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A method for translational rat ex vivo lung perfusion experimentation.
Ohsumi, Akihiro; Kanou, Takashi; Ali, Aadil; Guan, Zehong; Hwang, David M; Waddell, Thomas K; Juvet, Stephen; Liu, Mingyao; Keshavjee, Shaf; Cypel, Marcelo.
  • Ohsumi A; Latner Thoracic Surgery Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.
  • Kanou T; Department of Thoracic Surgery, Kyoto University Hospital, Kyoto, Japan.
  • Ali A; Latner Thoracic Surgery Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.
  • Guan Z; Latner Thoracic Surgery Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.
  • Hwang DM; Latner Thoracic Surgery Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.
  • Waddell TK; Latner Thoracic Surgery Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.
  • Juvet S; Latner Thoracic Surgery Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.
  • Liu M; Latner Thoracic Surgery Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.
  • Keshavjee S; Latner Thoracic Surgery Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.
  • Cypel M; Latner Thoracic Surgery Research Laboratories, Toronto General Hospital Research Institute, Toronto, Ontario, Canada.
Am J Physiol Lung Cell Mol Physiol ; 319(1): L61-L70, 2020 07 01.
Article en En | MEDLINE | ID: mdl-32233924
ABSTRACT
The application of ex vivo lung perfusion (EVLP) has significantly increased the successful clinical use of marginal donor lungs. While large animal EVLP models exist to test new strategies to improve organ repair, there is currently no rat EVLP model capable of maintaining long-term lung viability. Here, we describe a new rat EVLP model that addresses this need, while enabling the study of lung injury due to cold ischemic time (CIT). The technique involves perfusing and ventilating male Lewis rat donor lungs for 4 h before transplanting the left lung into a recipient rat and then evaluating lung function 2 h after reperfusion. To test injury within this model, lungs were divided into groups and exposed to different CITs (i.e., 20 min, 6 h, 12 h, 18 h and 24 h). Experiments involving the 24-h-CIT group were prematurely terminated due to the development of severe edema. For the other groups, no differences in the ratio of arterial oxygen partial pressure to fractional inspired oxygen ([Formula see text]/[Formula see text]) were observed during EVLP; however, lung compliance decreased over time in the 18-h group (P = 0.012) and the [Formula see text]/[Formula see text] of the blood from the left pulmonary vein 2 h after transplantation was lower compared with 20-min-CIT group (P = 0.0062). This new model maintained stable lung function during 4-h EVLP and after transplantation when exposed to up to 12 h of CIT.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Perfusión / Trasplante de Pulmón / Investigación Biomédica Traslacional / Pulmón Límite: Animals Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Perfusión / Trasplante de Pulmón / Investigación Biomédica Traslacional / Pulmón Límite: Animals Idioma: En Año: 2020 Tipo del documento: Article