Publication:
Immunomodulation of Oxidative Stress during Organ Donation Process: Preliminary Results.

dc.contributor.authorPalomo-López, Nora
dc.contributor.authorRodríguez-Rodríguez, Ana
dc.contributor.authorMartín-Villén, Luis
dc.contributor.authorMendoza-Prieto, María
dc.contributor.authorRuiz de Azúa-López, Zaida
dc.contributor.authorSempere-Bordes, Lluis
dc.contributor.authorBoyero-Corral, Laura
dc.contributor.authorDaga-Ruiz, Domingo
dc.contributor.authorGordillo-Brenes, Antonio
dc.contributor.authorPacheco-Sánchez, María
dc.contributor.authorPerez-Villares, José Miguel
dc.contributor.authorVilches-Arenas, Ángel
dc.contributor.authorEgea-Guerrero, Juan José
dc.date.accessioned2023-05-03T13:54:21Z
dc.date.available2023-05-03T13:54:21Z
dc.date.issued2022-04-20
dc.description.abstractThe objective was to quantify oxidative stress resulting from ischemia during the donation process, using malondialdehyde (MDA) measurement, and its modulation by the administration of melatonin. We designed a triple-blind clinical trial with donors randomized to melatonin or placebo. We collected donors by donation after brain death (DBD) and controlled donation after circulatory death (DCD), the latter maintained by normothermic regional perfusion (NRP). Melatonin or placebo was administered prior to donation or following limitation of therapeutic effort (LTE). Demographic variables and medical history were collected. We also collected serial measurements of MDA, at 60 and 90 min after melatonin or placebo administration. A total of 53 donors were included (32 from DBD and 21 from DCD). In the DBD group, 17 donors received melatonin, and 15 placebo. Eight DCD donors were randomized to melatonin and 13 to placebo. Medical history and cause for LTE were similar between groups. Although MDA values did not differ in the DBD group, statistical differences were observed in DCD donors during the 0-60 min interval: -4.296 (-6.752; -2.336) in the melatonin group and -1.612 (-2.886; -0.7445) in controls. Given the antioxidant effect of melatonin, its use could reduce the production of oxidative stress in controlled DCD.
dc.identifier.doi10.3390/healthcare10050762
dc.identifier.issn2227-9032
dc.identifier.pmcPMC9141959
dc.identifier.pmid35627899
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9141959/pdf
dc.identifier.unpaywallURLhttps://www.mdpi.com/2227-9032/10/5/762/pdf?version=1650433040
dc.identifier.urihttp://hdl.handle.net/10668/20993
dc.issue.number5
dc.journal.titleHealthcare (Basel, Switzerland)
dc.journal.titleabbreviationHealthcare (Basel)
dc.language.isoen
dc.organizationHospital Universitario Puerta del Mar
dc.organizationHospital Universitario Virgen de las Nieves
dc.organizationHospital Universitario Virgen de la Victoria
dc.organizationHospital Universitario Virgen de la Victoria
dc.organizationHospital Universitario Virgen del Rocío
dc.organizationInstituto de Biomedicina de Sevilla-IBIS
dc.organizationCATA - Coordinación Autonómica de Trasplantes de Andalucía
dc.pubmedtypeJournal Article
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectantioxidant effect
dc.subjectbrain death donor
dc.subjectdonation after circulatory death
dc.subjectischemia
dc.subjectmalondialdehyde
dc.subjectmelatonin
dc.subjectoxidative stress
dc.titleImmunomodulation of Oxidative Stress during Organ Donation Process: Preliminary Results.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number10
dspace.entity.typePublication

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