The mouse aortocaval fistula recapitulates human arteriovenous fistula maturation

Author:

Yamamoto Kota1234,Protack Clinton D.23,Tsuneki Masayuki25,Hall Michael R.23,Wong Daniel J.23,Lu Daniel Y.23,Assi Roland23,Williams Willis T.23,Sadaghianloo Nirvana236,Bai Hualong23,Miyata Tetsuro4,Madri Joseph A.25,Dardik Alan123

Affiliation:

1. Veterans Affairs Connecticut Healthcare Systems, West Haven, Connecticut;

2. Vascular Biology and Therapeutics Program, Yale University School of Medicine, New Haven, Connecticut;

3. Department of Surgery, Yale University School of Medicine, New Haven, Connecticut;

4. Division of Vascular Surgery, Department of Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan;

5. Department of Pathology, Yale University School of Medicine, New Haven, Connecticut; and

6. University Hospital of Nice, Nice, France

Abstract

Several models of arteriovenous fistula (AVF) have excellent patency and help in understanding the mechanisms of venous adaptation to the arterial environment. However, these models fail to exhibit either maturation failure or fail to develop stenoses, both of which are critical modes of AVF failure in human patients. We used high-resolution Doppler ultrasound to serially follow mice with AVFs created by direct 25-gauge needle puncture. By day 21, 75% of AVFs dilate, thicken, and increase flow, i.e., mature, and 25% fail due to immediate thrombosis or maturation failure. Mature AVF thicken due to increased amounts of smooth muscle cells. By day 42, 67% of mature AVFs remain patent, but 33% of AVFs fail due to perianastomotic thickening. These results show that the mouse aortocaval model has an easily detectable maturation phase in the first 21 days followed by a potential failure phase in the subsequent 21 days. This model is the first animal model of AVF to show a course that recapitulates aspects of human AVF maturation.

Publisher

American Physiological Society

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

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