Figure 5
Figure 5. Both lengthier FeCl3 treatment and elevated FVIII increase thrombus stability. C57Bl/6 mice were infused with saline or FVIII to 285% of normal. Thrombosis was induced by 10% FeCl3 application to the carotid artery for the indicated time (3 or 2 minutes). After stable occlusion, flow was monitored for 5 minutes to count embolic events (defined as a rapid increase in blood flow of at least 0.2 mL/min). (A-B) Representative flow tracings after 3- (A) and 2-minute (B) FeCl3 application to control (saline-infused) mice, respectively. Gray shaded area represents time of vessel drying, FeCl3 administration and vessel washing, during which flow could not be monitored. Brackets indicate the time from FeCl3 placement to the time of vessel occlusion. Arrows show emboli (marked with E) in the 5 minutes after stable occlusion. (C) Quantification of embolization data. Each point represents a separate mouse. Mice that did not achieve stable occlusion were excluded. Lines show mean values. *P < .05.

Both lengthier FeCl3 treatment and elevated FVIII increase thrombus stability. C57Bl/6 mice were infused with saline or FVIII to 285% of normal. Thrombosis was induced by 10% FeCl3 application to the carotid artery for the indicated time (3 or 2 minutes). After stable occlusion, flow was monitored for 5 minutes to count embolic events (defined as a rapid increase in blood flow of at least 0.2 mL/min). (A-B) Representative flow tracings after 3- (A) and 2-minute (B) FeCl3 application to control (saline-infused) mice, respectively. Gray shaded area represents time of vessel drying, FeCl3 administration and vessel washing, during which flow could not be monitored. Brackets indicate the time from FeCl3 placement to the time of vessel occlusion. Arrows show emboli (marked with E) in the 5 minutes after stable occlusion. (C) Quantification of embolization data. Each point represents a separate mouse. Mice that did not achieve stable occlusion were excluded. Lines show mean values. *P < .05.

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