Coenzyme Q10 Upregulates Platelet cAMP/PKA Pathway and Attenuates Integrin αIIbβ3 Signaling and Thrombus Growth. Issue 23 (3rd October 2019)

• Record Type: Journal Article
• Authors: Ya, Fuli; Xu, Xiaohong Ruby; Shi, Yilin; Gallant, Reid C.; Song, Fenglin; Zuo, Xiao; Zhao, Yimin; Tian, Zezhong; Zhang, Cheng; Xu, Xiping; Ling, Wenhua; Ni, Heyu; Yang, Yan
• Is Part Of: Molecular nutrition & food research. Volume 63:Issue 23(2019)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2019-10-03
• Subjects: cAMP/PKA pathway -- coenzyme Q10 -- dyslipidemic patients -- integrin αIIbβ3 -- platelets; Food -- Biotechnology -- Periodicals; Food -- Microbiology -- Periodicals; Nutrition -- Periodicals; Food -- Toxicology -- Periodicals; Nutrition -- Periodicals; Food Microbiology -- Periodicals; Food Technology -- Periodicals; Molecular Biology -- Periodicals; 664.0705
• DOI: 10.1002/mnfr.201900662
• Languages: English
• ISSNs: 1613-4125

Abstract

Abstract : Scope: Platelet integrin αIIbβ3 is the key mediator of atherothrombosis. Supplementation of coenzyme Q10 (CoQ10), a fat‐soluble molecule that exists in various foods, exerts protective cardiovascular effects. This study aims to investigate whether and how CoQ10 acts on αIIbβ3 signaling and thrombosis, the major cause of cardiovascular diseases. Methods and results: Using a series of platelet functional assays in vitro, it is demonstrated that CoQ10 reduces human platelet aggregation, granule secretion, platelet spreading, and clot retraction. It is further demonstrated that CoQ10 inhibits platelet integrin αIIbβ3 outside‐in signaling. These inhibitory effects are mainly mediated by upregulating cAMP/PKA pathway, where CoQ10 stimulates the A2A adenosine receptor and decreases phosphodiesterase 3A phosphorylation. Moreover, CoQ10 attenuates murine thrombus growth and vessel occlusion in a ferric chloride (FeCl3 )‐induced thrombosis model in vivo. Importantly, the randomized, double‐blind, placebo‐controlled clinical trial in dyslipidemic patients demonstrates that 24 weeks of CoQ10 supplementation increases platelet CoQ10 concentrations, enhances the cAMP/PKA pathway, and attenuates αIIbβ3 outside‐in signaling, leading to decreased platelet aggregation and granule release. Conclusion: Through upregulating the platelet cAMP/PKA pathway, and attenuating αIIbβ3 signaling and thrombus growth, CoQ10 supplementation may play an important protective role in patients with risks of cardiovascular diseases. Abstract : The extracellular coenzyme Q10 (CoQ10) stimulates platelet A2A adenosine receptor (A2A AR) and the intracellular CoQ10 inhibits phosphodiesterases 3A (PDE3A) activity, which contribute to the activation of the cAMP/PKA pathway. These effects result in attenuating platelet integrin αIIbβ3 outside‐in signaling and platelet function, and thus inhibiting thrombosis. Moreover, CoQ10‐enhanced cAMP/PKA pathway may also lead to the attenuation of αIIbβ3 inside‐out signaling.