雷贝拉唑对大鼠体内氯吡格雷抗血小板聚集作用和代谢的影响研究
蔡薇薇中圖分类号 R965 文献标志码 A 文章编号 1001-0408(2018)17-2342-05
DOI 10.6039/j.issn.1001-0408.2018.17.09
摘 要 目的:研究雷贝拉唑(RPZ)对大鼠体内氯吡格雷(CLP)抗血小板聚集作用和代谢的影响。方法:将40只SD大鼠随机分为空白对照组、RPZ组、CLP组、RPZ+CLP组、CLP+RPZ组,每组8只,CLP和RPZ 的给药剂量分别为6.75、0.9 mg/kg,两药给药间隔2 h,连续给药14 d。检测各组大鼠血小板聚集率(MPA)、血小板活化指数(PRI)、胃黏膜损伤评分以及血药浓度[氯吡格雷羧酸(CA)及CLP活性巯基代谢物衍生物(AM)],并采用Pearson相关性分析法分析MPA和PRI分别与CA、AM的关系。结果:与空白对照组比较,CLP组、RPZ+CLP组和CLP+RPZ组大鼠的MPA、PRI均明显降低(P0.05)。与CLP组比较,RPZ+CLP组和CLP+RPZ组大鼠的MPA、PRI均明显升高(P0.05)。MPA和PRI均与AM呈负相关性(r=-0.689、-0.765,P0.05)。结论:RPZ对CLP的抗血小板作用、致胃黏膜损伤有一定的抑制作用,两药的给药顺序不影响CLP的代谢。
关键词 氯吡格雷;雷贝拉唑;抗血小板聚集;代谢;相互作用;大鼠
ABSTRACT OBJECTIVE: To study the effects of rabeprazole (RPZ) on in vivo anti-platelet aggregation and metabolism of clopidogrel in rats. METHODS: Totally 40 SD rats were randomly divided into blank control group, RPZ group, CLP group, RPZ+CLP group and CLP+RPZ group, with 8 rats in each group. The dose of CLP and RPZ were 6.75 and 0.9 mg/kg, with medication interval of 2 h, for consecutive 14 d. The maximal platelet aggregation (MPA), platelet reaction index (PRI), gastric mucosal injury score and blood concentration [carboxylic acid of clopidogrel (CA) and active metabolite of clopidogrel (AM) were detected. The relationship of MPA and PRI with CA and AM were analyzed by Pearson relation analysis. RESULTS: Compared with blank control group ......
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