Bulut Gulay, Kurdoglu Zehra, Dönmez Yeliz Bozdemir, Kurdoglu Mertihan, Erten Remzi
Department of Pathology, Yuzuncu Yil University Faculty of Medicine Van, Turkey.
Department of Obstetrics and Gynecology, Ankara Education and Research Hospital Ankara, Turkey.
Int J Clin Exp Pathol. 2015 Aug 1;8(8):8774-85. eCollection 2015.
In our study, we aimed to investigate the effects of Jun N-terminal kinase inhibitor (SP600125) on fibrosis and inflammation in rats with polycystic ovary syndrome (PCOS).
50 Wistar-albino rats were divided into five groups (n=10 each): control group, sham group, PCOS group, SP600125+ PCOS group and SP600125 group. In the estradiol valerate (EV)-treated group in which PCOS was injected with a single 4 mg/kg i.p. of EV in 0.2 ml sesame oil and the rats were sacrificed on day 60. The estradiol valerate (EV)-treated + SP600125-treated group was injected with a single 4 mg/kg i.p. of EV in 0.2 ml sesame oil. As of day 60, the treatment group was additionally given 15 mg/kg i.p. of SP600125 once daily for 4 consecutive days and the rats were sacrificed on day 65. Histopathological findings (ovarian morphology, edema, inflammatory cell infiltration, vascular congestion and hyperemia) and collagen type IV immunoexpression were assessed.
The SP600125+ PCOS group showed a significant level of improvement in ovarian follicle morphology, edema, inflammatory infiltrate, vascular congestion and hyperemia as compared with the PCOS group. Furthermore, collagen type IV immunoexpression showed a significant reduction in staining intensity on the theca cell layer and ovary stroma as compared to the PCOS group.
This study demonstrates the therapeutic effect of SP600125 in the prevention of PCOS in an experimental model.
在我们的研究中,我们旨在研究Jun氨基末端激酶抑制剂(SP600125)对多囊卵巢综合征(PCOS)大鼠纤维化和炎症的影响。
将50只Wistar白化大鼠分为五组(每组n = 10):对照组、假手术组、PCOS组、SP600125 + PCOS组和SP600125组。在戊酸雌二醇(EV)处理组中,给大鼠腹腔注射一次4 mg/kg的EV(溶于0.2 ml芝麻油中),并在第60天处死大鼠。戊酸雌二醇(EV)处理 + SP600125处理组腹腔注射一次4 mg/kg的EV(溶于0.2 ml芝麻油中)。从第60天起,治疗组每天额外腹腔注射15 mg/kg的SP600125,连续4天,并在第65天处死大鼠。评估组织病理学结果(卵巢形态、水肿、炎性细胞浸润、血管充血和淤血)以及IV型胶原免疫表达。
与PCOS组相比,SP600125 + PCOS组在卵巢卵泡形态、水肿、炎性浸润、血管充血和淤血方面有显著改善。此外,与PCOS组相比,IV型胶原免疫表达显示在卵泡膜细胞层和卵巢基质上的染色强度显著降低。
本研究证明了SP600125在实验模型中预防PCOS的治疗效果。