References
- Thygesen K., Alpert J.S., Jaffe A.S., Chaitman B.R., Bax J.J., Morrow D.A., White H.D. et al. Fourth universal definition of myocardial infarction. Circulation. 2018;138(20):e618–e651. doi: 10.1161/CIR.0000000000000617
- Nepomniashchikh L.M., Lushnikova E.L., Semenov D.E. Regenerativno-plasticheskaia nedostatochnost' serdtsa: Morfologicheskie osnovy i molekuliarnye mekhanizmy (Regenerative-plastic heart failure: Morphological bases and molecular mechanisms). Moscow, 2003 (in Russ.).
- Kunita Y., Nakajima K., Nakata T., Kudo T., Kinuya S. Prediction of multivessel coronary artery disease and candidates for stress-only imaging using multivariable models with myocardial perfusion imaging. Annals of Nuclear Medicine. 2022;36:674–683. doi: 10.1007/s12149-022-01751-7
- Stähli B.E., Varbella F., Schwarz B., Nordbeck P., Felix S.B., Lang I.M., Toma A., Moccetti M., Valina C., Vercellino M. et al. Rationale and design of the MULTISTARS AMI Trial: A randomized comparison of immediate versus staged complete revascularization in patients with ST-segment elevation myocardial infarction and multivessel disease. American Heart Journal. 2020;228:98–108. doi: 10.1016/j.ahj.2020.07.016
- Lee S.H., Jeong M.H., Ahn J.H., Hyun D.Y, Cho K.H., Kim M.C., Sim D.S., Hong Y.J., Kim J.H., Ahn Y. et al. Predictors of recurrent acute myocardial infarction despite successful percutaneous coronary intervention. Korean J. Intern. Med. 2022;37(4):777–785. doi: 10.3904/kjim.2021.427
- Troidl C., Mӧllmann H., Nef H., Masseli F., Voss S., Szardien S., Willmer M., Rolf A., Rixe J., Troidl K. et al. Classically and alternatively activated macrophages contribute to tissue remodelling after myocardial infarction. J. Cell. Mol. Med. 2009;13(9B):3485–3496. doi: 10.1111/j.1582-4934.2009.00707.x
- Saxena A., Russo I., Frangogiannis N.G. Inflammation as a therapeutic target in myocardial infarction: learning from past failures to meet future challenges. Translat. Res. 2016;167(1):52–166. doi: 10.1016/j.trsl.2015.07.002
- Stafeev I.S., Menshikov M.Y., Tkachuk V.A., Parfyonova Ye.V. The Role of Macrophages in Repair of Injured Myocardium and Perspectives of Metabolic Reprogramming of Immune Cells for Myocardial Post-Infarction Recovery. Kardiologiia. 2017;57(12):53–59. doi: 10.18087/cardio.2017.12.10067
- Malyshev I.Yu. Phenomena and signaling mechanisms of macrophage reprogramming. Patologicheskaya Fiziologiya i Eksperimental'naya Terapiya (Pathological physiology and experimental therapy). 2015;59(2):99–111 (in Russ.).
- Fedorov A.A., Ermak N.A., Gerashchenko T.S., Topolnitskii E.B., Shefer N.A., Rodionov E.O., Stakheyeva M.N. Polarization of macrophages: mechanisms, markers and factors of induction. Siberian Journal of Oncology. 2022;21(4):124–136 (in Russ.). doi: 10.21294/1814-4861-2022-21-4-124-136
- Chen M., Li X., Wang S., Yu L., Tang J., Zhou S. The Role of Cardiac Macrophage and Cytokines on Ventricular Arrhythmias. Front. Physiol. 2020;11. Article No. 1113. doi: 10.3389/fphys.2020.01113
- Lafuse W.P., Wozniak D.J., Rajaram M.V.S. Role of cardiac macrophages on cardiac inflammation, fibrosis and tissue repair. Cells. 2020;10(51). doi: 10.3390/cells10010051
- Kim Y., Nurakhayev S., Nurkesh A., Zharkinbekov Z., Saparov A. Macrophage polarization in cardiac tissue repair following myocardial infarction. Int. J. Molecular Sciences. 2021;22. Article No. 2715. doi: 10.3390/ijms22052715
- Wang Y., Hou M., Duan S., Zhao Z., Wu X., Chen Y., Yin L. Macrophage-targeting gene silencing orchestrates myocardial microenvironment remodeling toward the anti-inflammatory treatment of ischemia-reperfusion (IR) injury. Bioactive Materials. 2022;17:320–333. doi: 10.1016/j.bioactmat.2022.01.026
- Fontaine M.A.C., Jin H., Gagliardi M., Rousch M., Wijnands E., Stoll M., Li X., Schurgers L., Reutelingsperger C., Schalkwijk C. et al. Blood Milieu in Acute Myocardial Infarction Reprograms Human Macrophages for Trauma Repair. Advanced Science. 2023;10. Article No. 2203053. doi: 10.1002/advs.202203053
- Voropaeva O.F., Tsgoev Ch.A. A numerical model of inflammation dynamics in the core of myocardial infarction. J. Appl. Industr. Math. 2019;13(2):372–383. doi: 10.1134/S1990478919020182
- Tsgoev C.A., Voropaeva O.F., Shokin Y.I. Mathematical modelling of acute phase of myocardial infarction. Russian Journal of Numerical Analysis and Mathematical Modelling. 2020;35(2):111–126. doi: 10.1515/rnam-2020-0009
- Voropaeva O.F., Tsgoev C.A., Shokin Yu.I. Numerical simulation of the inflammatory phase of myocardial infarction. Journal of Applied Mechanics and Technical Physics. 2021;62(3):441–450. doi: 10.1134/S002189442103010X
- Voropaeva O.F., Tsgoev Ch.A. Numerical Modelling of Myocardial Infarction. I. Analysis of Spatiotemporal Aspects of the Local Inflammatory Response. Mathematical Biology and Bioinformatics. 2023;18(1):49–71. doi: 10.17537/2023.18.49
- Voropaeva O.F., Tsgoev Ch.A. Numerical modelling of myocardial infarction. II. Analysis of macrophage polarization mechanism as a therapeutic target. Mathematical Biology and Bioinformatics. 2023;18(2):367–404. doi: 10.17537/2023.18.367
- Voropaeva O.F., Tsgoev Ch.A. Numerical Modeling of Myocardial Infarction in Multivessel Coronary Lesion. I. Analysis of Some Model Scenarios. Mathematical Biology and Bioinformatics. 2024;19(1):183–211. doi: 10.17537/2024.19.183
- Chen J., Ceholski D.K., Liang L., Fish K., Hajjar R.J. Variability in coronary artery anatomy affects consistency of cardiac damage after myocardial infarction in mice. Am. J. Physiol. Heart Circ. Physiol. 2017;313:H275–H282. doi: 10.1152/ajpheart.00127.2017
- Anderson R.H., Ho S.Y., Redmann K., Sanchez-Quintana D., Lunkenheimer P.P. The anatomical arrangement of the myocardial cells making up the ventricular mass. European Journal of Cardio-thoracic Surgery. 2005;28:517–525. doi: 10.1016/j.ejcts.2005.06.043
- Gouda Z.A., Elewa Y.H. A., Selim A.O. Histological architecture of cardiac myofibers composing the left ventricle of murine heart. Journal of Histology & Histopathology. 2015;2. Article No. 2. doi: 10.7243/2055-091X-2-2
- Lin P.-C., Kreutzer U., Jue T. Anisotropy and temperature dependence of myoglobin translational diffusion in myocardium: implication for oxygen transport and cellular architecture. Biophysical Journal. 2007;92:2608–2620. doi: 10.1529/biophysj.106.094458
- Strijkers G.J., Bouts A., Blankesteijn W.M., Peeters T.H., Vilanova A., van Prooijen M.C., Sanders H.M., Heijman E., Nicolay K. Diffusion tensor imaging of left ventricular remodeling in response to myocardial infarction in the mouse. NMR in Biomedicine. 2009;22:182–190. doi: 10.1002/nbm.1299
- Hsu E.W., Xue R., Holmes A., Forder J.R. Delayed reduction of tissue water diffusion after myocardial ischemia. Am. J. Physiol. 1998;275:H697–H702. doi: 10.1152/ajpheart.1998.275.2.H697
- Beyhoff N., Lohr D., Foryst-Ludwig A., Klopfleisch R., Brix S., Grune J., Thiele A., Erfinanda L., Tabuchi A., Kuebler W.M., Pieske B., Schreiber L.M., Kintscher U. Characterization of myocardial microstructure and function in an experimental model of isolatedsubendocardial damage. Hypertension. 2019;74:295–304. doi: 10.1161/HYPERTENSIONAHA.119.12956
- Saxena A., Bujak M., Frunza O., Dobaczewski M., Gonzalez-Quesada C., Lu B., Gerard C., Frangogiannis N.G. CXCR3-independent actions of the CXC chemokine CXCL10 in the infarcted myocardium and in isolated cardiac fibroblasts are mediated through proteoglycans. Cardiovascular Research. 2014;103:217–227. doi: 10.1093/cvr/cvu138
- Bujak M., Dobaczewski M., Chatila K., Mendoza L.H., Li N., Reddy A., Frangogiannis N.G. Interleukin-1 Receptor type I signaling critically regulates infarct healing and cardiac remodeling. Am. J. Pathol. 2008;173:57–67. doi: 10.2353/ajpath.2008.070974
- Zuylen V.-L., Haan M., Roelofs H., Fibbe W.E., Schalij M.J., Atsma D.E. Myocardial infarction models in NOD/Scid mice for cell therapy research: permanent ischemia vs ischemia-reperfusion. SpringerPlus. 2015;4. Article No. 336. doi: 10.1186/s40064-015-1128-y
- Jin Y.-F., Han H.-C., Berger J., Dai Q., Lindsey M.L. Combining experimental and mathematical modeling to reveal mechanisms of macrophage-dependent left ventricular remodeling. BMC Systems Biology. 2011;5. Article No. 60. doi: 10.1186/1752-0509-5-60
- Wang Y., Yang T., Ma Y., Halade G.V., Zhang J., Lindsey M.L., Jin Y.-F. Mathematical modeling and stability analysis of macrophage activation in left ventricular remodeling post-myocardial infarction. BMC Genomics. 2012;13. doi: 10.1186/1471-2164-13-S6-S21
- Yanenko N.N. The Method of Fractional Steps, the Solution of Problems of Mathematical Physics in Several Variables. Berlin: Springer-Verlag, 1971.
- Tikhonov A.N., Samarskii A.A. Homogeneous difference schemes. USSR Comput. Math. Math. Phys. 1962;1(1):5–67. doi: 10.1016/0041-5553(62)90005-8
- Voropaeva O.F., Chernykh G.G. Evoliutsiia zony turbulentnogo smesheniia v zhidkosti s nelineinoi stratifikatsiei. Modelirovanie v mekhanike: (Modeling in Mechanics): Coll. of scientific works of the USSR Academy of Sciences. Siberian Branch. Computer Center, ITPM. 1989;3(5):3–29 (in Russ.).
- Voropaeva O.F. Anisotropic turbulence decay in a far momentumless wake in a stratified medium. Mathematical Models and Computer Simulations. 2009;1(5):605–619. doi: 10.1134/S207004820905007X
- Cremer S., Schloss M.J., Vinegoni C., Foy B.H., Zhang S., Rohde D., Hulsmans M., Feruglio P.F., Schmidt S., Wojtkiewicz G., Higgins J.M., Weissleder R., Swirski F. K., Nahrendorf M. Diminished Reactive Hematopoiesis and Cardiac Inflammation in a Mouse Model of Recurrent Myocardial Infarction. J. Am. Coll. Cardiol. 2020;75:901–915. doi: 10.1016/j.jacc.2019.12.056
|
|
|