The Role of the Complement Cascade in Ischemia/Reperfusion Injury: Implications for Neuroprotection
Open Access
- 1 June 2001
- journal article
- review article
- Published by Springer Nature in Molecular Medicine
- Vol. 7 (6) , 367-382
- https://doi.org/10.1007/bf03402183
Abstract
The complement cascade plays a deleterious role in multiple models of ischemia/reperfusion (I/R) injury, including stroke. Investigation of the complement cascade may provide a critical approach to identifying neuroprotective strategies that can be effective at clinically relevant time points in cerebral ischemia. This review of the literature describes the deleterious effects of complement activation in systemic I/R models and previous attempts at therapeutic complement inhibition, with a focus on the potential role of complement inhibition in ischemic neuroprotection. Translation of these concepts into ischemic stroke models and exploration of related neuroprotective strategies are also reviewed. We performed a MEDLINE search to identify any studies published between 1966 and 2001 dealing with complement activation in the setting of I/R injury. We also searched for studies demonstrating up-regulation of any complement components within the central nervous system during inflammation and/or ischemia. The temporal and mechanistic overlap of the complement cascade with other biochemical events occurring in cerebral I/R injury is quite complex and is only beginning to be understood. However, there is compelling evidence that complement is quite active in the setting of acute stroke, suggesting that anticomplement strategies should be further investigated through genetic analysis, nonhuman primate models, and clinical investigations.Keywords
This publication has 126 references indexed in Scilit:
- Proteasome Inhibitor PS519 Reduces Infarction and Attenuates Leukocyte Infiltration in a Rat Model of Focal Cerebral IschemiaStroke, 2000
- Increased IL-1β, IL-8, and IL-17 mRNA Expression in Blood Mononuclear Cells Observed in a Prospective Ischemic Stroke StudyStroke, 1999
- CD18-Mediated Neutrophil Recruitment Contributes to the Pathogenesis of Reperfused but Not Nonreperfused StrokeStroke, 1999
- Inducible Nitric Oxide Synthase Gene Expression in Vascular Cells After Transient Focal Cerebral IschemiaStroke, 1996
- P-selectin and intercellular adhesion molecule-1 expression after focal brain ischemia and reperfusion.Stroke, 1994
- Polymorphonuclear leukocytes and monocytes/macrophages in the pathogenesis of cerebral ischemia and stroke.Stroke, 1992
- Polymorphonuclear leukocytes occlude capillaries following middle cerebral artery occlusion and reperfusion in baboons.Stroke, 1991
- Biology of complement: the overtureImmunology Today, 1991
- The role of complement in inflammation and phagocytosisImmunology Today, 1991
- The role of neutrophils and platelets in a rabbit model of thromboembolic stroke.Stroke, 1991