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کلیدواژهها
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folliculogenesis, inflammation, ischemia–reperfusion, L-carnitine, mouse, ovary transplantation, oxidative stress, stereology.
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چکیده
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Context. Ovarian tissue transplantation is performed to preserve fertility in patients undergoing chemotherapy and radiotherapy. However, the ischemia-reperfusion injury which occurs after the ovarian tissue transplantation causes follicular depletion and apoptosis. L -Carnitine has antioxidant and anti-inflammation properties. Aims. Therefore, we aimed to investigate the beneficial effect of L -carnitine on mouse ovaries following heterotopic autotransplantation. Methods. Mice were randomly divided into three groups (six mice per group): control, autografted and autografted + L -carnitine (200 mg/kg daily intraperitoneal injections). Seven days after ovary autografting, the serum levels of malondialdehyde (MDA), total antioxidant capacity, tumor necrosis factor alpha (TNF-α), interleukin (IL)-6 and IL-10 were measured. Ovary histology, serum concentrations of progesterone and estradiol were also measured 28 days after autotransplantation. Data were analysed using one-way analysis of variance (ANOVA) and Tukey test, and the means were considered significantly different at P < 0.05. Key results. In the autografted + L -carnitine group, the total volume of the ovary, the volume of the cortex, the number of follicles, the serum concentrations of IL-10, estradiol and progesterone significantly increased compared to the autografted group. In the autografted + L -carnitine group, serum concentrations of IL-6, TNF-α and MDA were significantly decreased compared to the autografted group. Conclusions. Our results indicated that L -carnitine can ameliorate the consequences of ischemia-reperfusion on the mice ovarian tissue following autotransplantation. Implications. L -carnitine improves the structure and function of transplanted ovaries.
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