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Inhibition of bradykinin receptor B1 protects mice from focal brain injury by reducing blood-brain barrier leakage and inflammation

Item Type:Article
Title:Inhibition of bradykinin receptor B1 protects mice from focal brain injury by reducing blood-brain barrier leakage and inflammation
Creators Name:Raslan, F. and Schwarz, T. and Meuth, S.G. and Austinat, M. and Bader, M. and Renne, T. and Roosen, K. and Stoll, G. and Siren, A.L. and Kleinschnitz, C.
Abstract:Kinins are proinflammatory and vasoactive peptides that are released during tissue damage and may contribute to neuronal degeneration, inflammation, and edema formation after brain injury by acting on discrete bradykinin receptors, B1R and B2R. We studied the expression of B1R and B2R and the effect of their inhibition on lesion size, blood-brain barrier (BBB) disruption, and inflammatory processes after a focal cryolesion of the right parietal cortex in mice. B1R and B2R gene transcripts were significantly induced in the lesioned hemispheres of wild-type mice (P<0.05). The volume of the cortical lesions and neuronal damage at 24 h after injury in B1R(-/-) mice were significantly smaller than in wild-type controls (2.5+/-2.6 versus 11.5+/-3.9 mm(3), P<0.001). Treatment with the B1R antagonist R-715 1 h after lesion induction likewise reduced lesion volume in wild-type mice (2.6+/-1.4 versus 12.2+/-6.1 mm(3), P<0.001). This was accompanied by a remarkable reduction of BBB disruption and tissue inflammation. In contrast, genetic deletion or pharmacological inhibition of B2R had no significant impact on lesion formation or the development of brain edema. We conclude that B1R inhibition may offer a novel therapeutic strategy after acute brain injuries.
Keywords:Endothelin-1, Evan's Blue, IL-1, Macrophages, TBI, TNF, Animals, Mice
Source:Journal of Cerebral Blood Flow and Metabolism
ISSN:0271-678X
Publisher:Nature Publishing Group (U.S.A.)
Volume:30
Number:8
Page Range:1477-1486
Date:August 2010
Official Publication:https://doi.org/10.1038/jcbfm.2010.28
PubMed:View item in PubMed

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