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Protective effects of a hydrogen-rich solution during cold ischemia in rat lung transplantation.
Saito, Masao; Chen-Yoshikawa, Toyofumi F; Takahashi, Mamoru; Kayawake, Hidenao; Yokoyama, Yuhei; Kurokawa, Ryosuke; Hirano, Shin-Ichi; Date, Hiroshi.
Afiliação
  • Saito M; Department of Thoracic Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Chen-Yoshikawa TF; Department of Thoracic Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan. Electronic address: fengshic@kuhp.kyoto-u.ac.jp.
  • Takahashi M; Department of Thoracic Surgery, Kyoto Katsura Hospital, Kyoto, Japan.
  • Kayawake H; Department of Thoracic Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Yokoyama Y; Department of Thoracic Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Kurokawa R; MiZ Co, Ltd, Kanagawa, Japan.
  • Hirano SI; MiZ Co, Ltd, Kanagawa, Japan.
  • Date H; Department of Thoracic Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
J Thorac Cardiovasc Surg ; 159(5): 2110-2118, 2020 05.
Article em En | MEDLINE | ID: mdl-31780065
BACKGROUND: Molecular hydrogen can reduce the oxidative stress of ischemia-reperfusion injury in various organs for transplantation and potentially improve survival rates in recipients. This study aimed to evaluate the protective effects of a hydrogen-rich preservation solution against ischemia-reperfusion injury after cold ischemia in rat lung transplantation. METHODS: Lewis rats were divided into a nontransplant group (n = 3), minimum-ischemia group (n = 3), cold ischemia group (n = 6), and cold ischemia with hydrogen-rich (more than 1.0 ppm) preservation solution group (n = 6). The rats in the nontransplant group underwent simple thoracotomy, and the rats in the remaining 3 groups underwent orthotopic left lung transplantation. The ischemic time was <30 minutes in the minimum-ischemia group and 6 hours in the cold ischemia groups. After 2-hour reperfusion, we evaluated arterial blood gas levels, pulmonary function, lung wet-to-dry weight ratio, and histologic features of the lung tissue. The expression of proinflammatory cytokines was measured using quantitative polymerase chain reaction assays, and 8-hydroxydeoxyguanosine levels were evaluated using enzyme-linked immunosorbent assays. RESULTS: When compared with the nontransplant and minimum-ischemia groups, the cold ischemia group had lower dynamic compliance, lower oxygenation levels, and higher wet-to-dry weight ratios. However, these variables were significantly improved in the cold ischemia with hydrogen-rich preservation solution group. This group also had fewer signs of perivascular edema, lower interleukin-1ß messenger RNA expression, and lower 8-hydroxydeoxyguanosine levels than the cold ischemia group. CONCLUSIONS: The use of a hydrogen-rich preservation solution attenuates ischemia-reperfusion injury in rat lungs during cold ischemia through antioxidant and anti-inflammatory effects.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Pulmão / Soluções para Preservação de Órgãos / Substâncias Protetoras / Isquemia Fria / Hidrogênio Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Thorac Cardiovasc Surg Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Pulmão / Soluções para Preservação de Órgãos / Substâncias Protetoras / Isquemia Fria / Hidrogênio Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Thorac Cardiovasc Surg Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão