Background: The role of complement in ischaemia-reperfusion injury has not been well investigated. 512 is a monoclonal antibody (mAb) directed against a rat membrane inhibitor of the C3 convertase step, which is the rat counterpart of mouse Crry/p65. 6D1 is a mAb against rat CD59 which inhibits the formation of membrane attack complexes. Methods:We visualized the tissue distribution of these membrane inhibitors in rat gastrointestinal tract by immunohistochemical staining with the appropriate mAb. Then, we tested the hypothesis that complement regulatory proteins protect rat gastric mucosa against ischaemia-reperfusion stress by using these mAbs. Gastric mucosal integrity was continuously monitored by measuring the blood-to-lumen clearance of [Cr-51]-labelled ethylenediaminetetraacetic acid (EDTA) under control conditions, during ischaemia and after reperfusion. Results: Rat 6D1 and 512 antigens were both widely distributed and predominantly expressed on smooth muscle and endothelial cells in gastrointestinal tracts. Blockade of complement regulatory proteins with 512 and 6D1 mAbs resulted in a significant increase in [Cr-51]-EDTA clearance after reperfusion. Conclusions: These findings support the hypothesis that endogenous complement regulatory proteins may act as important protective factors against ischaemia-reperfusion stress in rat gastric mucose. (C) 1999 Blackwell Science Asia Pty Ltd.
机构:
Charles Univ Prague, Dept Pharmacol, Fac Med Hradec Kralove, Hradec Kralove 50038, Czech RepublicAcad Sci Czech Republ, Inst Physiol, CR-14220 Prague 4, Czech Republic
Sterba, Martin
Popelova, Olga
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机构:
Charles Univ Prague, Dept Pharmacol, Fac Med Hradec Kralove, Hradec Kralove 50038, Czech RepublicAcad Sci Czech Republ, Inst Physiol, CR-14220 Prague 4, Czech Republic
机构:
Charles Univ Prague, Dept Pharmacol, Fac Med Hradec Kralove, Hradec Kralove 50038, Czech RepublicAcad Sci Czech Republ, Inst Physiol, CR-14220 Prague 4, Czech Republic