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  Ribonuclease (RNase) Prolongs Survival of Grafts in Experimental Heart Transplantation

Kleinert, E., Langenmayer, M. C., Reichart, B., Kindermann, J., Griemert, B., Blutke, A., et al. (2016). Ribonuclease (RNase) Prolongs Survival of Grafts in Experimental Heart Transplantation. JOURNAL OF THE AMERICAN HEART ASSOCIATION, 5(5): e003429. doi:10.1161/JAHA.116.003429.

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 Creators:
Kleinert, Eike, Author
Langenmayer, Martin C., Author
Reichart, Bruno, Author
Kindermann, Jana, Author
Griemert, Barbara, Author
Blutke, Andreas, Author
Troidl, Kerstin1, Author           
Mayr, Tanja, Author
Grantzow, Tobias, Author
Noyan, Fatih, Author
Abicht, Jan-Michael, Author
Fischer, Silvia, Author
Preissner, Klaus T., Author
Wanke, Ruediger, Author
Deindl, Elisabeth, Author
Guethoff, Sonja, Author
Affiliations:
1Pharmacology, Max Planck Institute for Heart and Lung Research, Max Planck Society, ou_2591696              

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Free keywords: HUMAN PANCREATIC RIBONUCLEASE; CARDIAC ALLOGRAFT VASCULOPATHY; ENDOTHELIAL GROWTH-FACTOR; EXTRACELLULAR RNA; JOINT PUBLICATION; REVISED GUIDES; NACAD GROUPS; VASCULAR SYSTEM; RATS; MICECardiovascular System & Cardiology; edema; extracellular RNA; ischemia/reperfusion injury; ribonuclease; transplantation;
 Abstract: Background-Cell damage, tissue and vascular injury are associated with the exposure and release of intracellular components such as RNA, which promote inflammatory reactions and thrombosis. Based on the counteracting anti-inflammatory and cardioprotective functions of ribonuclease A (RNase A) in this context, its role in an experimental model of heart transplantation in rats was studied. Methods and Results-Inbred BN/OrlRj rat cardiac allografts were heterotopically transplanted into inbred LEW/OrlRj rats. Recipients were intravenously treated every other day with saline or bovine pancreatic RNase A (50 mu g/kg). Toxic side effects were not found (macroscopically and histologically). Heart tissue flow cytometry and quantitative morphological analyses of explanted hearts at postoperative day 1 or postoperative day 4 showed reduced leukocyte infiltration, edema, and thrombus formation in RNase A-treated rats. In allogeneic mixed lymphocyte reactions, RNase A decreased the proliferation of effector T cells. RNase A treatment of rats resulted in prolonged median graft survival up to 10.5 days (interquartile range 1.8) compared to 6.5 days (interquartile range 1.0) in saline treatment (P=0.001). Treatment of rats with a new generated (recombinant) human pancreatic RNase 1 prolonged median graft survival similarly, unlike treatment with (recombinant) inactive human RNase 1 (each 50 mu g/kg IV every other day, 11.0 days, interquartile range 0.3, versus 8.0 days, interquartile range 0.5, P=0.007). Conclusions-Upon heart transplantation, RNase administration appears to present a promising and safe drug to counteract ischemia/reperfusion injury and graft rejection. Furthermore, RNase treatment may be considered in situations of critical reperfusion after percutaneous coronary interventions or in cardiac surgery using the heart-lung machine.

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Language(s): eng - English
 Dates: 2016
 Publication Status: Published online
 Pages: 13
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: ISI: 000386711200050
DOI: 10.1161/JAHA.116.003429
 Degree: -

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Title: JOURNAL OF THE AMERICAN HEART ASSOCIATION
Source Genre: Journal
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Publ. Info: 111 RIVER ST, HOBOKEN 07030-5774, NJ USA : WILEY
Pages: - Volume / Issue: 5 (5) Sequence Number: e003429 Start / End Page: - Identifier: ISSN: 2047-9980