Effects of carvedilol on an ischemia/reperfusion model: Biochemical, histopathological and immunohistochemical evaluation.

Özsoy, Asker Zeki; Nursal, Ayşe Feyda; Arıcı, Akgül; Bütün, İlknur; Uysal, Murat; Irmak Sapmaz, Hilal; Kunt İşgüder, Çiğdem; Yılmaz Doğru, Hatice; Taş, Ufuk

Aim The aim of this study was to investigate the effects of carvedilol (CVD) on experimentally induced ovarian ischemia/reperfusion (I/R) injury in rats. Methods An ovarian I/R model was applied to rats, classified into three groups: 1 ( n = 7), sham operated (control); 2 ( n = 7), 3 h ischemia 3 h reperfusion (I/R); 3 ( n = 7), 3 h ischemia CVD 3 h reperfusion (I/R CVD). Malondialdehyde (MDA) levels and glutathione peroxidase (GSH-Px) and superoxide dismutase (SOD) activities in ovarian tissues and serum were measured. Tissue damage was examined histopathologically; Bax and caspase-3 expression was determined immunhistochemically. Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assay was performed to show apoptotic cell death. Results MDA levels in ovarian tissues were significantly increased in the I/R group compared with the control. CVD administration significantly decreased tissue MDA levels in the I/R CVD in comparison with the I/R group. GSH-Px activities in serum were higher in the I/R CVD than in the I/R group. SOD activities in tissue and serum were significantly decreased in the I/R compared with the control group. Histological examination showed a significant improvement in ovarian morphology in the I/R CVD compared with the I/R group. Bax and caspase-3 protein was more strongly expressed in the I/R group compared with the control and I/R CVD groups. Apoptotic index detected by TUNEL assay was significantly increased in the I/R and decreased in the I/R CVD group. Conclusion Our results suggest that CVD reduces the deleterious effects of oxidative damage on ovaries in a rat I/R model.

PROTEIN analysis; TISSUE analysis; BLOOD serum analysis; ADRENERGIC beta blockers; ANIMAL experimentation; APOPTOSIS; GENE expression; HISTOLOGY; IMMUNOHISTOCHEMISTRY; OXIDOREDUCTASES; RATS; REPERFUSION injury; SUPEROXIDE dismutase; UTERINE diseases; MALONDIALDEHYDE; OXIDATIVE stress; TORSION abnormality (Anatomy); CARVEDILOL; PHARMACODYNAMICS

Journal of Obstetrics & Gynaecology Research, 2016, Vol 42, Issue 9, p1132

1341-8076

Academic Journal

10.1111/jog.13028