番茄红素对高脂血症大鼠血凝及纤溶的影响
番茄红素;,高脂血症;,血凝;,纤维蛋白溶解,,番茄红素;,高脂血症;,血凝;,纤维蛋白溶解,1材料与方法,2结果,3讨论,参考文献:
摘要:目的研究番茄红素(lycopene, LP)对高脂血症大鼠血脂、血凝及纤溶的影响。方法建立大鼠的高脂血症模型,同时连续ig 给予LP(20 mg/kg)或空白溶媒30 d,测定大鼠血浆总胆固醇(TC)、甘油三酯(TG)、高密度脂蛋白胆固醇(HDLC)、低密度脂蛋白胆固醇(LDLC)、凝血酶原时间(prothrombin time, PT)、活化部分凝血活酶时间(activated partial thrombplastin time, APTT)、 组织型纤溶酶原激活物 (tissue plasminogen activator, tPA) 活性及纤溶酶原激活物抑制剂1(plasminogen activator inhibitor1, PAI1)活性。结果与饲HFD组比较, 饲HFD大鼠在连续ig给予LP(20 mg/kg)30 d后,大鼠血浆TG含量平均下降27%,TC含量平均下降21%,LDLC含量平均下降39%,HDLC含量平均增加24%;血浆APTT显著延长而PAI1活性降低(P<0.05),t-PA活性显著增加(P<0.01)。结论 番茄红素不但能有效降低高脂血症大鼠血脂,而且可能通过防止脂质过氧化而有效改善动物血凝系统。关键词:番茄红素; 高脂血症; 血凝; 纤维蛋白溶解
Effects of Lycopene on Blood Coagulation and Fibrinolysis in Hyperlipidemia Rats
DENG ZuYue,XIN Yanfei
(Zhejiang Provincial Institute for Drug Control, Hangzhou 310004,China; Zhejiang Academy of Medical Sciences, Hangzhou 310013,China)
Abstract:ObjectiveTo explore the effects of lycopene (LP) on lipidemia, blood coagulation and fibrinolysis in experimental hyperlipidemia rats. MethodsExperimental hyperlipidemia rats were i.g. administration of LP (20 ml·kg1·d1) or vehicle (0.5% CMC, 10 ml·kg1·d1) for 30 d. The levels of plasma triglyceride (TG), total cholesterol (TC), high density lipoprotein cholesterol (HDLC), low density lipoprotein cholesterol (LDLC), prothrombin time (PT), activated partial thrombplastin time (APTT), plasminogen activator inhibitor 1 (PAI1) activity and tissue plasminogen activator (tPA) activity were measured. ResultsPlasma TG and HDL-C of the rats fed high fat diet (HFD) and dosed LP (20 mg/kg·d) was 27% lower and 24% higher than that of the HFD group rats. The APTT of LP and HFD group rats were significantly longer than that of the HFD group (P<0.05). The PAI1 in LP and HFD group was higher (P<0.05) and the tPA in LP and HFD group was lower than that of the HFD group (P<0.01). ConclusionBlood clotting system in experimental hyperlipidemia rats was improved by i.g. administration of LP. The results from the experiments may be helpful for the use of LP as an antiatherogenesis drug. ......
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