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- W2023573949 abstract "Objective: EGF-R is expressed in the murine ovary and ligand (EGF, TGFa) activation plays a role in normal folliculogenesis. In this study, we investigated the effect of ovulation induction with exogenous gonadotropins on in vivo EGF-R expression in rat ovarian follicles during the estrous cycle.Design: Prospective, randomized, controlled murine study, approved by the animal IRB, at an academic institution.Materials/Methods: Adult female Wistar rats were housed on a 12-hour light/12-hour dark schedule. Estrous cycles were monitored by vaginal smears. Animals were separated into two groups: rats in the study group were injected intraperitoneally with 10 IU PMSG in early proestrus followed by 10 IU hCG 56 hours after PMSG; rats in the control group were injected with 0.9% saline only. Three animals in each group were euthanized according to their vaginal smears at late proestrus, estrus and metestrus. The ovaries were cryopreserved. Immunohistochemistry was performed using a monoclonal anti-EGF-R antibody (Clone no. 29.1, mouse IgG) and a peroxidase-labeled goat anti-mouse IgG, as the secondary antibody. A chromogenic reaction was developed by incubation with a solution of 3-Amino-9-ethylcarbazole for 15 minutes. All sections were counterstained with Mayer’s hematoxylin and evaluated by light microscopy. The intensity of EGF-R immunostaining in the ovarian follicles was assessed by using a computer-assisted image analysis and results were expressed as “pixels per area (ppa)”. Statistical analysis was done with the Wilcoxon test and ANOVA with post-hoc tests, where appropriate. P value of <0.05 was considered significant.Results: In late proestrus, there was a weak EGF-R expression in the control group, while moderate staining was seen in the study group (P = 0.06). During estrus, EGF-R expression significantly increased in the control group (p < 0.05 vs proestrus), while it decreased in the PMSG stimulated group (P = NS vs proestrus). EGF-R staining was lower during estrus in the PMSG stimulated group when compared to that in the control group (p < 0.05). Following ovulation, during metestrus, EGF-R expression decreased in the control group, although not significantly (P = NS, vs estrus), and it increased in the study group (p < 0.05, vs estrus). However, the EGF-R staining during metestrus was comparable between control and study groups (P = NS).Conclusions: Exogenous gonadotropin administration to cycling rats significantly modulates EGF-R expression in ovarian follicles in vivo when compared to cycling controls. We postulate that changes in EGF-R expression in the granulosa and theca cells during gonadotropin stimulation may modulate ligand (EGF and TGFa) tissue effects during folliculogenesis.Supported By: University of Illinois Campus Research Board, Chicago, Illinois Objective: EGF-R is expressed in the murine ovary and ligand (EGF, TGFa) activation plays a role in normal folliculogenesis. In this study, we investigated the effect of ovulation induction with exogenous gonadotropins on in vivo EGF-R expression in rat ovarian follicles during the estrous cycle. Design: Prospective, randomized, controlled murine study, approved by the animal IRB, at an academic institution. Materials/Methods: Adult female Wistar rats were housed on a 12-hour light/12-hour dark schedule. Estrous cycles were monitored by vaginal smears. Animals were separated into two groups: rats in the study group were injected intraperitoneally with 10 IU PMSG in early proestrus followed by 10 IU hCG 56 hours after PMSG; rats in the control group were injected with 0.9% saline only. Three animals in each group were euthanized according to their vaginal smears at late proestrus, estrus and metestrus. The ovaries were cryopreserved. Immunohistochemistry was performed using a monoclonal anti-EGF-R antibody (Clone no. 29.1, mouse IgG) and a peroxidase-labeled goat anti-mouse IgG, as the secondary antibody. A chromogenic reaction was developed by incubation with a solution of 3-Amino-9-ethylcarbazole for 15 minutes. All sections were counterstained with Mayer’s hematoxylin and evaluated by light microscopy. The intensity of EGF-R immunostaining in the ovarian follicles was assessed by using a computer-assisted image analysis and results were expressed as “pixels per area (ppa)”. Statistical analysis was done with the Wilcoxon test and ANOVA with post-hoc tests, where appropriate. P value of <0.05 was considered significant. Results: In late proestrus, there was a weak EGF-R expression in the control group, while moderate staining was seen in the study group (P = 0.06). During estrus, EGF-R expression significantly increased in the control group (p < 0.05 vs proestrus), while it decreased in the PMSG stimulated group (P = NS vs proestrus). EGF-R staining was lower during estrus in the PMSG stimulated group when compared to that in the control group (p < 0.05). Following ovulation, during metestrus, EGF-R expression decreased in the control group, although not significantly (P = NS, vs estrus), and it increased in the study group (p < 0.05, vs estrus). However, the EGF-R staining during metestrus was comparable between control and study groups (P = NS). Conclusions: Exogenous gonadotropin administration to cycling rats significantly modulates EGF-R expression in ovarian follicles in vivo when compared to cycling controls. We postulate that changes in EGF-R expression in the granulosa and theca cells during gonadotropin stimulation may modulate ligand (EGF and TGFa) tissue effects during folliculogenesis. Supported By: University of Illinois Campus Research Board, Chicago, Illinois" @default.
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- W2023573949 title "Effect of exogenous gonadotropins on in vivo epidermal growth factor receptor (EGF-R) expression in murine ovarian follicles throughout the estrous cycle." @default.
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