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The effect of leptin on luteal angiogenic factors during the luteal phase of the estrous cycle in goats

机译:瘦素对山羊发情周期黄体期黄体血管生成因子的影响

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摘要

Fibroblast growth factor 2 (FGF2), angiopoietin 1 (Ang1), and vascular endothelial growth factor (VEGF) are angiogenic factors implicated in the vascular development of the corpus luteum (CL). Each factor is regulated or influenced by leptin in non-ovarian tissues. Moreover, leptin and its receptor, ObRb, have been identified in luteal tissue throughout the luteal phase. Therefore, leptin is hypothesized to influence luteal vasculature through the regulation of FGF2, Ang1, and VEGF. Multiparous, cycling crossbred female goats (does) were allocated to early (n=12), mid (n=8), and late (n=11) stages of the luteal phase for CL collection. Luteal tissue was harvested and either snap frozen in liquid N2, paraffin embedded, or cultured with leptin (0, 10−12, 10−11, 10−10, 10−9, 10−8 M). Tissue was analyzed for FGF2, Ang1, VEGF, ObRb, and leptin expression. Angiopoietin 1, FGF2, VEGF expression was higher (P≤0.001) in the mid-luteal stage than the early stage. Expression decreased (P≤0.001) during the late luteal stage with the exception of VEGF, which remained elevated. In contrast, leptin and ObRb were lowest (P≤0.003) during the mid-luteal stage compared to the early and late stages. All factors were detected in and/or around vessels in early stage tissue compared to mid and late stages. Leptin stimulated (P≤0.02) Ang1, FGF2, and VEGF expression only in early stage luteal cultures. Collectively, these data provide evidence that leptin may be involved in the luteal angiogenic process during the early stage of CL formation.
机译:成纤维细胞生长因子2(FGF2),血管生成素1(Ang1)和血管内皮生长因子(VEGF)是与黄体(CL)血管发育有关的血管生成因子。每种因子在非卵巢组织中受瘦素调节或影响。此外,在整个黄体期都在黄体组织中发现了瘦素及其受体ObRb。因此,假设瘦蛋白可通过调节FGF2,Ang1和VEGF影响黄体血管。将多胎,循环杂交的雌性山羊(种)分配到黄体期的早期(n = 12),中期(n = 8)和后期(n = 11)进行CL收集。收获黄体组织并在液态N2中速冻,石蜡包埋或与瘦素一起培养(0、10 -12 ,10 -11 ,10 -10 ,10 −9 ,10 −8 M)。分析组织的FGF2,Ang1,VEGF,ObRb和瘦蛋白表达。黄体中部血管生成素1,FGF2,VEGF的表达高于早期(P≤0.001)。在黄体后期,表达降低(P≤0.001),但VEGF除外,VEGF仍然升高。相比之下,与早期和晚期相比,在黄体中期阶段,瘦素和ObRb最低(P≤0.003)。与中晚期相比,在早期组织中和/或周围的血管中检测到所有因素。瘦素仅在早期黄体培养物中刺激(P≤0.02)Ang1,FGF2和VEGF表达。总体而言,这些数据提供了证据,表明瘦素可能在CL形成的早期参与黄体血管生成过程。

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