肿瘤化疗相关的结构改变:GnRH拮抗剂在卵巢卵泡中的作用

Pub Date : 2022-07-27 DOI:10.15296/ijwhr.2022.36
D. Mohammadnejad, Faeze Daghigh, A. Hamzehzadeh
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引用次数: 0

摘要

目的:近年来研究表明化疗对颗粒细胞增殖的不良影响。促性腺激素释放激素(GnRH)拮抗剂对颗粒细胞对化疗副作用的保护作用。在本研究中,我们的目的是评估cetrorelix对雌性小鼠卵巢颗粒细胞在给予硫替帕后增殖的影响。材料与方法:实验选用5-8周龄、体重24-28 g的Balb/c成年雌性小鼠30只,随机分为3组(对照组、t组、c组),每组10只。t组给予硫替帕2.5 mg/kg,连续4 d。c组在给药前、给药同时、给药结束后1周给予头孢瑞克(0.25 mg/kg)。在调查结束时,卵巢被用于定量和免疫组织化学研究。结果:t组原始、初级、次级、三级毛囊的平均数量明显低于对照组(P=0.02)。Cetrorelix通过增加卵巢皮质中卵泡的平均数量(P=0.04)对硫替帕诱导的损伤具有保护作用。结论:cetrorelix作为GnRH拮抗剂,可被认为是保护肿瘤细胞免受化疗损伤的有效药物之一。
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Chemotherapy-Related Structural Changes in Cancer: Effect of GnRH Antagonist in the Ovarian Follicles
Objectives: The adverse effect of chemotherapy on the proliferation of granulosa cells has been indicated in recent studies. Gonadotropin-releasing hormone (GnRH) antagonists exert protective effects on granulosa cells against the side effects of chemotherapy. In the present study, we aimed to evaluate the impact of cetrorelix on the proliferation of ovarian granulosa cells following administration of thiotepa in the ovaries of female mice. Materials and Methods: In this experimental study, 30 adult Balb/c female mice (5-8 weeks old, weighing 24-28 g) were divided into three groups (n=10/ each group) (Control group, T. group, and C. group). T. group received 2.5 mg/kg of thiotepa for four consecutive days. The C. group received cetrorelix (0.25 mg/kg) before and at the same time as thiotepa administration and a week after the end of thiotepa administration. Ovaries were used for quantitative and immunohistochemical studies at the end of the investigation. Results: The mean numbers of follicles such as primordial, primary, secondary, and tertiary significantly decreased in the T. group than control group (P=0.02). Cetrorelix treatment exerted a protective effect against thiotepa-induced damage by increasing the mean numbers of follicles in the ovarian cortex (P=0.04). Conclusions: As a GnRH antagonist, cetrorelix can be considered as one of the effective drugs to protect the granulosa cells against chemotherapy-induced damages in cancer disease.
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