Extravascular perivenous fibrin support leads to aneurysmal degeneration and intimal hyperplasia in arterialized vein grafts in the rat
- 557 Downloads
Background and aims
External support of vein grafts by fibrin glue possibly prevents overdistension, vascular remodeling, and neointimal hyperplasia. Previous animal models of neointimal hyperplasia showed conflicting results. Here, long-term effects of external fibrin glue support were studied in a new rat model of jugular vein to abdominal aorta transposition.
Materials and methods and methods
In male Wistar rats (250–300 g) right jugular vein (1.0–1.5 cm) was transposed to the infrarenal aorta. Fibrin glue (0.25 ml) covered the vein before releasing the vascular clamps (n = 6). Control vein grafts were exposed directly to blood pressure. After 16 weeks vein grafts were pressure-fixed for histology. Intima thickness, luminal and intimal area were measured by planimetry and elastic fibers demonstrated by Elastica van Giesson staining.
Intimal thickness (74.04 ± 6.7 µm vs 1245 ± 187 µm, control vs fibrin treatment; p < 0.001), intimal area (2517.16 ± 355 mm2 vs 18424 ± 4927 mm2, control vs fibrin treatment; p < 0.05) and luminal area (2184.75 ± 347 mm2 vs 7231.85 ± 1782 mm2, control vs fibrin treatment; p < 0.05) were significantly increased, elastic fibers in the vessel wall were diminished and the vessel wall infiltrated by mononuclear cells in fibrin glue supported veins.
External support of vein grafts by fibrin glue leads to aneurysmal degeneration and intimal hyperplasia, thereby possibly jeopardizing long-term graft patency.
KeywordsFibrin support Vein graft failure Neointima formation
Vein grafts for bypass grafting in vascular and cardiovascular surgery exert good long-term patency and show far better patency rates than synthetic grafts in peripheral vascular surgery . However, after 10 years 40% of vein grafts in coronary artery surgery  and 50% of peripheral venous grafts fail, mainly due to the development of neointimal hyperplasia, especially at sites of anastomosis . Vein graft damage after implantation is believed to be due to arterial pressure, thereby increasing wall tension, shear stress and pulsatile blood flow. This ultimately leads to overdistension of the vein graft promoting intimal hyperplasia through a remodeling process, which involves proliferation and migration of vascular smooth muscle cells (VSMC) as well as myofibroblast to the vein graft . To reduce wall shear stress and to prevent the proposed negative effects of early vein graft distension due to arterial pressure, several ‘extra vascular support’ strategies have been introduced. These include the placement of a porous, non-restrictive, polyester stent [5, 6, 7], or a bio absorbable sheath  or the use of perivenous application of fibrin glue . Perivenous fibrin glue has been used in a variety of experimental models and for different follow-up times [10, 11, 12]. The results of these studies were conflicting in terms of the development of intimal hyperplasia at different time points. Because endpoints were relatively early after venous grafting we sought to test longer follow-up times in a new model of arterialized jugular vein transposition to the infrarenal aorta.
Material and methods
Male Wistar rats, body weight 250–350 g, were purchased from Charles River Laboratories (Sulzfeld, Germany). Rats were fed standard laboratory chow and were kept according to the German legislation on the protection of animals at a 12-h day-and-night shift. The protocol was approved by the local authorities on the protection of animals (Niedersächsisches Landesamt für Verbraucherschutz und Lebensmittelsicherheit/Tierschutz, AZ: 33.42502–046/06, 29.06.06).
This model has been used in mice, but has not been described in rats and offers a complete arterialized graft exposed to the arterial blood pressure .
After Sevoflurane anesthesia, right jugular vein was freed from surrounding tissue and small vein branches. It was then harvested at a length of 1.0–1.5 cm. The vein was flushed gently free from blood with 4°C Ringer solution with a syringe and stored in cold Ringer solution until implantation. Then the abdominal aorta was separated from the infrarenal cava vein. A corresponding segment of 1-cm aorta was excised and the jugular vein interposed with interrupted 8-0 nylon sutures.
N = 6 animals each were assigned to the following groups:
Before declamping 0.25 ml of Fibrin glue (Tissucol Duo S 0.5 ml Immuno, Baxter Deutschland GmbH Edisonstraße 4 85716 Unterschleißheim, Germany) was applied onto the transposed vein graft. Then the blood flow was restored. Animals were followed for 16 weeks and killed thereafter.
Blood flow was restored without application of Fibrin glue. Animals were followed as described for the Fibrin group.
Fibrin control group: the jugular vein was freed as for transposition but left in place and covered with 0.25 ml of Fibrin glue (Tissucol Duo S 0.5 ml Immuno, Baxter Deutschland GmbH Edisonstraße 4 85716 Unterschleißheim, Germany)
Histology and morphometry
The vein segment was pressure fixated for 15 min with 4% Phosphate buffered Formalin at a hydrostatic pressure of 100 mmHg by flushing the formalin through the abdominal aorta replacing the entire blood volume by formalin. The probes were then stored for 36 h in formalin. For wax embedding, three segments were removed from each vein graft, dehydrated, and embedded in paraffin wax with their axis perpendicular to the cutting plane. Sections were stained with hematoxylin and eosin and elastic van Gieson for examination under light microscopy.
Each segment was analyzed in a blinded fashion. Vessel wall dimensions, intimal and luminal areas were measured by computer-aided planimetry with use of an Olympus® BH-2 microscope video camera, head (JVC TK-870E), computer (Victor V386A, Victor Technologies), SoftaOlympus DP-Soft 3.1® software and image-analysis system (Olympus Europe Holding GmbH, Hamburg, Germany). The area enclosed by the endothelium defined the lumen. The area enclosed between the internal elastic lamina and the lumen defined the intima. Measurements of perimeters of the lumen, intimal thickness, and total wall thickness were obtained. Mean values of luminal and intimal circumferences, as well as intimal and total wall thickness, were then calculated for all sections from the same graft.
All values are presented as mean ± standard error of the mean (SEM). Data were analyzed for statistical difference by aid of the computer software GraphPad Instat® Version 3.05. Non-parametric statistic test Mann–Whitney was used to detect statistical differences. A two-tailed p value < 0.05 was accepted statistically significant.
Fibrin supported vessels showed a dense infiltration of mononuclear cells and foam cells and a disruption of vessel architecture. Neointimal formation was demonstrated in both groups, but fibrin glue supported veins showed an excessive formation of neointima and aneurysmal degeneration in four of six animals (Fig. 3A–C). Control vessels, in comparison, showed a preserved vessel architecture with no or minimal infiltration of mononuclear cells and much less development of intimal hyperplasia (Fig. 3D, E). Analyzing the fibrin control group without transposition revealed a damage in vessel wall architecture showing a scattered appearance with some degree of inflammation (Fig 3F)
In addition to the increase of luminal area, the intima showed a significant increase in the intimal area measured in the fibrin groups compared to control, which also showed development of neointima, 2,517.16 ± 356 mm2 vs 18,424 ± 4,927 mm2, control vs fibrin treatment; p < 0.05, (Fig. 1, second column).
Total wall thickness
Corresponding to the increase in total wall thickness and increase in intimal area, the intima thickened significantly in fibrin-supported veins compared to control grafts with a lesser degree of neointimal proliferation 74.04 ± 6.7 μm vs 1245 ± 187 μm control vs fibrin treatment; p < 0.05 (Fig. 2B).
Macroscopically, the elastin fibers in fibrin-supported veins were strongly diminished compared to control and foam cells were present only in fibrin-treated veins (Fig. 4). In the fibrin control group without transposition, elastic fibers were disrupted, causing loss of continuity within the vessel wall (Fig. 4C).
Vein graft failure due to intimal hyperplasia jeopardizes long-term patency of vein grafts in peripheral vascular and cardiovascular surgery. Early graft damage is believed to be due to surgical trauma and overdistension-inducing mechanisms, which ultimately lead to intimal hyperplasia. Therefore, protecting vein grafts from early pressure-related distension injury is considered an important step toward longer vein graft function. External fibrin glue support could possibly counteract the intravenous arterial pressure thereby possibly preventing early vein graft overdistension. On the other hand, fibrin application could be used as a vehicle to transport therapeutic agents to prevent intimal hyperplasia at the site of action .
However, at later time points it was demonstrated that external fibrin support showed negative or even detrimental effects on vein grafts . In the experiments reported here, we could demonstrate a negative effect of external vein graft support in the rat. We used a new rat model of jugular vein transposition, which displayed a neointimal formation at 16 weeks follow-up. In our hands, external fibrin support leads to aneurysmal degeneration, excessive neointimal formation, and to an inflammatory response with the detection of foam cells and loss of elastin fibers. Control grafts also showed neointimal formation but without disruption of vessel wall architecture or aneurysmal degeneration.
In the fibrin control group without transposition, a similar disruption of elastic fibers within the vein graft was noted pointing toward a detrimental effect of fibrin on vessel wall architecture. This is in conjunction to previous reports in a pig model  showing an interspecies reproducible effect. It was stated that inflammation and infiltration of macrophages to vascular tissue is associated with fibrin . As we could demonstrate the appearance of foam cells in fibrin supported grafts, we therefore hypothesize that in the process of fibrin degradation the inflammatory response with accumulation of macrophages and excretion of a variety of cytokines and elastases leads to lysis of elastin fibers. This could explain aneurysmal degeneration and intense accumulation of neointimal hyperplasia because in a distorted vessel architecture blood flow cannot be expected to be laminar, and vessel wall shear stress is likely to be greater and not predictable, leading to higher adaptive responses of the vessel and to excessive neointimal formation.
We conclude that in our hands external support of vein grafts by application of fibrin glue does not prevent neointimal hyperplasia in the long term, but, on the contrary, leads to an intense neointimal hyperplasia possibly due to the inflammatory response leading to cellular proliferation (smooth muscle cells [SMC], myofibroblasts), cell migration (SMC from the media, myofibroblasts from the periadventitia, macrophages from luminal and adventitial side, platelets from luminal side), extracellular matrix deposition, and inflammatory processes (leukocytes, platelets, growth factors, cytokines). Disrupted elastin fibers within the vein vessel wall in fibrin control veins add data to the possible detrimental effect of fibrin. This could possibly be a factor, which contributes to long-term vein graft failure. Our data raise the question whether the possible detrimental effects of local fibrin application on vein grafts contradict the theoretical advantages of drug delivery through local fibrin application. These experimental data are supported by clinical observations showing an unfavorable risk—benefit relation for the intraoperative use of fibrin glue [16, 17]
The expert technical assistance of Mrs. Waldmann-Beushausen is gratefully acknowledged.
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
- 6.Angelini GD, Lloyd C, Bush R, Johnson J, Newby AC (2002) An external, oversized, porous polyester stent reduces vein graft neointima formation, cholesterol concentration, and vascular cell adhesion molecule 1 expression in cholesterol-fed pigs. J Thorac Cardiovasc Surg 124(5):950PubMedCrossRefGoogle Scholar