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纸质出版日期:2015
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朴新新, 汪宁, 汪光云, 等. 脑络欣通胶囊对脑缺血再灌注模型大鼠血小板聚集及血栓形成的影响[J]. 中国实验方剂学杂志, 2015,21(22):26-30.
PIAO Xin-xin, WANG Ning, WANG Guang-yun, et al. Effects of Naoluo Xintong Capsules on Platelet Aggregation and Thrombus Formation in Rats with Focal Cerebral Ischemia/Reperfusion[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(22): 26-30.
朴新新, 汪宁, 汪光云, 等. 脑络欣通胶囊对脑缺血再灌注模型大鼠血小板聚集及血栓形成的影响[J]. 中国实验方剂学杂志, 2015,21(22):26-30. DOI: 10.13422/j.cnki.syfjx.2015220026.
PIAO Xin-xin, WANG Ning, WANG Guang-yun, et al. Effects of Naoluo Xintong Capsules on Platelet Aggregation and Thrombus Formation in Rats with Focal Cerebral Ischemia/Reperfusion[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(22): 26-30. DOI: 10.13422/j.cnki.syfjx.2015220026.
目的:观察脑络欣通胶囊对局灶性脑缺血再灌注损伤大鼠血小板聚集和血栓形成的影响。方法:雄性SD大鼠
随机分为假手术组10只
造模组60只
线栓法制备大脑中动脉闭塞缺血-再灌注(MCAO/R)模型
将造模成功的大鼠随机分为模型组
阿司匹林组(0.010 g·kg-1)
脑络欣通高、中、低剂量组(4.500
2.250
1.125 g·kg-1)。透射电子显微镜观察海马神经元超微结构变化
检测各组血清中血栓素B2(TXB2)
6-酮前列腺素F1α(6-keto-PGF1α)
血小板聚集率及体内血栓形成时间。结果:与假手术组比较
模型组损伤大鼠的神经元的病理形态损坏严重
大鼠血清中TXB2水平明显升高
6-keto-PGF1α水平明显降低
模型组大鼠血小板在1
2
5 min的聚集率和最大聚集率明显升高(P<0.05
P<0.01);与模型组比较
脑络欣通胶囊低、中、高剂量组损伤大鼠的神经元的病理形态学均有明显改善
明显降低大鼠血清中TXB2水平
明显升高6-keto-PGF1α水平
1
2 min时
脑络欣通3个剂量组均明显降低大鼠血小板的聚集率
5 min时
低、高剂量组均明显降低大鼠血小板聚集率
低、中剂量组5 min内的最大聚集率
脑络欣通胶囊低、中剂量组大鼠体内血栓形成时间显著延长(P<0.05
P<0.01)。结论:脑络欣通胶囊具有抑制脑缺血再灌注损伤模型大鼠血小板的聚集和血栓形成
对缺血性脑血管疾病具有一定的保护作用。
Objective: The present study was designed to investigate the effects of Naoluo Xintong capsules on platelet aggregation and thrombus formation in rats with focal cerebral ischemia/reperfusion injury. Method: Male SD rats were randomly divided into sham operation group (n=10)
modeling group (n=60). Middle cerebral artery occlusion/reperfusion (MCAO/R) models were induced by the intraluminal suture method. The successfully modeled rats were randomly divided into model group
Aspirin group (0.010 g·kg-1)
Naoluo Xintong capsules high
middle and low dose groups (4.500
2.250
1.125 g·kg-1). Transmission electron microscope was used to observe the ultrastructure changes of hippocampal neurons. The levels of serum thromboxane B2(TXB2)
6-keto prostaglandin F1α(6-keto-PGF1α)
platelet aggregation rate and in vivo thrombus formation time were detected. Result: Compared with the sham operation group
pathological changes of the neurons in model group were severely damaged
TXB2 level in serum was significantly increased
6-keto-PGF1α level was significantly reduced
and platelet aggregation rates at 1
2
5 min and maximum aggregation rate in model group were significantly increased (P<0.05
P<0.01). Compared with the model group
pathological morphology of neurons in Naoluo Xintong capsules groups (1.125
2.250
4.500 g·kg-1) was significantly improved. After Naoluo Xintong capsules treatment
the serum TXB2 level was significantly decreased. In contrast
the level of serum 6-keto-PGF1α was increased. The platelet aggregation rate in Naoluo Xintong capsules low
middle and high dose groups in 1 min and 2 min was significantly lower than that in the model group
and the platelet aggregation rate in Naoluo Xintong capsules low and high dose groups and maximum aggregation rate in low and the middle dose groups in 5 min were significantly decreased. The thrombus formation time in Naoluo Xintong capsules low and middle dose groups was markedly prolonged (P<0.05
P<0.01). Conclusion: Naoluo Xintong capsules can inhibit the platelet aggregation and thrombus formation in focal cerebral ischemia/reperfusion injury models
with certain protection effect for ischemic cerebral vascular diseases.
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