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本文引用的文献

1
Extension of longevity and reduction of inflammation is ovarian-dependent, but germ cell-independent in post-reproductive female mice.延长寿命和减少炎症是卵巢依赖性的,但在生殖后雌性小鼠中与生殖细胞无关。
Geroscience. 2019 Feb;41(1):25-38. doi: 10.1007/s11357-018-0049-4. Epub 2018 Dec 13.
2
Rapamycin increases oxidative metabolism and enhances metabolic flexibility in human cardiac fibroblasts.雷帕霉素可增加人心脏成纤维细胞的氧化代谢并增强代谢灵活性。
Geroscience. 2018 Jun 21;40(3):243-56. doi: 10.1007/s11357-018-0030-2.
3
Rapamycin treatment attenuates age-associated periodontitis in mice.雷帕霉素治疗可减轻小鼠与年龄相关的牙周炎。
Geroscience. 2017 Aug;39(4):457-463. doi: 10.1007/s11357-017-9994-6. Epub 2017 Sep 9.
4
Short-term rapamycin treatment increases ovarian lifespan in young and middle-aged female mice.短期雷帕霉素治疗可延长年轻和中年雌性小鼠的卵巢寿命。
Aging Cell. 2017 Aug;16(4):825-836. doi: 10.1111/acel.12617. Epub 2017 May 22.
5
A randomized controlled trial to establish effects of short-term rapamycin treatment in 24 middle-aged companion dogs.一项随机对照试验,旨在确定短期雷帕霉素治疗对 24 只中年伴侣犬的影响。
Geroscience. 2017 Apr;39(2):117-127. doi: 10.1007/s11357-017-9972-z. Epub 2017 Apr 3.
6
The role of transplanted visceral fat from the long-lived growth hormone receptor knockout mice on insulin signaling.长寿生长激素受体基因敲除小鼠移植内脏脂肪对胰岛素信号的作用。
Geroscience. 2017 Feb;39(1):51-59. doi: 10.1007/s11357-017-9957-y. Epub 2017 Jan 18.
7
Ovarian aging and the activation of the primordial follicle reserve in the long-lived Ames dwarf and the short-lived bGH transgenic mice.长寿 Ames 矮鼠和短命 bGH 转基因鼠的卵巢衰老与原始卵泡储备的激活。
Mol Cell Endocrinol. 2017 Nov 5;455:23-32. doi: 10.1016/j.mce.2016.10.015. Epub 2016 Oct 19.
8
Ovarian transcriptome associated with reproductive senescence in the long-living Ames dwarf mice.长寿艾姆斯侏儒小鼠中与生殖衰老相关的卵巢转录组
Mol Cell Endocrinol. 2017 Jan 5;439:328-336. doi: 10.1016/j.mce.2016.09.019. Epub 2016 Sep 20.
9
Age at menarche and age at natural menopause in East Asian women: a genome-wide association study.东亚女性初潮年龄和自然绝经年龄:一项全基因组关联研究。
Age (Dordr). 2016 Dec;38(5-6):513-523. doi: 10.1007/s11357-016-9939-5. Epub 2016 Sep 14.
10
Next Generation Sequencing-Based Comprehensive Chromosome Screening in Mouse Polar Bodies, Oocytes, and Embryos.基于新一代测序技术的小鼠极体、卵母细胞和胚胎全染色体筛查
Biol Reprod. 2016 Apr;94(4):76. doi: 10.1095/biolreprod.115.135483. Epub 2016 Feb 24.

热量限制和雷帕霉素对小鼠卵巢衰老的影响。

Effect of caloric restriction and rapamycin on ovarian aging in mice.

机构信息

Faculdade de Nutrição, Universidade Federal de Pelotas, Pelotas, RS, Brazil.

Faculdade de Medicina Veterinária, Universidade Federal de Pelotas, Pelotas, RS, Brazil.

出版信息

Geroscience. 2019 Aug;41(4):395-408. doi: 10.1007/s11357-019-00087-x. Epub 2019 Jul 29.

DOI:10.1007/s11357-019-00087-x
PMID:31359237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6815295/
Abstract

Caloric restriction (CR) increases the preservation of the ovarian primordial follicular reserve, which can potentially delay menopause. Rapamycin also increases preservation on the ovarian reserve, with similar mechanism to CR. Therefore, the aim of our study was to evaluate the effects of rapamycin and CR on metabolism, ovarian reserve, and gene expression in mice. Thirty-six female mice were allocated into three groups: control, rapamycin-treated (4 mg/kg body weight every other day), and 30% CR. Caloric restricted females had lower body weight (P < 0.05) and increased insulin sensitivity (P = 0.003), while rapamycin injection did not change body weight (P > 0.05) and induced insulin resistance (P < 0.05). Both CR and rapamycin females displayed a higher number of primordial follicles (P = 0.02 and 0.04, respectively), fewer primary, secondary, and tertiary follicles (P < 0.05) and displayed increased ovarian Foxo3a gene expression (P < 0.05). Despite the divergent metabolic effects of the CR and rapamycin treatments, females from both groups displayed a similar increase in ovarian reserve, which was associated with higher expression of ovarian Foxo3a.

摘要

热量限制(CR)增加了卵巢原始卵泡储备的保存,这可能会延迟绝经。雷帕霉素也通过与 CR 相似的机制增加卵巢储备的保存。因此,我们的研究目的是评估雷帕霉素和 CR 对代谢、卵巢储备和基因表达的影响。将 36 只雌性小鼠分配到三组:对照组、雷帕霉素处理组(每天 4mg/kg 体重,每隔一天)和 30%CR 组。CR 组的雌性小鼠体重较低(P<0.05),胰岛素敏感性增加(P=0.003),而雷帕霉素注射没有改变体重(P>0.05),并诱导胰岛素抵抗(P<0.05)。CR 和雷帕霉素组的雌性小鼠原始卵泡数量更多(P=0.02 和 0.04),初级、次级和三级卵泡数量更少(P<0.05),卵巢 Foxo3a 基因表达增加(P<0.05)。尽管 CR 和雷帕霉素治疗的代谢效应不同,但两组雌性小鼠的卵巢储备都有相似的增加,这与卵巢 Foxo3a 表达的增加有关。