streptozotocin-Induced Diabetic Rats.

Cell Physiol Biochem. 2016

[8]
Inhibitory effects of resveratrol on the adhesion, migration and invasion of human bladder cancer cells.

Mol Med Rep. 2017-2

[9]
Resveratrol supplementation of high-fat diet-fed pregnant mice promotes brown and beige adipocyte development and prevents obesity in male offspring.

J Physiol. 2017-3-1

[10]
Resveratrol enhances brown adipocyte formation and function by activating AMP-activated protein kinase (AMPK) α1 in mice fed high-fat diet.

Mol Nutr Food Res. 2017-4

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