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dc.contributor.authorDíaz Morales, Noelia 
dc.contributor.authorSancho Martínez, Sandra María 
dc.contributor.authorBaranda Alonso, Eva María 
dc.contributor.authorFuentes Calvo, Isabel 
dc.contributor.authorSidhu-Muñoz, Rebeca S
dc.contributor.authorMartín Fernández, Nuria
dc.contributor.authorLópez Hernández, Francisco José 
dc.contributor.authorMartínez Salgado, José Carlos 
dc.date.accessioned2026-06-19T08:36:08Z
dc.date.available2026-06-19T08:36:08Z
dc.date.issued2025-03
dc.identifier.citationDiaz-Morales, N., Sancho-Martinez, S. M., Baranda-Alonso, E. M., Fuentes-Calvo, I., Sidhu-Munoz, R. S., Martin-Fernandez, N., ... & Martinez-Salgado, C. (2025). Age and hypertension synergize with dehydration to cause renal frailty in rats and predispose them to intrinsic acute kidney injury. Laboratory Investigation, 105(3), 102211.es_ES
dc.identifier.issn0023-6837
dc.identifier.urihttp://hdl.handle.net/10366/171876
dc.description.abstract[EN]Acute kidney frailty (AKF) is a condition of increased susceptibility to acute kidney injury (AKI), an abrupt impairment of renal excretory function potentially leading to severe complications. Prevention of AKI relies on the recognition of risk factors contributing to AKF. At the population level, dehydration constitutes a predisposing factor for AKI. However, renal frailty may be context-specific, with variations among patients in the types of damage and the distinct pathological mechanisms. In this regard, we studied the combined effect of dehydration with other factors on renal homeostasis, such as increasing age and hypertension. AKF status was studied in rats bearing risk factors individually and in combination and was evaluated as the level of AKI induced by a triggering dose of cisplatin, which is known to be mildly nephrotoxic for young, healthy rats. AKI was assessed through parameters of renal function (including creatinine, urea, creatinine clearance, proteinuria, and fractional excretion of sodium) and histopathology of renal tissue specimens. The hydration status was measured by bioelectric impedance and other techniques. Water deprivation induces a dehydration state characterized by reductions in body weight and urinary flow and increases in hematocrit and plasma and urine osmolality. Bioelectric impedance showed a net loss of body water after water deprivation with no relevant changes in body mass distribution. Dehydration is not sufficient to predispose young control rats to intrinsic AKI. However, the combination of dehydration with advanced age or hypertension induces AKF evidenced by a magnified response of renal dysfunction (reduced filtration and tubular function) and tubular necrosis caused by low-dose cisplatin treatment. This study highlights the relevance of addressing AKF as a premorbid condition providing prophylactic opportunities and shows that dehydration differentially predisposes to prerenal and intrinsic AKI.es_ES
dc.description.sponsorshipInstituto de Salud Carlos III (ISCIII) (Cofinanciado por la Unión Europea-NextGenerationEU), Junta de Castilla y León (Consejería de Educación), Fondo Europeo de Desarrollo Regional (FEDER), Ministerio de Ciencia e Innovaciónes_ES
dc.format.mimetypeapplication/pdf
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationales_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/es_ES
dc.subjectacute kidney frailtyes_ES
dc.subjectagees_ES
dc.subjectcisplatines_ES
dc.subjectdehydrationes_ES
dc.subjecthypertensiones_ES
dc.subjectacute kidney injuryes_ES
dc.subjectfragilidad renal agudaes_ES
dc.subjectdaño renal agudoes_ES
dc.subjectedades_ES
dc.subjectenvejecimientoes_ES
dc.subjectcisplatinoes_ES
dc.subjectdeshidrataciónes_ES
dc.subjecthipertensiónes_ES
dc.subject.meshCisplatin *
dc.subject.meshAcute Kidney Injury *
dc.subject.meshRats *
dc.subject.meshAnimals *
dc.subject.meshKidney *
dc.subject.meshDehydration *
dc.subject.meshHypertension *
dc.subject.meshAging *
dc.subject.meshKidney Diseases *
dc.titleAge and hypertension synergize with dehydration to cause renal frailty in rats and predispose them to intrinsic acute kidney injuryes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1016/j.labinv.2024.102211es_ES
dc.subject.unesco3209 Farmacologíaes_ES
dc.subject.unesco5206.03 Envejecimiento de la Poblaciónes_ES
dc.subject.unesco2411 Fisiología Humanaes_ES
dc.subject.unesco3207 Patologíaes_ES
dc.identifier.doi10.1016/j.labinv.2024.102211
dc.relation.projectIDPI21/01226es_ES
dc.relation.projectIDPI21/00548es_ES
dc.relation.projectIDRICORS2040es_ES
dc.relation.projectIDRD21/0005/0004es_ES
dc.relation.projectIDIES160P20es_ES
dc.relation.projectIDFJC2020-043205-Ies_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.essn1530-0307
dc.journal.titleLaboratory Investigationes_ES
dc.volume.number105es_ES
dc.issue.number3es_ES
dc.page.initial102211es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decsriñón *
dc.subject.decsanimales *
dc.subject.decsdeshidratación *
dc.subject.decscisplatino *
dc.subject.decslesión renal aguda *
dc.subject.decsratas *
dc.subject.decsenvejecimiento *
dc.subject.decshipertensión *
dc.subject.decsenfermedades renales *


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Attribution-NonCommercial-NoDerivatives 4.0 International
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