Abstract
Blood flow arrest and reperfusion during myocardial infarction (MI) cause myocyte and endothelium injury through oxidative stress and inflammation, both of which involve Reactive Oxygen Species (ROS) and peroxides that consume antioxidant defenses. The aim of this study was to determine whether serum from the occluded coronary vessel has impaired anti-oxidative defenses as compared to serum from aortic blood or from the periphery of healthy controls. Forty-seven patients (44 men) were included for study. Inclusion criteria were chest pain, ST elevation, and cardiac troponin increase. A photoreaction producing a standardized amount of singlet oxygen (1O2), an excited form of oxygen, was performed in serum samples obtained during primary percutaneous coronary intervention (PCI). Immediately after laser light delivery to 5 % sera containing 5 µg/mL rose bengal, dichloro-dihydro-fluorescein (DCFH) was added and its post-oxidation transformation into the fluorescent DCF, was recorded. At least 5 h after the start of symptoms, the mean secondary ROS production after 1O2 delivery was increased in coronary sera (p < 0.001), but in aortic blood remained similar to that of healthy controls. The peak troponin value correlated with DCF fluorescence throughout the interval between symptoms onset and PCI. A high fluorescence was associated with a higher risk of MACE. These results show that oxidants secondary to 1O2 are increased in occluded vessels during AMI in parallel to c-troponin, demonstrating that antioxidants are consumed. A O2 increase during reperfusion would thus extend the damage resulting from IDM necrosis. The effect of conditioning during PCI could be studied using the described method.
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Abbreviations
- 1O2 :
-
Singlet oxygen
- AMI:
-
Acute myocardial infarction
- AUC:
-
Area under the curve
- DCF:
-
Dichlorofluorescein (oxidized, fluorescent)
- DCF-DA:
-
Dichlorofluorescein diacetate
- DCFH:
-
Dichlorofluorescein (reduced, non fluorescent)
- MACE:
-
Major adverse cardiac events
- RB:
-
Rose bengal
- ROS:
-
Reactive oxygen species
- SD:
-
Standard deviation
- SOS:
-
Secondary reactive oxygen species and peroxides
References
Fearon IM, Faux SP (2009) Oxidative stress and cardiovascular disease: novel tools give (free) radical insight. J Mol Cell Cardiol 47(3):372–381
Svilaas T, Vlaar PJ, van der Horst IC, Diercks GF, de Smet BJ, van den Heuvel AF, Anthonio RL, Jessurun GA, Tan ES, Suurmeijer AJ, Zijlstra F (2008) Thrombus aspiration during primary percutaneous coronary intervention. N Engl J Med 358(6):557–567
Vlaar PJ, Svilaas T, van der Horst IC, Diercks GF, Fokkema ML, de Smet BJ, van den Heuvel AF, Anthonio RL, Jessurun GA, Tan ES, Suurmeijer AJ, Zijlstra F (2008) Cardiac death and reinfarction after 1 year in the Thrombus Aspiration during Percutaneous coronary intervention in Acute myocardial infarction Study (TAPAS): a 1-year follow-up study. Lancet 371(9628):1915–1920
Perrelli MG, Pagliaro P, Penna C (2011) Ischemia/reperfusion injury and cardioprotective mechanisms: role of mitochondria and reactive oxygen species. World J Cardiol 3(6):186–200
Becker LB (2004) New concepts in reactive oxygen species and cardiovascular reperfusion physiology. Cardiovasc Res 61(3):461–470
Ovize M, Baxter GF, Di Lisa F, Ferdinandy P, Garcia-Dorado D, Hausenloy DJ, Heusch G, Vinten-Johansen J, Yellon DM, Schulz R (2010) Postconditioning and protection from reperfusion injury: where do we stand? Position paper from the Working Group of Cellular Biology of the Heart of the European Society of Cardiology. Cardiovasc Res 87(3):406–423
Harling L, Rasoli S, Vecht JA, Ashrafian H, Kourliouros A, Athanasiou T (2011) Do antioxidant vitamins have an anti-arrhythmic effect following cardiac surgery? A meta-analysis of randomised controlled trials. Heart 97(20):1636–1642
Dhalla NS, Elmoselhi AB, Hata T, Makino N (2000) Status of myocardial antioxidants in ischemia-reperfusion injury. Cardiovasc Res 47(3):446–456
Andersen HR, Nielsen JB, Nielsen F, Grandjean P (1997) Antioxidative enzyme activities in human erythrocytes. Clin Chem 43(4):562–568
Olivier D, Douillard S, Lhommeau I, Bigot E, Patrice T (2009) Secondary oxidants in human serum exposed to singlet oxygen: the influence of hemolysis. Photochem Photobiol Sci 8(10):1476–1486
Redmond RW, Gamlin JN (1999) A compilation of singlet oxygen yields from biologically relevant molecules. Photochem Photobiol 70(4):391–475
McColl AJ, Keeble T, Hadjinikolaou L, Cohen A, Aitkenhead H, Glenville B, Richmond W (1998) Plasma antioxidants: evidence for a protective role against reactive oxygen species following cardiac surgery. Ann Clin Biochem 35(Pt 5):616–623
Yusuf S, Dagenais G, Pogue J, Bosch J, Sleight P (2000) Vitamin E supplementation and cardiovascular events in high-risk patients. The Heart Outcomes Prevention Evaluation Study Investigators. N Engl J Med 342(3):154–160
De Vecchi E, Pala MG, Di Credico G, Agape V, Paolini G, Bonini PA, Grossi A, Paroni R (1998) Relation between left ventricular function and oxidative stress in patients undergoing bypass surgery. Heart 79(3):242–247
Bartosz G (2010) Non-enzymatic antioxidant capacity assays: limitations of use in biomedicine. Free Radic Res 44(7):711–720
Waring WS, Mishra V, Maxwell SR (2003) Comparison of spectrophotometric and enhanced chemiluminescent assays of serum antioxidant capacity. Clin Chim Acta 338(1–2):67–71
Tsimikas S (2006) Measures of oxidative stress. Clin Lab Med 26 (3):571–590, v–vi
Snyder JW, Skovsen E, Lambert JD, Poulsen L, Ogilby PR (2006) Optical detection of singlet oxygen from single cells. Phys Chem Chem Phys 8(37):4280–4293
Douillard S, Lhommeau I, Foursac A, Aillet L, Bigot E, Patrice T (2010) Biophysical parameters influencing secondary oxidants activation in human serum exposed to singlet oxygen. J Photochem Photobiol B 102(3):224–231
Huang D, Ou B, Prior RL (2005) The chemistry behind antioxidant capacity assays. J Agric Food Chem 53(6):1841–1856
Kon T, Tanigawa T, Hayamizu K, Shen M, Tsuji T, Naito Y, Yoshikawa T (2004) Singlet oxygen quenching activity of human serum. Redox Rep 9(6):325–330
Tanielian C, Mechin R, Seghrouchni R, Schweitzer C (2000) Mechanistic and kinetic aspects of photosensitization in the presence of oxygen. Photochem Photobiol 71(1):12–19
Girotti AW (2008) Translocation as a means of disseminating lipid hydroperoxide-induced oxidative damage and effector action. Free Radic Biol Med 44(6):956–968
Wright A, Hawkins CL, Davies MJ (2003) Photo-oxidation of cells generates long-lived intracellular protein peroxides. Free Radic Biol Med 34(6):637–647
Badwey JA, Karnovsky ML (1980) Active oxygen species and the functions of phagocytic leukocytes. Annu Rev Biochem 49:695–726
Kanofsky JR (1989) Singlet oxygen production by biological systems. Chem Biol Interact 70(1–2):1–28
Hampton MB, Kettle AJ, Winterbourn CC (1998) Inside the neutrophil phagosome: oxidants, myeloperoxidase, and bacterial killing. Blood 92(9):3007–3017
Weishaupt KR, Gomer CJ, Dougherty TJ (1976) Identification of singlet oxygen as the cytotoxic agent in photoinactivation of a murine tumor. Cancer Res 36(7 Pt 1):2326–2329
Hafer K, Iwamoto KS, Schiestl RH (2008) Refinement of the dichlorofluorescein assay for flow cytometric measurement of reactive oxygen species in irradiated and bystander cell populations. Radiat Res 169(4):460–468
Summa D, Spiga O, Bernini A, Venditti V, Priora R, Frosali S, Margaritis A, Di Giuseppe D, Niccolai N, Di Simplicio P (2007) Protein-thiol substitution or protein dethiolation by thiol/disulfide exchange reactions: the albumin model. Proteins 69(2):369–378
Wu G, Fang YZ, Yang S, Lupton JR, Turner ND (2004) Glutathione metabolism and its implications for health. J Nutr 134(3):489–492
Kip KE, Hollabaugh K, Marroquin OC, Williams DO (2008) The problem with composite end points in cardiovascular studies: the story of major adverse cardiac events and percutaneous coronary intervention. J Am Coll Cardiol 51(7):701–707
Moe KT, Wong P (2010) Current trends in diagnostic biomarkers of acute coronary syndrome. Ann Acad Med Singapore 39(3):210–215
Pahor M, Elam MB, Garrison RJ, Kritchevsky SB, Applegate WB (1999) Emerging noninvasive biochemical measures to predict cardiovascular risk. Arch Intern Med 159(3):237–245
Lhommeau I, Douillard S, Bigot E, Benoit I, Krempf M, Patrice T (2011) Serum resistance to singlet oxygen in patients with diabetes mellitus in comparison to healthy donors. Metabolism 60(9):1340–1348
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Acknowledgments to the Fondation pour la Recherche Médicale, the Ligue Nationale contre le Cancer, the Etablissement Français du Sang and Dr J Ashton-Chess for English translation.
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Guerin, P., Bigot, E. & Patrice, T. Evidence for antioxidants consumption in the coronary blood of patients with an acute myocardial infarction. J Thromb Thrombolysis 35, 41–47 (2013). https://doi.org/10.1007/s11239-012-0774-y
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DOI: https://doi.org/10.1007/s11239-012-0774-y