阿魏油胶树脂对来曲唑诱导的多囊卵巢综合征大鼠的治疗作用。

IF 1.8 Q3 OBSTETRICS & GYNECOLOGY
Amir Shieh, Seyyed Majid Bagheri, Maryam Yadegari, Davoud Javidmehr, Zeinab Farhadi
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引用次数: 2

摘要

目的:阿魏是一种从阿魏中提取的口香糖,在伊朗传统医学中用于治疗一些生殖系统疾病。在大鼠模型中,研究了刺尾草对卵巢组织、多囊卵巢综合征(PCOS)相关基因表达以及肝、肾和血细胞因子水平的影响。方法:将30只大鼠分为正常组、多囊组和三种剂量(12.5、25、50 mg/kg)给药3周的多囊卵巢综合征诱导组。来曲唑以1mg /kg剂量口服,连续3周诱导PCOS。取血样,摘除卵巢,准备进行组织形态学检查。测量肝脏和肾脏参数。实时聚合酶链反应测定促黄体生成素受体、CYP11A1、单磷酸腺苷活化蛋白激酶、脂联素及脂联素受体1和2的mRNA表达水平。结果:治疗组与对照组肝、肾、血液指标无明显差异。在25和50 mg/kg剂量下,卵巢组织病理学,特别是卵泡膜和颗粒层的厚度,相对于PCOS组有显著改善。25和50 mg/kg处理组靶基因的表达也有所改善。结论:Asafoetida可作为PCOS常规治疗的补充手段。Asafoetida似乎通过调节和激活代谢和卵巢周期酶起作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Therapeutic effect of Ferula assa-foetida oleo-gum resin in rats with letrozole-induced polycystic ovary syndrome.

Therapeutic effect of Ferula assa-foetida oleo-gum resin in rats with letrozole-induced polycystic ovary syndrome.

Therapeutic effect of Ferula assa-foetida oleo-gum resin in rats with letrozole-induced polycystic ovary syndrome.

Therapeutic effect of Ferula assa-foetida oleo-gum resin in rats with letrozole-induced polycystic ovary syndrome.

Objective: Asafoetida is a gum derived from Ferula assa-foetida, which is used in traditional Iranian medicine to treat some reproductive system disorders. The effects of asafoetida on ovarian tissue, expression of certain genes associated with polycystic ovary syndrome (PCOS), and levels of liver, kidney, and blood cell factors after treatment in a rat model were investigated.

Methods: Thirty rats were divided into five groups: normal, polycystic, and treatment with three doses of asafoetida (12.5, 25, and 50 mg/kg for 3 weeks after PCOS induction). PCOS was induced by letrozole at a dose of 1 mg/kg administered orally for 3 weeks. Blood samples were taken, and the ovaries were removed and prepared for histomorphometric examination. Liver and kidney parameters were measured. The mRNA expression levels of luteinizing hormone receptor, CYP11A1, adenosine monophosphate-activated protein kinase, adiponectin, and adiponectin receptors 1 and 2 were also measured by real-time polymerase chain reaction.

Results: The levels of liver, kidney, and blood parameters did not significantly differ between the treatment groups and the control group. At doses of 25 and 50 mg/kg, ovarian histopathology, especially the thicknesses of the theca and granulosa layers, was significantly improved relative to the PCOS group. The expression of target genes also improved in the 25 and 50 mg/kg treatment groups.

Conclusion: Asafoetida can be used to treat PCOS as a complementary approach to conventional therapies. Asafoetida appears to act by regulating and activating metabolic and ovarian cycle enzymes.

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