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白藜芦醇通过减少DNA损伤并经由磷脂酰肌醇3激酶途径增强颗粒细胞增殖,从而促进体外培养的绵羊原始卵泡的激活。

Resveratrol promotes in vitro activation of ovine primordial follicles by reducing DNA damage and enhancing granulosa cell proliferation via phosphatidylinositol 3-kinase pathway.

作者信息

Bezerra Maria Éllida S, Gouveia Bruna B, Barberino Ricássio S, Menezes Vanúzia G, Macedo Taís J S, Cavalcante Agnes Y P, Monte Alane P O, Santos Jamile M S, Matos Maria Helena T

机构信息

Nucleus of Biotechnology Applied to Ovarian Follicle Development, Federal University of São Francisco Valley, Petrolina, PE, Brazil.

出版信息

Reprod Domest Anim. 2018 Dec;53(6):1298-1305. doi: 10.1111/rda.13274. Epub 2018 Aug 13.

Abstract

We aimed to study the effects of resveratrol on the morphology, DNA fragmentation, follicular activation and cell proliferation after in vitro culture of ovine ovarian tissue, and to verify if PI3K pathway is involved in resveratrol action in the sheep ovary. Ovaries were collected and divided into fragments. One fragment was fixed for histology (fresh control). The remaining fragments were cultured for 7 days in control medium (α-MEM ) alone or with resveratrol (2, 10 or 30 µM). After culture, ovarian tissue was destined to morphological analysis. TUNEL and proliferating cell nuclear antigen (PCNA) analyses were performed in the fresh control, α-MEM and 2 µM resveratrol. Inhibition of PI3K activity was performed through pre-treatment with LY294002. The percentage of normal follicles was similar between α-MEM and 2 µM resveratrol, and higher than those in other resveratrol treatments. An increase in follicular activation was observed in all treatments compared to fresh control. DNA fragmentation decreased in tissues cultured in 2 µM resveratrol compared to α-MEM . Moreover, PCNA-positive cells were higher in 2 µM resveratrol than in α-MEM . LY294002 inhibited follicular activation stimulated by α-MEM and 2 µM resveratrol. In conclusion, 2 µM resveratrol promotes primordial follicle activation compared to the fresh control by reducing DNA fragmentation and stimulating granulosa cell proliferation through activation of the PI3K pathway.

摘要

我们旨在研究白藜芦醇对绵羊卵巢组织体外培养后的形态、DNA片段化、卵泡激活和细胞增殖的影响,并验证PI3K信号通路是否参与白藜芦醇在绵羊卵巢中的作用。采集卵巢并切成碎片。一片碎片用于组织学固定(新鲜对照)。其余碎片在单独的对照培养基(α-MEM)或含白藜芦醇(2、10或30 μM)的培养基中培养7天。培养后,对卵巢组织进行形态学分析。在新鲜对照、α-MEM和2 μM白藜芦醇组中进行TUNEL和增殖细胞核抗原(PCNA)分析。通过用LY294002预处理来抑制PI3K活性。α-MEM组和2 μM白藜芦醇组的正常卵泡百分比相似,且高于其他白藜芦醇处理组。与新鲜对照相比,所有处理组的卵泡激活均增加。与α-MEM组相比,2 μM白藜芦醇培养的组织中DNA片段化减少。此外,2 μM白藜芦醇组的PCNA阳性细胞高于α-MEM组。LY294002抑制了α-MEM和2 μM白藜芦醇刺激的卵泡激活。总之,与新鲜对照相比,2 μM白藜芦醇通过减少DNA片段化并通过激活PI3K信号通路刺激颗粒细胞增殖,从而促进原始卵泡激活。

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