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. 2015 Aug 1;8(8):8774-85.
eCollection 2015.

Effects of jnk inhibitor on inflammation and fibrosis in the ovary tissue of a rat model of polycystic ovary syndrome

Affiliations

Effects of jnk inhibitor on inflammation and fibrosis in the ovary tissue of a rat model of polycystic ovary syndrome

Gulay Bulut et al. Int J Clin Exp Pathol. .

Abstract

Objective: 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).

Method: 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.

Results: 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.

Conclusion: This study demonstrates the therapeutic effect of SP600125 in the prevention of PCOS in an experimental model.

Keywords: Fibrosis; Jun N-terminal kinase inhibitor; inflammation; polycystic ovary syndrome.

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Figures

Figure 1
Figure 1
A. Section of an ovary from group 3 (H&E, ×40). B. Cystic degenerating follicles showing a thin granulosa layer and debris in follicular fluid (H&E, ×100). C. An atretic secondary follicle with granulosa cells showing signs of atresia and intact theca cells (H&E, ×200).
Figure 2
Figure 2
Histological examination of normal ovaries. Different developmental stages of follicles were detected in group 1 (A) (H&E, ×40), group 2 (B) (H&E, ×40), group 4 (C) (H&E, ×40), group 5 (D) (H&E, ×40).
Figure 3
Figure 3
Distribution of degree of edema of ovarian stroma.
Figure 4
Figure 4
Distribution of degree of vascular congestion and hyperemia.
Figure 5
Figure 5
Distribution of degree of inflammation.
Figure 6
Figure 6
Distribution of staining intensities among groups with collagen type IV staining in the ovarian stroma.
Figure 7
Figure 7
Distribution of staining intensities among groups with collagen type IV staining in the theca cell layer.
Figure 8
Figure 8
Expression of collagen type IV in rat ovaries. Group1 (A) (collagen type IV, ×100), group 2 (B) (collagen type IV, ×100) , group 5 (C) (collagen type IV, ×100), group 4 (D) (collagen type IV, ×100), group 3 (E, F) (collagen type IV, ×100, ×200).

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