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Cilastatin as a Potential Anti-Inflammatory and Neuroprotective Treatment in the Management of Glaucoma

dc.contributor.authorMartínez López, Miguel Ángel
dc.contributor.authorRubio Casado, Sara
dc.contributor.authorSan Felipe Riba, Diego
dc.contributor.authorMartín Sánchez, Beatriz
dc.contributor.authorFernández Albarral, José
dc.contributor.authorGarcía Martín, Elena Salobrar
dc.contributor.authorMatamoros, José Antonio
dc.contributor.authorRamírez Sebastián, José Manuel
dc.contributor.authorHoz Montañana, María Rosa De
dc.contributor.authorSalazar Corral, Juan José
dc.contributor.authorMarco López, Eva María
dc.contributor.authorLázaro Fernández, Alberto
dc.contributor.authorLópez Gallardo, Meritxell
dc.contributor.authorRamírez Sebastián, Ana Isabel
dc.date.accessioned2024-03-12T17:51:29Z
dc.date.available2024-03-12T17:51:29Z
dc.date.issued2024-03-07
dc.descriptionSubmission received: 10 January 2024 / Revised: 26 February 2024 / Accepted: 5 March 2024 / Published: 7 March 2024 (This article belongs to the Special Issue Advanced Research in Retina 2.0)
dc.description.abstractGlaucoma is a neurodegenerative disease that causes blindness. In this study, we aimed to evaluate the protective role of cilastatin (CIL), generally used in the treatment of nephropathologies associated with inflammation, in an experimental mouse model based on unilateral (left) laser-induced ocular hypertension (OHT). Male Swiss mice were administered CIL daily (300 mg/kg, i.p.) two days before OHT surgery until sacrifice 3 or 7 days later. Intraocular Pressure (IOP), as well as retinal ganglion cell (RGC) survival, was registered, and the inflammatory responses of macroglial and microglial cells were studied via immunohistochemical techniques. Results from OHT eyes were compared to normotensive contralateral (CONTRA) and naïve control eyes considering nine retinal areas and all retinal layers. OHT successfully increased IOP values in OHT eyes but not in CONTRA eyes; CIL did not affect IOP values. Surgery induced a higher loss of RGCs in OHT eyes than in CONTRA eyes, while CIL attenuated this loss. Similarly, surgery increased macroglial and microglial activation in OHT eyes and to a lesser extent in CONTRA eyes; CIL prevented both macroglial and microglial activation in OHT and CONTRA eyes. Therefore, CIL arises as a potential effective strategy to reduce OHT-associated damage in the retina of experimental mice.
dc.description.departmentDepto. de Inmunología, Oftalmología y ORL
dc.description.departmentUnidad Docente de Inmunología, Oftalmología y ORL
dc.description.departmentDepto. de Fisiología
dc.description.departmentDepto. de Genética, Fisiología y Microbiología
dc.description.facultyFac. de Medicina
dc.description.facultyInstituto de Investigaciones Oftalmológicas Ramón Castroviejo
dc.description.facultyFac. de Ciencias Biológicas
dc.description.facultyFac. de Óptica y Optometría
dc.description.refereedTRUE
dc.description.sponsorshipUniversidad Complutense deMadrid (España)
dc.description.sponsorshipMinisterio de Ciencia, Innovación y Universidades de España
dc.description.sponsorshipInstituto de Salud Carlos III (España)
dc.description.sponsorshipFondo Europeo de Desarrollo Regional (FEDER)
dc.description.sponsorshipComisión Europea
dc.description.sponsorshipComunidad de Madrid (España)
dc.description.statuspub
dc.identifier.citationMartínez-López, M.A.; Rubio-Casado, S.; San Felipe, D.; Martín-Sánchez, B.; Fernández-Albarral, J.A.; Salobrar-García, E.; Matamoros, J.A.; Ramírez, J.M.; de Hoz, R.; Salazar, J.J.; et al. Cilastatin as a Potential Anti-Inflammatory and Neuroprotective Treatment in the Management of Glaucoma. Int. J. Mol. Sci. 2024, 25, 3115. https://doi.org/10.3390/ijms25063115
dc.identifier.doi10.3390/ijms25063115
dc.identifier.officialurlhttps://doi.org/10.3390/ijms25063115
dc.identifier.relatedurlhttps://www.mdpi.com/1422-0067/25/6/3115#
dc.identifier.urihttps://hdl.handle.net/20.500.14352/102168
dc.issue.number6
dc.journal.titleInternational Journal of Molecular Sciences
dc.language.isoeng
dc.page.initial3115
dc.publisherMDPI
dc.relation.projectIDUCM Research Groups 951579
dc.relation.projectIDUCM Research Group 920105
dc.relation.projectIDSNEO-20222384
dc.relation.projectIDinfo:eu-repo/grantAgreement/ISCIII/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020 (ISCIII)/PI20%2F01577/ES/EL CONTROL DE LA APOPTOSIS RENAL BLOQUEA EL INFLAMASOMA Y EVITA EL DAÑO ORGANICO A DISTANCIA/
dc.relation.projectIDISCIII-RICORS2040
dc.relation.projectIDRD21/0005/0029
dc.relation.projectID2022/BMD-7223
dc.relation.projectIDPID2022-140535NB-I00
dc.relation.projectIDCT15/23
dc.relation.projectIDCT63/19-CT64/19
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.cdu617.7-007.681
dc.subject.cdu616.8-002
dc.subject.cdu611.8.018.24
dc.subject.keywordRetina
dc.subject.keywordGlaucoma
dc.subject.keywordOcular hypertension (OHT)
dc.subject.keywordRetinal ganglion cells (RGCs)
dc.subject.keywordMacroglial cells
dc.subject.keywordMicroglial cells
dc.subject.keywordNeuroinflammation
dc.subject.keywordCilastatin
dc.subject.keywordTherapeutic approach
dc.subject.keywordNeuroprotection
dc.subject.ucmOftalmología
dc.subject.ucmMedicamentos
dc.subject.ucmBiología celular (Biología)
dc.subject.unesco3201.09 Oftalmología
dc.subject.unesco3208 Farmacodinámica
dc.subject.unesco2407 Biología Celular
dc.titleCilastatin as a Potential Anti-Inflammatory and Neuroprotective Treatment in the Management of Glaucoma
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number25
dspace.entity.typePublication
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