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首页> 外文期刊>Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis >Dietary Nitrate Supplementation Reduces Circulating Platelet-Derived Extracellular Vesicles in Coronary Artery Disease Patients on Clopidogrel Therapy: A Randomised, Double-Blind, Placebo-Controlled Study
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Dietary Nitrate Supplementation Reduces Circulating Platelet-Derived Extracellular Vesicles in Coronary Artery Disease Patients on Clopidogrel Therapy: A Randomised, Double-Blind, Placebo-Controlled Study

机译:膳食硝酸盐补充减少冠状动脉疾病患者氯吡格雷治疗中的循环血小板衍生细胞外囊泡:随机,双盲,安慰剂对照研究

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Extracellular vesicles (EVs) are implicated in the pathogenesis of cardiovascular disease (CVD). Specifically, platelet-derived EVs are highly pro-coagulant, promoting thrombin generation and fibrin clot formation. Nitrate supplementation exerts beneficial effects in CVD, via an increase in nitric oxide (NO) bioavailability. Clopidogrel is capable of producing NO-donating compounds, such as S-nitrosothiols (RSNO) in the presence of nitrite and low pH. The aim this study was to assess the effect of nitrate supplementation with versus without clopidogrel therapy on circulating EVs in coronary artery disease (CAD) patients. In this randomized, double-blind, placebo-controlled study, CAD patients with (n = 10) or without (n = 10) clopidogrel therapy received a dietary nitrate supplement (SiS nitrate gel) or identical placebo. NO metabolites and platelet activation were measured using ozone-based chemiluminescence and multiple electrode aggregometry. EV concentration and origin were determined using nanoparticle tracking analysis and time-resolved fluorescence. Following nitrate supplementation, plasma RSNO was elevated (4.7 +/- 0.8 vs 0.2 +/- 0.5 nM) and thrombin-receptor mediated platelet aggregation was reduced (-19.9 +/- 6.0 vs 4.0 +/- 6.4 U) only in the clopidogrel group compared with placebo. Circulating EVs were significantly reduced in this group (-1.183e(11) +/- 3.15e(10) vs -9.93e(9) +/- 1.84e(10) EVs/mL), specifically the proportion of CD41+ EVs (-2,120 +/- 728 vs 235 +/- 436 RFU [relative fluorescence unit]) compared with placebo. In vitro experiments demonstrated clopidogrel-SNO can reduce platelet-EV directly (6.209e(10) +/- 4.074e(9) vs 3.94e(11) +/- 1.91e(10) EVs/mL). In conclusion, nitrate supplementation reduces platelet-derived EVs in CAD patients on clopidogrel therapy, increasing patient responsiveness to clopidogrel. Nitrate supplementation may represent a novel approach to moderating the risk of thrombus formation in CAD patients.
机译:细胞外囊泡(EVS)涉及心血管疾病(CVD)的发病机制。具体而言,血小板衍生的EV是高度凝结剂,促进凝血酶产生和纤维蛋白凝块形成。硝酸盐补充在CVD中施加有益效果,通过增加一氧化氮(NO)生物利用度。氯吡格雷能够在亚硝酸盐和低pH存在下生产不含含量的化合物,例如S-亚硝基硫醇(RSNO)。本研究的目的是评估硝酸盐补充剂与冠状动脉疾病(CAD)患者循环EVS的影响。在该随机,双盲,安慰剂对照研究中,CAD患者(n = 10)或没有(n = 10)氯丙基菌疗法接受膳食硝酸盐补充剂(Sis硝酸盐凝胶)或相同的安慰剂。使用基于臭氧的化学发光和多电极聚集体测量没有代谢物和血小板活化。使用纳米颗粒跟踪分析和时间分辨荧光测定EV浓度和起源。在硝酸盐补充后,血浆RSNO升高(4.7 +/- 0.8 Vs 0.2 +/- 0.5nm),并且仅在氯吡格雷中降低了凝血酶 - 受体介导的血小板聚集(-19.9 +/- 6.0 vs.4.0 +/- 6.4 u)与安慰剂相比。该组循环EVS显着降低(-1.183e(11)+/- 3.15e(10)vs -9.93e(9)+/- 1.84e(10)EVS / ml),特别是CD41 + EV的比例(与安慰剂相比,-2,120 +/- 728 vs 235 +/- 436 RFU [相对荧光单位])。体外实验证明了氯吡格雷 - SnO可以直接减少血小板-eV(6.209E(10)+/- 4.074e(9)Vs 3.94e(11)+/- 1.91e(10)EVS / ml)。总之,硝酸盐补充减少了CAD患者的血小板衍生EV,对氯吡格雷氏症的患者,增加对氯吡格雷的患者反应性。硝酸盐补充剂可以代表一种新的方法来调节CAD患者中血栓形成风险的方法。

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