从甘蔗蜡中纯化的新物质d-003对健康志愿者血小板聚集和花生四烯酸代谢物血浆水平的影响

M L Arruzazabala, R Mas, V Molina, D Carbajal, L Fernández, J Illnait, G Castaño, J Fernández, S Mendoza
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引用次数: 0

摘要

D-003是一种从甘蔗蜡中提纯的高分子量脂肪酸混合物,具有实验和临床研究证明的降胆固醇和抗血小板作用。实验证据表明,D-003诱导的血小板聚集抑制与血栓素B2 (TxB2)的降低和前列环素(Pgl2)的升高有关。这项双盲、随机、安慰剂对照研究旨在研究D-003 (20 mg/天)是否能改变人类健康志愿者血清中TxB2和Pgl2的水平,并抑制血小板聚集。31名受试者随机分为安慰剂组或D-003组,剂量为20mg /天,持续14天。测定血清TxB2、Pgl2水平及血小板对花生四烯酸(AA) (1.75 mM)和胶原(1 μ g/ml)的聚集。与基线相比,D-003 (20 mg/天)显著降低了36.4%的txb2 (p < 0.001),增加了31%的Pgl2血清水平,这些变化与安慰剂不同。正如预期的那样,D-003显著抑制血小板聚集到AA(81.9-65.6%)和胶原(75.3-62.3%)(p < 0.001)。没有受试者退出研究。未观察到与药物相关的干扰。我们得出结论,D-003 20 mg/天,连续14天显著抑制血小板对AA和胶原的聚集,降低TxB2,增加Pgl2血清水平。这些结果与实验模型的结果一致,表明D-003的抗血小板作用与观察到的AA代谢物水平的变化有关。然而,进一步的研究应该更深入地探讨这一作用的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of d-003, a new substance purified from sugar cane wax, on platelet aggregation and plasma levels of arachidonic acid metabolites in healthy volunteers.

D-003 is a mixture of very high molecular weight aliphatic acids purified from sugar cane wax showing cholesterol-lowering and antiplatelet effects proven in experimental and clinical studies. Experimental evidence indicates that inhibition of platelet aggregation induced by D-003 is associated with a reduction of thromboxane B2 (TxB2) and an increase of prostacyclin (Pgl2) serum levels. This double-blinded, randomized, placebo-controlled study was undertaken to investigate whether D-003 (20 mg/day) modifies serum levels of TxB2 and Pgl2 and inhibits platelet aggregation in human healthy volunteers. Thirty-one subjects were randomized to placebo or D-003 at 20 mg/day for 14 days. Serum levels of TxB2 and Pgl2 and platelet aggregation to arachidonic acid (AA) (1.75 mM) and collagen (1 microg/ml) were assessed. D-003 (20 mg/day) significantly reduced (p < 0.001) TxB2by 36.4% and increased Pgl2 serum levels by 31% compared with baseline, and these changes were different from placebo. As expected, D-003 significantly inhibited (p < 0.001) platelet aggregation to AA (81.9-65.6%) and to collagen (75.3-62.3%). No subject withdrew from the study. No drug-related disturbances were observed. We conclude that D-003 at 20 mg/day for 14 days significantly inhibited platelet aggregation to AA and collagen and reduced TxB2 and increased Pgl2 serum levels. These results are consistent with those observed in experimental models, indicating that the antiplatelet effect of D-003 is associated with the observed changes on the levels of AA metabolites. Further studies, however, should explore the mechanism involved in this action in greater depth.

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