首页> 外文期刊>Bulgarian journal of veterinary medicine. >HISTOMORPHOMETRIC ANALYSIS OF GOAT UTERINE TISSUE ON?IN VITRO?EXPOSURE WITH OVARIAN HORMONES AND MIFEPRISTONE
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HISTOMORPHOMETRIC ANALYSIS OF GOAT UTERINE TISSUE ON?IN VITRO?EXPOSURE WITH OVARIAN HORMONES AND MIFEPRISTONE

机译:山羊子宫组织的组织形态分析?卵巢激素和米非司酮暴露

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Uterus, the largest reproductive tract organ in female mammals, is the site of implantation of fertilised egg and foetus development. Uterus is a dynamic reproductive organ; its morphology alters with reproductive phase and steroidal cues. The aim of the present study was to assess the effects of progesterone (P4), estrogen (E2) and antiprogestogen i.e., mifepristone on goat’s uterine histoarchitecture in in vitro short term culture. Uterine tissue slices were cultured in the presence of E2, P4 and mifepristone at the dose of 10–9 M, 10–7 M and 10–6 M respectively for 24 hours. Uterine morphology of E2- and P4-treated groups did not reveal marked changes from that of control group. Mifepristone treatment caused conspicuous changes in uterine histoarchitecture, led to congested endometrium, regressed uterine glands and constricted blood vessels. The changes observed in morphometry after E2 and P4 exposure included increased uterine gland diameter (47.00 and 45.95 μm respectively) and glandular epithelial cell height (18.37 and 17.43 μm respectively) while the mifepristone treatment resulted in significant reduction of gland diameter (34.95 μm) as well as epithelium height (14.25 μm) as compared to those in control group (39.9 and 15.56 μm respectively). These morphometrical changes revealed prominent regressive changes in anti-progestin treated group while E2 and P4 showed prolific effects in in vitro culture. Thus it is envisaged that E2 and P4 induced characteristic progressive changes in the histologic structure especially in endometrial glands of the goat uterus while anti-steroidogenic formulation i.e. mifepristone severely reduced the normal histoarchitecture of the uterus which is a prerequisite for implantation.
机译:女性哺乳动物最大的生殖道器官子宫,是植入受精卵和胎儿发育的部位。子宫是一种动态生殖器官;它的形态学改变了生殖期和甾体提示。本研究的目的是评估孕酮(P4),雌激素(E2)和抗溶剂I.E.,米非司酮对山羊子宫组培养物中的山羊母细胞构建的影响。在e2,p4和vifepristone的存在下分别在10-9μm,10-7m和10-6m的剂量下培养子宫组织切片24小时。 E2-和P4治疗组的子宫形态并未显示对照组的显着变化。米非司酮治疗引起子宫组织建筑的显着变化,导致拥挤的子宫内膜,回归子宫腺和收缩血管。在E2和P4暴露之后,在形态学中观察到的变化包括增加的子宫腺直径(分别为47.00和45.95μm)和腺上皮细胞高度(分别分别为18.37和17.43μm),而米非司治疗导致腺体直径(34.95μm)显着降低与对照组(分别为39.9和15.56μm)相比,与上皮高度(14.25μm)相比。这些形态学变化揭示了抗孕激素治疗组的突出渐变变化,而E2和P4在体外培养方面表现出多平性。因此,设想E2和P4诱导组织学结构的特征性逐渐变化,特别是在山羊子宫的子宫内膜腺体中,而抗分原制剂I.。米非司酮严重降低了子宫的正常组织建筑,这是植入的先决条件。

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