The role of the complement cascade in ischemia/reperfusion injury: Implications for neuroprotection

被引:111
作者
D'Ambrosio, AL [1 ]
Pinsky, DJ [1 ]
Connolly, ES [1 ]
机构
[1] Columbia Univ, Dept Neurol Surg, Inst Neurol, New York, NY 10032 USA
关键词
D O I
10.1007/BF03402183
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: 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. Summary of Review: 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. Conclusions: 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.
引用
收藏
页码:367 / 382
页数:16
相关论文
共 145 条
  • [1] Localization and cell association of C1q in Alzheimer's disease brain
    Afagh, A
    Cummings, BJ
    Cribbs, DH
    Cotman, CW
    Tenner, AJ
    [J]. EXPERIMENTAL NEUROLOGY, 1996, 138 (01) : 22 - 32
  • [2] ALBRECHT P, 1978, AM J CLIN PATHOL, V70, P175
  • [3] AMES A, 1968, AM J PATHOL, V52, P437
  • [4] LIMITATION OF REPERFUSION INJURY BY A MONOCLONAL-ANTIBODY TO C5A DURING MYOCARDIAL-INFARCTION IN PIGS
    AMSTERDAM, EA
    STAHL, GL
    PAN, HL
    RENDIG, SV
    FLETCHER, MP
    LONGHURST, JC
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1995, 268 (01): : H448 - H457
  • [5] BALLOW M, 1969, J IMMUNOL, V103, P944
  • [6] Inhibition of complement as a therapeutic approach in inflammatory central nervous system (CNS) disease
    Barnum, SR
    [J]. MOLECULAR MEDICINE, 1999, 5 (09) : 569 - 582
  • [7] Bartko D, 1997, Bratisl Lek Listy, V98, P321
  • [8] THE ROLE OF NEUTROPHILS AND PLATELETS IN A RABBIT MODEL OF THROMBOEMBOLIC STROKE
    BEDNAR, MM
    RAYMOND, S
    MCAULIFFE, T
    LODGE, PA
    GROSS, CE
    [J]. STROKE, 1991, 22 (01) : 44 - 50
  • [9] Bednar MM, 1997, NEUROL RES, V19, P588
  • [10] Activation of complement by tissue plasminogen activator, but not acute cerebral ischemia, in a rabbit model of thromboembolic stroke
    Bednar, MM
    Gross, CE
    Russell, SR
    Short, D
    Giclas, PC
    [J]. JOURNAL OF NEUROSURGERY, 1997, 86 (01) : 139 - 142