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Brain inflammation is induced by co-morbidities and risk factors for stroke

Drake, C; Boutin, H; Jones, M S; Denes, A; McColl, B W; Selvarajah, J R; Hulme, S; Georgiou, R F; Hinz, R; Gerhard, A; Vail, A; Prenant, C; Julyan, P; Maroy, R; Brown, G; Smigova, A; Herholz, K; Kassiou, M; Crossman, D; Francis, S; Proctor, S D; Russell, J C; Hopkins, S J; Tyrrell, P J; Rothwell, N J; Allan, S M

Brain Behav Immun. 2011;25(6):1113-22.

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Abstract

Chronic systemic inflammatory conditions, such as atherosclerosis, diabetes and obesity are associated with increased risk of stroke, which suggests that systemic inflammation may contribute to the development of stroke in humans. The hypothesis that systemic inflammation may induce brain pathology can be tested in animals, and this was the key objective of the present study. First, we assessed inflammatory changes in the brain in rodent models of chronic, systemic inflammation. PET imaging revealed increased microglia activation in the brain of JCR-LA (corpulent) rats, which develop atherosclerosis and obesity, compared to the control lean strain. Immunostaining against Iba1 confirmed reactive microgliosis in these animals. An atherogenic diet in apolipoprotein E knock-out (ApoE(-/-)) mice induced microglial activation in the brain parenchyma within 8weeks and increased expression of vascular adhesion molecules. Focal lipid deposition and neuroinflammation in periventricular and cortical areas and profound recruitment of activated myeloid phagocytes, T cells and granulocytes into the choroid plexus were also observed. In a small, preliminary study, patients at risk of stroke (multiple risk factors for stroke, with chronically elevated C-reactive protein, but negative MRI for brain pathology) exhibited increased inflammation in the brain, as indicated by PET imaging. These findings show that brain inflammation occurs in animals, and tentatively in humans, harbouring risk factors for stroke associated with elevated systemic inflammation. Thus a "primed" inflammatory environment in the brain may exist in individuals at risk of stroke and this can be adequately recapitulated in appropriate co-morbid animal models.

Bibliographic metadata

Type of resource:
Content type:
Published date:
Language:
eng
Journal title:
Volume:
25
Issue:
6
Start page:
1113
End page:
22
Total:
-1090
Pagination:
1113-22
Digital Object Identifier:
S0889-1591(11)00058-4 [pii] 10.1016/j.bbi.2011.02.008
ISI Accession Number:
21356305
Related website(s):
  • Related website http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=21356305
General notes:
  • Drake, Caroline Boutin, Herve Jones, Matthew S Denes, Adam McColl, Barry W Selvarajah, Johann R Hulme, Sharon Georgiou, Rachel F Hinz, Rainer Gerhard, Alexander Vail, Andy Prenant, Christian Julyan, Peter Maroy, Renaud Brown, Gavin Smigova, Alison Herholz, Karl Kassiou, Michael Crossman, David Francis, Sheila Proctor, Spencer D Russell, James C Hopkins, Stephen J Tyrrell, Pippa J Rothwell, Nancy J Allan, Stuart M United States Brain, behavior, and immunity Brain Behav Immun. 2011 Aug;25(6):1113-22. Epub 2011 Feb 26.
Access state:
Active

Institutional metadata

University researcher(s):

Record metadata

Manchester eScholar ID:
uk-ac-man-scw:128095
Created by:
Herholz, Karl
Created:
27th July, 2011, 12:55:20
Last modified by:
Herholz, Karl
Last modified:
27th July, 2011, 12:55:20

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