Selenium Nanoparticles Modulate Steroidogenesis-Related Genes and Improve Ovarian Functions via Regulating Androgen Receptors Expression in Polycystic Ovary Syndrome Rat Model

被引:15
作者
Abdallah, Ahmed B. E. [1 ]
El-Ghannam, Mohammed A. [1 ]
Hasan, Azza A. [2 ]
Mohammad, Lamiaa G. [1 ]
Mesalam, Noura M. [3 ]
Alsayed, Radwa M. [1 ]
机构
[1] Zagazig Univ, Fac Med, Dept Physiol, Zagazig, Egypt
[2] Zagazig Univ, Fac Pharm, Dept Pharmaceut, Zagazig, Egypt
[3] Egyptian Atom Energy Author, Nucl Res Ctr, Biol Applicat Dept, Cairo 13759, Egypt
关键词
PCOS; Selenium nanoparticles; Steroidogenesis; mRNA expression; Androgen receptors; Ovarian histopathology and immunohistochemistry; GRANULOSA-CELLS; FOLLICULAR STRUCTURES; HORMONE; INSULIN; DIAGNOSIS; AROMATASE; WOMEN; HYPERANDROGENISM; INCREASES; DIET;
D O I
10.1007/s12011-023-03616-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Polycystic ovary syndrome (PCOS) occurs during the reproductive period in women and is characterized by reproductive, endocrine, and metabolic disorders. Androgen plays a decisive role in its pathogenesis due to the interaction between hyperandrogenism and insulin resistance, which might be improved by selenium nanoparticles (SeNPs). The present study aimed to clarify the effect of SeNPs on androgen synthesis and action in the PCOS model and the resulting effect on ovarian function. Fifty-five 7-week-old female albino rats (90-105 g) were divided equally into five groups: control (C), fed a standard diet for 11 weeks; high-fat diet (HFD) group, fed HFD for 11 weeks; HFD and letrozole (L) (HFD + L), fed HFD for 11 weeks and administrated orally with L, at a daily dose of 1 mg/kg BW, for three weeks from the 7th to 9th week of the trial; HFD + L + 0.1SeNPs and HFD + L + 0.2SeNPs groups, treated the same as HFD + L group and orally gavaged SeNPs at daily doses of 0.1 and 0.2 mg/kg BW, respectively, during the last 14 day of the experiment. Daily determination of estrous cycle was performed, and at the end of the experimental period, BMI, serum glucose, insulin, HOMA-IR, lipid profile, sex hormones, TNF-alpha, IL6, oxidative stress biomarkers, ovarian mRNA expression of different proteins and enzymes involved in steroidogenesis, pathological examination, and immunohistochemical staining for androgen receptor (AR) were evaluated. Treatment of SeNPs restored estrous cyclicity, decreased BMI, and insulin resistance, improved dyslipidemia, reduced serum testosterone, and improved ovarian histopathology in PCOS rats. Furthermore, the anti-inflammatory and antioxidant impacts of SeNPs were remarkably noticed. Administration of SeNPs decreased androgen synthesis and expression of ovarian AR protein by decreasing the mRNA expression of STAR, Cyp11A1, Cyp17A1, and HSD17B3 and increasing the expression of Cyp19 alpha 1. Conclusively, SeNPs decreased androgen synthesis and blocked the vicious circle initiated by excessive androgen secretion via decreased AR expression. Thus, it may effectively treat PCOS cases by eliminating its reproductive, endocrine, and metabolic dysfunctions.
引用
收藏
页码:5721 / 5733
页数:13
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