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Peer-reviewed veterinary case report

Protective Effects of a Hydrogen-Rich Preservation Solution in a Canine Lung Transplantation Model.

Journal:
The Annals of thoracic surgery
Year:
2021
Authors:
Kayawake, Hidenao et al.
Affiliation:
Department of Thoracic Surgery · Japan
Species:
dog

Abstract

BACKGROUND: Molecular hydrogen (H) has protective effects against ischemia-reperfusion injury in various organs. Because they are easier to transport and safer to use than inhaled H, H-rich solutions are suitable for organ preservation. In this study, we examined the protective effects of an H-rich solution for lung preservation in a canine left lung transplantation (LTx) model. METHODS: Ten beagles underwent orthotopic left LTx after 23 hours of cold ischemia followed by reperfusion for 4 hours. Forty-five minutes after reperfusion, the right main pulmonary artery was clamped to evaluate the function of the implanted graft. The beagles were divided into two groups: control group (n&#xa0;= 5), and Hgroup (n&#xa0;= 5). In the control group, the donor lungs were flushed and immersed during cold preservation at 4&#xb0;C using ET-Kyoto solution, and in the Hgroup, these were flushed and immersed using H-rich ET-Kyoto solution. Physiologic assessments were performed during reperfusion. After reperfusion, the wet-to-dry ratios were determined, and histology examinations were performed. RESULTS: Significantly higher partial pressure of arterial oxygen and significantly lower partial pressure of carbon dioxide were observed in the Hgroup than in the control group (P&#xa0;= .045 and P < .001, respectively). The wet-to-dry ratio was significantly lower in the Hgroup than in the control group (P&#xa0;= .032). Moreover, in histology examination, less lung injury and fewer apoptotic cells were observed in the Hgroup (P < .001 and P < .001, respectively). CONCLUSIONS: Our results demonstrated that the H-rich preservation solution attenuated ischemia-reperfusion injury in a canine left LTx model.

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Original publication: https://pubmed.ncbi.nlm.nih.gov/32649946/