低剂量阿司匹林、血小板功能和前列腺素合成:肾上腺素和α -肾上腺素能阻断的影响

Gundu H.R. Rao , Ratnammal K. Reddy , James G. White
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引用次数: 24

摘要

本研究评估了低剂量口服阿司匹林对血小板前列腺素合成和功能的影响。给成人服用整片(80毫克)或半片(40毫克)婴儿阿司匹林对血小板对凝血酶、ADP和肾上腺素的反应没有影响,但在摄入后16-20小时选择性地抑制花生四烯酸阈值浓度诱导的聚集。大剂量的花生四烯酸酯克服了低剂量阿司匹林的抑制作用,但成人阿司匹林片(600毫克)却没有。由于肾上腺素浓度过低,不会引起聚集,它恢复了阿司匹林处理过的血小板对花生四烯酸酯的敏感性。对a-肾上腺素能激动剂、拮抗剂和钙通道阻滞剂的研究表明,肾上腺素的纠正作用是通过a-肾上腺素受体对血小板膜钙调节的影响来介导的。
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Low dose aspirin, platelet function and prostaglandin synthesis: Influence of epinephrine and alpha adrenergic blockade

The present investigation has evaluated the effects of low doses of oral aspirin on platelet prostaglandin synthesis and function. Whole (80 mg) or half (40 mg) tablets of baby aspirin given to adults had no effect on the response of their platelets to thrombin, ADP and epinephrine, but selectively inhibited aggregation induced by threshold concentrations of arachidonate 16–20 hours after ingestion. Larger amounts of arachidonate overcame the inhibition imposed by low dose aspirin, but not by adult aspirin tablets (600 mg). Epinephrine, in concentrations too low to cause aggregation, restored the sensitivity of aspirin-treated platelets to arachidonate. Studies with a-adrenergic agonists, antagonists and calcium channel blockers demonstrated that the corrective effect of epinephrine was mediated by an a-adrenergic receptor influence on calcium modulation of the platelet membrane.

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