Assessment of glial activation response in the progress of natural scrapie after chronic dexamethasone treatment

Guijarro, Isabel M. (Universidad de Zaragoza) ; Garcés, Moisés (Universidad de Zaragoza) ; Andrés-Benito, Pol ; Marín, Belén (Universidad de Zaragoza) ; Otero, Alicia (Universidad de Zaragoza) ; Barrio, Tomás ; Carmona, Margarita ; Ferrer, Isidro ; Badiola, Juan J. (Universidad de Zaragoza) ; Monzón, Marta (Universidad de Zaragoza)
Assessment of glial activation response in the progress of natural scrapie after chronic dexamethasone treatment
Resumen: Neuroinflammation has been correlated with the progress of neurodegeneration in many neuropathologies. Although glial cells have traditionally been considered to be protective, the concept of them as neurotoxic cells has recently emerged. Thus, a major unsolved question is the exact role of astroglia and microglia in neurodegenerative disorders. On the other hand, it is well known that glucocorticoids are the first choice to regulate inflammation and, consequently, neuroglial inflammatory activity. The objective of this study was to determine how chronic dexamethasone treatment influences the host immune response and to characterize the beneficial or detrimental role of glial cells. To date, this has not been examined using a natural neurodegenerative model of scrapie. With this aim, immunohistochemical expression of glial markers, prion protein accumulation, histopathological lesions and clinical evolution were compared with those in a control group. The results demonstrated how the complex interaction between glial populations failed to compensate for brain damage in natural conditions, emphasizing the need for using natural models. Additionally, the data showed that modulation of neuroinflammation by anti-inflammatory drugs might become a research focus as a potential therapeutic target for prion diseases, similar to that considered previously for other neurodegenerative disorders classified as prion-like diseases.
Idioma: Inglés
DOI: 10.3390/ijms21093231
Año: 2020
Publicado en: International Journal of Molecular Sciences 21, 9 (2020), 3231 [23 pp.]
ISSN: 1661-6596

Factor impacto JCR: 5.923 (2020)
Categ. JCR: BIOCHEMISTRY & MOLECULAR BIOLOGY rank: 67 / 297 = 0.226 (2020) - Q1 - T1
Categ. JCR: CHEMISTRY, MULTIDISCIPLINARY rank: 49 / 178 = 0.275 (2020) - Q2 - T1

Factor impacto SCIMAGO: 1.455 - Catalysis (Q1) - Computer Science Applications (Q1) - Inorganic Chemistry (Q1) - Spectroscopy (Q1) - Molecular Biology (Q1) - Organic Chemistry (Q1) - Physical and Theoretical Chemistry (Q1) - Medicine (miscellaneous) (Q1)

Financiación: info:eu-repo/grantAgreement/EUR/INTERREG-POCTEFA/EFA-148-16 REDPRION
Financiación: info:eu-repo/grantAgreement/ES/MEC/FPU15-03524
Tipo y forma: Artículo (Versión definitiva)
Área (Departamento): Área Sanidad Animal (Dpto. Patología Animal)
Área (Departamento): Area Histología (Dpto. Anatom.Histolog.Humanas)
Área (Departamento): Area Medicina (Dpto. Medicina, Psiqu. y Derm.)


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