Effects of nitric oxide on microviscosity and polarity of erythrocyte membranes in experiment
https://doi.org/10.18699/SSMJ20230612
Abstract
Enhancement of methods for protecting target organs during coronary artery bypass surgery determined the development of a technology for delivering nitric oxide (NO) to the systemic blood flow using a cardiopulmonary bypass (CB) apparatus, which makes NO available to all organs and tissues.
The aim of the study was to access the effect of perioperative NO conditioning on the coefficients of microviscosity and polarity of sheep etythrocyte membranes during experimental surgical intervention using CB.
Material and methods. Study was carried out on 20 sheep weighing 30–34 kg. Two groups were formed. In the CB group, 10 sheep underwent the standard clinical protocol of artificial lung ventilation (ALV) and CB. In the CB + NO group, 10 sheep received NO at a dose of 80 ppm through the circuit of ALV apparatus immediately after tracheal intubation. At the start of CB, NO was delivered to the extracorporeal circulation circuit at a dose of 80 ppm for 90 min. After disconnection from CB, NO supply continued through the ALV apparatus at a dose of 80 ppm for 60 min. The coefficients of microviscosity and polarity of sheep erythrocyte membranes were determined by spectrofluorimetry using pyrene probe.
Results and discussion. The implementation of CB was accompanied by a statistically significant decrease in the microviscosity coefficient in the zones of proteinlipid contact of sheep erythrocyte membranes. In the zone of total lipids, the microviscosity coefficient did not change after CB implementation. The membrane polarity coefficient at the final stage of the surgery increased significantly in the zone of annular lipids and did not change in the zone of total lipids. NO supply to the circuit of the extracorporeal circulation neutralizes the revealed increase in the microviscosity and polarity of the annular lipids.
Conclusions. The introduction of NO into the extracorporeal circulation circuit at the concentration of 80 ppm prevents a decrease in the coefficients of microviscosity and polarity of annular lipids of erythrocyte membranes that occurs during cardiac surgery.
About the Authors
T. Yu. RebrovaRussian Federation
Tatiana Yu. Rebrova - candidate of medical sciences.
634012, Tomsk, Kievskaya st., 111a
Yu. K. Podoksenov
Russian Federation
Yuriy K. Podoksenov - doctor of medical sciences.
634012, Tomsk, Kievskaya st., 111a
S. A. Afanasiev
Russian Federation
Sergey A. Afanasiev - doctor of medical sciences.
634012, Tomsk, Kievskaya st., 111a
N. O. Kamenshchikov
Russian Federation
Nikolay O. Kamenshchikov - candidate of medical sciences.
634012, Tomsk, Kievskaya st., 111a
V. A. Korepanov
Russian Federation
Vyacheslav A. Korepanov
634012, Tomsk, Kievskaya st., 111a
M. L. Diakova
Russian Federation
Mariya L. Diakova - candidate of medical sciences.
634012, Tomsk, Kievskaya st., 111a
References
1. Yu L., Zhu K., Du N., Si Y., Liang J., Shen R., Chen B. Comparison of hybrid coronary revascularization versus coronary artery bypass grafting in patients with multivessel coronary artery disease: a metaanalysis. J. Cardiothorac. Surg. 2022;17(1):147. doi: 10.1186/s13019-022-01903-w
2. van den Eynde J., Bomhals K., Noé D., Jacquemyn X., McCutcheon K., Bennett J., Puskas J.D., Oosterlinck W. Revascularization strategies in patients with multivessel coronary artery disease: a Bayesian network meta-analysis. Interact. Cardiovasc. Thorac. Surg. 2022;34(6):947–957. doi: 10.1093/icvts/ivab376
3. Kalogeris T., Baines C.P., Krenz M., Korthuis R.J. Ischemia/Reperfusion. Compr. Physiol. 2016;7(1):113– 170. doi: 10.1002/cphy.c160006
4. Cadenas S. ROS and redox signaling in myocardial ischemia-reperfusion injury and cardioprotection. Free Radic. Biol. Med. 2018;117:76–89. doi: 10.1016/j.freeradbiomed.2018.01.024
5. Szocs K. Endothelial dysfunction and reactive oxygen species production in ischemia/reperfusion and nitrate tolerance. Gen. Physiol. Biophys. 2004;23(3):265–295.
6. Radi R. Oxygen radicals, nitric oxide, and peroxynitrite: Redox pathways in molecular medicine. Proc. Natl. Acad. Sci. USA. 2018;115(23):5839–5848. doi: 10.1073/pnas.1804932115
7. Malakhova Z.L., Vasina E.Yu., Vlasov T.D. Endothelium-dependent vasodilatation of the skin of a healthy man: nitrogen oxide or hyperpolarizing factor? Rossiyskiy fiziologicheskiy zhurnal imeni Ivana Mikhaylovicha Sechenova = Russian Journal of Physiology. [In Russian]. 2017;103(8):930–939.
8. Guide for the care and use of laboratory animals: Eighth Edition. Washington: The National Academies Press, 2011.
9. Rebrova T.Yu., Afanasiev S.A., Putrova O.D., Popov S.V. Age-related features of erythrocyte membrane microviscosity in experimental cardiosclerosis. Adv. Gerontol. 2013;3:211–214. doi: 10.1134/S2079057013030119
10. Оhnishi S.T., Barr J.K. A simplified method of quantitating protein using the biuret and phenol reagents. Anal. Biochem. 1978;86(1):193–200. doi: 10.1016/0003-2697(78)90334-2
11. Dobretsov G.E. Fluorescent probes in the study of cells, membranes and lipoproteins. Moscow: Nauka, 1989. 277 p. [In Russian].
12. Rebrova T.Yu., Afanasiev S.A., Putrova O.D., Repin A.N. Microviscosity of erythrocyte membranes in chronic coronary insufficiency in patients of middle and older age groups. Adv. Gerontol. 2015;5:45–49. doi: 10.1134/S2079057015010099
13. Sezgin E., Levental I., Mayor S., Eggeling C. The mystery of membrane organization: composition, regulation and roles of lipid rafts. Nat. Rev. Mol. Cell. Biol. 2017;18(6):361–374. doi: 10.1038/nrm.2017.16
14. Revin V.V., Gromova N.V., Revina E.S., Prosnikova K.V., Revina N.V., Bochkareva S.S., Stepushkina O.G., Grunyushkin I.P., Tairova M.R., Incina V.I. Effects of polyphenol compounds and nitrogen oxide donors on lipid oxidation, membrane-skeletal proteins, and erythrocyte structure under hypoxia. Biomed. Res. Int. 2019;2019:6758017. doi: 10.1155/2019/6758017
15. Akagawa M. Protein carbonylation: molecular mechanisms, biological implications, and analytical approaches. Free Radic. Res. 2021;55(4):307–320. doi: 10.1080/10715762.2020.1851027
16. Ochoa J.J., Vílchez M.J., Palacios M.A., García J.J., Reiter R.J., Muñoz-Hoyos A. Melatonin protects against lipid peroxidation and membrane rigidity in erythrocytes from patients undergoing cardiopulmonary bypass surgery. J. Pineal. Res. 2003;35(2):104– 108. doi: 10.1034/j.1600-079x.2003.00061.x
17. Rebrova T.Yu., Shipulin V.M., Afanasiev S.A., Vorobieva E.V., Kiyko O.G. The experience of the application of ascorbinic acid as antioxidant after coronary artery surgery with use of cardiopulmonary bypass. Kardiologiya = Cardiology. 2012;52(7):73–76. [In Russian].
18. Widmer C.C., Pereira C.P., Gehrig P., Vallelian F., Schoedon G., Buehler P.W., Schaer D.J. Hemoglobin can attenuate hydrogen peroxide-induced oxidative stress by acting as an antioxidative peroxidase. Antioxid. Redox. Signal. 2010;12(2):185–198. doi: 10.1089/ars.2009.2826
19. Nasybullina E.I., Kosmachevskaya O.V., Topunov A.F. Effect of nitric oxide metabolites on the formation of membranebound hemoglobin under carbonyl stress. Trudy Karel’skogo nauchnogo tsentra RAN = Proceedings of the Karelian Scientific Center of the Russian Academy of Sciences. 2018;(4):93–104. [In Russian]. doi: 10.17076/them814
20. Filippova O.N., Shperling I.A., Rogov O.A., Saprykina E.V., Ryazantseva N.V., Novitsky V.V. Mechanisms of erythrocytes’ damage after toxic effects of methemoglobin poisons. Byulleten’ sibirskoy meditsiny = Bulletin of Siberian Medicine. 2006;5(1):32–37. [In Russian].