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大型动物慢性肺动脉高压模型开发中的挑战。

Challenges in the development of chronic pulmonary hypertension models in large animals.

作者信息

Rothman Abraham, Wiencek Robert G, Davidson Stephanie, Evans William N, Restrepo Humberto, Sarukhanov Valeri, Mann David

机构信息

Children's Heart Center Nevada, Las Vegas, NV, USA.

University of Nevada, School of Medicine, Department of Pediatrics, Las Vegas, NV, USA.

出版信息

Pulm Circ. 2017 Feb 1;7(1):156-166. doi: 10.1086/690099. eCollection 2017 Mar.

DOI:10.1086/690099
PMID:28680575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5448539/
Abstract

Pulmonary hypertension (PH) results in significant morbidity and mortality. Chronic PH animal models may advance the study of PH's mechanisms, evolution, and therapy. In this report, we describe the challenges and successes in developing three models of chronic PH in large animals: two models (one canine and one swine) utilized repeated infusions of ceramic microspheres into the pulmonary vascular bed, and the third model employed a surgical aorto-pulmonary shunt. In the canine model, seven dogs underwent microsphere infusions that resulted in progressive elevation of pulmonary arterial pressure over a few months. In this model, pulmonary endoarterial tissue was obtained for histology. In the aorto-pulmonary shunt swine model, 17 pigs developed systemic level pulmonary pressures after 2-3 months. In this model, pulmonary endoarterial tissue was sequentially obtained to assess for changes in gene and microRNA expression. In the swine microsphere infusion model, three pigs developed only a modest chronic increase in pulmonary arterial pressure, despite repeated infusions of microspheres (up to 40 in one animal). The main purpose of this model was for vasodilator testing, which was performed successfully immediately after acute microsphere infusions. Chronic PH in large animal models can be successfully created; however, a model's characteristics need to match the investigational goals.

摘要

肺动脉高压(PH)会导致显著的发病率和死亡率。慢性PH动物模型可能会推动对PH机制、演变及治疗的研究。在本报告中,我们描述了在大型动物中建立三种慢性PH模型的挑战与成功之处:两种模型(一种犬类模型和一种猪类模型)通过向肺血管床反复注入陶瓷微球来构建,第三种模型采用手术建立主动脉-肺动脉分流。在犬类模型中,七只狗接受了微球注入,导致肺动脉压在几个月内逐渐升高。在该模型中,获取了肺内动脉组织用于组织学检查。在主动脉-肺动脉分流猪类模型中,17头猪在2至3个月后出现了体循环水平的肺动脉压。在该模型中,依次获取肺内动脉组织以评估基因和微小RNA表达的变化。在猪类微球注入模型中,尽管反复注入微球(一只动物最多注入40次),但三头猪仅出现了适度的慢性肺动脉压升高。该模型的主要目的是进行血管扩张剂测试,在急性微球注入后立即成功进行了此项测试。大型动物模型中的慢性PH可以成功建立;然而,模型的特性需要与研究目标相匹配。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ff/5448539/bc37409eaf4a/10.1086_690099-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ff/5448539/be88ab9cf911/10.1086_690099-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ff/5448539/3c0c0ffbbb98/10.1086_690099-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ff/5448539/74194bd2cbee/10.1086_690099-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ff/5448539/0a70e46cf299/10.1086_690099-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ff/5448539/0016f0265062/10.1086_690099-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ff/5448539/660cd8aa6f68/10.1086_690099-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ff/5448539/bc37409eaf4a/10.1086_690099-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ff/5448539/be88ab9cf911/10.1086_690099-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ff/5448539/3c0c0ffbbb98/10.1086_690099-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ff/5448539/74194bd2cbee/10.1086_690099-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ff/5448539/0a70e46cf299/10.1086_690099-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ff/5448539/0016f0265062/10.1086_690099-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ff/5448539/660cd8aa6f68/10.1086_690099-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92ff/5448539/bc37409eaf4a/10.1086_690099-fig8.jpg

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