Key result
Pentamethylquercetin (PMQ) significantly inhibited thrombus formation in vivo and platelet aggregation in vitro, protecting mice from collagen-epinephrine-induced thromboembolic death.
Why the study?
Does pentamethylquercetin (PMQ) reduce thrombus formation and inhibit platelet function in preclinical models?
Does pentamethylquercetin (PMQ) reduce thrombus formation and inhibit platelet function in preclinical models?
p-value: p=<0.001
PMQ demonstrates potent anti-thrombotic activity in vivo and inhibits platelet function in vitro by suppressing PI3K/Akt-GSK3β and Syk-PLCγ2-Erk signaling cascades, suggesting potential as a therapeutic candidate for thrombotic disorders.
Flavonoids exert both anti-oxidant and anti-platelet activities in vitro and in vivo. Pentamethylquercetin (PMQ), a polymethoxylated flavone derivative, has been screened for anti-carcinogenic and cardioprotective effects. However, it is unclear whether PMQ has anti-thrombotic effects. In the present study, PMQ (20 mg/kg) significantly inhibited thrombus formation in the collagen- epinephrine- induced acute pulmonary thrombosis mouse model and the ferric chloride-induced carotid injury model. To explore the mechanism, we evaluated the effects of PMQ on platelet function. We found that PMQ inhibited platelet aggregation and granule secretion induced by low dose agonists, including ADP, collagen, thrombin and U46619. Biochemical analysis revealed that PMQ inhibited collagen-, thrombin- and U46619-induced activation of Syk, PLCγ2, Akt, GSK3β and Erk1/2. Therefore, we provide the first report to show that PMQ possesses anti-thrombotic activity in vivo and inhibited platelet function in vitro, suggesting that PMQ may represent a potential therapeutic candidate for the prevention or treatment of thrombotic disorders.
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Liang et al. (2015) studied Thrombosis. Pentamethylquercetin (PMQ) vs. Vehicle was evaluated on Survival in collagen-epinephrine-induced acute pulmonary thrombosis mouse model (p=<0.001). Pentamethylquercetin (PMQ) significantly inhibited thrombus formation in vivo and platelet aggregation in vitro, protecting mice from collagen-epinephrine-induced thromboembolic death.
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