Figure 7.
ACC1 pKO mice exhibited reduced arterial thrombosis while maintaining normal hemostasis. (A) Tail bleeding times of ACC1flx/flx, GPIb-Cre+/−, and ACC1 pKO mice in saline solution preheated at 37°C. Results are expressed as mean ± SEM (n ≥ 23). Data were analyzed via 1-way ANOVA. (B-D) Mice were subjected to thrombosis induced in vivo by FeCl3 application to the carotid artery (10% of FeCl3 during 5 minutes). Thrombus formation was visualized using intravital microscopy analyzing exogenous platelet accumulation stained with carboxyfluorescein succinimidyl ester. (B-C) Thrombus growth area quantification over time. Data are expressed as mean ± SEM (n ≥ 6). #P ≤.05 relative to ACC1flx/flx mice. Data were analyzed using unpaired t test comparing area under the curve. (D) Representative pictures of thrombus formation over time (1, 5, 9, 15, and 19 minutes) after FeCl3 injury.

ACC1 pKO mice exhibited reduced arterial thrombosis while maintaining normal hemostasis. (A) Tail bleeding times of ACC1flx/flx, GPIb-Cre+/−, and ACC1 pKO mice in saline solution preheated at 37°C. Results are expressed as mean ± SEM (n ≥ 23). Data were analyzed via 1-way ANOVA. (B-D) Mice were subjected to thrombosis induced in vivo by FeCl3 application to the carotid artery (10% of FeCl3 during 5 minutes). Thrombus formation was visualized using intravital microscopy analyzing exogenous platelet accumulation stained with carboxyfluorescein succinimidyl ester. (B-C) Thrombus growth area quantification over time. Data are expressed as mean ± SEM (n ≥ 6). #P ≤.05 relative to ACC1flx/flx mice. Data were analyzed using unpaired t test comparing area under the curve. (D) Representative pictures of thrombus formation over time (1, 5, 9, 15, and 19 minutes) after FeCl3 injury.

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