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Behav Brain Res ; 302: 171-4, 2016 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-26778788

RESUMEN

Peripheral administration of lipopolysaccharide (LPS) elevates production of pro-inflammatory cytokines, and motivates the expression of sickness behaviors. In this study, we tested the ability of an LPS-derived adjuvant, monophosphoryl lipid A (MPLA), to prevent LPS-induced sickness behaviors in a burrowing paradigm. Testing occurred over a three-day period. Animals received a single injection of either MPLA or saline the first two days of testing. On day three, animals received either LPS or saline. Tissue from the dorsal hippocampus was collected for qRT-PCR to assess expression of IL-1ß and IL-4. Results indicate that, during the pre-treatment phase, administration of MPLA induces an immune response sufficient to trigger sickness behaviors. However, we observed that animals pre-treated with MPLA for two days were resistant to LPS-induced sickness behaviors on day three. Results from the qRT-PCR analysis indicated that LPS-treated animals pre-treated with MPLA expressed significantly less IL-1ß compared to LPS-treated animals pre-treated with saline. However, we did not observe a significant difference in IL-4 expression between groups. Therefore, results indicate that under the given parameters of the study, MPLA pre-treatment protects against LPS-induced sickness behaviors, at least in part, by decreasing expression of the pro-inflammatory cytokine IL-1ß.


Asunto(s)
Adyuvantes Inmunológicos/farmacología , Regulación de la Expresión Génica/efectos de los fármacos , Hipocampo/efectos de los fármacos , Conducta de Enfermedad/efectos de los fármacos , Interleucina-1beta/metabolismo , Lípido A/análogos & derivados , Adyuvantes Inmunológicos/administración & dosificación , Animales , Modelos Animales de Enfermedad , Esquema de Medicación , Interleucina-1beta/genética , Interleucina-4/genética , Interleucina-4/metabolismo , Lípido A/administración & dosificación , Lípido A/farmacología , Lipopolisacáridos/toxicidad , Ratones , Ratones Endogámicos C57BL , ARN Mensajero/metabolismo
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