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灵长类动物卵巢中血管生成因子的调节与作用

Regulation and action of angiogenic factors in the primate ovary.

作者信息

Stouffer R L, Martínez-Chequer J C, Molskness T A, Xu F, Hazzard T M

机构信息

Division of Reproductive Sciences, Oregon Regional Primate Research Center/Oregon Health Sciences University, Beaverton, OR 97006, USA.

出版信息

Arch Med Res. 2001 Nov-Dec;32(6):567-75. doi: 10.1016/s0188-4409(01)00323-x.

Abstract

The ephemerality of the maturing follicle and subsequent corpus luteum as they perform their gametogenic and/or endocrine functions during the ovarian cycle is associated with remarkable changes in local vasculature. Studies on the angiogenic and angiolytic process in the ovary, rare in healthy adult tissues, complement recent efforts to understand vasculogenesis in embryonic tissues and to control angiogenesis in pathologic states such as cancer. Several reports indicate that the newly discovered vascular-specific angiogenic factors are expressed in the ovary, notably members of the vascular endothelial growth factor (VEGF) and angiopoietin (Ang) families plus their receptors (VEGF-Rs, neuropilins, Tie). Unlike in many other tissues, gonadotropic hormones (particularly luteinizing hormone, [LH]) are major stimulators of angiogenesis and VEGF/Ang expression in the ovary. However, local factors such as insulin-like growth factors or oxygen tension likely modulate the angiogenic processes. Recent studies employing systemic or local administration of anti-angiogenic drugs (TNP-470 or fumagillin) or specific VEGF antagonists (VEGF antibody or soluble VEGFR-1) demonstrate a vital role for normal angiogenesis and VEGF action in follicle development, ovulation, or corpus luteum function. Further studies discerning the various angiogenic factors and their roles in controlling the growth, maturation, function, and regression of the vasculature in ovarian compartments during the menstrual cycle could yield novel strategies for manipulating fertility or for alleviating infertility.

摘要

成熟卵泡及随后的黄体在卵巢周期中执行配子发生和/或内分泌功能时的短暂性与局部血管系统的显著变化相关。卵巢中血管生成和血管溶解过程的研究在健康成年组织中较为罕见,它补充了近期在理解胚胎组织血管生成以及控制癌症等病理状态下血管生成方面所做的努力。一些报告表明,新发现的血管特异性血管生成因子在卵巢中表达,特别是血管内皮生长因子(VEGF)和血管生成素(Ang)家族的成员及其受体(VEGF-Rs、神经纤毛蛋白、Tie)。与许多其他组织不同,促性腺激素(特别是黄体生成素,[LH])是卵巢血管生成和VEGF/Ang表达的主要刺激因素。然而,胰岛素样生长因子或氧张力等局部因素可能会调节血管生成过程。最近使用抗血管生成药物(TNP-470或夫马洁林)或特异性VEGF拮抗剂(VEGF抗体或可溶性VEGFR-1)进行全身或局部给药的研究表明,正常血管生成和VEGF作用在卵泡发育、排卵或黄体功能中起着至关重要的作用。进一步研究识别各种血管生成因子及其在月经周期中控制卵巢各部分血管系统生长、成熟、功能和退化方面的作用,可能会产生操纵生育或缓解不孕的新策略。

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