Diversity of coronary arterial tree in laboratory mice

• Autorzy: Klosinska D. , Ciszek B. , Majchrzak B. , Badurek I. , Ratajska A.
• Języki publikacji: EN

Abstrakty

EN

Background: Research on the development and topography of mouse coronary arteries has been conducted for many years. Patterns of the course of these vessels have been described in various mouse strains. Our research focused on hearts of MIZZ mice. Materials and methods: We visualised the coronary artery system by means of latex dye perfusion via the aorta. The injected latex did not reach the capillary vessel system. Results: The heart of MIZZ mice is supplied with blood by two main coronary arteries: the right and the left one. They deliver blood to the right and left part of the heart, respectively. The right coronary artery arises from the right sinus of the aorta and the left coronary artery from the left sinus. The interventricular septum is usually supplied by the septal artery, which is the main branch of the right coronary artery. All arteries of the coronary system run intramurally. The number of branches and the location of their ostia differed among the examined individuals. Conclusions: Detailed information about the normal topography of coronary arteries, the number and course of their branches, as well as the area of the heart which is vascularised by these vessels constitutes the basic knowledge necessary to conduct further experiments. (Folia Morphol 2020; 79, 2: 255–264)

• Wydawca: -
• Czasopismo: Folia Morphologica
• Rocznik: 2020
• Tom: 79
• Numer: 2
• Opis fizyczny: p.255-264,fig.,ref.

Twórcy

autor

Klosinska D.

• Division of Histology and Embryology, Department of Morphological Sciences, Faculty of Veterinary Medicine, Warsaw University of Life Sciences, Warsaw, Poland

autor

Ciszek B.

• Department of Clinical Anatomy, Medical University of Warsaw, Poland

autor

Majchrzak B.

• Department of Pathology, Medical University of Warsaw, Poland

autor

Badurek I.

• Department of Pathology, Medical University of Warsaw, Poland

autor

Ratajska A.

• Department of Pathology, Medical University of Warsaw, Poland

Bibliografia

• 1. Ahmed SH, Rakhawy MT, Abdalla A, et al. The comparative anatomy of the blood supply of cardiac ventricles in the albino rat and guinea-pig. J Anat. 1978; 126(Pt 1): 51–57, indexed in Pubmed: 649502.
• 2. Andrade JN, Tang J, Hensley MT, et al. Rapid and efficient production of coronary artery ligation and myocardial infarction in mice using surgical clips. PLoS One. 2015; 10(11): e0143221, doi: 10.1371/journal.pone.0143221, indexed in Pubmed: 26599500.
• 3. Arque JM, Cruz V, Rosado LM, et al. Congenital anomalies of coronary arteries in rodents. Am J Cardiol. 1986; 57(6): 498–499, doi: 10.1016/0002-9149(86)90789-7, indexed in Pubmed: 3946275.
• 4. Barth C, Roberts W. Left main coronary artery originating from the right sinus of valsalva and coursing between the aorta and pulmonary trunk. J Am Coll Cardiol. 1986; 7(2): 366–373, doi: 10.1016/s0735-1097(86)80507-1.
• 5. Basso C, Maron B, Corrado D, et al. Clinical profile of congenital coronary artery anomalies with origin from the wrong aortic sinus leading to sudden death in young competitive athletes. J Am Coll Cardiol. 2000; 35(6): 1493–1501, doi: 10.1016/s0735-1097(00)00566-0.
• 6. Becker AE. Variations of the main coronary arteries. In: Becker AE, Losekoot G, Marcelletti C, Anderson RH, editors. Paediatric Cardiology. 1981: 263–277.
• 7. Buehler A, Martire A, Strohm C, et al. Angiogenesisindependent cardioprotection in FGF-1 transgenic mice. Cardiovasc Res. 2002; 55(4): 768–777, doi: 10.1016/s0008-6363(02)00494-7.
• 8. Cheitlin MD, De Castro CM, McAllister HA. Sudden death as a complication of anomalous left coronary origin from the anterior sinus of Valsalva, A not-so-minor congenital anomaly. Circulation. 1974; 50(4): 780–787, doi: 10.1161/01.cir.50.4.780, indexed in Pubmed: 4419670.
• 9. Cheng K, Ibrahim A, Hensley MT, et al. Relative roles of CD90 and c-kit to the regenerative efficacy of cardiosphere-derived cells in humans and in a mouse model of myocardial infarction. J Am Heart Assoc. 2014; 3(5): e001260, doi: 10.1161/JAHA.114.001260, indexed in Pubmed: 25300435.
• 10. Ciszek B, Skubiszewska D, Ratajska A. The anatomy of the cardiac veins in mice. J Anat. 2007; 211(1): 53–63, doi: 10.1111/j.1469-7580.2007.00753.x, indexed in Pubmed: 17553104.
• 11. Clauss SB, Walker DL, Kirby ML, et al. Patterning of coronary arteries in wildtype and connexin43 knockout mice. Dev Dyn. 2006; 235(10): 2786–2794, doi: 10.1002/dvdy.20887, indexed in Pubmed: 16802337.
• 12. Desmet W, Vanhaecke J, Vrolix M, et al. Isolated single coronary artery: a review of 50,000 consecutive coronary angiographies. Eur Heart J. 1992; 13(12): 1637–1640, doi: 10.1093/oxfordjournals.eurheartj.a060117, indexed in Pubmed: 1289093.
• 13. Durán AC, Fernández-Gallego T, Fernández B, et al. Solitary coronary ostium in the aorta in Syrian hamsters. A morphological study of 130 cases. Cardiovasc Pathol. 2005; 14(6): 303–311, doi: 10.1016/j.carpath.2005.07.001, indexed in Pubmed: 16286039.
• 14. Durán A, Sans-Coma V, Arqué J, et al. Blood supply to the interventricular septum of the heart in rodents with intramyocardial coronary arteries. Acta Zoologica. 1992; 73(4): 223–229, doi: 10.1111/j.1463-6395.1992. tb01086.x.
• 15. Fernández B, Durán AC, Fernández MC, et al. The coronary arteries of the C57BL/6 mouse strains: implications for comparison with mutant models. J Anat. 2008; 212(1): 12–18, doi: 10.1111/j.1469-7580.2007.00838.x, indexed in Pubmed: 18067545.
• 16. Fernandez B, Duran AC. How many coronary arteries are there in mammals? J Morphol. 2007; 268(1072).
• 17. Flaht-Zabost A, Gula G, Ciszek B, et al. Cardiac mouse lymphatics: developmental and anatomical update. Anat Rec (Hoboken). 2014; 297(6): 1115–1130, doi: 10.1002/ar.22912, indexed in Pubmed: 24700724.
• 18. González-Iriarte M, Carmona R, Pérez-Pomares JM, et al. Development of the coronary arteries in a murine model of transposition of great arteries. J Mol Cell Cardiol. 2003; 35(7): 795–802, doi: 10.1016/s0022-2828(03)00134-2, indexed in Pubmed: 12818570.
• 19. Guinovart MP, Vilallonga JR. Arterias coronarias: aspectos anatomo-clínicos:. Ediciones Científicas y Técnicas. 1993.
• 20. Guo Y, Wu WJ, Qiu Y, et al. Demonstration of an early and a late phase of ischemic preconditioning in mice. Am J Physiol. 1998; 275(4): H1375–H1387, doi: 10.1152/ajpheart.1998.275.4.H1375, indexed in Pubmed: 9746488.
• 21. Icardo JM, Colvee E. Origin and course of the coronary arteries in normal mice and in iv/iv mice. J Anat. 2001; 199(Pt 4): 473–482, doi: 10.1046/j.1469-7580.2001.19940473.x, indexed in Pubmed: 11693308.
• 22. Jones SP, Tang XL, Guo Y, et al. The NHLBI-sponsored Consortium for preclinicAl assESsment of cARdioprotective therapies (CAESAR): a new paradigm for rigorous, accurate, and reproducible evaluation of putative infarct-sparing interventions in mice, rabbits, and pigs. Circ Res. 2015; 116(4): 572–586, doi: 10.1161/CIRCRESAHA.116.305462, indexed in Pubmed: 25499773.
• 23. Juszyński M, Ciszek B, Stachurska E, et al. Development of lymphatic vessels in mouse embryonic and early postnatal hearts. Dev Dyn. 2008; 237(10): 2973–2986, doi: 10.1002/dvdy.21693, indexed in Pubmed: 18816838.
• 24. Kolesová H, Bartoš M, Hsieh WC, et al. Novel approaches to study coronary vasculature development in mice. Dev Dyn. 2018; 247(8): 1018–1027, doi: 10.1002/dvdy.24637, indexed in Pubmed: 29770532.
• 25. Lewis FT. The question of Sinusoids. Anat Anz. 1904; 25: 261–269.
• 26. Li WE, Waldo K, Linask KL, et al. An essential role for connexin43 gap junctions in mouse coronary artery development. Development. 2002; 129(8): 2031–2042, indexed in Pubmed: 11934868.
• 27. Liberthson RR, Dinsmore RE, Fallon JT. Aberrant coronary artery origin from the aorta. Report of 18 patients, review of literature and delineation of natural history and management. Circulation. 1979; 59(4): 748–754, doi: 10.1161/01.cir.59.4.748, indexed in Pubmed: 421315.
• 28. López-García A, Soto-Navarrete MT, Fernández MC, et al. Unusual anatomical origins of the coronary arteries in C57BL/6 mice. Are they strain-specific? J Anat. 2016; 229(5): 703–709, doi: 10.1111/joa.12512, indexed in Pubmed: 27345017.
• 29. Makkar RR, Smith RR, Cheng Ke, et al. Intracoronary cardiosphere-derived cells for heart regeneration after myocardial infarction (CADUCEUS): a prospective, randomised phase 1 trial. Lancet. 2012; 379(9819): 895–904, doi: 10.1016/S0140-6736(12)60195-0, indexed in Pubmed: 22336189.
• 30. Michael LH, Entman ML, Hartley CJ, et al. Myocardial ischemia and reperfusion: a murine model. Am J Physiol. 1995; 269(6 Pt 2): H2147–H2154, doi: 10.1152/ajpheart.1995.269.6.H2147, indexed in Pubmed: 8594926.
• 31. Ratajska A, Gula G, Flaht-Zabost A, et al. Comparative and developmental anatomy of cardiac lymphatics. Scien World J. 2014; 2014: 183170, doi: 10.1155/2014/183170, indexed in Pubmed: 24592145.
• 32. Salto-Tellez M, Lim SY, Oakley REl, et al. Myocardial infarction in the C57BL/6J mouse. Cardiovasc Pathol. 2004; 13(2): 91–97, doi: 10.1016/s1054-8807(03)00129-7.
• 33. Sans-Coma V, Arqué JM, Durán AC, et al. The coronary arteries of the Syrian hamster, Mesocricetus auratus (Waterhouse 1839). Ann Anatom. 1993; 175(1): 53–57, doi: 10.1016/s0940-9602(11)80239-6.
• 34. Vandergriff AC, Hensley TM, Henry ET, et al. Magnetic targeting of cardiosphere-derived stem cells with ferumoxytol nanoparticles for treating rats with myocardial infarction. Biomaterials. 2014; 35(30): 8528–8539, doi: 10.1016/j.biomaterials.2014.06.031, indexed in Pubmed: 25043570.
• 35. Wollert KC, Drexler H. Clinical applications of stem cells for the heart. Circ Res. 2005; 96(2): 151–163, doi: 10.1161/01. RES.0000155333.69009.63, indexed in Pubmed: 15692093.

Identyfikatory

DOI

10.5603/FM.a2019.0070