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DOI: 10.1055/s-0031-1299571
Hemolysis Compromises Nitric Oxide-Dependent Vasodilatory Responses in Patients Undergoing Major Cardiovascular Surgery
Publication History
18 May 2011
29 September 2011
Publication Date:
12 March 2012 (online)
Abstract
Background The hemolytic products cell-free oxyhemoglobin (FHb) and arginase-1 reduce nitric oxide (NO) bioavailability by scavenging NO and by degrading the NO precursor arginine to ornithine, respectively. In this study we evaluated the relevance of hemolysis to NO-dependent blood flow in patients undergoing cardiovascular surgery.
Methods Plasma FHb, arginase-1, and amino acid concentrations were measured perioperatively. Forearm blood flow (FBF) responses to the intra-arterial administered NO-donor sodium nitroprusside (SNP) and the endothelium-dependent vasodilator acetylcholine (ACh) were measured by venous occlusion plethysmography.
Results When peak values plasma FHb and arginase-1 were found, vascular dilatation to SNP, but not ACh, was significantly reduced compared with 1 day postoperatively, when FHb had returned to baseline levels (p < 0.05). Interestingly, plasma FHb concentration was inversely correlated to FBF responses to SNP (r −0.93, p < 0.001). In contrast, the increase in arginase-1 was not biologically relevant as the ratio of plasma arginine to ornithine remained constant.
Conclusion We conclude that hemolysis with concomitant release of FHb during cardiovascular surgery is associated with impaired NO-dependent forearm blood flow.
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References
- 1 Rother RP, Bell L, Hillmen P, Gladwin MT. The clinical sequelae of intravascular hemolysis and extracellular plasma hemoglobin: a novel mechanism of human disease. JAMA 2005; 293 (13) 1653-1662
- 2 Maruyama O, Numata Y, Nishida M , et al. Hemolysis caused by surface roughness under shear flow. J Artif Organs 2005; 8 (4) 228-236
- 3 Koch CG, Li L, Sessler DI , et al. Duration of red-cell storage and complications after cardiac surgery. N Engl J Med 2008; 358 (12) 1229-1239
- 4 Serrick CJ, Scholz M, Melo A, Singh O, Noel D. Quality of red blood cells using autotransfusion devices: a comparative analysis. J Extra Corpor Technol 2003; 35 (1) 28-34
- 5 Jacobs MJ, Mommertz G, Koeppel TA , et al. Surgical repair of thoracoabdominal aortic aneurysms. J Cardiovasc Surg (Torino) 2007; 48 (1) 49-58
- 6 Hanssen SJ, Derikx JP, Vermeulen Windsant IC , et al. Visceral injury and systemic inflammation in patients undergoing extracorporeal circulation during aortic surgery. Ann Surg 2008; 248 (1) 117-125
- 7 Cruz-Landeira A, Bal MJ, Quintela López-Rivadulla M. Determination of methemoglobin and total hemoglobin in toxicological studies by derivative spectrophotometry. J Anal Toxicol 2002; 26 (2) 67-72
- 8 Ikemoto M, Tsunekawa S, Awane M , et al. A useful ELISA system for human liver-type arginase, and its utility in diagnosis of liver diseases. Clin Biochem 2001; 34 (6) 455-461
- 9 van Eijk HM, Rooyakkers DR, Deutz NE. Rapid routine determination of amino acids in plasma by high-performance liquid chromatography with a 2-3 microns Spherisorb ODS II column. J Chromatogr A 1993; 620 (1) 143-148
- 10 Houben AJ, Schaper NC, de Haan CH , et al. Local 24-h hyperglycemia does not affect endothelium-dependent or -independent vasoreactivity in humans. Am J Physiol 1996; 270 (6 Pt 2) H2014-H2020
- 11 Reiter CD, Wang X, Tanus-Santos JE , et al. Cell-free hemoglobin limits nitric oxide bioavailability in sickle-cell disease. Nat Med 2002; 8 (12) 1383-1389
- 12 Taddei S, Virdis A, Ghiadoni L, Versari D, Salvetti A. Which endothelium-derived factors are really important in humans?. Biol Chem 2006; 387 (2) 151-157
- 13 Minneci PC, Deans KJ, Zhi H , et al. Hemolysis-associated endothelial dysfunction mediated by accelerated NO inactivation by decompartmentalized oxyhemoglobin. J Clin Invest 2005; 115 (12) 3409-3417
- 14 Morris CR, Kato GJ, Poljakovic M , et al. Dysregulated arginine metabolism, hemolysis-associated pulmonary hypertension, and mortality in sickle cell disease. JAMA 2005; 294 (1) 81-90
- 15 Nishiyama T, Hanaoka K. Free hemoglobin concentrations in patients receiving massive blood transfusion during emergency surgery for trauma. Can J Anaesth 2000; 47 (9) 881-885
- 16 Tanaka K, Kanamori Y, Sato T , et al. Administration of haptoglobin during cardiopulmonary bypass surgery. ASAIO transactions/American Society for Artificial Internal Organs 1991; 37: M482-483
- 17 Schaer DJ, Schaer CA, Buehler PW , et al. CD163 is the macrophage scavenger receptor for native and chemically modified hemoglobins in the absence of haptoglobin. Blood 2006; 107 (1) 373-380
- 18 van de Poll MC, Hanssen SJ, Berbée M , et al. Elevated plasma arginase-1 does not affect plasma arginine in patients undergoing liver resection. Clin Sci (Lond) 2008; 114 (3) 231-241
- 19 Meyer C, Heiss C, Drexhage C , et al. Hemodialysis-induced release of hemoglobin limits nitric oxide bioavailability and impairs vascular function. J Am Coll Cardiol 2010; 55 (5) 454-459
- 20 Schechter AN, Gladwin MT. Hemoglobin and the paracrine and endocrine functions of nitric oxide. N Engl J Med 2003; 348 (15) 1483-1485
- 21 Takaki A, Morikawa K, Tsutsui M , et al. Crucial role of nitric oxide synthases system in endothelium-dependent hyperpolarization in mice. J Exp Med 2008; 205 (9) 2053-2063
- 22 Barr FE, Beverley H, VanHook K , et al. Effect of cardiopulmonary bypass on urea cycle intermediates and nitric oxide levels after congenital heart surgery. J Pediatr 2003; 142 (1) 26-30
- 23 Welborn MB, Oldenburg HS, Hess PJ , et al. The relationship between visceral ischemia, proinflammatory cytokines, and organ injury in patients undergoing thoracoabdominal aortic aneurysm repair. Crit Care Med 2000; 28 (9) 3191-3197
- 24 Vermeulen Windsant IC, Snoeijs MG, Hanssen SJ , et al. Hemolysis is associated with acute kidney injury during major aortic surgery. Kidney Int 2010; 77 (10) 913-920
- 25 Vermeulen Windsant IC, Hanssen SJ, Buurman WA, Jacobs MJ. Cardiovascular surgery and organ damage: time to reconsider the role of hemolysis. J Thorac Cardiovasc Surg 2011; 142 (1) 1-11