A novel vein graft model: adaptation to differential flow environments.

Accelerated intimal hyperplasia in response to altered flow environment is critical to the process of vein bypass graft failure. Lack of a reproducible animal model for dissecting the mechanisms of vein graft (VG) remodeling has limited progress toward solving this clinically significant problem. Combining a cuffed anastomotic technique with other surgical manipulations, we developed a well-defined, more robust method for studying hemodynamic factors in VG arterialization. VG with fistula placement, complete occlusion, or partial distal branch ligation (DBL) was performed in the carotid artery of 56 rabbits. Extensive hemodynamic and physiological analyses were performed to define the hemodynamic forces and histological adaptations of the wall at 1-28 days. Anastomotic time averaged 12 min, with 100% patency of bilateral grafts and unilateral grafts plus no adjunct or delayed fistula. Bilateral VG-DBL resulted in an immediate disparity in wall shear (0.8 +/- 0.1 vs. 12.4 +/- 1.1 dyn/cm2, ligated vs. contralateral graft). Grafts exposed to low shear stress responded primarily through enhanced intimal thickening (231 +/- 35 vs. 36 +/- 18 microm, low vs. high shear). High-shear-stress grafts adapted through enhanced outward remodeling, with a 24% increase in lumen diameter at 28 days (3.0 +/- 0.1 vs. 3.7 +/- 0.2 mm, low vs. high shear). We have taken advantage of the cuffed anastomotic technique and combined it with a bilateral VG-DBL model to dissect the impact of hemodynamic forces on VG arterialization. This novel model offers a robust, clinically relevant, statistically powerful small animal model for evaluation of high- and low-shear-regulated VG remodeling.

[1]  G. L’italien,et al.  Matched elastic properties and successful arterial grafting. , 1980, Archives of surgery.

[2]  C. Zarins,et al.  Carotid Bifurcation Atherosclerosis: Quantitative Correlation of Plaque Localization with Flow Velocity Profiles and Wall Shear Stress , 1983, Circulation research.

[3]  A. Murday,et al.  Intimal hyperplasia in arterial autogenous vein grafts: a new animal model. , 1983, Cardiovascular research.

[4]  D. Ku,et al.  Pulsatile Flow and Atherosclerosis in the Human Carotid Bifurcation: Positive Correlation between Plaque Location and Low and Oscillating Shear Stress , 1985, Arteriosclerosis.

[5]  V. Bernhard,et al.  Six-year prospective multicenter randomized comparison of autologous saphenous vein and expanded polytetrafluoroethylene grafts in infrainguinal arterial reconstructions. , 1986, Journal of vascular surgery.

[6]  M. Adams,et al.  Kinetics of vein graft hyperplasia: association with tangential stress. , 1987, Journal of vascular surgery.

[7]  A. Clowes,et al.  Atherosclerosis in Rabbit Vein Grafts , 1989, Arteriosclerosis.

[8]  Y. Kawashima,et al.  Simplified rat lung transplantation using a cuff technique. , 1989, The Journal of thoracic and cardiovascular surgery.

[9]  A. Clowes,et al.  The effect of rigid external support on vein graft adaptation to the arterial circulation. , 1989, Journal of vascular surgery.

[10]  P. Hagen,et al.  Myointimal thickening in experimental vein grafts is dependent on wall tension. , 1992, Journal of vascular surgery.

[11]  R J Wagner,et al.  Differential response of arteries and vein grafts to blood flow reduction. , 1993, Journal of vascular surgery.

[12]  W J Keon,et al.  Coronary bypass graft fate and patient outcome: angiographic follow-up of 5,065 grafts related to survival and reoperation in 1,388 patients during 25 years. , 1996, Journal of the American College of Cardiology.

[13]  Amit Kumar,et al.  Remodeling with neointima formation in the mouse carotid artery after cessation of blood flow. , 1997, Arteriosclerosis, thrombosis, and vascular biology.

[14]  M. Mann,et al.  Genetic manipulation of vein grafts. , 1997, Current opinion in cardiology.

[15]  D. Giddens,et al.  Pulsatile flow in an end-to-side vascular graft model: comparison of computations with experimental data. , 2001, Journal of biomechanical engineering.

[16]  S Glagov,et al.  The effects of extremely low shear stress on cellular proliferation and neointimal thickening in the failing bypass graft. , 2001, Journal of vascular surgery.

[17]  M. Mann,et al.  Long-term stabilization of vein graft wall architecture and prolonged resistance to experimental atherosclerosis after E2F decoy oligonucleotide gene therapy. , 2001, The Journal of thoracic and cardiovascular surgery.

[18]  R. Mulligan,et al.  Genetic interventions for vein bypass graft disease: a review. , 2002, Journal of vascular surgery.