Qi R, Liao F, Inoue K, Yatomi Y, Sato K, Ozaki Y
Department of Clinical and Laboratory Medicine, Yamanashi Medical University, Yamanashi, Japan.
Biochem Pharmacol. 2000 Nov 15;60(10):1475-83. doi: 10.1016/s0006-2952(00)00467-6.
Garlic has been used in herbal medicine for thousands of years. Some reports have shown that garlic has protective effects against atherosclerosis and inhibits platelet function. In this study, we investigated the mechanism by which diallyl trisulfide (DT), a component of garlic, inhibits platelet function. DT inhibited platelet aggregation and Ca(2+) mobilization in a concentration-dependent manner without increasing intracellular cyclic AMP and cyclic GMP. DT also had no inhibitory effects on thromboxane A(2) (TXA(2)) production in cell-free systems. Collagen-related peptide (CRP)-induced Ca(2+) mobilization is regulated by phospholipase C-gamma2 (PLC-gamma2) activation. We evaluated the effect of DT on tyrosine phosphorylation of PLC-gamma2 and the production of inositol-1,4,5-trisphosphate (IP(3)). DT at concentrations that inhibited platelet aggregation and Ca(2+) mobilization had no effects on tyrosine phosphorylation of PLC-gamma2 or on the formation of IP(3) induced by CRP. Similar results were obtained with thrombin-induced platelet activation. DT inhibited platelet aggregation and Ca(2+) mobilization induced by thrombin without affecting the production of IP(3.) We then evaluated the effect of DT on the binding of IP(3) to its receptor. DT at high concentrations partially blocked the binding of IP(3) to its receptor. Taken together, our findings suggest that the agent suppresses Ca(2+) mobilization at a step distal to IP(3) formation. DT may provide a good tool for investigating Ca(2+) mobilization.
大蒜用于草药已有数千年历史。一些报告显示,大蒜对动脉粥样硬化具有保护作用,并能抑制血小板功能。在本研究中,我们探究了大蒜成分二烯丙基三硫化物(DT)抑制血小板功能的机制。DT以浓度依赖的方式抑制血小板聚集和Ca(2+)动员,且不增加细胞内环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)。DT在无细胞体系中对血栓素A(2)(TXA(2))的产生也没有抑制作用。胶原相关肽(CRP)诱导的Ca(2+)动员受磷脂酶C-γ2(PLC-γ2)激活调控。我们评估了DT对PLC-γ2酪氨酸磷酸化和肌醇-1,4,5-三磷酸(IP(3))产生的影响。抑制血小板聚集和Ca(2+)动员浓度的DT对PLC-γ2的酪氨酸磷酸化或CRP诱导的IP(3)形成没有影响。凝血酶诱导的血小板激活也得到了类似结果。DT抑制凝血酶诱导的血小板聚集和Ca(2+)动员,但不影响IP(3)的产生。然后我们评估了DT对IP(3)与其受体结合的影响。高浓度的DT部分阻断了IP(3)与其受体的结合。综上所述,我们的研究结果表明,该药物在IP(3)形成的下游步骤抑制Ca(2+)动员。DT可能为研究Ca(2+)动员提供一个良好的工具。