The protective effect of erythropoietin on ischemia- reperfusion injury caused by ovarian torsion-detorsion in the experimental rat model.

Pub Date : 2023-06-01 DOI:10.1080/01478885.2022.2122653
Bahar Kartal, Mehmet Fatih Bozkurt, Ebru Alimoğullari, Uygar Saçık
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引用次数: 1

Abstract

Ovarian torsion is one of the most dangerous gynecological emergencies requiring surgery. A total of 50%-90% ovarian torsion cases are caused by physiological cysts, endometriosis, and other benign or malignant ovarian neoplasms. The aim of the study was to investigate the effects of erythropoietin (EPO) treatment on ischemia/reperfusion (IR) injury caused by ovarian torsion/detorsion (T/D) injury. Thirty female Wistar albino rats were divided into five groups as follows: Group I: Control; Group II: Torsion (T); Group III: Torsion/Detorsion(T/D); Group IV: Torsion/Detorsion (T/D) + EPO; Group V: EPO. Sections of the ovaries were evaluated for histopathological changes with hematoxylin and eosin stain, a immunohistochemical assay for caspase 3 expression, and the TUNEL assay for apoptosis. Ovarian sections from torsion/detorsion and torsion groups showed more hemorrhage, vascular congestion, edema, degenerative granulosa, and stromal cells. Fewer histopathological changes were found in EPO and T/D + EPO groups. Caspase 3 and TUNEL positive cells were significantly increased in the torsion/detorsion group as compared with the other groups (p < 0.05). Treatment with erythropoietin decreased the number of caspase 3 and TUNEL positive cells. The results of the study showed that erythropoietin administration is effective for recovery from degenerative changes in the ovary induced by the torsion-detorsion injury.

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促红细胞生成素对实验性大鼠卵巢扭扭所致缺血再灌注损伤的保护作用。
卵巢扭转是最危险的妇科急症之一,需要手术治疗。50%-90%的卵巢扭转病例是由生理性囊肿、子宫内膜异位症和其他卵巢良恶性肿瘤引起的。本研究旨在探讨促红细胞生成素(EPO)治疗对卵巢扭转/扭转(T/D)损伤所致缺血/再灌注(IR)损伤的影响。雌性Wistar白化大鼠30只,随机分为5组:第一组:对照组;第二组:扭转(T);第三组:扭转/变形(T/D);IV组:扭转/扭转(T/D) + EPO;V组:EPO。卵巢切片采用苏木精和伊红染色、caspase 3表达的免疫组织化学检测和TUNEL细胞凋亡检测来评估组织病理学变化。扭转/扭转组和扭转组卵巢切片显示出血、血管充血、水肿、变性颗粒和间质细胞较多。EPO组和T/D + EPO组组织病理改变较少。与其他组相比,扭转/扭转组Caspase 3和TUNEL阳性细胞显著增加(p
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