Effects of D-003, a mixture of very long chain fatty acids purified from sugar cane wax, at 5 and 10 mg/day on platelet aggregation in healthy volunteers.

M L Arruzazabala, V Molina, D Carbajal, L Fernández, R Mas, G Castaño, J Illnait, S Mendoza, J Fernańdez
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Abstract

D-003 is a mixture of high molecular weight aliphatic primary acids purified from sugar cane wax with antiplatelet and cholesterol-lowering effects. Previous studies showed that D-003 (10-20 mg/day) administered for a short time inhibits platelet aggregation, 14 days being the longest duration investigated. This study was conducted to investigate the effects of D-003 (5 and 10 mg/day) for 30 days on platelet aggregation in normocholesterolemic subjects. This report shows the effects of D-003 on platelet aggregation to arachidonic acid (AA) (1.5 mM), collagen (2 microg/ml) and adenosine 5'-diphosphate ADP (2 microM) assessed at baseline and at treatment completion. Fifty-four subjects were randomized to placebo or D-003 (5 or 10 mg/day) for 30 days. Platelet aggregation to AA, collagen and ADP were assessed. D-003 at the lowest dose (5 mg/day) significantly but modestly inhibited (p < 0.01) platelet aggregation to AA (5.0%) and (p < 0.01) to collagen (7.5%). D-003 at 10 mg/day inhibited (p < 0.001) platelet aggregation to AA and collagen (p < 0.01) by 20.3% and 14.7%, respectively. ADP-induced aggregation, however, was unchanged. D-003 at 10 mg/day, but not at 5 mg/day, lowered (p < 0.01) plasma fibrinogen. D-003 (5 and 10 mg/day) reduced low-density lipoprotein cholesterol (LDL-C) by 17.7% and 26.4%, respectively, and total cholesterol (TC) by 14.5% and 18.5%, while at 10 mg/day, but not at 5 mg/day, it increased high-density lipoprotein cholesterol (HDL-C) by 9.6%. Triglycerides, however, were unchanged with D-003. No disturbances in safety indicators were induced with D-003. One subject (D-003 5 mg/day) discontinued the study and four patients (three taking D-003 and one taking placebo) reported adverse effects (AE) (headache in two patients taking D-003 and one patient taking placebo, and polyphagia in one patient taking D-003). In conclusion, D-003 (5-10 mg/day) for 30 days inhibited platelet aggregation to AA and collagen but not to ADP Therefore, the antiplatelet effect was present with the longer treatment, even at a dose of 5 mg/day. The cholesterol-lowering effects of D-003 were consistent with those expected for such a short treatment. In addition, D-003 at 10 mg/day significantly lowered plasma fibrinogen. The treatment was well tolerated.

D-003是一种从甘蔗蜡中纯化的长链脂肪酸混合物,5和10毫克/天对健康志愿者血小板聚集的影响。
D-003是从甘蔗蜡中提纯的高分子量脂肪族伯酸的混合物,具有抗血小板和降胆固醇的作用。先前的研究表明,D-003 (10- 20mg /天)短时间给药可抑制血小板聚集,最长时间为14天。本研究旨在探讨D-003(5和10毫克/天)对正常胆固醇血症患者血小板聚集的影响。该报告显示了D-003在基线和治疗结束时对花生四烯酸(AA) (1.5 mM)、胶原(2微克/毫升)和腺苷5'-二磷酸ADP(2微米)血小板聚集的影响。54名受试者被随机分配到安慰剂或D-003组(5或10毫克/天),持续30天。观察血小板对AA、胶原和ADP的聚集情况。最低剂量(5 mg/d) D-003对AA(5.0%)和胶原(7.5%)的血小板聚集有极显著(p < 0.01)和中度抑制(p < 0.01)。D-003对AA和胶原聚集的抑制作用(p < 0.01)分别为20.3%和14.7%。然而,adp诱导的聚集没有变化。D-003在10 mg/d组降低了血浆纤维蛋白原,而在5 mg/d组没有降低(p < 0.01)。D-003(5和10 mg/d)分别使低密度脂蛋白胆固醇(LDL-C)降低17.7%和26.4%,总胆固醇(TC)降低14.5%和18.5%,而在10 mg/d组,高密度脂蛋白胆固醇(HDL-C)升高9.6%,但在5 mg/d组没有。然而,甘油三酯与D-003没有变化。D-003对安全指标无干扰。一名受试者(D-003 5毫克/天)停止了研究,四名患者(三名服用D-003,一名服用安慰剂)报告了不良反应(AE)(两名服用D-003的患者头痛,一名服用安慰剂的患者,一名服用D-003的患者多食)。综上所述,D-003 (5-10 mg/d)治疗30 d可抑制血小板对AA和胶原的聚集,但对ADP无抑制作用。因此,即使在5 mg/d的剂量下,随着治疗时间的延长,抗血小板作用仍然存在。D-003的降胆固醇效果与预期的短期治疗一致。此外,D-003在10 mg/d时显著降低血浆纤维蛋白原。这种治疗耐受性良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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