Successful Six‐Day Kidney Preservation Using Trophic Factor Supplemented Media and Simple Cold Storage

This study examined the effect of trophic factor supplementation [TFS; bovine neutrophil peptide‐1 (bactenecin), 1 mg/L; substance P, 2.5 mg/L; nerve growth factor, 20 μg/L; epidermal growth factor, 10 μg/L; insulin‐like growth factor‐1, 10 μg/L] during cold storage with UW lactobionate solution. Do...

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Veröffentlicht in:American journal of transplantation 2002-09, Vol.2 (8), p.712-718
Hauptverfasser: McAnulty, Jonathan F., Reid, Ted W., Waller, Ken R., Murphy, Christopher J.
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Sprache:eng
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Zusammenfassung:This study examined the effect of trophic factor supplementation [TFS; bovine neutrophil peptide‐1 (bactenecin), 1 mg/L; substance P, 2.5 mg/L; nerve growth factor, 20 μg/L; epidermal growth factor, 10 μg/L; insulin‐like growth factor‐1, 10 μg/L] during cold storage with UW lactobionate solution. Dogs transplanted with kidneys stored for 4 days in TFS‐UW had significantly lower peak serum creatinine values (mean 2.9 ± 0.2 mg/dL) and returned to normal values faster (6 days) than kidneys stored for 3 days in unmodified UW solution (4.2 ± 0.3 mg/dL and 14 days, respectively). Kidneys stored for 5 days in TFS‐UW (mean peak creatinine 3.7 ± 0.3) functioned equivalently to kidneys stored for 3 days and better than kidneys stored for 4 days in UW alone. Dogs with kidneys stored for 6 days in TFS‐UW had mean peak creatinines of 5.7 ± 0.4 mg/dL. These returned to normal creatinine values in 14 days, equal to 3‐day stored and significantly better than kidneys stored for 4 days in UW alone (20 days recovery time). This study shows trophic factor deprivation appears to be a critical mechanism of injury in organ preservation with current synthetic storage media, and marks the initial development of a synthetic biologically active preservation solution, the next generation of preservation media.
ISSN:1600-6135
1600-6143
DOI:10.1034/j.1600-6143.2002.20805.x