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dc.contributor.authorArévalo, Ana Paula-
dc.contributor.authorPagotto, Romina-
dc.contributor.authorPórfido Barayoli, Jorge Luis-
dc.contributor.authorDaghero Villanueva, Hellen-
dc.contributor.authorSegovia, Mercedes-
dc.contributor.authorYamasaki, Kanji-
dc.contributor.authorVarela Cruces, María Belén-
dc.contributor.authorHill, Marcelo-
dc.contributor.authorVerdes García, José Manuel-
dc.contributor.authorDuhalde Vega, Maite-
dc.contributor.authorBollati-Fogolín, Mariela-
dc.contributor.authorCrispo, Martina-
dc.date.accessioned2025-02-11T15:26:47Z-
dc.date.available2025-02-11T15:26:47Z-
dc.date.issued2021-
dc.identifier.citationArévalo, A, Pagotto, R, Pórfido Barayoli, J, Daghero Villanueva, H, Segovia, M, Yamasaki, K, Varela Cruces, M, Hill, M, Verdes García, J, Duhalde Vega, M, Bollati-Fogolín, M y Crispo, M. Ivermectin reduces in vivo coronavirus infection in a mouse experimental model. Scientific Reports. [en línea] 2021, 11(7132), 1-12es
dc.identifier.urihttps://hdl.handle.net/20.500.12008/48337-
dc.description.abstractThe objective of this study was to test the effectiveness of ivermectin for the treatment of mouse hepatitis virus (MHV), a type 2 family RNA coronavirus similar to SARS-CoV-2. Female BALB/cJ mice were infected with 6,000 PFU of MHV-A59 (group infected, n = 20) or infected and then immediately treated with a single dose of 500 μg/kg ivermectin (group infected + IVM, n = 20) or were not infected and treated with PBS (control group, n = 16). Five days after infection/treatment, the mice were euthanized and the tissues were sampled to assess their general health status and infection levels. Overall, the results demonstrated that viral infection induced typical MHV-caused disease, with the livers showing severe hepatocellular necrosis surrounded by a severe lymphoplasmacytic inflammatory infiltration associated with a high hepatic viral load (52,158 AU), while mice treated with ivermectin showed a better health status with a lower viral load (23,192 AU; p < 0.05), with only a few having histopathological liver damage (p < 0.05). No significant differences were found between the group infected + IVM and control group mice (P = NS). Furthermore, serum transaminase levels (aspartate aminotransferase and alanine aminotransferase) were significantly lower in the treated mice than in the infected animals. In conclusion, ivermectin diminished the MHV viral load and disease in the mice, being a useful model for further understanding this therapy against coronavirus diseases.es
dc.format.extent12 pes
dc.format.mimetypeapplication/pdfes
dc.language.isoenes
dc.relation.ispartofScientific Reports, 2021, 11(7132), 1-12es
dc.rightsLas obras depositadas en el Repositorio se rigen por la Ordenanza de los Derechos de la Propiedad Intelectual de la Universidad de la República.(Res. Nº 91 de C.D.C. de 8/III/1994 – D.O. 7/IV/1994) y por la Ordenanza del Repositorio Abierto de la Universidad de la República (Res. Nº 16 de C.D.C. de 07/10/2014)es
dc.subject.otherINFECCION EXPERIMENTALes
dc.subject.otherRATONESes
dc.subject.otherIVERMECTINAes
dc.subject.otherCORONAVIRUS CAUSANTE DEL SINDROME RESPIRATORIO AGUDO SEVEROes
dc.subject.otherTERAPIAes
dc.titleIvermectin reduces in vivo coronavirus infection in a mouse experimental modeles
dc.typeArtículoes
dc.contributor.filiacionArévalo Ana Paula, Institut Pasteur de Montevideo (Uruguay). Transgenic and Experimental Animal Unit-
dc.contributor.filiacionPagotto Romina, Institut Pasteur de Montevideo (Uruguay). Cell Biology Unit-
dc.contributor.filiacionPórfido Barayoli Jorge Luis, Institut Pasteur de Montevideo (Uruguay). Transgenic and Experimental Animal Unit / Institut Pasteur de Montevideo (Uruguay). Worm Biology Laboratory / Universidad de la República (Uruguay). Faculty of Chemistry. Department of Biosciences-
dc.contributor.filiacionDaghero Villanueva Hellen, Institut Pasteur de Montevideo (Uruguay). Cell Biology Unit-
dc.contributor.filiacionSegovia Mercedes, Institut Pasteur de Montevideo (Uruguay). Laboratory of Immunoregulation and Inflammation / Universidad de la República (Uruguay). Faculty of Medicine. Immunobiology Department-
dc.contributor.filiacionYamasaki Kanji, Universidad de la República (Uruguay). Veterinary Faculty. Department of Pathobiology. Pathology Unit-
dc.contributor.filiacionVarela Cruces María Belén, Universidad de la República (Uruguay). Veterinary Faculty. Department of Pathobiology. Pathology Unit-
dc.contributor.filiacionHill Marcelo, Institut Pasteur de Montevideo (Uruguay). Laboratory of Immunoregulation and Inflammation / Universidad de la República (Uruguay). Faculty of Medicine. Immunobiology Department-
dc.contributor.filiacionVerdes García José Manuel, Universidad de la República (Uruguay). Veterinary Faculty. Department of Pathobiology. Pathology Unit-
dc.contributor.filiacionDuhalde Vega Maite, Institut Pasteur de Montevideo (Uruguay). Laboratory of Immunoregulation and Inflammation / University of Buenos Aires (Buenos Aires, Argentina). School of Pharmacy and Biochemistry. Institute of Biological Chemistry and Chemical Physics (UBA‑CONICET)-
dc.contributor.filiacionBollati-Fogolín Mariela, Institut Pasteur de Montevideo (Uruguay). Cell Biology Unit-
dc.contributor.filiacionCrispo Martina, Institut Pasteur de Montevideo (Uruguay). Transgenic and Experimental Animal Unit-
dc.rights.licenceLicencia Creative Commons Atribución (CC - By 4.0)es
dc.identifier.doihttps://doi.org/10.1038/s41598-021-86679-0-
Aparece en las colecciones: Publicaciones académicas y científicas - Facultad de Veterinaria

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