机构地区:[1]北京大学药学院天然药物及仿生药物国家重点实验室,北京100191 [2]北京大学临床肿瘤学院,北京100142 [3]北京大学基础医学院血液流变学中心,北京100191
出 处:《中国药理学与毒理学杂志》2009年第3期183-187,共5页Chinese Journal of Pharmacology and Toxicology
基 金:国家杰出青年科学基金资助课题(30525043)~~
摘 要:目的观察三七总皂苷(PNS)对急性血瘀大鼠血液流变学的影响。方法大鼠随机分为正常对照组、模型组、阿司匹林100mg·kg-1阳性对照组、PNS50和100mg·kg-1组,每日早晚ig给药各1次,共7次。第5次给药后,除正常对照组外,其余4组大鼠sc给予肾上腺素加冰浴造成急性血瘀模型。在切变率200~1s-1范围内采用锥板法测定全血粘度和血浆粘度;微量毛细管法测定红细胞压积;光电比浊法测定二磷酸腺苷(ADP)诱导的血小板凝聚和光电电磁法测定凝血参数。结果模型组大鼠全血粘度和血浆粘度升高,红细胞聚集指数和血小板凝聚率增加,红细胞压积升高,纤维蛋白原含量增加,凝血酶时间、活化部分凝血活酶时间和凝血酶原时间均显著缩短。而与模型组相比,大鼠ig给予PNS50和100mg·kg-1均能显著降低全血粘度200s-1:(4.5±0.4)vs(4.1±0.4),(4.0±0.3)mPa.s;100s-1:(5.0±0.4)vs(4.4±0.5),(4.4±0.4)mPa.s;50s-1:(5.6±0.5)vs(4.9±0.6),(4.9±0.4)mPa.s;1s-1:(27.1±3.0)vs(22.2±4.6),(22.0±3.5)mPa·s及血浆粘度50s-1:(1.51±0.14)vs(1.33±0.10),(1.32±0.08)mPa.s,明显降低红细胞压积0.49±0.02vs0.45±0.03,0.44±0.03、红细胞聚集指数(5.5±0.4)vs(5.0±0.5),(5.0±0.6)和血小板凝聚率(32±3)% vs(26±3)%,(24±4)%;明显降低纤维蛋白原含量(4.8±0.3)vs(4.2±0.4),(4.1±0.3)g·L-1,以及延长凝血酶时间(25.2±2.7)vs(30.5±4.7),(31.2±3.9)s和凝血酶原时间(14.5±1.1)vs(15.7±1.1),(15.8±1.0)s。结论PNS能显著改善血瘀大鼠血液流变学异常。AIM To evaluate effects of Panax notoginseng saponins (PNS) on the hemorheo- logical abnormality in rats with acute blood sta- sis. METHODS The rats were randomly di- vided into normal control, model, aspirine 100 mg·kg-1, PNS 50 and 100 mg·kg-1 groups. The rats were ig given PNS or aspirin twice a day, altogether 7 times. After the 5th adminis- tration, the acute blood stasis model was in- duced by adrenaline and ice water soaking. The control group treated with the same procedure except sc normal saline. Whole blood viscosity and plasma viscosity were evaluated by cone- plate viscometer, hematocrit was determined by micro-capillary method, platelet aggregation was measured by photoelectric turbidimetry and coagulation parameters were evaluated by opti- cal electromagnetic method. RESULTS Com- pared with normal control group, whole blood viscosity and plasma viscosity of rats in blood stasis model group were significantly increased; erythrocyte aggregation index (EAI) and the platelet aggregation rate were also significantly elevated. Meanwhile, hematocrit and fibrino- gen (Fib) content were also increased, while prothrombin time ( PT ) , activated partial thromboplastin time (AlYlW) and thrombin time (TT) were shortened. Compared with model group, PNS 50 and 100 rag-kg-1 could significantly decrease whole blood viscosity [ 200 s-1 (4.5±0.4) vs (4.1±0.4) (4.0± 0.3)mPa.s;100 s-1 : (5.0 ±0.4) vs (4.4 ± 0.5),(4.4 ±0.4)mPa.s;50 s-1:(5.6 ± 0.5) vs (4.9 ±0.6) , (4.9 ±0.4)mPa-s; 1 s-1:(27.1±3.0) vs (22.2±4.6),(22.0± 3.5)mPa.s3 and plasma viscosity [50 s-1 (1.51±0.14) vs (1.33±0.10), (1.32± 0.08)mPa-s3; inhibit EAI [(5.5 ±0.4) vs (5.0 ± 0.5 ), (5.0 ± 0.6) 3 and ADP-indueed platelet aggregation rate [ ( 32 ± 3) % vs (26 ± 3 ) %, (24 ± 4) % 3 ; reduce hematoerit (0.49 ± 0.02 vs 0.45 .±0.03, 0.44 ±0.03 and Fib content [(4.8 ±0.3) vs (4.2 ±0.4), (4.1_ 0.3)g·L-1]; howeve
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