Background. We hypothesize that arterial wall hypoxia incites the pathologic formation of intimal hyperplasia at an artery anastomosis. We have determined from previous studies performed in our laboratory, the oxygen tension profiles of the artery wall at various times after vascular anastomosis. The purpose of this study is to determine the rate of cellular proliferation at an artery anastomosis when the artery wall is most hypoxic. Materials and methods. Expanded polytetrafluoroethylene (ePTFE) grafts were placed end to end in the infrarenal aorta of 27 New Zealand white rabbits. The anastomotic aortic wall oxygen (O2) tensions were measured with an O2 microelectrode in rabbits 0, 7, 14, 29, and 42 days after surgery. O2 tensions were also measured in 4 control rabbits for comparison. 5-Bromo-2'- deoxyuridine (BrDU) was injected intraperitoneally 24 h prior to rabbit sacrifice. After O2 tension measurements, the rabbits were sacrificed and the aortic grafts were harvested. Bioquant morphometrics was used to measure cells with BrDU counter-staining and intimal thickness in 17 rabbits: in control (n = 4), Day 0 (n = 4), 7 (n = 5), and 42 (n = 4). Student's t test was used to compare O2 tensions, cellular proliferation, and intimal hyperplasia between days. Results. The pO2 levels at the outer layers of the aorta, 1 mm distal to the distal aortic graft anastomosis, were 61.0 ± 2 (±SE) mm Hg for controls, 19.8 ± 1 mm Hg for Day 7 (P < 0.0001), 19.0 ± 1 mm Hg for Day 14, 39.2 ± 1 mm Hg for Day 28, and 58.5 ± 1 mm Hg for Day 42 aortic grafts. BrDU-staining ratios in the intima were significantly higher in the Day 7 aortic grafts, 28.6 ± 3%, versus BrDU-staining ratio, 1.4 ± 1%, in Day 42 aortic grafts (P < 0.0002). Conclusions. Cellular proliferation is highest at Day 7 when the artery wall is most hypoxic and returns to baseline as O2 tensions normalize. (C) 2000 Academic Press.
|Original language||English (US)|
|Number of pages||6|
|Journal||Journal of Surgical Research|
|State||Published - Jun 1 2000|
Bibliographical noteFunding Information:
This work was supported by a Veterans Affairs Merit Review Grant (S.M.S.) and by a National Institutes of Health Service Award 5F32HL10076-02 (E.S.L.). The authors thank W.L. Gore & Associates, Inc., for providing the vascular grafts and Jeannie Emmanual for technical assistance. We thank Connie M. Lindberg for editorial assistance.
- Intimal hyperplasia
- Smooth muscle cells