4.6 Article

A rodent model of human dose-equivalent progestin-only implantable contraception

期刊

出版社

BMC
DOI: 10.1186/s12958-021-00729-w

关键词

Hormonal contraception; Long-acting reversible contraception; Progestin; Etonogestrel; Estrus cycle; Ovarian function; Ultrasound biomicroscopy

资金

  1. Translational Research Institute for Space Health Postdoctoral Fellowship [NNX16AO69A]

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The study demonstrated that the implantation of etonogestrel (ENG) LARC pellets affects the estrus cycle in rodents, with different doses of pellets having dose-dependent effects on the time spent in diestrus and estrus. Additionally, alterations in ovarian function were observed following pellet implantation.
Background Long-acting, reversible contraceptives (LARC; progestin only) are an increasingly common hormonal contraceptive choice in reproductive aged women looking to suppress ovarian function and menstrual cyclicity. The overall objective was to develop and validate a rodent model of implanted etonogestrel (ENG) LARC, at body size equivalent doses to the average dose received by women during each of the first 3 years of ENG subdermal rod LARC use. Methods Intact, virgin, female Sprague-Dawley rats (16-wk-old) were randomized to 1 of 4 groups (n = 8/group) of ENG LARC (high-0.30 mu g/d, medium-0.17 mu g/d, low-0.09 mu g/d, placebo-0.00 mu g/d) via a slow-release pellet implanted subcutaneously. Animals were monitored for 21 days before and 29 days following pellet implantation using vaginal smears, ultrasound biomicroscopy (UBM), saphenous blood draws, food consumption, and body weights. Data were analyzed by chi-square, non-parametric, univariate, and repeated measures 2-way ANOVA. Results Prior to pellet implantation there was no difference in time spent in estrus cycle phases among the treatment groups (p > 0.30). Following pellet implantation there was a dose-dependent impact on the time spent in diestrus and estrus (p < 0.05), with the high dose group spending more days in diestrus and fewer days in estrus. Prior to pellet insertion there was not an association between treatment group and estrus cycle classification (p = 0.57) but following pellet implantation there was a dose-dependent association with cycle classification (p < 0.02). Measurements from the UBM (ovarian volume, follicle count, corpora lutea count) indicate an alteration of ovarian function following pellet implantation. Conclusion Assessment of estrus cyclicity indicated a dose-response relationship in the shift to a larger number of acyclic rats and longer in duration spent in the diestrus phase. Therefore, each dose in this model mimics some of the changes observed in the ovaries of women using ENG LARC and provides an opportunity for investigating the impacts on non-reproductive tissues in the future.

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