Have a personal or library account? Click to login
The morphological response of the heart and spleen following acute myocardial infarction-induced sterile inflammation: a clinicopathological study Cover

The morphological response of the heart and spleen following acute myocardial infarction-induced sterile inflammation: a clinicopathological study

Open Access
|Dec 2020

References

  1. 1. Vos T, Allen C, Arora M, Barber RM, Bhutta ZA, Brown A, et al. Global, regional, and national incidence, prevalence, and years lived with disability for 310 diseases and injuries, 1990-2015: a systematic analysis for the Global Burden of Disease Study 2015. Lancet. 2015; 388 (10053): 1545–1602. doi: 10.1016/S0140-6736(16)31678-610.1016/S0140-6736(16)31678-6
  2. 2. Bordejevic DA, Florina C, Mornos C, Olariu I, Petrescu L, Tomescu MC, Citu I, Mavrea A, Pescariu S. Prognostic impact of blood pressure and heart rate at admission on in-hospital mortality after primary percutaneous intervention for acute myocardial infarction with ST-segment elevation in western Romania. Ther Clin Risk Manag. 2017; 13: 1061–1068. doi: 10.2147/TCRM.S14131210.2147/TCRM.S141312557468128883734
  3. 3. Becker D., Merkely, B. [Current therapy of the acute coronary syndrome – 2016]. Orv. Hetil. 2016; 157(38), 1500–1506.
  4. 4. Coppin E, Florentin J, Vasamsetti SB, Arunkumar A, Sembrat J, Rojas M, Dutta P. Splenic hematopoietic stem cells display a pre-activated phenotype. Immunol Cell Biol. 2018; 96(7): 772-784. doi: 10.1111/imcb.12035.10.1111/imcb.12035637914729526053
  5. 5. Wang Z, He D, Zeng YY, Zhu L, Yang C, Lu YJ, Huang JQ, Cheng XY, Huang XH, Tan XJ. The spleen may be an important target of stem cell therapy for stroke. J Neuroinflammation. 2019;16(1):20. doi: 10.1186/s12974-019-1400-0.10.1186/s12974-019-1400-0635244930700305
  6. 6. Vahidy FS, Parsha KN, Rahbar MH, Lee M, Bui T-T, Nguyen C, Savitz SI. Acute splenic responses in patients with ischemic stroke and intracerebral hemorrhage. J Cereb Blood Flow Metabo. 2015; 36(6), 1012–1021. doi: 10.1177/0271678x1560788010.1177/0271678X15607880490862026661179
  7. 7. Kim E, Yang J, Beltran CD, Cho S. Role of Spleen-Derived Monocytes/Macrophages in Acute Ischemic Brain Injury. J Cereb Blood Flow Metab. 2014; 34(8), 1411–1419. doi: 10.1038/jcbfm.2014.10110.1038/jcbfm.2014.101412608724865998
  8. 8. Swirski FK, Nahrendorf M, Etzrodt M, Wildgruber M, Cortez-Retamozo V, Panizzi P, Figueiredo JL, Kohler RH, Chudnovskiy A, Waterman P, Aikawa E, Mempel TR, Libby P, Weissleder R, Pittet MJ. Identification of splenic reservoir monocytes and their deployment to inflammatory sites. Science. 2009;325:612–616. doi: 10.1126/science.1175202.10.1126/science.1175202280311119644120
  9. 9. Zouggari Y, Ait-Oufella H, Bonnin P, et al. B lymphocytes trigger monocyte mobilization and impair heart function after acute myocardial infarction. Nat Med. 2013;19:1273–1280. doi: 10.1038/nm.3284.10.1038/nm.3284404292824037091
  10. 10. Prabhu SD, Frangogiannis NG. The Biological Basis for Cardiac Repair After Myocardial Infarction. Circ Res. 2016; 119(1), 91-112. doi: 10.1161/circresaha.116.30357710.1161/CIRCRESAHA.116.303577492252827340270
  11. 11. Frangogiannis NG. Cell biological mechanisms in regulation of the post-infarction inflammatory response. Cur Opin Physiol. 2018; 7–13. doi: 10.1016/j.cophys.2017.09.00110.1016/j.cophys.2017.09.001585146829552674
  12. 12. Sprogøe-Jakobsen S, Sprogøe-Jakobsen U. The weight of the normal spleen. Forensic Sci Int. 1997;88(3):215-23.10.1016/S0379-0738(97)00103-5
  13. 13. Ferreira T., Rasband W. Image J User Guide. Image Processing and Analysis in Java. National Institutes of Health. 2012. http://rsb.info.nih.gov/ij.
  14. 14. Sejrup JK, Morelli VM, Løchen M-L, Njølstad I, Mathiesen EB, WilsgaardT, Braekkan SK. Myocardial infarction, prothrombotic genotypes, and venous thrombosis risk: The Tromsø Study. Res Prac Thromb Haemost. 2020; 4(2), 247– 254. doi: 10.1002/rth2.1230610.1002/rth2.12306704054732110755
  15. 15. Jortveit J, Govatsmark RE, Langørgen J, Hole T, Mannsverk J, Olsen S, Risøe C, Halvorsen S. Gender differences in the assessment and treatment of myocardial infarction. Tidsskr Nor Laegeforen. 2016;136(14-15):1215-22. doi: 10.4045/tidsskr.16.0224.10.4045/tidsskr.16.022427554562
  16. 16. Pedersen LR, Frestad D, Michelsen MM, Mygind ND, Rasmusen H, Suhrs HE, Prescott E. Risk Factors for Myocardial Infarction in Women and Men: A Review of the Current Literature. Curr Pharm Des. 2016;22(25):3835-52.10.2174/138161282266616030911531826956230
  17. 17. Liang Y, Chen H, Wang P. Correlation of Leukocyte and Coronary Lesion Severity of Acute Myocardial Infarction. Angiology. 2018; 69(7), 591–599. doi: 10.1177/000331971774078210.1177/000331971774078229130316
  18. 18. Yuan D, Tie J, Xu Z, Liu G, Ge X, Wang Z, Zhou X.. Dynamic Profile of CD4+ T-Cell-Associated Cytokines/Chemokines following Murine Myocardial Infarction/Reperfusion. Mediators of Inflamm. 2019; 2019:9483647. doi: 10.1155/2019/948364710.1155/2019/9483647644249231011288
  19. 19. Avci E, Kiris T, Çelik A, Variş E, Esin FK, Köprülü D, Kadi H. Prognostic value of rising mean platelet volume during hospitalization in patients with ST-segment elevation myocardial infarction treated with primary percutaneous coronary intervention. BMC Cardiovasc Disord. 2018;18(1):226. doi: 10.1186/s12872-018-0970-6.10.1186/s12872-018-0970-6628655930526502
  20. 20. Fang L, Moore XL, Dart MA, Wang LM. Systemic Inflammatory Response Following Acute Myocardial Infarction. J Geriatr Cardiol. 2015;12(3): 305-12. doi: 10.11909/j.issn.1671-5411.2015.03.020.
  21. 21. Van Amerongen MJ, Harmsen MC, van Rooijen N, Petersen AH, van Luyn MJ. Macrophage depletion impairs wound healing and increases left ventricular remodeling after myocardial injury in mice. Am J Pathol. 2007; 170(3):818-29. doi: 10.2353/ajpath.2007.06054710.2353/ajpath.2007.060547186489317322368
  22. 22. Horváth E., Orădan A., Chiriac L., Dobreanu M., Nagy EE., Voidăzan S., Berei R., Muntean DL., Huțanu A. Fish-oil Preconditioning Up-regulates Expression of Splenic Arg1 Positive M2 Type Macrophages and the Arg1/Inos2 Ratio After Experimental Induced Transient Cerebral Ischemia. Farmacia, 2019; 67(5): 820-829.10.31925/farmacia.2019.5.10
  23. 23. O’Malley DP, George TI, Orazi A, Abbondanzo SL. Benign and Reactive Conditions of Lymph Node and Spleen (Atlas of Nontumor Pathology). Amer Registry of Pathology. 1 edition. 2009; 10-15, 75-93.
  24. 24. Prabhu SD. The Cardiosplenic Axis is Essential for the Pathogenesis of Ischemic Heart Failure. Trans Am Clin Climatol Assoc. 2018; 129:202-214.
  25. 25. Courties G, Herisson F, Sager HB, Ye Y, Wei Y, Sun Y, Severe N, Dutta P, Scharff J, Scadden DT, Weissleder R, Swirski FK, Moskowitz MA, Nahrendorf M. Ischemic Stroke Activates Hematopoietic Bone Marrow Stem Cells. Circ Res. 2015; 116(3): 407–417. doi: 10.1161/CIRCRESAHA.116.305207.10.1161/CIRCRESAHA.116.305207431251125362208
  26. 26. Horváth E, Huțanu A, Orădan A, Chiriac L, Muntean DL, Nagy EE, Dobreanu M. N-3 polyunsaturated fatty acids induce granulopoiesis and early monocyte polarization in the bone marrow of a tMCAO rat model. N-3 polyunsaturated fatty acids induce granulopoiesis and early monocyte polarization in the bone marrow of a tMCAO rat model. Revista Română de Medicină de Laborator (Romanian Journal of Laboratory Medicine). 2019; 27(1): 1841-6624. doi.10.2478/rrlm-2019-0004.wwwww10.2478/rrlm-2019-0004
DOI: https://doi.org/10.2478/orvtudert-2019-0015 | Journal eISSN: 2537-5059 | Journal ISSN: 1453-0953
Language: English
Page range: 105 - 112
Published on: Dec 3, 2020
Published by: Transylvanian Museum Society
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year

© 2020 Harsa Mihai Iuliu, Bányai-Kovács Nándor, Horváth Emőke, published by Transylvanian Museum Society
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.