Skip to main content
Log in

Role of Myeloperoxidase, Paraoxonase, and Nitric Oxide System in the Blood and Pericardial Fluid of Patients with Ischemic Heart Disease after Direct Myocardial Revascularization

  • Published:
Advances in Gerontology Aims and scope Submit manuscript

Abstract

To study the role of paraoxonase, myeloperoxidase, arginase, asymmetric dimethylarginine, and nitric oxide in the mechanisms of the pathogenesis of postpericardiotomy syndrome (PPCS), 76 patients with ischemic heart disease (IHD) who underwent coronary artery bypass grafting were examined. Patients were divided into two groups: Group 1, IHD patients who were not diagnosed with PPCS as a result of clinical studies, and Group 2, IHD patients who were diagnosed with PPCS. The results indicate that the postoperative period after coronary artery bypass grafting is associated with the inhibition of paraoxonase, the activation of myeloperoxidase, enhanced arginase activity, increased nitrite/nitrate and asymmetric dimethylarginine levels; it may also be accompanied by the development of endothelial dysfunction and increased systemic inflammatory response. In the present work, inverse correlations were found between the paraoxonase aryl esterase activity and myeloperoxidase activity in plasma, as well as the paraoxonase aryl esterase activity in blood plasma and arginase activity in erythrocytes in patients of both groups. Tests to predict the development of postpericardiotomy syndrome were developed based on the ratio of activity of the studied enzymes.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1.
Fig. 2.
Fig. 3.
Fig. 4.
Fig. 5.
Fig. 6.
Fig. 7.
Fig. 8.

Similar content being viewed by others

REFERENCES

  1. Golikov, P.P. and Nikolaeva, N.Yu., Determination of nitrite/nitrate (NOx) in blood serum, Vopr. Biomed. Khim., 2004, no. 1, pp. 79–83.

  2. Kolb, V.G. and Kamyshnikov, V.S., Spravochnik po klinicheskoi khimii (Handbook on Clinical Chemistry), Minsk: Belarus’, 1982, pp. 290–292.

  3. Saidov, M.Z. and Pinegin, B.V., Spectrophotometric determination of myeloperoxidase in phagocytic cells, Lab. Delo, 1991, no. 3, pp. 56–59.

  4. Shumakov, K.V., Lefterova, N.P., Pak, N.L., et al., Coronary artery bypass in conditions of artificial blood circulation and on open heart: a comparative analysis of the immediate and long-term results and postoperative complications (cardiac arrhythmias, cognitive and neurological disorders, rheological features, and the state of the homeostasis system), Kreativn. Kardiol., 2009, no. 1, pp. 28–50.

  5. Alam, S.R., Lewis, S.C., Zamvar, V., et al., Perioperative elafin for ischaemia-reperfusion injury during coronary artery bypass graft surgery: a randomized-controlled trial, Heart, 2015, vol. 101, no. 20, pp. 1639–1645.

    Article  CAS  Google Scholar 

  6. Aviram, M., Introduction to paraoxonases, J. Lipids, 2012, vol. 2012, pp. 1–2.

    Article  Google Scholar 

  7. Bayrak, T., Bayrak, A., Iş ı ldak, M., et al., Increased asymmetric dimethylarginine (ADMA) levels and decreased homocysteine thiolactonase/paraoxonase (HTLase/PONase) activities are related to the risk of cardiovascular disease in prediabetic/diabetic patients, Turk. J. Biochem., 2014, vol. 39, no. 3, pp. 270–276.

    Article  CAS  Google Scholar 

  8. Brener, S., Frequency and long-term impact of myonecrosis after coronary stenting, Eur. Heart J., 2002, vol. 23, pp. 869–876.

    Article  CAS  Google Scholar 

  9. Butts, B., Goeddel, L.A., George, D.J., et al., Increased inflammation in pericardial fluid persists 48 hours after cardiac surgery, Circulation, 2017, vol. 136, pp. 2284–2286.

    Article  Google Scholar 

  10. Emami Razavi, E.A., Basati, G., Varshosaz, J., et al., Association between HDL particles size and myeloperoxidase/paraoxonase-1 (MPO/PON1) ratio in patients with acute coronary syndrome, Acta Med. Iran., 2013, vol. 51, no. 6, pp. 365–371.

    PubMed  Google Scholar 

  11. Gad, M.Z., Abdel-Maksoud, S.M., Hassanein, S.I., et al., Nitric oxide regulating proteins as biochemical and genetic markers of coronary artery disease, in Biomarkers in Cardiovascular Disease, Patel, V.B. and Preedy, V.R., Eds., Dordrecht: Springer-Verlag, 2016, pp. 1–27. https://doi.org/10.1007/978-94-007-7741-5_34-1

    Google Scholar 

  12. Hernandez, A.F., Pla, A., Valenzuela, A., et al., Paraoxonase activity in human pericardial fluid: its relationship to coronary artery disease, Int. J. Leg. Med., 1993, vol. 105, pp. 321–324.

    Article  CAS  Google Scholar 

  13. Huang, Y., Wu Z., Riwanto M., et al., Myeloperoxidase, paraoxonase-1, and HDL form a functional ternary complex, J. Clin. Invest., 2013, vol. 123, no. 9, pp. 3815–3828.

    Article  CAS  Google Scholar 

  14. Hueb, W., Lopes, N.H., Gersh, B.J., et al., Five-year follow-up of the Medicine, Angioplasty, or Surgery Study (MASS II): a randomized controlled clinical trial of 3 therapeutic strategies for multivessel coronary artery disease, Circulation, 2007, vol. 115, no. 9, pp. 1082–1089.

    Article  Google Scholar 

  15. Keshari, R.S., Jyoti, A., Dubey, M., Kothari, N., et al., Cytokines induced neutrophil extracellular traps formation: implication for the inflammatory disease condition, PLoS One, 2012, no. 7, pp. 48111–48118.

  16. Kilic, S.S., Aydin, S., Kilic, N. Serum arylesterase and paraoxonase activity in patients with chronic hepatitis, World J. Gastroenterol., 2005, vol. 11, pp. 7351–7354.

    Article  CAS  Google Scholar 

  17. Li, H. and Förstermann, U., Uncoupling of endothelial NO synthase in atherosclerosis and vascular disease, Curr. Opin. Pharmacol., 2013, vol. 13, no. 2, pp. 161–167.

    Article  Google Scholar 

  18. Loria, V., Dato, I., Graziani, F., et al., Myeloperoxidase: a new biomarker of inflammation in ischemic heart disease and acute coronary syndromes, Mediators Inflammation, 2008, vol. 2008, pp. 1–4.

    Article  Google Scholar 

  19. Nguyen, S.D. and Sok, D.E., Oxidative inactivation of paraoxonase1, an antioxidant protein and its effect on antioxidant action, Free Radical Res., 2003, vol. 37, no. 12, pp. 1319–1330.

    Article  CAS  Google Scholar 

  20. Plicner, D., Mazura, P., Sadowski, J., et al., Asymmetric dimethylarginine and oxidative stress following coronary artery bypass grafting: associations with postoperative outcome, Eur. J. Cardio-Thoracic Surg., 2014, vol. 45, pp. 1–6.

    Article  Google Scholar 

  21. Preeshagul, I., Gharbaran, R., Jeong, K.H., et al., Potential biomarkers for predicting outcomes in CABG cardiothoracic surgeries, J. Cardiothorac. Surg., 2013, vol. 8, no. 176, pp. 1–12.

    Article  Google Scholar 

  22. Rath, M., Müller, I., Kropf, P., et al., Metabolism via arginase or nitric oxide synthase: two competing arginine pathways in macrophages, Front. Immunol., 2014, vol. 5, no. 532, pp. 1–10.

    Article  Google Scholar 

  23. Santhanam, L., Lim, H.K., Lim, H. K., et al., Inducible NO synthase dependent S-nitrosylation and activation of arginase1 contribute to age-related endothelial dysfunction, Circ. Res., 2007, vol. 101, pp. 692–702.

    Article  CAS  Google Scholar 

  24. Schindhelm, R.K., Zwan, L.P., Teerlink, T., et al., Myeloperoxidase: a useful biomarker for cardiovascular disease risk stratification?, Clin. Chem., 2009, vol. 55, no. 8, pp. 1462–1470.

    Article  CAS  Google Scholar 

  25. Schlüter, K.-D., Schulz, R., and Schreckenberg, R., Arginase induction and activation during ischemia and reperfusion and functional consequences for the heart, Front. Physiol., 2015, vol. 6, no. 65, pp. 1–8.

    Article  Google Scholar 

  26. Sibal, L., Agarwal, S.C., Home, P.D., et al., The role of asymmetric dimethylarginine (ADMA) in endothelial dysfunction and cardiovascular disease, Curr. Cardiol. Rev., 2010, vol. 6, no. 2, pp. 82–90.

    Article  CAS  Google Scholar 

  27. Simundic, A.M., Diagnostic accuracy—Part 1 Basic concepts: sensitivity and specificity, ROC analysis, STARD statement, Point Care, 2012, vol. 11, pp. 6–8.

    Google Scholar 

  28. Sydow, K. and Böger, R.H., Reloaded: ADMA and oxidative stress are responsible for endothelial dysfunction in hyperhomocyst(e)inaemia: effects of L-arginine and B vitamins, Cardiovasc. Res., 2012, vol. 96, pp. 167–171.

    Article  CAS  Google Scholar 

  29. Trocha, M., Merwid-Ląd, A., Szuba, A., et al., Effect of selected drugs on plasma asymmetric dimethylarginine (ADMA) levels, Adv. Clin. Exp. Med., 2010, vol. 19, no. 2, pp. 233–243.

    Google Scholar 

  30. Vanhoutte, P.M., Shimokawa, H., and Tang, E.H.C., Endothelial dysfunction and vascular disease, Acta Physiol., 2009, vol. 196, pp. 193–222.

    Article  CAS  Google Scholar 

  31. Wysocka, A., Cybulski, M., Berbe, H., et al., Prognostic value of paraoxonase 1 in patients undergoing coronary artery bypass grafting surgery, Med. Sci. Monit., 2014, vol. 11, no. 20, pp. 594–600.

    Google Scholar 

  32. Yang, Z. and Ming, X.-F., Arginase: the emerging therapeutic target for vascular oxidative stress and inflammation, Front. Immunol., 2013, vol. 4, pp. 1–11.

    Article  Google Scholar 

  33. Zhu, C., Yu, Y., Montani, J.-P., et al., Arginase-I enhances vascular endothelial inflammation and senescence through eNOS-uncoupling, BMC Res. Notes, 2017, vol. 10, no. 82, pp. 1–8.

    Article  Google Scholar 

Download references

ACKNOWLEDGMENTS

The study was performed on the equipment of the High Technologies Center for Collective Use at Southern Federal University.

Funding

The study was carried out in the framework of the basic part of the State Assignment of the Ministry of Education and Science of the Russian Federation (projects no. 1878 and no. 6.6762.2017/BCh).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to V. V. Vnukov.

Ethics declarations

Conflict of interests. The authors declare that they have no conflict of interest.

Statement of compliance with standards of research involving humans as subjects. All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. Informed consent was obtained from all individual participants involved in the study.

Additional information

Translated by G. Levit

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Vnukov, V.V., Sidorov, R.V., Gvaldin, D.Y. et al. Role of Myeloperoxidase, Paraoxonase, and Nitric Oxide System in the Blood and Pericardial Fluid of Patients with Ischemic Heart Disease after Direct Myocardial Revascularization. Adv Gerontol 9, 426–433 (2019). https://doi.org/10.1134/S2079057019040167

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S2079057019040167

Keywords:

Navigation