Abstract

BackgroundPlatelet activation is relevant to a variety of coronary heart diseases. Our previous studies revealed that sesamol possesses potent antiplatelet activity through increasing cyclic AMP formation. Although platelets are anucleated cells, they also express the transcription factor, NF-κB, that may exert non-genomic functions in platelet activation. Therefore, we further investigated the inhibitory roles of sesamol in NF-κB-mediated platelet function.MethodsPlatelet aggregation, Fura 2-AM fluorescence, and immunoblotting analysis were used in this study.ResultsNF-κB signaling events, including IKKβ phosphorylation, IκBα degradation, and p65 phosphorylation, were markedly activated by collagen (1 μg/ml) in washed human platelets, and these signaling events were attenuated by sesamol (2.5~25 μM). Furthermore, SQ22536 and ODQ, inhibitors of adenylate cyclase and guanylate cyclase, respectively, strongly reversed the sesamol (25 μM)-mediated inhibitory effects of IKKβ phosphorylation, IκBα degradation, and p65 phosphorylation stimulated by collagen. The protein kinase A (PKA) inhibitor, H89, also reversed sesamol-mediated inhibition of IκBα degradation. Moreover, BAY11-7082, an NF-κB inhibitor, abolished IκBα degradation, phospholipase C (PLC)γ2 phosphorylation, protein kinase C (PKC) activation, [Ca2+]i mobilization, and platelet aggregation stimulated by collagen. Preincubation of platelets with the inhibitors, SQ22536 and H89, both strongly reversed sesamol-mediated inhibition of platelet aggregation and [Ca2+]i mobilization.ConclusionsSesamol activates cAMP-PKA signaling, followed by inhibition of the NF-κB-PLC-PKC cascade, thereby leading to inhibition of [Ca2+]i mobilization and platelet aggregation. Because platelet activation is not only linked to hemostasis, but also has a relevant role in inflammation and metastasis, our data demonstrating that inhibition of NF-κB interferes with platelet function may have a great impact when these types of drugs are considered for the treatment of cancer and various inflammatory diseases.

Highlights

  • Platelet activation is relevant to a variety of coronary heart diseases

  • Concentration- and time-dependent effects of sesamol on collagen-induced nuclear factor-kappa B (NF-B) activation in washed human platelets In our previous report [11], sesamol (1~5 μM) exhibited potent activity of inhibiting platelet aggregation stimulated by collagen (1 μg/ml); it significantly inhibited platelet aggregation stimulated by arachidonic acid (AA)

  • Sesamol (2.5~25 μM) concentration-dependently reversed the degradation of IBa protein at 10 min after collagen stimulation (Figure 1C). These results suggest that IKKb phosphorylation and subsequent IBa degradation in collagen-stimulated platelets may contribute to sesamol’s inhibitory actions on NF-B signaling

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Summary

Introduction

Platelet activation is relevant to a variety of coronary heart diseases. Our previous studies revealed that sesamol possesses potent antiplatelet activity through increasing cyclic AMP formation. Platelets are anucleated cells, they express the transcription factor, NF-B, that may exert non-genomic functions in platelet activation. We further investigated the inhibitory roles of sesamol in NF-B-mediated platelet function. Sesamol is a potent phenolic antioxidant contained only in processed sesame oil. Sesame seed oil was used to remove wrinkles and prevent aging, Arterial thrombosis is quite distinct from venous thrombosis in that arterial thrombosis is mostly composed of platelets that adhere to ruptured endothelial surfaces [9]. Platelet aggregation may play a crucial role in the atherothrombotic process [10]

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