Document Type : Original Article

Authors

1 Graduate Student, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran

2 Department of Surgery and Diagnostic Imaging, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran

3 Department of Internal Medicine and Clinical Pathology, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran

4 Department of Surgery and Radiology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran

Abstract

Echocardiography is a non-invasive method of cardiac evaluation in most species. Echocardiographic reference parameters are poorly documented in sheep and not documented in Ghezel sheep. The purpose of this study was to determine reference ranges of normal echocardiographic parameters using two-dimensional and M-mode techniques in Ghezel sheep. In 15 healthy female Ghezel sheep aged between 15 and 18 months, echocardiography was performed in standing position from left and right parasternal approach focused at 3rd - 5th intercostal spaces using a 2.50 - 5.00 MHz phased array transducer. The following parameters were measured in two-dimensional echocardiography: left atrial diameter (LAD), mitral valve annulus (MVA), aortic sinus (AoS), aortic valve (AoV), pulmonary sinus (PuS), and pulmonary valve (PuV); and in M-mode echocardiography: interventricular septum (IVS), left ventricular internal diameter (LVID), left ventricular free wall (LVFW), right ventricle free wall (RVFW), right ventricle internal diameter (RVID). Calculated variables included the ratios LAD/Ao and Pu/AoS, and the fractional shortening (FS), end diastolic volume (EDV), end systolic volume (ESV), ejection fraction (EF), stroke volume (SV) and cardiac output (CO) of the left ventricle. In conclusion, echocardiographic parameters could be reliably assessed in Ghezel sheep and our study provided some normal echocardiographic reference ranges that might be useful in proper identification, visualization, and measurements of cardiac structures. Such findings could be useful to assess and to diagnose the specific heart diseases in sheep practice and also for experimental studies in sheep as an animal model used for research purposes in cardiovascular studies of human.

Keywords

  1. Amory H, Kafidi N, Lekeux P. Echocardiographic evaluation of cardiac morphologic and functional variables in double - muscled calves. Am J Vet Res 1992;53(9):1540-1547.
  2. Amory H, Lekeux P. Effect of growth on functional and morphological echocardiographic variables in Friesian calves. Vet Rec 1991;128(15):349-354.
  3. Crippa L, Ferro E, Melloni E, Brambilla P, et al. Echocardiographic parameters and indices in normal beagle dog. Lab Anim 1992;26(3):190-195.
  4. Dancea A, Fouron JC, Miró J, et al. Correlation between electrocardiographic and ultrasonographic time -interval measurements in fetal lamb heart. Pediatr Res 2000; 47(3):324-328.
  5. Veille JC, Sivakoff M, Nemeth M. Accuracy of echocardiography measurements in the fetal lamb. Am J Obstet Gynecol 1988; 158(5):1225-1232.
  6. Hong T, Maish MS, Cohen J, et al. Reproducible echo-cardiography in juvenile sheep and its application in the evaluation of a pulmonary valve homograft implant. Contemp Top Lab Anim Sci 2000; 39(5):20-25.
  7. Olsson K, Hansson A, Hydbring E, et al. A serial study of heart function during pregnancy, lactation and the dry period in dairy goats using echocardiography. Exp Physiol 2001; 86(1):93-99.
  8. Leroux AA, Moonen ML, Farnir F, et al. Two - dimensional and M - mode echocardiographic reference values in healthy adult Saanen goats. Vet Rec 2012; 170(6):154. doi: 10.1136/vr.100192.
  9. Acorda JA, Pajas AMGA. M - mode echocardiographic values in male and female Philippine sheep (Ovis aries) (Artiodactyla: Bovidae) by age and status of lactation and pregnancy. Philipp J Vet Med 2015; 52(1), 11-20.
  10. Reef VB, McGuirk SM. Diseases of the cardiovascular system. In: Bradford PS (Ed). Large animal internal medicine. 3rd St. Louis, USA: Mosby 2002:447-468.
  11. Hartley WJ, Kater JC. Perinatal disease conditions of sheep in New Zealand. N Z Vet J 1964; 12(3):49-57.
  12. Dennis SM, Leipold HW. Congenital cardiac defects in lambs. Am J Vet Res 1968; 29(12):2337-2340.
  13. Shivaprakesh BV, Gopalakrishna Rao D. Local anaesthetic toxicity in a sheep with patent ductus arteriosus. Indian Vet J 1997; 74:901-902.
  14. Locatelli P, Olea FD, De Lorenzi A, et al. Reference values for echocardiographic parameters and indexes of left ventricular function in healthy, young adult sheep used in translational research: comparison with standardized values in humans. Int J Clin Exp Med 2011; 4(4): 258-264.
  15. Boudjemline Y, Agnoletti G, Bonnet D, et al. Percutaneous pulmonary valve replacement in a large right ventricular outflow tract: an experimental study. J Am Coll Cardiol 2004; 43(6):1082-1087.
  16. Attmann T, Jahnke T, Quaden R, et al. Advances in experimental percutaneous pulmonary valve replacement. Ann Thorac Surg 2005; 80(3): 969-975.
  17. Quinn RW, Hilbert SL, Bert AA, et al. Performance and morphology of decellularized pulmonary valves implanted in juvenile sheep. Ann Thorac Surg 2011; 92(1): 131-137.
  18. Mason IL. A world dictionary, of livestock breeds: types and varieties. 4th Oxon, UK: CAB International 1996; 273.
  19. Nabavi Alijani S, Rafat, SA et al. Genetic analysis of ewe productivity traits in ‎Ghezel sheep using linear and threshold models. Slovak J Anim Sci 2015; 48(3): 103-‎‎109‎.
  20. Kirberger RM, van den Berg JS. Pulsed wave Doppler echocardiographic evaluation of intracardiac blood flow in normal sheep. Res Vet Sci 1993; 55(2):189-194.
  21. Hallowell GD, Potter TJ, Bowen IM. Reliability of quantitative echocardiography in adult sheep and goats. BMC Vet Res. 2012; 8:181. doi: 10.1186/1746-6148-8-181.
  22. Boon JA. Veterinary echocardiography. 2nd New Jersey, USA: Wiley - Blackwell 2011; 61-183.
  23. Szaluś-Jordanow O, Czopowicz M, Witkowski L, et al. Reference intervals of echocardiographic measurments in healthy adult dairy goats. PloS One 2017;12(8): e0183293. doi: 10.1371/journal.pone. 0183293.
  24. Dukes - McEwan J, Borgarelli M, Tidholm A, et al. Proposed guidelines for the diagnosis of canine idiopathic dilated cardiomyopathy. J Vet Cardiol 2003; 5(2):7-19.
  25. Yadegari M. Normal echocardiographic findings in Lori - Bakhtiari sheep. Hum Vet Med 2014; 6(2):45-48.
  26. Al - Haidar A, Farnir F, Deleuze S, et al. Effect of breed, sex, age and body weight on echocardiographic measurements in the equine species. Res Vet Sci 2013;95(1): 255 -260.
  27. Morrison SA, Moise NS, Scarlett J, et al. Effect of breed and body weight on echocardiographic values in four breeds of dogs of differing somatotype. J Vet Intern Med 1992; 6(4):220-224.
  28. Sisson D, Schaeffer D. Changes in linear dimensions of the heart, relative to body weight, as measured by M - mode echocardiography in growing dogs. Am J Vet Res 1991; 52(10):1591-1596.
  29. Vloumidi EI, Fthenakis GC. Ultrasonographic examination of the heart in sheep. Small Ruminant Res 2017; 152:119-127.
  30. Ikeda Y, Yutani C, Huang Y, et al. Histological remodeling in an ovine heart failure model resembles human ischemic cardiomyopathy. Cardiovasc Pathol 2001;10(1):19-27.
  31. Moainie SL, Gorman III JH, Guy TS, et al. An ovine model of postinfarction dilated cardiomyopathy. Ann Thorac Surg. 2002; 74(3):753-760.
  32. Ghanta RK, Rangaraj A, Umakanthan R, et al. Adjustable, physiological ventricular restraint improves left ventricular mechanics and reduces dilatation in an ovine model of chronic heart failure. Circulation. 2007; 115(10):1201-1210.
  33. Mattoon JS, Nyland TG. Small animal diagnostic ultrasound. 3rd Pennsylvania, USA: Saunders 2014; 354-367.