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Title

Peripheral inflammation increases the deleterious effect of CNS inflammation on the nigrostriatal dopaminergic system

AuthorsHernández-Romero, M. C.; Machado de la Quintana, Alberto ; Pablos, Rocío M. de; Espinosa-Oliva, Ana M.; Argüelles, Sandro; Villarán, Ruth F.; Venero, José L.; Herrera, Antonio J. ; Delgado-Cortés, María José; Sarmiento, Manuel; Mauriño, Raquel; Santiago, Marti; Cano, Josefina
Issue Date2012
PublisherElsevier
CitationNeuroToxicology 33(3): 347-360 (2012)
AbstractEvidence supports the role of inflammation in the development of neurodegenerative diseases. In this work, we are interested in inflammation as a risk factor by itself and not only as a factor contributing to neurodegeneration. We tested the influence of a mild to moderate peripheral inflammation (injection of carrageenan into the paws of rats) on the degeneration of dopaminergic neurons in an animal model based on the intranigral injection of lipopolysaccharide (LPS), a potent inflammatory agent. Overall, the treatment with carrageenan increased the effect of the intranigral injection of LPS on the loss of dopaminergic neurons in the SN along with all the other parameters studied, including: serum levels of the inflammatory markers TNF-α, IL-1β, IL-6 and C-reactive protein; activation of microglia, expression of proinflammatory cytokines, the adhesion molecule ICAM and the enzyme iNOS, loss of astrocytes and damage to the blood brain barrier (BBB). The possible implication of BBB rupture in the increased loss of dopaminergic neurons has been studied using another Parkinson's disease animal model based on the intraperitoneal injection of rotenone. In this experiment, loss of dopaminergic neurons was also strengthened by carrageenan, without affecting the BBB. In conclusion, our data show that a mild to moderate peripheral inflammation can exacerbate the degeneration of dopaminergic neurons caused by a harmful stimulus. © 2012 Elsevier Inc.
URIhttp://hdl.handle.net/10261/62922
DOI10.1016/j.neuro.2012.01.018
Identifiersdoi: 10.1016/j.neuro.2012.01.018
issn: 0161-813X
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