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dc.contributor.authorLeón-Rodríguez, Ana
dc.contributor.authorFernández-Arjona, María del Mar
dc.contributor.authorMateos-Grondona, Jesús 
dc.contributor.authorPedraza-Benítez, María del Carmen 
dc.contributor.authorLópez-Ávalos, María Dolores 
dc.date.accessioned2024-11-25T10:12:10Z
dc.date.available2024-11-25T10:12:10Z
dc.date.issued2022-07-08
dc.identifier.citationLeón-Rodríguez, A., Fernández-Arjona, M., Grondona, J.M. et al. Anxiety-like behavior and microglial activation in the amygdala after acute neuroinflammation induced by microbial neuraminidase. Sci Rep 12, 11581 (2022). https://doi.org/10.1038/s41598-022-15617-5es_ES
dc.identifier.urihttps://hdl.handle.net/10630/35276
dc.description.abstractShort-term behavioral alterations are associated with infection and aid the recovery from sickness. However, concerns have raised that sustained behavioral disturbances after acute neuroinflammation could relate to neurological diseases in the long run. We aimed to explore medium- and longterm behavioral disturbances after acute neuroinflammation in rats, using a model based on the intracerebroventricular administration of the enzyme neuraminidase (NA), which is part of some pathogenic bacteria and viruses. Neurological and behavioral assessments were performed 2 and 10 weeks after the injection of NA, and neuroinflammation was evaluated by gene expression and histology. No alterations were observed regarding basic neurological functions or locomotor capacity in NA-injected rats. However, they showed a reduction in unsupported rearing, and increased grooming and freezing behaviors, which indicate anxiety-like behavior. A principal component analysis including a larger set of parameters further supported such anxiety-like behavior. The anxiety profile was observed 2 weeks after NA-injection, but not after 10 weeks. Concomitantly, the amygdala presented increased number of microglial cells showing a morphologic bias towards an activated state. A similar but subtler tendency was observed in hypothalamic microglia located in the paraventricular nucleus. Also, in the hypothalamus the pattern recognition receptor toll-like receptor 4 (TLR4) was slightly overexpressed 2 weeks after NA injection. These results demonstrate that NA-induced neuroinflammation provokes anxiety-like behavior in the medium term, which disappears with time. Concurrent microgliosis in the amygdala could explain such behavior. Further experiments should aim to explore subtle but long-lasting alterations observed 10 weeks after NA injection, both in amygdala and hypothalamus, as well as mild behavioral changes.es_ES
dc.description.sponsorshipThis work was supported by funding from Spanish Government: Ministerio de Economía, Industria y Competitividad (grant number SAF2017-83645) and Ministerio de Ciencia e Innovación (grant number PID2020-117464RB-I00). ALR received fellowships from Ministerio de Educación y Formación Profesional (Spanish Government) and from Plan Propio de Investigación y Transferencia (Universidad de Málaga, Spain). Authors are grateful to D. Navas-Fernández (Servicios Centrales de Apoyo a la Investigación, Universidad de Málaga) for his help with the acquisition of images with scanner microscope and with confocal microscope. The Leica confocal microscope (SP5 II) was acquired with FEDER funds of the European Union.es_ES
dc.language.isoenges_ES
dc.publisherSpringer Naturees_ES
dc.rightsAttribution 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectSistema nervioso - Inflamaciónes_ES
dc.subjectNeurogliaes_ES
dc.subjectVirulencia (Microbiología)es_ES
dc.subjectNúcleo amigdalinoes_ES
dc.subject.otherMicrogliaes_ES
dc.subject.otherNeuroinflammationes_ES
dc.subject.otherNeuraminidasees_ES
dc.subject.otherAnxiety behaviores_ES
dc.subject.otherAmigdalaes_ES
dc.subject.otherRatses_ES
dc.titleAnxiety‑like behavior and microglial activation in the amygdala after acute neuroinflammation induced by microbial neuraminidase.es_ES
dc.typejournal articlees_ES
dc.centroFacultad de Cienciases_ES
dc.identifier.doi10.1038/s41598-022-15617-5
dc.type.hasVersionVoRes_ES
dc.departamentoBiología Celular, Genética y Fisiología
dc.rights.accessRightsopen accesses_ES


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