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大鼠诱导性多囊卵巢中生长因子的卵巢内定位

Intraovarian localization of growth factors in induced cystic ovaries in rats.

作者信息

Ortega H H, Salvetti N R, Amable P, Dallard B E, Baravalle C, Barbeito C G, Gimeno E J

机构信息

Department of Anatomy and Histology, National University of Litoral, Santa Fe, Argentina.

出版信息

Anat Histol Embryol. 2007 Apr;36(2):94-102. doi: 10.1111/j.1439-0264.2006.00726.x.

Abstract

We hypothesized that the special hormonal environment present in animals with cystic ovarian disease (COD) interferes with cellular production of growth factors (GFs). The objective of the present study was to characterize the expression of insulin-like growth factor (IGF)-I, fibroblast growth factor (FGF)-2 and vascular endothelial growth factor (VEGF) in induced COD using immunohistochemistry. We used an experimental model based on the exposure to constant light of adult rats during 15 weeks. We quantified the expression of GFs in cystic and normal ovaries by the Immunohistochemical Stained Area (IHCSA). In animals with COD, a significant reduction in the IHCSA of IGF-I in the follicular fluid, theca and granulosa layers of cysts occurred; and an increase in the interstitial tissue with regard to the control group. We found moderate immunoreactivity of FGF-2 in granulosa and theca layers of secondary and tertiary follicles and lower expression in the granulosa and theca interna layers of cystic follicles. Immunoexpression of VEGF was found in granulosa and theca cells of secondary and tertiary follicles. This study shows changes in the ovarian expression of IGF-I, FGF-2 and VEGF in induced COD. We can propose that an alteration in the control of the follicular dynamic, through the GFs, added to other features, could be involved in the ovarian cyst pathogenesis.

摘要

我们推测,患有囊性卵巢疾病(COD)的动物体内存在的特殊激素环境会干扰生长因子(GFs)的细胞生成。本研究的目的是利用免疫组织化学方法对诱导性COD中胰岛素样生长因子(IGF)-I、成纤维细胞生长因子(FGF)-2和血管内皮生长因子(VEGF)的表达进行表征。我们使用了一个基于成年大鼠连续15周暴露于持续光照下的实验模型。我们通过免疫组织化学染色面积(IHCSA)对囊性和正常卵巢中GFs的表达进行了量化。在患有COD的动物中,囊肿的卵泡液、卵泡膜和颗粒层中IGF-I的IHCSA显著降低;与对照组相比,间质组织增加。我们发现FGF-2在次级和三级卵泡的颗粒层和卵泡膜层有中度免疫反应性,而在囊性卵泡的颗粒层和卵泡内膜层表达较低。在次级和三级卵泡的颗粒细胞和卵泡膜细胞中发现了VEGF的免疫表达。本研究显示了诱导性COD中卵巢IGF-I、FGF-2和VEGF表达的变化。我们可以提出,通过GFs对卵泡动态控制的改变,加上其他特征,可能参与了卵巢囊肿的发病机制。

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