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dc.contributor.authorLópez-Novoa, José M.
dc.contributor.authorQuirós Luis, Yaremi
dc.contributor.authorVicente Vicente, Rosa Laura 
dc.contributor.authorMorales Martín, Ana Isabel 
dc.contributor.authorLópez Hernández, Francisco José 
dc.date.accessioned2026-01-21T09:07:58Z
dc.date.available2026-01-21T09:07:58Z
dc.date.issued2011-01
dc.identifier.citationLopez-Novoa, J. M., Quiros, Y., Vicente, L., Morales, A. I., & Lopez-Hernandez, F. J. (2011). [Rev. of New insights into the mechanism of aminoglycoside nephrotoxicity: An integrative point of view]. Kidney International, 79(1), 33-45. https://doi.org/10.1038/KI.2010.337. Epub 2010 Sep 22. PMID: 20861826es_ES
dc.identifier.issn0085-2538
dc.identifier.urihttp://hdl.handle.net/10366/169111
dc.description.abstract[EN]Nephrotoxicity is one of the most important side effects and therapeutical limitations of aminoglycoside antibiotics, especially gentamicin. Despite rigorous patient monitoring, nephrotoxicity appears in 10-25% of therapeutic courses. Traditionally, aminoglycoside nephrotoxicity has been considered to result mainly from tubular damage. Both lethal and sub-lethal alterations in tubular cells handicap reabsorption and, in severe cases, may lead to a significant tubular obstruction. However, a reduced glomerular filtration is necessary to explain the symptoms of the disease. Reduced filtration is not solely the result of tubular obstruction and tubular malfunction, resulting in tubuloglomerular feedback activation; renal vasoconstriction and mesangial contraction are also crucial to fully explain aminoglycoside nephrotoxicity. This review critically presents an integrative view on the interactions of tubular, glomerular, and vascular effects of gentamicin, in the context of the most recent information available. Moreover, it discusses therapeutic perspectives for prevention of aminoglycoside nephrotoxicity derived from the pathophysiological knowledge.es_ES
dc.description.sponsorshipInstituto de Salud Carlos III (Retic 016/2006, RedinRen to JML-N, and FIS grant PI081900 to FJL-H), Junta de Castilla y Leon (Excellence Group GR-100), and Ministerio de Ciencia y Tecnología (BFU2004-00285/BFI and SAF2007-63893). REFERENCESes_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAminoglycoside antibioticses_ES
dc.subjectGentamicines_ES
dc.subjectNephrotoxicityes_ES
dc.subjectPathophysiologyes_ES
dc.subjectPreventiones_ES
dc.subject.meshGentamicins *
dc.subject.meshKidney Tubules *
dc.subject.meshAnti-Bacterial Agents *
dc.subject.meshHumans *
dc.subject.meshKidney Glomerulus *
dc.subject.meshAminoglycosides *
dc.subject.meshKidney Diseases *
dc.subject.meshRenal Circulation *
dc.titleNew insights into the mechanism of aminoglycoside nephrotoxicity: an integrative point of viewes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1038/KI.2010.337es_ES
dc.subject.unesco3209 Farmacologíaes_ES
dc.identifier.doi10.1038/ki.2010.337
dc.relation.projectIDRetic 016/2006es_ES
dc.relation.projectIDFIS grant PI081900es_ES
dc.relation.projectIDBFU2004-00285/BFIes_ES
dc.relation.projectIDSAF2007-63893es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.pmid20861826
dc.identifier.essn1523-1755
dc.journal.titleKidney Internationales_ES
dc.volume.number79es_ES
dc.issue.number1es_ES
dc.page.initial33es_ES
dc.page.final45es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decstúbulos renales *
dc.subject.decshumanos *
dc.subject.decsglomérulos renales *
dc.subject.decsantibacterianos *
dc.subject.decsgentamicinas *
dc.subject.decsaminoglicósidos *
dc.subject.decscirculación renal *
dc.subject.decsenfermedades renales *


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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