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Mouse Myocardial performance

Isolated Perfused Heart (SP-65)

 

Applications

This model is useful in the study of the pathophysiology of myocardial ischemia and reperfusion and vascular resistance.

Background

The Langendorff preparation consists of a retrograde system which perfuses the coronary vascular system of an isolated heart via the aorta with blood (by donor rat) or other oxygenated fluid (such as Krebs-Henseleit) from a reservoir to study coronary flow during cardiac activity. Models are maintained at constant mean pressure (controlled by a balloon placed in the left ventricle) or constant mean flow (using an in-line flowprobe inserted into the perfusion line).

Variations to the Langendorff preparation are made so the left ventricle performs pressure-volume work for the study of myocardial performance. Retrograde perfusion through the aortic cannula is reversed when the heart resumes contractions and antegrade perfusion is established via a cannula into the pulmonary vein or left atrium to produce a work-performing heartAortic flow plus coronary sinus effluent equals cardiac output. Flow in the aortic cannula and venous cannula can be accurately measured with inline flowprobes. Coronary flow can be collected and weighed or be derived from aortic flow and venous return. Other cardiac parameters can be calculated from the pressure-flow relationships: heart rate, contractility, stoke volume and stroke work.

Preparation

Probe Style:
In-line Flowprobes (N-Series)
1N 
1N for 0.46 inch (1.2mm) tubing ID

isolated_heart_graphicweb

Anesthetize the mouse with pentobarbital (60 mg/kg IP). To prevent coagulation, administer heparin (1000 IU/kg) intravenously in the right femoral vein. A cannula is placed in the trachea for ventilation. Make a longitudinal skin and muscle incision opening the abdomen from the diaphragm to the throat. Cut the diaphragm free from the ribs. Open the thorax following the bone-cartilage border on the left and right sides parallel to the sternum from the diaphragm cranially to the first rib. Turn the complete anterior thoracic wall upwards over the head to expose the heart. Remove the pericardium. Separate the ascending aorta from connective tissue and the pulmonary artery using blunt dissection. Preplace a thread around the aorta.

Prepare for insertion of the aortic cannula: Prime the cannula to remove air bubbles and allow a small stream of perfusate during insertion. Clamp the vena cava above the diaphragm to minimize bleeding. Sprinkle the heart with cold physiological saline (4º C) so the heart slows down and stops beating. Incise the pulmonary artery to avoid distension of the right ventricle. Incise the aorta as far cranially as possible and insert the cannula, taking care that the position of the cannula is not too low to impede the aortic valves or the coronary ostia. Tighten the thread around the end of the cannula. Fully perfuse the heart. Completely isolate and remove the heart for transfer to the Langendorff apparatus.

Transonic Systems' research flowmeters operate inline (flow through) flowprobes for high resolution volume flow measurements in extracorporeal circuits. Ultrasonic transit time flowprobes can measure blood, buffer solutions and other non-aerated liquids used in perfused organ studies. A dual channel or dual module flowmeter will operate two 1N flowprobes to simultaneously measure aortic flow and venous return for cardiac output.

  • direct volumetric flow measurement
  • high resolution and sensitivity for low flow conditions
  • exceptional electrical and zero baseline stability
  • measures blood, saline & other non-aerated liquids

References List updated in June 2002

1087A Chen, E.P., Bittner, H.B., Davis, R.D., Van Trigt, P., Folz, R.J., "Physiologic Effects of Extracellular Superoxide Dismutase Transgene Overexpression of Myocardial Function after Ischemia and Reperfusion," Journal of Thoracic and Cardiovascular Surgery, Vol. 115, p. 450-459, 1998. (isolated heart, mouse, 2N probe)

Bittner, H.B., Chen, E.P., Peterseim, D.S., Van Trigt, P., "A Work-Performing Heart Preparation for Myocardial Performance Analysis in Murine Hearts," Journal of Surgical Research, Vol 64, p. 57-62, 1996.

Grupp, I.L., Subramaniam, A., Hewett, T.E., Robbins, J., Grupp, G., "Comparison of Normal, Hypodynamic and Hyperdynamic Mouse Hearts Using Isolated Work-Performing Heart Preparations," American Journal of Physiology, Vol 265, p. H1401-1410, 1993.

Lu, W., Grupp, I.L., Harrer, J., Ponniah, S., Grupp, G., Duffy, J.J., Doetschman, T., Kranias, E.G., "Targeted Ablation of the Phospholamban Gene Is Associated with Markedly Enhanced Myocardial Contractility and Loss of -Agoinist Stimulation ," Circulation Research, Vol. 75, p. 401-409, 1994.

Mutchuchamy, M., Grupp, I.L., Grupp, G., O'Toole, B., Kier, A.B., Boivin, G.P., Neumann, J., Wieczorek, D.F., "Molecular and Physiological Effectts of Overexpressing Striated Muscle -Tropomyosin in the Adult Murine Heart ," The Journal of Biological Chemistry, Vol. 270, No. 51, p. 30593-30603, 1995.Döring, H.J., Dehnert, H., The Isolated Perfused Heart According to Langendorff, English edition, Biomesstechnick-Verlag, West Germany, 1988, (available from Transonic Systems).

Rev 3/97

 

 

 
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