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枸橼酸氯米酚和来曲唑对人原始卵丘细胞凋亡途径和细胞周期的影响及雌二醇的保护作用。

The Effect of Clomiphene Citrate and Letrozole in Apoptotic Pathways and Cell Cycle in Human Primary Cumulus Cells and the Protective Effect of Estradiol.

机构信息

Department of Obstetrics and Gynecology, Federal University of Minas Gerais, Belo Horizonte, Brazil.

Fertibaby Clinic, Belo Horizonte, Brazil.

出版信息

Reprod Sci. 2022 Aug;29(8):2272-2281. doi: 10.1007/s43032-022-00961-8. Epub 2022 May 5.

Abstract

Clomiphene citrate (CC) and letrozole are ovulatory stimulants that, despite high ovulation rates, achieve low pregnancy rates. This study aimed to investigate the in vitro effects of CC and letrozole, alone or in combination with estradiol, on apoptosis in human cumulus cells. We performed a controlled prospective study using primary cumulus cell cultures from patients undergoing in vitro fertilization (n=22). Alpha-inhibin immunocytochemistry was used to assess cell culture purity and morphology. Cell viability was evaluated by MTT assay, cell cycle status by flow cytometry, and Caspase-3, Bax and SOD-2, and S26 gene expression by qPCR. Cells were treated for 24 hours in 5 conditioned media: CC, CC + estradiol, letrozole, letrozole + estradiol and control. None of the treatments affected cell viability, but letrozole reduced the mean percentage of cells in the S phase compared to control (24.79 versus 21.70, p=0.0014). Clomiphene treatment increased mRNA expression of Bax (4 fold) and SOD-2 (2 fold), which was reversed by co-treatment with estradiol. SOD-2 expression increased in cells treated with letrozole compared to control (4 fold), which was also reversed by estradiol. These findings suggest that clomiphene citrate and letrozole do not significantly affect the viability of human cumulus cells. Still, the expression of genes involved in apoptosis was modulated by these drugs alone and in association with estradiol, suggesting that CC and letrozole may have direct effects on cumulus cells beyond their known mechanisms of action.

摘要

枸橼酸氯米酚(CC)和来曲唑是促排卵药物,尽管排卵率高,但妊娠率低。本研究旨在探讨 CC 和来曲唑单独或与雌二醇联合应用对人卵丘细胞凋亡的体外影响。我们进行了一项使用接受体外受精的患者的原代卵丘细胞培养的对照前瞻性研究(n=22)。α-抑制素免疫细胞化学用于评估细胞培养纯度和形态。通过 MTT 测定评估细胞活力,通过流式细胞术评估细胞周期状态,通过 qPCR 评估 Caspase-3、Bax 和 SOD-2 以及 S26 基因表达。将细胞用 5 种条件培养基处理 24 小时:CC、CC+雌二醇、来曲唑、来曲唑+雌二醇和对照。这些处理均未影响细胞活力,但与对照相比,来曲唑降低了 S 期细胞的平均百分比(24.79%比 21.70%,p=0.0014)。CC 处理增加了 Bax(4 倍)和 SOD-2(2 倍)的 mRNA 表达,这一表达被雌二醇的共同处理所逆转。与对照相比,来曲唑处理的细胞中 SOD-2 的表达增加(4 倍),这也被雌二醇逆转。这些发现表明,枸橼酸氯米酚和来曲唑对人卵丘细胞的活力没有显著影响。然而,这些药物单独和与雌二醇联合应用时,参与凋亡的基因表达受到调节,这表明 CC 和来曲唑可能对卵丘细胞具有超出其已知作用机制的直接影响。

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