Protective effect of C5a receptor inhibition after murine reperfused stroke
Document Type
Article
Abstract
OBJECTIVE: The complement cascade has been implicated in cerebral ischemia/reperfusion injury. To develop clinically useful therapies that successfully manipulate the complement cascade, the individual roles of its components must be clearly defined. Previous studies have shown that C5 inhibition improves outcome after experimental stroke. In this study, we investigated the role of C5a in stroke injury by inhibiting its activity at the receptor level. METHODS: C5a receptor antagonist or vehicle was administered to mice before temporary middle cerebral artery occlusion. Stroke outcomes were assessed 24 hours later in all mice using both neurological deficit scores and cerebral infarct volumes. RESULTS: Animals treated with C5a receptor antagonist experienced significantly decreased infarct volume and demonstrated an improving trend in neurological function. CONCLUSION: These findings demonstrate that modulation of C5a receptor activity significantly alters the degree of neurological damage after experimental reperfused stroke.
Medical Subject Headings
Animals; Brain Ischemia (pathology, physiopathology, prevention & control); Complement C5a (antagonists & inhibitors, physiology); Male; Mice; Mice, Inbred C57BL; Peptides (pharmacology, therapeutic use); Receptor, Anaphylatoxin C5a (antagonists & inhibitors, physiology); Reperfusion Injury (pathology, physiopathology, prevention & control); Stroke (pathology, physiopathology, prevention & control)
Publication Date
7-1-2008
Publication Title
Neurosurgery
E-ISSN
1524-4040
Volume
63
Issue
1
First Page
122
Last Page
5; discussion 125
PubMed ID
18728577
Digital Object Identifier (DOI)
10.1227/01.NEU.0000335079.70222.8D
Recommended Citation
Kim, Grace H.; Mocco, J; Hahn, David K.; Kellner, Christopher P.; Komotar, Ricardo J.; Ducruet, Andrew F.; Mack, William J.; and Connolly, E Sander, "Protective effect of C5a receptor inhibition after murine reperfused stroke" (2008). Translational Neuroscience. 2151.
https://scholar.barrowneuro.org/neurobiology/2151