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首页> 外文期刊>International immunopharmacology >The antiplatelet activity of Geiji-Bokryung-Hwan, Korean traditional formulation, is mediated through inhibition of phospholipase C and inhibition of TxB(2) synthetase activity.
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The antiplatelet activity of Geiji-Bokryung-Hwan, Korean traditional formulation, is mediated through inhibition of phospholipase C and inhibition of TxB(2) synthetase activity.

机译:Geiji-Bokryung-Hwan(韩国传统制剂)的抗血小板活性是通过抑制磷脂酶C和抑制TxB(2)合成酶的活性来介导的。

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摘要

Geiji-Bokryung-Hwan (GBH), consisting of herbes of Cinnamomi ramulus (Geiji), Poria cocos (Bokryun), Mountan cortex radicis (Mokdanpi), Paeoniae radix (Jakyak), and Persicae semen (Doin), on antiplatelet activity in human platelet suspensions was studied. The mechanism involved in the antiplatelet activity of GBH in human platelet suspensions was investigated. GBH did not significantly affect the thromboxane synthetase activity of aspirin-treated platelet microsomes and GBH (15 and 30 microg/ml) significantly inhibited [3H]arachidonic acid released in collagen-activated platelets but not in unactivated-platelets. Nitric oxide (NO) production in human platelets was measured by a chemiluminesence detection method in this study. GBH did not significantly affect nitrate production in collagen (10 microg/ml)-induced human platelet aggregation. Various concentrations of GBH (0, 5, 10, 15, and 30 microg/ml) dose-dependently inhibited [3H]inositol monophosphate formation stimulated by collagen (10 microg/ml) in [3H]myoinositol-loaded platelets at different incubation times (1, 2, 3, and 5 min). These results indicated that the antiplatelet activity of GBH may possibly be due to the inhibition of phospholipase C (PLC) activity, leading to reduce phosphoinositide breakdown, followed by the inhibition of thromboxane A(2) formation, and then inhibition of [Ca(2+)](i) mobilization of platelet aggregation stimulated by agonists. In conclusion, GBH suppressed PLC in a dose-dependent manner, and may have pharmaceutical applications. These data suggest that GBH extracts merit investigation as a potential anti-atherosclerogenic agent in humans.
机译:Geiji-Bokryung-Hwan(GBH),由Cinnamomi ramulus(Geiji),Poria cocos(Bokryun),Mountan cortex radicis(Mokdanpi),Paeoniae radix(Jakyak)和Persicae精液(Doin)组成,它们具有抗人血小板活性。研究了血小板悬浮液。研究了人血小板悬浮液中GBH抗血小板活性的机制。 GBH不会显着影响阿司匹林治疗的血小板微粒体的血栓烷合成酶活性,GBH(15和30微克/毫升)显着抑制胶原激活的血小板中释放的[3H]花生四烯酸,而未激活的血小板则没有。在这项研究中,通过化学发光检测方法测量了人体血小板中一氧化氮(NO)的产生。 GBH不会显着影响胶原蛋白(10微克/毫升)诱导的人血小板聚集中硝酸盐的产生。不同浓度的GBH(0、5、10、15和30 microg / ml)剂量依赖性地抑制胶原蛋白(10 microg / ml)在[3H]肌醇加载的血小板中在不同的孵育时间刺激的[3H]肌醇单磷酸的形成。 (1、2、3和5分钟)。这些结果表明,GBH的抗血小板活性可能是由于抑制了磷脂酶C(PLC)的活性,导致减少了磷酸肌醇的降解,继而抑制了血栓烷A(2)的形成,然后抑制了[Ca(2) +)](i)动员激动剂刺激的血小板聚集。总之,GBH以剂量依赖性方式抑制PLC,并且可能具有药物应用。这些数据表明,GBH可作为人类潜在的抗动脉粥样硬化剂进行研究。

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