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. 2019 Apr 1;10(2):429–462. doi: 10.14336/AD.2019.0119

Table 4.

sCR1 treatment for ischemic stroke.

Animals Stroke models Time of administration Routes of injection Time point of observations Outcomes Mechanisms Refs
Sprague-Dawley rats 1 h MCAO 1 h before surgery Intravenous injection of sCR1 1 h, 24 h after surgery Reduced brain infarct volume and neurological motor deficits Reduced neutrophil accumulation and inflammation; Reduced C4b deposition in the cortex [387]
Sprague-Dawley rats 2 h MCAO 1 h before surgery Intravenous injection of sCR1 2 h, 24 h after surgery Reduced brain infarct size and neurological deficit scores Inhibited neutrophil infiltration and C3b deposition in the brain [388]
Adult male baboons 1.25 h MCAO 45 min before surgery Intravenous injection of sCR1-sLex 2 h, 6 h, 12 h, 72 h and 10 days of post-ischemia Increased brain infarct volume;
Did not improve neurological functions
Not studied [390]
Adult male baboons 1.25 h MCAO 45 min before surgery Intravenous injection of sCR1 72 h and 10 days of post-surgery Did not affect brain infarct volume and neurological scores Not studied [389]
7-day-old rats Unilateral carotid artery ligation followed by transient hypoxia 24 h before surgery Intraperitoneal injection of sCR1 or sCR1-sLex 24 h after surgery Did not reduce infarct volume Not studied [300]
Mice 0.75 h MCAO Immediately before MCAO Administration of sCR1 or sCR1-sLex 24 h after stroke Reduced brain infarct volume and neurological deficit score Inhibited neutrophil and platelet accumulation in the brain [24]