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使用渗透泵皮下输注血管紧张素II可诱导小鼠主动脉瘤形成。

Subcutaneous Angiotensin II Infusion using Osmotic Pumps Induces Aortic Aneurysms in Mice.

作者信息

Lu Hong, Howatt Deborah A, Balakrishnan Anju, Moorleghen Jessica J, Rateri Debra L, Cassis Lisa A, Daugherty Alan

机构信息

Saha Cardiovascular Research Center, University of Kentucky.

Department of Pharmacology and Nutritional Sciences, University of Kentucky.

出版信息

J Vis Exp. 2015 Sep 28(103):53191. doi: 10.3791/53191.

DOI:10.3791/53191
PMID:26436287
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4692630/
Abstract

Osmotic pumps continuously deliver compounds at a constant rate into small animals. This article introduces a standard protocol used to induce aortic aneurysms via subcutaneous infusion of angiotensin II (AngII) from implanted osmotic pumps. This protocol includes calculation of AngII amount and dissolution, osmotic pump filling, implantation of osmotic pumps subcutaneously, observation after pump implantation, and harvest of aortas to visualize aortic aneurysms in mice. Subcutaneous infusion of AngII through osmotic pumps following this protocol is a reliable and reproducible technique to induce both abdominal and thoracic aortic aneurysms in mice. Infusion durations range from a few days to several months based on the purpose of the study. AngII 1,000 ng/kg/min is sufficient to provide maximal effects on abdominal aortic aneurysmal formation in male hypercholesterolemic mouse models such as apolipoprotein E deficient or low-density lipoprotein receptor deficient mice. Incidence of abdominal aortic aneurysms induced by AngII infusion via osmotic pumps is 5-10 times lower in female hypercholesterolemic mice and also lower in both genders of normocholesterolemic mice. In contrast, AngII-induced thoracic aortic aneurysms in mice are not hypercholesterolemia or gender-dependent. Importantly, multiple features of this mouse model recapitulate those of human aortic aneurysms.

摘要

渗透泵能以恒定速率持续向小动物输送化合物。本文介绍了一种通过植入的渗透泵皮下输注血管紧张素II(AngII)来诱导主动脉瘤的标准方案。该方案包括AngII用量的计算与溶解、渗透泵填充、渗透泵皮下植入、泵植入后的观察以及收获主动脉以观察小鼠主动脉瘤。按照此方案通过渗透泵皮下输注AngII是一种在小鼠中诱导腹主动脉瘤和胸主动脉瘤的可靠且可重复的技术。根据研究目的,输注持续时间从几天到几个月不等。对于雄性高胆固醇血症小鼠模型,如载脂蛋白E缺乏或低密度脂蛋白受体缺乏小鼠,1000 ng/kg/min的AngII足以对腹主动脉瘤形成产生最大影响。通过渗透泵输注AngII诱导的腹主动脉瘤在雌性高胆固醇血症小鼠中的发生率比雄性低5至10倍,在正常胆固醇血症小鼠的两性中发生率也较低。相比之下,AngII诱导的小鼠胸主动脉瘤与高胆固醇血症或性别无关。重要的是,该小鼠模型的多个特征与人类主动脉瘤的特征相似。

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Arterioscler Thromb Vasc Biol. 2015 Feb;35(2):378-88. doi: 10.1161/ATVBAHA.114.304389. Epub 2014 Dec 18.
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Genomic Editing of a Pathogenic Mutation in ACTA2 Rescues Multisystemic Smooth Muscle Dysfunction Syndrome in Mice.对ACTA2致病突变进行基因组编辑可挽救小鼠的多系统平滑肌功能障碍综合征。
Circulation. 2025 May 16. doi: 10.1161/CIRCULATIONAHA.125.074218.
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