• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

一种用于人类先兆子痫的新动物模型:对妊娠大鼠输注超低剂量内毒素

A new animal model for human preeclampsia: ultra-low-dose endotoxin infusion in pregnant rats.

作者信息

Faas M M, Schuiling G A, Baller J F, Visscher C A, Bakker W W

机构信息

Department of Pathology, University of Groningen, The Netherlands.

出版信息

Am J Obstet Gynecol. 1994 Jul;171(1):158-64. doi: 10.1016/0002-9378(94)90463-4.

DOI:10.1016/0002-9378(94)90463-4
PMID:8030692
Abstract

OBJECTIVE

An animal model for preeclampsia was developed by means of an ultra-low-dose endotoxin infusion protocol in conscious pregnant rats.

STUDY DESIGN

Rats received a permanent jugular vein cannula on day 0 of pregnancy, through which endotoxin (1.0 micrograms/kg body weight) (n = 10) or saline solution (n = 6) was infused during 1 hour on day 14 of pregnancy. Blood pressure, albuminuria, and platelet counts were measured, and histopathologic studies was performed in these rats.

RESULTS

A significant increase of blood pressure (p < 0.05) and of urinary albumin excretion (p < 0.05) was observed in endotoxin-treated pregnant animals, in contrast to control pregnant rats receiving saline solution. Platelet coagulopathy was found and glomerular fibrinogen deposits could be detected only in the endotoxin-treated pregnant rats. In addition, the activity of the glomerular antithrombotic enzyme adenosine diphosphatase was decreased in endotoxin-treated pregnant rats compared with saline solution-treated pregnant rats.

CONCLUSION

Because histopathologic and clinical events in this model mimic predominant features of human preeclampsia, this model may enable further study into the pathophysiologic mechanisms of this complication of pregnancy.

摘要

目的

通过对清醒妊娠大鼠采用超低剂量内毒素输注方案建立子痫前期动物模型。

研究设计

大鼠在妊娠第0天接受永久性颈静脉插管,在妊娠第14天通过该插管在1小时内输注内毒素(1.0微克/千克体重)(n = 10)或生理盐水(n = 6)。测量血压、蛋白尿和血小板计数,并对这些大鼠进行组织病理学研究。

结果

与接受生理盐水的对照妊娠大鼠相比,在内毒素处理的妊娠动物中观察到血压显著升高(p < 0.05)和尿白蛋白排泄显著增加(p < 0.05)。仅在内毒素处理的妊娠大鼠中发现血小板凝血病且可检测到肾小球纤维蛋白原沉积。此外,与生理盐水处理的妊娠大鼠相比,内毒素处理的妊娠大鼠肾小球抗血栓酶腺苷二磷酸酶的活性降低。

结论

由于该模型中的组织病理学和临床事件模拟了人类子痫前期的主要特征,该模型可能有助于进一步研究妊娠该并发症的病理生理机制。

相似文献

1
A new animal model for human preeclampsia: ultra-low-dose endotoxin infusion in pregnant rats.一种用于人类先兆子痫的新动物模型:对妊娠大鼠输注超低剂量内毒素
Am J Obstet Gynecol. 1994 Jul;171(1):158-64. doi: 10.1016/0002-9378(94)90463-4.
2
Experimental endotoxemia in pregnancy: in situ glomerular microthrombus formation associated with impaired glomerular adenosine diphosphatase activity.孕期实验性内毒素血症:与肾小球腺苷二磷酸酶活性受损相关的原位肾小球微血栓形成。
J Lab Clin Med. 1989 Nov;114(5):531-7.
3
Aspirin treatment of the low-dose-endotoxin-treated pregnant rat: pathophysiologic and immunohistologic aspects.低剂量内毒素处理的妊娠大鼠的阿司匹林治疗:病理生理学和免疫组织学方面
J Lab Clin Med. 1997 Nov;130(5):496-508. doi: 10.1016/s0022-2143(97)90126-8.
4
Superoxide-mediated glomerulopathy in the endotoxin-treated pregnant rat.内毒素处理的妊娠大鼠中的超氧化物介导的肾小球病。
Kidney Blood Press Res. 1998;21(6):432-7. doi: 10.1159/000025896.
5
Evaluation of low-dose endotoxin administration during pregnancy as a model of preeclampsia.孕期低剂量内毒素给药作为子痫前期模型的评估。
Anesthesiology. 2000 Dec;93(6):1446-55. doi: 10.1097/00000542-200012000-00017.
6
The role of AT1 angiotensin receptor activation in the pathogenesis of preeclampsia.AT1血管紧张素受体激活在子痫前期发病机制中的作用。
Am J Obstet Gynecol. 1998 Jun;178(6):1307-12. doi: 10.1016/s0002-9378(98)70337-0.
7
Altered monocyte function in experimental preeclampsia in the rat.大鼠实验性先兆子痫中单核细胞功能的改变
Am J Obstet Gynecol. 2004 Oct;191(4):1192-8. doi: 10.1016/j.ajog.2004.03.041.
8
Glomerular inflammation in pregnant rats after infusion of low dose endotoxin. An immunohistological study in experimental pre-eclampsia.低剂量内毒素输注后孕鼠的肾小球炎症。子痫前期实验的免疫组织学研究。
Am J Pathol. 1995 Nov;147(5):1510-8.
9
Extracellular ATP induces albuminuria in pregnant rats.细胞外 ATP 可诱导孕鼠出现白蛋白尿。
Nephrol Dial Transplant. 2010 Aug;25(8):2468-78. doi: 10.1093/ndt/gfq095. Epub 2010 Mar 11.
10
Reproductive condition, glomerular adenosine diphosphatase activity, and platelet aggregation in the rat: effect of endotoxin.大鼠的生殖状况、肾小球腺苷二磷酸酶活性及血小板聚集:内毒素的影响
Biol Reprod. 1993 Dec;49(6):1303-9. doi: 10.1095/biolreprod49.6.1303.

引用本文的文献

1
Circular RNA circ_0022707 impedes the progression of preeclampsia via the miR-3135b/GHR/PI3K/Akt axis.环状 RNA circ_0022707 通过 miR-3135b/GHR/PI3K/Akt 轴阻碍子痫前期的进展。
Funct Integr Genomics. 2024 Nov 5;24(6):208. doi: 10.1007/s10142-024-01490-0.
2
A comparison of rat models that best mimic immune-driven preeclampsia in humans.比较最能模拟人类免疫驱动性子痫前期的大鼠模型。
Front Endocrinol (Lausanne). 2023 Sep 28;14:1219205. doi: 10.3389/fendo.2023.1219205. eCollection 2023.
3
Pre-Eclampsia: From Etiology and Molecular Mechanisms to Clinical Tools-A Review of the Literature.
子痫前期:从病因学、分子机制到临床工具——文献综述
Curr Issues Mol Biol. 2023 Jul 25;45(8):6202-6215. doi: 10.3390/cimb45080391.
4
RISING STARS: Approaches to modeling placental function in preeclampsia in vitro and in vivo.崭露头角的新星:体外和体内子痫前期胎盘功能建模方法。
J Endocrinol. 2023 Jun 9;258(1). doi: 10.1530/JOE-23-0008. Print 2023 Jul 1.
5
Cardiovascular Dysfunction in Intrauterine Growth Restriction.宫内生长受限的心血管功能障碍。
Curr Hypertens Rep. 2022 Dec;24(12):693-708. doi: 10.1007/s11906-022-01228-y. Epub 2022 Nov 2.
6
Animal Models of Preeclampsia: Mechanistic Insights and Promising Therapeutics.子痫前期的动物模型:发病机制的深入了解和有前景的治疗方法。
Endocrinology. 2022 Aug 1;163(8). doi: 10.1210/endocr/bqac096.
7
TLR4 Modulates Senescence and Paracrine Action in Placental Mesenchymal Stem Cells via Inhibiting Hedgehog Signaling Pathway in Preeclampsia.TLR4 通过抑制子痫前期中 Hedgehog 信号通路调节胎盘间充质干细胞衰老和旁分泌作用。
Oxid Med Cell Longev. 2022 Jun 14;2022:7202837. doi: 10.1155/2022/7202837. eCollection 2022.
8
The etiology of preeclampsia.子痫前期的病因。
Am J Obstet Gynecol. 2022 Feb;226(2S):S844-S866. doi: 10.1016/j.ajog.2021.11.1356.
9
Metformin Corrects Glucose Metabolism Reprogramming and NLRP3 Inflammasome-Induced Pyroptosis via Inhibiting the TLR4/NF-B/PFKFB3 Signaling in Trophoblasts: Implication for a Potential Therapy of Preeclampsia.二甲双胍通过抑制 TLR4/NF-B/PFKFB3 信号通路纠正葡萄糖代谢重编程和 NLRP3 炎性体诱导的滋养细胞细胞焦亡:子痫前期潜在治疗的意义。
Oxid Med Cell Longev. 2021 Nov 11;2021:1806344. doi: 10.1155/2021/1806344. eCollection 2021.
10
Current State of Preeclampsia Mouse Models: Approaches, Relevance, and Standardization.子痫前期小鼠模型的现状:方法、相关性及标准化
Front Physiol. 2021 Jul 2;12:681632. doi: 10.3389/fphys.2021.681632. eCollection 2021.