Inhaled carbon monoxide prevents graft-induced intimal hyperplasia in swine

被引:17
|
作者
Ramlawi, Basel
Scott, Jeffrey R.
Feng, Jun
Mieno, Shigetoshi
Raman, Kathleen G.
Gallo, David
Csizmadia, Eva
Chin, Beek Yoke
Bach, Fritz H.
Otterbein, Leo E.
Sellke, Frank W.
机构
[1] Beth Israel Deaconess Med Ctr, Div Cardiothorac Surg, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Div Transplantat, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
[4] Univ Pittsburgh, Sch Med, Dept Surg, Pittsburgh, PA 15260 USA
关键词
carbon monoxide; intimal hyperplasia; arteriovenous grafts; vascular smooth muscle proliferation; heme oxygenase-1; anastomosis;
D O I
10.1016/j.jss.2006.08.031
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. Arteriovenous grafts often fail due to stenosis caused by venous anastomotic intimal hyperplasia (IH) and vascular smooth muscle cell (VSMC) proliferation. We examined the effects of inhaled carbon monoxide (CO), a product of heme-oxygenase-1 degradation of heme, on IH in a porcine arteriovenous graft model. Materials and methods. Eighteen Yorkshire pigs were divided into three groups (N = 6/group): (1) CO 100 ppm preoperatively for 1 h; (2) CO 250 ppm preoperatively for 1 h and intraoperatively; and (3) airtreated controls. Animals underwent end-to-side placement of polytetrafluoroethylene grafts connecting the common femoral artery and vein in both groins. Intimal thickness of the venous anastomosis at 30 days was measured blinded. The effect of CO on pig VSMC proliferation was studied in cell culture using [H-3]thymidine incorporation. Results. Pigs in the group receiving CO 250 ppm showed significantly less IH compared to animals in the group receiving 100 ppm and the air-treated group (267.5 +/- 21.4, 824 +/- 145.8, and 914.8 +/- 133.7 pixels, respectively, P < 0.0001). This effect was not observed when comparing the 100 ppm group to the air-treated group. COHb levels were significantly elevated in the 100 ppm and 250 ppm compared to air-treated pigs (5.8 +/- 0.47, 13.2 +/- 1.0 versus 2.3 +/- 0.11%, respectively, P < 0.001). Oxygen saturation, respiratory rate, and hemodynamics were not significantly different between the groups. CO induced VSMC growth arrest compared to air in vitro (11.9 +/- 4 versus 20.3 +/- 5 10(3) counts/min/well, P < 0.01). Conclusion. A single exposure to a low concentration of inhaled CO (250 ppm) confers protection against intimal proliferation of VSMCs when given perioperatively in a clinically relevant model of arteriovenous grafts. These data are the first to suggest, in a clinically relevant model, the potential role for CO in clinical applications. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:121 / 127
页数:7
相关论文
共 50 条
  • [1] Inhaled carbon monoxide inhibits intimal hyperplasia and provides added benefit with nitric oxide
    Raman, Kathleen G.
    Barbato, Joel E.
    Ifedigbo, Emeka
    Ozanich, Brett A.
    Zenati, Mazen S.
    Otterbein, Leo E.
    Tzeng, Edith
    JOURNAL OF VASCULAR SURGERY, 2006, 44 (01) : 151 - 158
  • [2] Pioglitazone Prevents Intimal Hyperplasia In Experimental Rabbit Vein Graft
    Morisaki, Koichi
    Shibata, Rei
    Banno, Hiroshi
    Kobayashi, Masayoshi
    Yamamoto, Kiyohito
    Murohara, Toyoaki
    Komori, Kimihiro
    CIRCULATION, 2010, 122 (21)
  • [3] Inhaled carbon monoxide (CO) prevents lung oedema induced by endotoxic shock
    Mazzola, S
    Forni, M
    Albertini, M
    Bacci, ML
    Ciminaghi, B
    Lavitrano, M
    Seren, E
    Clement, MG
    VETERINARY RESEARCH COMMUNICATIONS, 2004, 28 (01) : 209 - 212
  • [4] Inhaled Carbon Monoxide (CO) Prevents Lung Oedema Induced by Endotoxic Shock
    S. Mazzola
    M. Forni
    M. Albertini
    M.L. Bacci
    B. Ciminaghi
    M. Lavitrano
    E. Seren
    M.G. Clement
    Veterinary Research Communications, 2004, 28 : 209 - 212
  • [5] Intraoperative Administration of Inhaled Carbon Monoxide Reduces Delayed Graft Function in Kidney Allografts in Swine
    Hanto, D. W.
    Maki, T.
    Yoon, M. H.
    Csizmadia, E.
    Chin, B. Y.
    Gallo, D.
    Konduru, B.
    Kuramitsu, K.
    Smith, N. R.
    Berssenbrugge, A.
    Attanasio, C.
    Thomas, M.
    Wegiel, B.
    Otterbein, L. E.
    AMERICAN JOURNAL OF TRANSPLANTATION, 2010, 10 (11) : 2421 - 2430
  • [6] Graft-Induced Midgap States in Functionalized Carbon Nanotubes
    Bouilly, Delphine
    Janssen, Jonathan Laflamme
    Cabana, Janie
    Cote, Michel
    Martel, Richard
    ACS NANO, 2015, 9 (03) : 2626 - 2634
  • [7] Biliverdin administration prevents the formation of intimal hyperplasia induced by vascular injury
    Nakao, A
    Murase, N
    Ho, C
    Toyokawa, H
    Billiar, TR
    Kanno, S
    CIRCULATION, 2005, 112 (04) : 587 - 591
  • [8] NFKB-induced gene expression in vein graft intimal hyperplasia
    Finch, J.
    Gregan, S.
    Foxwel, B.
    Haskard, D.
    Monac, C.
    Hornick, P.
    ATHEROSCLEROSIS SUPPLEMENTS, 2006, 7 (03) : 288 - 288
  • [9] MK2 inhibitory peptide delivered in nanopolyplexes prevents vascular graft intimal hyperplasia
    Evans, Brian C.
    Hocking, Kyle M.
    Osgood, Michael J.
    Voskresensky, Igor
    Dmowska, Julia
    Kilchrist, Kameron V.
    Brophy, Colleen M.
    Duvall, Craig L.
    SCIENCE TRANSLATIONAL MEDICINE, 2015, 7 (291)
  • [10] Free radical attenuation prevents thrombosis and enables photochemical inhibition of vein graft intimal hyperplasia
    Nigri, GR
    Kossodo, S
    Waterman, P
    Fungaloi, P
    LaMuraglia, GM
    JOURNAL OF VASCULAR SURGERY, 2004, 39 (04) : 843 - 849