Icaritin Sensitizes Thrombin- and TxA₂-Induced Platelet Activation and Promotes Hemostasis via Enhancing PLCγ2-PKC Signaling Pathways

 

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Abstract

Background Vascular injury results in uncontrollable hemorrhage in hemorrhagic diseases and excessive antithrombotic therapy. Safe and efficient hemostatic agents which can be orally administered are urgently needed. Platelets play indispensable roles in hemostasis, but there is no drug exerting hemostatic effects through enhancing platelet function.

Methods The regulatory effects of icaritin, a natural compound isolated from Herba Epimedii, on the dense granule release, thromboxane A₂ (TxA₂) synthesis, α-granule release, activation of integrin αIIbβ3, and aggregation of platelets induced by multiple agonists were investigated. The effects of icaritin on tail vein bleeding times of warfarin-treated mice were also evaluated. Furthermore, we investigated the underlying mechanisms by which icaritin exerted its pharmacological effects.

Results Icaritin alone did not activate platelets, but significantly potentiated the dense granule release, α-granule release, activation of integrin αIIbβ3, and aggregation of platelets induced by thrombin and U46619. Icaritin also shortened tail vein bleeding times of mice treated with warfarin. In addition, phosphorylated proteome analysis, immunoblotting analysis, and pharmacological research revealed that icaritin sensitized the activation of phospholipase Cγ2 (PLCγ2)-protein kinase C (PKC) signaling pathways, which play important roles in platelet activation.

Conclusion Icaritin can sensitize platelet activation induced by thrombin and TxA₂ through enhancing the activation of PLCγ2-PKC signaling pathways and promote hemostasis, and has potential to be developed into a novel orally deliverable therapeutic agent for hemorrhages.

Data Availability Statement

The datasets analyzed for the current study are available from the corresponding author on request.

Authors' Contribution

Z.Z., Y.L., H.L., R.G., D.H., Z.L., M.H., C.S., J.Y., and K.Z. performed most of the experiments, and contributed to the acquisition and analysis of data. Z.Z. designed the study and drafted the manuscript. N.W. contributed to the analysis of data and revised the manuscript. P.T. and G.Z. supervised the study team and revised the manuscript.

Publication History

Received: 03 April 2023

Accepted: 13 January 2024

Accepted Manuscript online:
15 January 2024

Article published online:
09 February 2024

© 2024. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

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