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去氢表雄酮诱导的多囊卵巢综合征小鼠模型需要持续治疗来维持生殖表型。

Dehydroepiandrosterone-induced polycystic ovary syndrome mouse model requires continous treatments to maintain reproductive phenotypes.

机构信息

Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University Health Science Center, No.38 Xueyuan Rd, Haidian District, Beijing, 100191, China.

出版信息

J Ovarian Res. 2023 Oct 25;16(1):207. doi: 10.1186/s13048-023-01299-8.

Abstract

BACKGROUND

Polycystic ovary syndrome (PCOS) is the most common endocrinopathy associated with infertility and metabolic disorder in women of reproductive age. Animal models have been developed and used as tools to unravel the pathogenesis of PCOS, among which most postnatal models employ continuing experimental manipulations. However, the persistence and stability of these animals after modeling is unknown. Dehydroepiandrosterone (DHEA)-induced PCOS mouse model is commonly used in PCOS studies. Thus the aim of the present study was to investigate the reproductive features of DHEA-induced PCOS mice fed a normal chow or an high-fat diet (HFD) with treatment withdrawal or consecutive treatments after PCOS mouse models were established.

METHODS

Prepubertal C57BL/6 J mice (age 25 days) were injected (s.c.) daily with DHEA on a normal chow or a 60% HFD for 20 consecutive days to induce PCOS mouse models. Mice injected with the vehicle sesame oil were used as controls. After 20 days, mice were divided into 2 groups, namely "Continue dosing group" and "Stop dosing group". The animals were consecutively treated with DHEA or DHEA + HFD, or housed without any treatment for 2 or 4 weeks. Estrous cycles were evaluated during this period. At the end of the experiment, serum testosterone (T) levels were measured and the morphology of ovaries was evaluated.

RESULTS

The mice in Continue dosing groups maintained reproductive phenotypes of PCOS mouse models. In contrast, 2 or 4 weeks after PCOS models were established, the mice with treatment withdrawal in Stop dosing groups exhibited normal serum testosterone levels, regular estrous cycle, and relatively normal ovarian morphology. In addition, even with consecutive treatments, there was no marked difference in body weight between DHEA mice on the normal chow or an HFD in Continue dosing groups and the control animals 3 weeks after modeling.

CONCLUSIONS

After PCOS mice were induced with DHEA or DHEA + HFD, the mice still need consecutive treatments to maintain reproductive phenotypes to be regarded as PCOS mice that meet the diagnostic criteria of PCOS defined by the 2003 Rotterdam criteria.

摘要

背景

多囊卵巢综合征(PCOS)是育龄妇女中最常见的与不孕和代谢紊乱相关的内分泌疾病。已经开发并使用动物模型作为揭示 PCOS 发病机制的工具,其中大多数产后模型采用持续的实验操作。然而,建模后这些动物的持久性和稳定性尚不清楚。脱氢表雄酮(DHEA)诱导的 PCOS 小鼠模型常用于 PCOS 研究。因此,本研究旨在探讨 DHEA 诱导的 PCOS 小鼠在建立 PCOS 模型后停止或连续治疗时,给予正常饲料或高脂肪饮食(HFD)的生殖特征。

方法

将 25 天大的 C57BL/6J 幼鼠(prepubertal)每天皮下注射(s.c.)DHEA,连续 20 天,以诱导 PCOS 小鼠模型。注射芝麻油溶剂的小鼠作为对照组。20 天后,将小鼠分为两组,即“继续给药组”和“停止给药组”。动物连续给予 DHEA 或 DHEA+HFD,或不给予任何处理 2 或 4 周。在此期间评估动情周期。实验结束时,测量血清睾酮(T)水平并评估卵巢形态。

结果

继续给药组的小鼠维持 PCOS 小鼠模型的生殖表型。相比之下,在停止给药组中停止治疗 2 或 4 周后,模型建立的小鼠血清睾酮水平正常,动情周期规律,卵巢形态相对正常。此外,即使连续治疗,在继续给药组中,给予正常饲料或 HFD 的 DHEA 小鼠与建模后 3 周的对照动物相比,体重无明显差异。

结论

用 DHEA 或 DHEA+HFD 诱导 PCOS 小鼠后,仍需要连续治疗才能维持符合 2003 年鹿特丹标准定义的 PCOS 诊断标准的生殖表型,才能被认为是 PCOS 小鼠。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3910/10599050/692b1c0d693a/13048_2023_1299_Fig1_HTML.jpg

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