Investigation of Therapeutic Effects of Erdosteine on Polycystic Ovary Syndrome in a Rat Model

被引:32
作者
Karateke, Atilla [1 ]
Dokuyucu, Recep [2 ]
Dogan, Hatice [3 ]
Ozgur, Tumay [4 ]
Tas, Zeynel Abidin [4 ]
Tutuk, Okan [3 ]
Agturk, Gokhan [3 ]
Tumer, Cemil [3 ]
机构
[1] Reyhanli Sevgi Hosp, Dept Obstet & Gynecol, TR-31000 Antakya, Hatay Province, Turkey
[2] Med Specialty Training Ctr, Dept Physiol, Ankara, Turkey
[3] Mustafa Kemal Univ, Sch Med, Dept Physiol, Antakya, Turkey
[4] Mustafa Kemal Univ, Sch Med, Dept Pathol, Antakya, Turkey
关键词
Polycystic ovary syndrome; Metformin; Erdosteine; Letrozole; ANTI-MULLERIAN HORMONE; ORAL-CONTRACEPTIVES; INSULIN-RESISTANCE; METFORMIN; EXPRESSION; WOMEN; ACID;
D O I
10.1159/000494300
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Polycystic ovary syndrome (PCOS) is a serious endocrine disorder. In the present study, we investigated the therapeutic effects of erdosteine in letrozole-induced PCOS in rats. Methods: Thirty-two Wistar albino female rats were grouped as control group (C), PCOS group (PCOS), PCOS-metformin group (PCOS+MET), and PCOS-erdosteine group (PCOS+Erd). PCOS was induced by administering letrozole; such rats presented with sex hormone disorder, abnormal estrous cycles determined by daily vaginal smear, large cystic follicles, and increasing fasting insulin levels. After induction of PCOS, metformin (500 mg/kg/day) and erdosteine (100 mg/kg/day) were given orally to the treatment groups for 30 days. Serum concentrations of glucose, total cholesterol, low-and high-density lipoprotein, triglyceride, as well as the total oxidant and antioxidant status, oxidative stress index, circulating estrone (E1), estradiol (E2), testosterone, and androstenedione were evaluated. The ovaries were graded histologically. Results: Weights of ovarian tissues (p < 0.05) and the number of atretic follicles (p < 0.001) and cystic follicles (p < 0.01) decreased in the PCOS+Erd group; the corpus luteum number was significantly higher in the PCOS+Erd group (p < 0.01) as compared with the PCOS group. Lipid parameters (total-C, LDL-C, and TG), E1 (estrone), E1/E2 ratio, testosterone, and androstenedione significantly decreased, while HDL-C and E2 (estradiol) significantly increased in the PCOS+Erd group as compared with the PCOS group. Moreover glucose, insulin, and HOMA-IR were reduced with treatment of erdosteine (p > 0.05, p < 0.001, and p < 0.001, respectively). Conclusion: It is suggested that erdosteine may be used in the treatment of PCOS as an alternative to metformin. It appears that our findings might be supported by clinical and molecular studies. (c) 2018 The Author(s) Published by S. Karger AG, Basel
引用
收藏
页码:515 / 522
页数:8
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