Macedo T J S, Barros V R P, Monte A P O, Gouveia B B, Bezerra M É S, Cavalcante A Y P, Barberino R S, Menezes V G, Matos M H T
Nucleus of Biotechnology Applied to Ovarian Follicle Development,Federal University of São Francisco Valley,Petrolina-PE,Brazil.
Universidade Federal do Vale do São Francisco (UNIVASF),Campus de Ciências Agrárias. Colegiado de Medicina Veterinária - Laboratório de Biologia Celular,Citologia e Histologia,Rodovia BR 407,Km 12,Lote 543 - Projeto de Irrigação Nilo Coelho - S/N,C1.,CEP: 56300-990 - Petrolina - PE-Brasil.
Zygote. 2017 Aug;25(4):434-442. doi: 10.1017/S0967199417000193. Epub 2017 Jul 11.
The worldwide consumption of red wine, nuts and grapes has resulted in increased human exposure to resveratrol, which could affect reproductive function. However, the effect of resveratrol on in vitro culture of early-stage ovarian follicles has never been investigated. The aims of the present study were to evaluate the effect of resveratrol on sheep secondary follicle morphology, growth, DNA fragmentation, intracellular levels of glutathione (GSH) and active mitochondria. Secondary follicles were isolated from the ovaries and cultured for 18 days in supplemented α-MEM+ (control medium) or in control medium containing resveratrol (2, 10 or 30 µM). The parameters analyzed were morphology, antrum formation, follicle diameter, DNA fragmentation, GSH levels and mitochondrial activity. After 18 days, all resveratrol groups significantly decreased the percentages of morphologically normal follicles compared with the control group (α-MEM+). Antrum formation was higher in both α-MEM+ and 2 µM resveratrol groups than in the 10 µM resveratrol group. In addition, 30 µM resveratrol increased the percentage of oocytes with DNA damage compared with the control. Oocytes from follicles treated with 10 or 30 µM resveratrol significantly decreased intracellular GSH levels compared with the 2 µM resveratrol group. Moreover, follicles in α-MEM+ (control) showed more active mitochondria than those in 10 or 30 µM resveratrol. In conclusion, ovine isolated secondary follicles are able to grow to the antral stage after in vitro culture in medium containing 2 µM resveratrol, maintaining the same rates of DNA damage, GSH levels and mitochondrial function as the control medium. However, the addition of 30 µM resveratrol increased DNA fragmentation and oxidative stress through decreasing mitochondrial activity.
全球范围内对红酒、坚果和葡萄的消费导致人类接触白藜芦醇的机会增加,而这可能会影响生殖功能。然而,白藜芦醇对早期卵巢卵泡体外培养的影响从未被研究过。本研究的目的是评估白藜芦醇对绵羊次级卵泡形态、生长、DNA片段化、细胞内谷胱甘肽(GSH)水平和活性线粒体的影响。从卵巢中分离出次级卵泡,并在添加了α-MEM+的培养基(对照培养基)或含有白藜芦醇(2、10或30μM)的对照培养基中培养18天。分析的参数包括形态、卵泡腔形成、卵泡直径、DNA片段化、GSH水平和线粒体活性。18天后,与对照组(α-MEM+)相比,所有白藜芦醇组形态正常卵泡的百分比均显著降低。α-MEM+组和2μM白藜芦醇组的卵泡腔形成均高于10μM白藜芦醇组。此外,与对照组相比,30μM白藜芦醇增加了DNA损伤的卵母细胞百分比。与2μM白藜芦醇组相比,用10或30μM白藜芦醇处理的卵泡中的卵母细胞细胞内GSH水平显著降低。此外,α-MEM+(对照)组的卵泡线粒体活性比10或30μM白藜芦醇组的卵泡更高。总之,绵羊分离的次级卵泡在含有2μM白藜芦醇的培养基中体外培养后能够生长到卵泡腔阶段,其DNA损伤率、GSH水平和线粒体功能与对照培养基相同。然而,添加30μM白藜芦醇会通过降低线粒体活性增加DNA片段化和氧化应激。