Literature DB >> 25650793

Adult mouse venous hypertension model: common carotid artery to external jugular vein anastomosis.

Shun-Tai Yang1, Ana Rodriguez-Hernandez2, Espen J Walker1, William L Young3, Hua Su1, Michael T Lawton4.   

Abstract

The understanding of the pathophysiology of brain arteriovenous malformations and arteriovenous fistulas has improved thanks to animal models. A rat model creating an artificial fistula between the common carotid artery (CCA) and the external jugular vein (EJV) has been widely described and proved technically feasible. This construct provokes a consistent cerebral venous hypertension (CVH), and therefore has helped studying the contribution of venous hypertension to formation, clinical symptoms, and prognosis of brain AVMs and dural AVFs. Equivalent mice models have been only scarcely described and have shown trouble with stenosis of the fistula. An established murine model would allow the study of not only pathophysiology but also potential genetic therapies for these cerebrovascular diseases. We present a model of arteriovenous fistula that produces a durable intracranial venous hypertension in the mouse. Microsurgical anastomosis of the murine CCA and EJV can be difficult due to diminutive anatomy and frequently result in a non-patent fistula. In this step-by-step protocol we address all the important challenges encountered during this procedure. Avoiding excessive retraction of the vein during the exposure, using 11-0 sutures instead of 10-0, and making a carefully planned end-to-side anastomosis are some of the critical steps. Although this method requires advanced microsurgical skills and a longer learning curve that the equivalent in the rat, it can be consistently developed. This novel model has been designed to integrate transgenic mouse techniques with a previously well-established experimental system that has proved useful to study brain AVMs and dural AVFs. By opening the possibility of using transgenic mice, a broader spectrum of valid models can be achieved and genetic treatments can also be tested. The experimental construct could also be further adapted to the study of other cerebrovascular diseases related with venous hypertension such as migraine, transient global amnesia, transient monocular blindness, etc.

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Year:  2015        PMID: 25650793      PMCID: PMC4354570          DOI: 10.3791/50472

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  16 in total

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3.  Transient global amnesia may be caused by cerebral vein thrombosis.

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Journal:  Med Hypotheses       Date:  2005-08-02       Impact factor: 1.538

4.  Development of acquired arteriovenous fistulas in rats due to venous hypertension.

Authors:  T Terada; R T Higashida; V V Halbach; C F Dowd; M Tsuura; N Komai; C B Wilson; G B Hieshima
Journal:  J Neurosurg       Date:  1994-05       Impact factor: 5.115

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6.  Nonischemic cerebral venous hypertension promotes a pro-angiogenic stage through HIF-1 downstream genes and leukocyte-derived MMP-9.

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Review 9.  Development of a cerebral microvascular dysplasia model in rodents.

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3.  Development of a murine iliac arteriovenous fistula model for examination of hemodialysis access-related limb pathophysiology.

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4.  Brain dural arteriovenous fistulas in the COVID-19 Era: A warning and rationale for association.

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Review 5.  New insight into DAVF pathology-Clues from meningeal immunity.

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