Pharmacological inhibition of PKM2 dimerization reduces susceptibility to acute venous thrombosis and improves vein wall response in the WT mice. (A) Thrombus incidence in vehicle- or ML265-treated mice 48 hours after IVC stenosis. (B) Representative IVC thrombus (top) harvested 48 hours after stenosis from vehicle- or ML265-treated mice (50 mg/kg) is shown, along with quantified thrombus weight and thrombus length (n = 12 per group; bottom). Values are mean ± SEM; Mann-Whitney U test. (C) The level of CitH3 was measured in the thrombus isolated from vehicle- and ML265-treated mice. A representative western blot for CitH3 is shown. β-actin was used as a loading control (n = 3 per group). Values are mean ± SEM; unpaired Student t test. (D) Fold increase in contraction (left) and percent of relaxation (right) measured by wire myograph (DMT 610M) in IVCs isolated from vehicle- and ML265 (50 mg/kg)-treated mice 48 hours after IVC stenosis. Phenylephrine (0.5 mM) and acetylcholine (1.62 mM) were used for contraction and relaxation, respectively (n = 8-9 per group). Values are mean ± SEM; unpaired Student t test and Mann-Whitney U test are used for the fold increase in contraction and percent of relaxation, respectively.