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RESEARCH PRODUCT
Histologic effects of university of wisconsin two-layer method preservation of rat pancreas.
Vincenzo Davide PalumboRoberta AltomareMaurizio BellaviaMaria Concetta GiovialeGabriele SpinelliGiuseppe DamianoRosario BaroneA.i. Lo MonteGiuseppe BuscemiFrancesco CacciabaudoRoberto PuleioGiovanni Cassatasubject
CryopreservationTransplantationPathologymedicine.medical_specialtybusiness.industryIn situ perfusionTwo layerOxygenationCryopreservationRatsTransplantationSettore MED/18 - Chirurgia Generalemedicine.anatomical_structureTwo-layer method; organ preservationMedicineRat PancreasAnimalsSurgeryRats Wistarorgan preservationbusinessPancreasTwo-layer methodPerfusionPancreasdescription
Marginal donors represent a poorly utilized source of organs for transplantation despite their availability. The key is to reduce the ischemic damage in the effort to improve organ quality. This study investigated the histologic effects after in situ perfusion of preservation with a two-layer method compared with the classic University of Wisconsin preservation in term of tissue integrity and number of viable exocrine cells in the rat pancreas both after exsanguination and at 8 weeks of cryopreservation. Pancreata harvested from 60 rats were collected using 3 methods: two-layer method following University of Wisconsin perfusion; exsanguination; and classic University of Wisconsin perfusion/storage. In addition to histologic analysis of collected pancreata, we analyzed the number of CK19(+) cells and their viability using chi-square tests with values P < .05 considered to be significant. Rat pancreas histology showed as University of Wisconsin in situ perfusion and preservation by the two-layer method to be more effective to maintain the morphologic integrity of both exocrine and endocrine tissues. There were a larger number of CK19(+) cells with good viability. Moreover, the effects of oxygenation were visible in pancreas biopsies preserved after exsanguination. In situ University of Wisconsin perfusion and preservation for 240 minutes with the two-layer method yielded greater numbers and viability of CK19(+) cells even after 8 weeks of cryopreservation.
year | journal | country | edition | language |
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2013-01-01 |