Venous Mechanical Properties After Arteriovenous Fistulae in Mice

J Surg Res. 2020 Apr:248:129-136. doi: 10.1016/j.jss.2019.12.007. Epub 2019 Dec 31.

Abstract

Background: An arteriovenous fistula (AVF) exposes the outflow vein to arterial magnitudes and frequencies of blood pressure and flow, triggering molecular pathways that result in venous remodeling and AVF maturation. It is unknown, however, how venous remodeling, that is lumen dilation and wall thickening, affects venous mechanical properties. We hypothesized that a fistula is more compliant compared with a vein because of altered contributions of collagen and elastin to the mechanical properties.

Methods: Ephb4+/- and littermate wild-type (WT) male mice were treated with sham surgery or needle puncture to create an abdominal aortocaval fistulae. The thoracic inferior vena cava was harvested 3 wk postoperatively for mechanical testing and histological analyses of collagen and elastin.

Results: Mechanical testing of the thoracic inferior vena cava from Ephb4+/- and WT mice showed increased distensibility and increased compliance of downstream veins after AVF compared with sham. Although Ephb4+/- veins were thicker than WT veins at the baseline, after AVF, both Ephb4+/- and WT veins showed similar wall thickness as well as similar collagen and elastin area fractions, but increased collagen undulation compared with sham.

Conclusions: Fistula-induced remodeling of the outflow vein results in circumferentially increased distensibility and compliance, likely due to post-translational modifications to collagen.

Keywords: Arteriovenous fistula; Collagen; Compliance; Elastin; EphB4; Stiffness; Venous remodeling.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Arteriovenous Shunt, Surgical*
  • Collagen / metabolism
  • Elasticity
  • Elastin / metabolism
  • Male
  • Mice, Inbred C57BL
  • Receptor, EphB4 / genetics
  • Vena Cava, Inferior / physiology*

Substances

  • Collagen
  • Elastin
  • Ephb4 protein, mouse
  • Receptor, EphB4