کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5534325 1550840 2017 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
The effects of levonorgestrel on FSH-stimulated primary rat granulosa cell cultures through gene expression profiling are associated to hormone and folliculogenesis processes
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیولوژی سلول
پیش نمایش صفحه اول مقاله
The effects of levonorgestrel on FSH-stimulated primary rat granulosa cell cultures through gene expression profiling are associated to hormone and folliculogenesis processes
چکیده انگلیسی


- Levonorgestrel inhibited hFSH-induced estradiol biosynthesis in rat granulosa cells.
- The mechanism of aromatase inhibition is post-cAMP at the level of gene transcription.
- Levonorgestrel alters FSH-responsive genes involved in folliculogenesis.
- Progesterone-mediated oocyte maturation genes are modified by levonorgestrel.
- The ovary is a target for levonorgestrel contraceptive effects.

Levonorgestrel (LNG), a synthetic progestin, is used in emergency contraception (EC). The mechanism is preventing or delaying ovulation at the level of the hypothalamic pituitary unit; however, little knowledge exists on LNG effects at the ovary. The aim of this study was to identify the effects of LNG on FSH-induced 17β-estradiol (E2) production, including LNG-mediated changes on global gene expression in rat granulosa cells (GC). Isolated GC from female Wistar rats were incubated in vitro in the presence or absence of human FSH and progestins. At the end of incubations, culture media and cells were collected for E2 and mRNA quantitation. The results showed the ability of LNG to inhibit both hFSH-induced E2 production and aromatase gene expression. Microarray analysis revealed that LNG treatment affects GC functionality particularly that related to folliculogenesis and steroid metabolism. These results may offer additional evidence for the mechanisms of action of LNG as EC.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Molecular and Cellular Endocrinology - Volume 439, 5 January 2017, Pages 337-345
نویسندگان
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