Non-volume-loaded heart provides a more relevant heterotopic transplantation model

Karis R. Tang-Quan, Jason Bartos, Tobias Deuse, Eric Churchill, Hansjörg Schäfer, Hermann Reichenspurner, Daria Mochly-Rosen, Robert C. Robbins, Sonja Schrepfer

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Background: We aimed to compare two techniques of heterotopic heart transplantation in rats. Non-volume-loaded (NL) and volume-loaded (VL) models were tested for their physiologic and immunologic properties to assess their suitability for transplant studies. Methods: Syngeneic heterotopic heart transplants were performed according to the techniques previously described by Ono (NL) and Yokoyama (VL). Grafts were followed over 90. days with sequential echocardiography. Ex-vivo Langendorff perfusion was used to gain functional data. Allogeneic heart transplants were done to determine whether chronic allograft vasculopathy (CAV) develops at a different pace in both transplant models. Results: The ischemic time during surgery was significantly longer using the VL model (p<0.001). The LV diameter of NL hearts decreased over time while that of the VL model significantly increased (p=0.004 on POD 90). Mean LV developed pressure and (d. P/. d. t)max were significantly higher with the NL model (61.1 ± 8.5. mmHg and 4261.7 ± 419.6. mmHg/s) than with VL hearts (19.9 ± 16.5. mmHg; p=0.011 and 924.8 ± 605.6. mmHg/s; p<0.001). The mean weight of NL hearts (0.45 ± 0.03. g) was significantly less than that of VL hearts (1.21 ± 0.16. g, p<0.001). Histology of syngeneic NL grafts showed healthy, but partly atrophic myocardium, whereas the LV myocardium of VL hearts showed dilation and scarring typical for chronic ischemic injury. Heart allografts similarly developed CAV with luminal narrowing of 37.2 ± 16.6% (NL) and 34.4 ± 21.4% (VL), respectively by POD 90 (p=0.807). Conclusions: Since the coronary arteries in the VL model get perfused with partly deoxygenated blood, the myocardium suffers from chronic ischemic injury. We recommend using the NL model in preclinical transplant studies.

Original languageEnglish (US)
Pages (from-to)65-70
Number of pages6
JournalTransplant Immunology
Volume23
Issue number1-2
DOIs
StatePublished - May 2010

Bibliographical note

Funding Information:
The authors thank Pauline Chu and Christiane Pahrmann for their excellent histological work. The present study was supported by the Falk Research Fund for the Department of Cardiothoracic Surgery at Stanford University School of Medicine, Stanford, CA, USA. Sonja Schrepfer has received a research grant from the Deutsche Forschungsgemeinschaft (DFG) ( SCHR992/3-1 ). The other authors have no disclosures to make.

Keywords

  • Chronic ischemia
  • Heterotopic heart transplantation
  • Immunology
  • Non-volume-loaded heart transplant model
  • Ono-Lindsey
  • Rat
  • Transplant vasculopathy
  • Volume-loaded heart transplant model
  • Yokoyama

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