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1
Exposure to ethinylestradiol during prenatal development and postnatal supplementation with testosterone causes morphophysiological alterations in the prostate of male and female adult gerbils.在产前发育过程中暴露于乙炔雌二醇,以及在产后用睾酮进行补充,会导致雄性和雌性成年沙鼠前列腺的形态生理学改变。
Int J Exp Pathol. 2011 Apr;92(2):121-30. doi: 10.1111/j.1365-2613.2010.00756.x. Epub 2011 Feb 12.
2
Microscopic comparative study of the exposure effects of testosterone cypionate and ethinylestradiol during prenatal life on the prostatic tissue of adult gerbils.睾酮 Cypionate 和乙炔雌二醇在产前生活中对成年沙鼠前列腺组织的暴露效应的微观比较研究。
Microsc Res Tech. 2012 Aug;75(8):1084-92. doi: 10.1002/jemt.22034. Epub 2012 Apr 5.
3
Prenatal exposure to ethinylestradiol alters the morphologic patterns and increases the predisposition for prostatic lesions in male and female gerbils during ageing.孕期暴露于炔雌醇会改变雄性和雌性沙鼠衰老过程中的形态模式,并增加前列腺病变的易感性。
Int J Exp Pathol. 2016 Feb;97(1):5-17. doi: 10.1111/iep.12153. Epub 2016 Feb 8.
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Neonatal exposure to ethinylestradiol increases ventral prostate growth and promotes epithelial hyperplasia and inflammation in adult male gerbils.新生期接触乙炔雌二醇会增加成年雄性沙鼠腹侧前列腺的生长,并促进其上皮增生和炎症。
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Pubertal exposure to ethinylestradiol promotes different effects on the morphology of the prostate of the male and female gerbil during aging.青春期接触乙炔雌二醇会对雄性和雌性沙鼠衰老过程中前列腺的形态产生不同影响。
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Prenatal and pubertal exposure to 17α-ethinylestradiol cause morphological changes in the prostate of old gerbils.孕前期和青春期接触 17α-乙炔基雌二醇会导致老年沙鼠前列腺发生形态变化。
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Ethinylestradiol and its effects on the macrophages in the prostate of adult and senile gerbils.炔雌醇及其对成年和老年沙鼠前列腺中巨噬细胞的影响。
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Prenatal testosterone exposure as a model for the study of endocrine-disrupting chemicals on the gerbil prostate.产前睾酮暴露作为研究内分泌干扰物对沙鼠前列腺影响的模型。
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Testosterone exposure in prenatal life disrupts epithelial nuclear morphology, smooth muscle layer pattern, and FGF10 and Shh expression in prostate.产前暴露于睾酮会破坏前列腺的上皮核形态、平滑肌层模式以及 FGF10 和 Shh 的表达。
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Tissue evidence of the testosterone role on the abnormal growth and aging effects reversion in the gerbil (Meriones unguiculatus) prostate.睾酮对沙鼠(长爪沙鼠)前列腺异常生长及衰老效应逆转作用的组织学证据。
Anat Rec A Discov Mol Cell Evol Biol. 2006 Nov;288(11):1190-200. doi: 10.1002/ar.a.20391.

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1
Prenatal and pubertal exposure to ethinylestradiol induces Long-Term stromal and epithelial changes in the gerbil dorsal prostate.孕期和青春期接触乙炔雌二醇会导致沙鼠背侧前列腺出现长期的基质和上皮变化。
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Dysregulation of AR and ERα caused ovarian alterations in gerbils prenatally exposed to 17α-ethinylestradiol and pequi oil.在产前暴露于17α-乙炔雌二醇和美洲苦配巴油的沙鼠中,雄激素受体(AR)和雌激素受体α(ERα)的失调导致了卵巢改变。
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Neonatal exposure to ethinylestradiol increases ventral prostate growth and promotes epithelial hyperplasia and inflammation in adult male gerbils.新生期接触乙炔雌二醇会增加成年雄性沙鼠腹侧前列腺的生长,并促进其上皮增生和炎症。
Int J Exp Pathol. 2016 Oct;97(5):380-388. doi: 10.1111/iep.12208. Epub 2016 Dec 5.
4
Prenatal exposure to ethinylestradiol alters the morphologic patterns and increases the predisposition for prostatic lesions in male and female gerbils during ageing.孕期暴露于炔雌醇会改变雄性和雌性沙鼠衰老过程中的形态模式,并增加前列腺病变的易感性。
Int J Exp Pathol. 2016 Feb;97(1):5-17. doi: 10.1111/iep.12153. Epub 2016 Feb 8.
5
Prepubertal exposure to bisphenol-A induces ERα upregulation and hyperplasia in adult gerbil female prostate.青春期前暴露于双酚A会导致成年沙鼠雌性前列腺中雌激素受体α上调和增生。
Int J Exp Pathol. 2015 Jun;96(3):188-95. doi: 10.1111/iep.12120. Epub 2015 Jun 22.

本文引用的文献

1
Disorders related with ageing in the gerbil female prostate (Skene's paraurethral glands).沙鼠女性前列腺(斯基恩氏尿道旁腺)与衰老相关的疾病。
Int J Exp Pathol. 2010 Apr;91(2):132-43. doi: 10.1111/j.1365-2613.2009.00685.x. Epub 2009 Dec 22.
2
Silver Impregnation of Reticulum in Paraffin Sections.石蜡切片中网织纤维的银浸染法
Am J Pathol. 1937 Nov;13(6):993-1002.5.
3
The dual, opposing roles of estrogen in the prostate.雌激素在前列腺中的双重、相反作用。
Ann N Y Acad Sci. 2009 Feb;1155:174-86. doi: 10.1111/j.1749-6632.2009.04360.x.
4
Hormonal oscillations during the estrous cycle influence the morphophysiology of the gerbil (Meriones unguiculatus) female prostate (skene paraurethral glands).发情周期中的激素振荡会影响沙鼠(长爪沙鼠)雌性前列腺(斯基恩尿道旁腺)的形态生理学。
Biol Reprod. 2008 Dec;79(6):1084-91. doi: 10.1095/biolreprod.108.070540. Epub 2008 Aug 6.
5
Estrogen-regulated development and differentiation of the prostate.雌激素对前列腺发育和分化的调节作用。
Differentiation. 2008 Jul;76(6):660-70. doi: 10.1111/j.1432-0436.2008.00291.x. Epub 2008 Jun 28.
6
Endocrine disruptors and prostate cancer risk.内分泌干扰物与前列腺癌风险
Endocr Relat Cancer. 2008 Sep;15(3):649-56. doi: 10.1677/ERC-08-0043. Epub 2008 Jun 4.
7
Perinatal exposure to oestradiol and bisphenol A alters the prostate epigenome and increases susceptibility to carcinogenesis.围产期暴露于雌二醇和双酚A会改变前列腺表观基因组并增加致癌易感性。
Basic Clin Pharmacol Toxicol. 2008 Feb;102(2):134-8. doi: 10.1111/j.1742-7843.2007.00166.x.
8
Age-related histopathological lesions in the Mongolian gerbil ventral prostate as a good model for studies of spontaneous hormone-related disorders.蒙古沙鼠腹侧前列腺中与年龄相关的组织病理学病变作为自发性激素相关疾病研究的良好模型。
Int J Exp Pathol. 2008 Feb;89(1):13-24. doi: 10.1111/j.1365-2613.2007.00550.x.
9
The role of estrogens and estrogen receptors in normal prostate growth and disease.雌激素及雌激素受体在前列腺正常生长与疾病中的作用。
Steroids. 2008 Mar;73(3):233-44. doi: 10.1016/j.steroids.2007.10.013. Epub 2007 Nov 12.
10
Prostatic hormonal carcinogenesis is mediated by in situ estrogen production and estrogen receptor alpha signaling.前列腺激素致癌作用由原位雌激素生成和雌激素受体α信号传导介导。
FASEB J. 2008 May;22(5):1512-20. doi: 10.1096/fj.07-9526com. Epub 2007 Nov 30.

在产前发育过程中暴露于乙炔雌二醇,以及在产后用睾酮进行补充,会导致雄性和雌性成年沙鼠前列腺的形态生理学改变。

Exposure to ethinylestradiol during prenatal development and postnatal supplementation with testosterone causes morphophysiological alterations in the prostate of male and female adult gerbils.

机构信息

Graduate Program in Cell and Structural Biology, Institute of Biology, Campinas State University, UNICAMP, Campinas, SP, Brazil.

出版信息

Int J Exp Pathol. 2011 Apr;92(2):121-30. doi: 10.1111/j.1365-2613.2010.00756.x. Epub 2011 Feb 12.

DOI:10.1111/j.1365-2613.2010.00756.x
PMID:21314741
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3081515/
Abstract

Steroids perform significant functions in prostatic development and growth, so that interferences of this equilibrium may predispose the gland to the development of diseases during the life. Embryonic and neonatal exposure to xenoestrogens, many of them with endocrine-disrupting potential, has been related to the induction of disturbances in reproductive system organs. Thus, this study aimed to analyse morphological and immunocytochemical aspects of prostate in both male and female adult gerbils either exposed to ethinylestradiol during the prenatal phase (pregnant females received 10 μg/kg, by gavage) (EE group) or exposed to testosterone (1 mg/kg) during the postnatal period (EE/T group). Serological analysis revealed a rise in estradiol levels in adult males and females of the EE group. A higher incidence of prostatic intraepithelial neoplasia (PIN) was observed in the male and female prostate of the treated groups, besides an increase in collagen and reticular fibres. Immunocytochemistry showed an increase in prostatic epithelial cells immunoreactive to AR and a presence of a smooth muscle layer, evidenced by α actin, in injured regions this way absent in prostatic epithelial buds. These pieces of evidence suggest that the alterations verified in the prostate in adulthood of both sexes may be due to the high oestrogen levels. Either males or females of the EE/T group showed normalized estradiol levels, although prostatic lesions could be observed. While the prostatic gland of male gerbils was more affected than the female prostate, this study showed that the exposure to EE during this critical period of development disrupts the prostate of both sexes in terms of prostatic lesions.

摘要

类固醇在前列腺的发育和生长中发挥着重要作用,因此这种平衡的干扰可能使前列腺在生命过程中易患疾病。胚胎和新生动物暴露于许多具有内分泌干扰潜力的外源性雌激素,与生殖系统器官发育紊乱的诱导有关。因此,本研究旨在分析雄性和雌性成年沙鼠前列腺的形态和免疫细胞化学方面,这些沙鼠在产前阶段(怀孕雌性通过灌胃接受 10μg/kg 的雌二醇)(EE 组)或在产后阶段(EE/T 组)暴露于睾丸酮(1mg/kg)。血清学分析显示 EE 组成年雄性和雌性的雌二醇水平升高。在处理组的雄性和雌性前列腺中观察到前列腺上皮内瘤形成(PIN)的发生率更高,此外胶原和网状纤维增加。免疫细胞化学显示 AR 阳性前列腺上皮细胞的数量增加,并且在受损区域存在平滑肌层,α 肌动蛋白证明了这一点,而在前列腺上皮芽中不存在平滑肌层。这些证据表明,两性成年期前列腺的改变可能是由于雌激素水平升高所致。EE/T 组的雄性或雌性动物的雌二醇水平正常,但仍可观察到前列腺病变。虽然雄性沙鼠的前列腺比雌性前列腺受影响更大,但本研究表明,在发育的这个关键时期暴露于 EE 会破坏两性前列腺的前列腺病变。