环磷酰胺对大鼠胎盘发育的影响。

IF 0.9 4区 医学 Q4 PATHOLOGY
Satoshi Furukawa, Naho Tsuji, Seigo Hayashi, Yusuke Kuroda, Masayuki Kimura, Chisato Kojima, Kazuya Takeuchi
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引用次数: 0

摘要

我们研究了环磷酰胺(CPA)对妊娠大鼠胎盘发育的形态学影响。妊娠大鼠单次腹腔注射CPA,剂量为0 mg/kg(对照组),妊娠第12天注射25 mg/kg (CPA GD 12治疗组),妊娠第14天注射25 mg/kg (CPA GD 14治疗组)。cppa处理组胎儿和胎盘重量下降,cpdp 12处理组胎儿从gdp 17开始完全吸收,cpdp 14处理组胎儿出现外部畸形。在组织病理学上,CPA诱导胎盘各部分细胞凋亡和/或细胞增殖抑制。在迷宫区,合胞滋养细胞选择性减少,形成小胎盘。在基底区,海绵滋养细胞数量减少,导致糖原细胞岛发育不全。此外,在GD 15时,少量间质滋养细胞从基区向子宫腺侵袭。这些病变的严重程度在CPA GD 12治疗组高于CPA GD 14治疗组。在子宫内膜腺中,子宫自然杀伤细胞数量减少,但不影响子宫内膜腺的发育。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of cyclophosphamide on rat placental development.

We examined the morphological effects of cyclophosphamide (CPA) on placental development in pregnant rats. CPA was administered as a single dose to pregnant rats intraperitoneally at 0 mg/kg (the control group), 25 mg/kg on gestation day (GD) 12 (the CPA GD 12-treated group), and 25 mg/kg on GD 14 (the CPA GD 14-treated group). The fetal and placental weight decreased in the CPA-treated groups, complete fetal resorption from GD 17 onwards in the CPA GD 12-treated group, and external malformations in the CPA GD 14-treated group. Histopathologically, CPA induced apoptosis and/or cell proliferation inhibition in each part of the placenta. In the labyrinth zone, syncytiotrophoblasts were selectively reduced, resulting in a small placenta. In the basal zone, the number of spongiotrophoblasts was reduced, resulting in hypoplasia of glycogen cell islands. In addition, a small number of interstitial trophoblasts invaded the metrial gland from the basal zone on GD 15. The severity of these lesions was higher in the CPA GD 12-treated group than in the CPA GD 14-treated group. In the metrial gland, although the number of uterine natural killer cells was reduced, metrial gland development was not affected.

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来源期刊
Journal of Toxicologic Pathology
Journal of Toxicologic Pathology PATHOLOGY-TOXICOLOGY
CiteScore
2.10
自引率
16.70%
发文量
22
审稿时长
>12 weeks
期刊介绍: JTP is a scientific journal that publishes original studies in the field of toxicological pathology and in a wide variety of other related fields. The main scope of the journal is listed below. Administrative Opinions of Policymakers and Regulatory Agencies Adverse Events Carcinogenesis Data of A Predominantly Negative Nature Drug-Induced Hematologic Toxicity Embryological Pathology High Throughput Pathology Historical Data of Experimental Animals Immunohistochemical Analysis Molecular Pathology Nomenclature of Lesions Non-mammal Toxicity Study Result or Lesion Induced by Chemicals of Which Names Hidden on Account of the Authors Technology and Methodology Related to Toxicological Pathology Tumor Pathology; Neoplasia and Hyperplasia Ultrastructural Analysis Use of Animal Models.
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