Subnormothermic perfusion with h2s donor ap39 improves dcd porcine renal graft outcomes in an ex vivo model of kidney preservation and reperfusion
dc.contributor.author | Juriasingani, S | |
dc.contributor.author | Ruthirakanthan, A | |
dc.contributor.author | Richard-Mohamed, M | |
dc.contributor.author | Akbari, M | |
dc.contributor.author | Aquil, S | |
dc.contributor.author | Patel, S | |
dc.contributor.author | Al-Ogaili, R | |
dc.contributor.author | Whiteman, M | |
dc.contributor.author | Luke, P | |
dc.contributor.author | Sener, A | |
dc.date.accessioned | 2021-04-20T06:15:58Z | |
dc.date.issued | 2021-03-17 | |
dc.description.abstract | Cold preservation is the standard of care for renal grafts. However, research on alterna-tives like perfusion at higher temperatures and supplementing preservation solutions with hydrogen sulfide (H2S) has gained momentum. In this study, we investigated whether adding H2S donor AP39 to porcine blood during subnormothermic perfusion at 21 °C improves renal graft outcomes. Porcine kidneys were nephrectomized after 30 min of clamping the renal pedicles and treated to 4 h of static cold storage (SCS) on ice or ex vivo subnormothermic perfusion at 21 °C with autologous blood alone (SNT) or with AP39 (SNTAP). All kidneys were reperfused ex vivo with autologous blood at 37 °C for 4 h. Urine output, histopathology and RNAseq were used to evaluate the renal graft function, injury and gene expression profiles, respectively. The SNTAP group exhibited significantly higher urine output than other groups during preservation and reperfusion, along with significantly lower apoptotic injury compared to the SCS group. The SNTAP group also exhibited differential pro-survival gene expression patterns compared to the SCS (downregulation of pro-apoptotic genes) and SNT (downregulation of hypoxia response genes) groups. Subnormothermic perfusion at 21 °C with H2S-supplemented blood improves renal graft outcomes. Further research is needed to facilitate the clinical translation of this approach. | en_GB |
dc.description.sponsorship | Medical Research Council (MRC) | en_GB |
dc.description.sponsorship | Physicians Services Incorporated (PSI) Foundation | en_GB |
dc.description.sponsorship | Lawson Research Institute | en_GB |
dc.identifier.citation | Vol. 11 (3), article 446 | en_GB |
dc.identifier.doi | 10.3390/biom11030446 | |
dc.identifier.grantnumber | Grant #18- 17 | en_GB |
dc.identifier.grantnumber | Spring 2017 Internal Research Fund Pilot Study Competition | en_GB |
dc.identifier.uri | http://hdl.handle.net/10871/125397 | |
dc.language.iso | en | en_GB |
dc.publisher | MDPI | en_GB |
dc.rights | This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited | en_GB |
dc.subject | AP39 | en_GB |
dc.subject | hydrogen sulfide | en_GB |
dc.subject | subnormothermic perfusion | en_GB |
dc.subject | kidney preservation | en_GB |
dc.subject | ischemia– reperfusion injury | en_GB |
dc.subject | donation after cardiac death | en_GB |
dc.subject | porcine model | en_GB |
dc.title | Subnormothermic perfusion with h2s donor ap39 improves dcd porcine renal graft outcomes in an ex vivo model of kidney preservation and reperfusion | en_GB |
dc.type | Article | en_GB |
dc.date.available | 2021-04-20T06:15:58Z | |
dc.identifier.issn | 2218-273X | |
dc.description | This is the final published version, also available from MDPI via the DOI in this record. | en_GB |
dc.identifier.journal | Biomolecules | en_GB |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | en_GB |
dcterms.dateAccepted | 2021-03-15 | |
exeter.funder | ::Medical Research Council (MRC) | en_GB |
rioxxterms.version | VoR | en_GB |
rioxxterms.licenseref.startdate | 2021-03-15 | |
rioxxterms.type | Journal Article/Review | en_GB |
refterms.dateFCD | 2021-04-20T06:12:28Z | |
refterms.versionFCD | VoR | |
refterms.dateFOA | 2021-04-20T06:16:17Z | |
refterms.panel | A | en_GB |
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