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

• Published in: Reproduction in domestic animals Vol. 53; no. 6; pp. 1298 - 1305
• Main Authors: 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.
• Format: Journal Article
• Language: English
• Published: Germany Blackwell Publishing Ltd 01.12.2018
• Subjects: 1-Phosphatidylinositol 3-kinase; Animals; apoptosis; Cell activation; Cell culture; Cell growth; Cell proliferation; Cell Proliferation - drug effects; Cytology; Deoxyribonucleic acid; DNA; DNA damage; DNA fragmentation; DNA Fragmentation - drug effects; Female; Follicles; Fragmentation; Fragments; growth; Histology; In Situ Nick-End Labeling - veterinary; Kinases; Morphology; oocyte; Ovarian Follicle - drug effects; Ovarian Follicle - physiology; Ovaries; Phosphatidylinositol 3-Kinase - physiology; PI3K; polyphenol; Proliferating cell nuclear antigen; Proliferating Cell Nuclear Antigen - metabolism; Resveratrol; Resveratrol - pharmacology; Sheep; Tissue culture; Tissue Culture Techniques - veterinary; apoptosis; growth; oocyte; PI3K; polyphenol
• ISSN: 0936-6768; 1439-0531
• DOI: 10.1111/rda.13274

Contents 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.