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作 者:谢笑龙[1] 吴敏[1] 吴芹[1] 黄燮南[1] 龚其海[1] 石京山[1]
机构地区:[1]遵义医学院药理学教研室,贵州遵义563000
出 处:《中国药理学与毒理学杂志》2008年第2期116-119,共4页Chinese Journal of Pharmacology and Toxicology
摘 要:目的研究异钩藤碱对血小板内游离钙离子浓度([Ca^2+]i)的影响,以探讨其抗血小板聚集作用的可能机制。方法比浊法测定家兔血小板聚集功能;双波长Fura-2荧光法测定血小板胞浆[Ca^2+]i。结果异钩藤碱0.33~1.30mmol·L-1体外给药对ADP和凝血酶引起的血小板聚集有浓度依赖性的抑制作用。存在细胞外钙时,异钩藤碱对基础状态血小板的[Ca^2+]i和ADP及凝血酶诱导的[Ca^2+]i水平有浓度依赖性的降低作用,而无细胞外钙存在时,则均无明显影响,表明其可抑制血小板的外钙内流,对内钙释放无明显抑制作用。结论异钩藤碱可抑制血小板聚集,其作用机制可能与其抑制血小板胞浆[Ca^2+]i升高有关。AIM Observing the effect of isorhynchophylline on cytoplasmic free calcium level ( [Ca^2+]i ) of platelets, to investigate the possible mechanism of its anti-platelet aggregation. METHODS Rabbit platelet aggregation and platelet [Ca^2+]i were determined by Born method and double beam fluorescence spectrophotometric method, respectively. RESULTS Isorhynchophylline 0. 33 - 1. 30 mmol. L-1 administered in vitro visibly inhibited the rabbit's platelet aggregation induced by ADP (15μmol.L^-1) and thrombin (3 kU.L-1) in a concentration-dependent manner. In the presence of extracellular [Ca^2+]i, isorhynchophylline inhibited the resting [Ca^2+]i and the increased [Ca^2+]i induced by ADP ( 15 μmol· L^-1 ) and thrombin (3 kU.L^-1) in a concentration-dependent manner, but had no effect on [Ca^2+]i in the absence of extracellular Ca^2+, which indicated that isorhynchophylline inhibited extracellular Ca^2+ influx in platelets, but had no inhibitory effect on intracellular Ca^2+ mobilization. CONCLUSION Isorhynchophylline markedly inhibits the rabbit platelet aggregation, and the mechanism may be related to its depression on the rise of platelet [Ca^2+]i.
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