Laboratory of Animal Reproduction (REPROA), State University of Londrina (UEL), Londrina, PR, Brazil.
Professional Master's in Veterinary Clinics, Laboratório de Biotecnologia da Reprodução Animal (REPROA), DCV, CCA, State University of Londrina (UEL), Londrina, PR, Cep: 86057-970, Brazil.
In Vitro Cell Dev Biol Anim. 2021 Oct;57(9):856-864. doi: 10.1007/s11626-021-00629-8. Epub 2021 Nov 8.
We evaluated the effect of quercetin on the in vitro culture of bovine ovarian fragments in relation to morphology, development, and oxidative stress. Ovaries (n = 12) from Nelore heifers (n = 6) were used. Each pair of ovaries was divided into nine fragments, and one fragment from each animal was fixed in Bouin solution for 24 h (histology control) or frozen (- 80°C; control for oxidative stress). Other ovarian fragments (n = 8) were distributed into concentrations of 0, 10, 25, and 50 μg/mL of quercetin added to the culture medium for 5 or 10 d. Data were analyzed by chi-square test or ANOVA followed by Tukey's test (P < 0.05). Treatment with 25 μg/mL quercetin resulted in the highest proportion of total intact follicles for 5 (67.3%) and 10 d (57.1%); the concentration of 25 μg/mL also presented the best proportion of developing follicles for 5 d (68.7%) and 10 d (62.8%). Treatment with 25 μg/mL quercetin resulted in significant ferric reduction for 10 d of culture, but not for 5 d. No difference (P > 0.1) was observed in the production of reactive oxygen species or in the oxidative degradation of lipids between treatments and non-cultivated controls. Treatment with 25 μg/mL quercetin preserved the morphological integrity of the developing follicles for 5 and 10 d of culture, in addition to promoting the best antioxidant potential after 10 d of culture in bovine ovarian fragments.
我们评估了槲皮素对牛卵巢组织体外培养的影响,涉及形态、发育和氧化应激。使用了来自内罗尔小母牛(n = 6)的卵巢(n = 12)。每对卵巢被分为 9 个片段,每个动物的一个片段固定在布因溶液中 24 小时(组织学对照)或在-80°C 下冷冻(氧化应激对照)。其他卵巢片段(n = 8)被分配到浓度为 0、10、25 和 50 μg/mL 的槲皮素添加到培养基中培养 5 或 10 天。数据通过卡方检验或方差分析后用 Tukey 检验进行分析(P < 0.05)。用 25 μg/mL 槲皮素处理可获得最多的总完整卵泡,分别为 5 天(67.3%)和 10 天(57.1%);浓度为 25 μg/mL 时,5 天(68.7%)和 10 天(62.8%)的发育卵泡比例也最好。用 25 μg/mL 槲皮素处理可导致培养 10 天的铁还原显著增加,但培养 5 天则不然。在培养期间,处理组与非培养对照组之间的活性氧产生或脂质氧化降解没有差异(P > 0.1)。用 25 μg/mL 槲皮素处理可保持发育卵泡的形态完整性,分别培养 5 天和 10 天,此外还可在牛卵巢片段培养 10 天后发挥最佳的抗氧化潜力。