南方医科大学学报 ›› 2014, Vol. 34 ›› Issue (08): 1162-.

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兔颈动脉球囊损伤后血小板聚集和活化及阿托伐他汀的作用

童保文,林志鸿,谢良地,许昌声   

  • 出版日期:2014-08-20 发布日期:2014-08-20

Atorvastatin inhibits platelet aggregation and activation following carotid balloon injury
in cholesterol-fed rabbits

  • Online:2014-08-20 Published:2014-08-20

摘要: 目的探讨高脂饮食的新西兰兔颈总动脉球囊损伤后急性期血小板聚集、活化及阿托伐他汀的作用。方法30只雄性新西
兰兔,随机分为5 组:对照组、高脂组、模型组、低剂量组[5 mg/(kg·d)阿托伐他汀治疗]、高剂量组[10 mg/(kg·d)阿托伐他汀治
疗],每组6只。比浊法检测血小板聚集率,ELISA法检测血清P-选择素(P-Selectin)、血栓素B2(Thromboxane B2, TXB2)水平。
结果(1)与对照组相比,高脂组血清P-Selectin 水平明显增加[(23.99±3.58)vs(16.72±1.76)pg/ml,P<0.01];血小板聚集率、
TXB2与对照组无明显差别;(2)模型组P-Selectin、TXB2表达及血小板聚集率均较高脂组显著增加(P<0.05),具有时效性,且在
术后24 h 达高峰[P-Selectin(35.26±4.93)vs(23.99±3.58)pg/ml;TXB2(264.33±27.68)vs(156.58±12.97)pg/ml;血小板聚集率
(58.59±10.78)vs(38.57±7.54)%;P<0.01];(3)与模型组相比,低剂量组显著降低兔血清P-Selectin、TXB2水平,同时抑制了血小
板聚集率[P-Selectin(28.14±5.05)比(35.26±4.93)pg/ml;TXB2(190.16±16.86)vs(264.33±27.67)pg/ml;血小板聚集率(47.21±
5.42)vs(58.59±10.77)%;均P<0.01];(4)与低剂量组相比,高剂量组血小板聚集和活化水平进一步降低[P-Selectin(22.74±
3.02)vs(28.14±5.05)pg/ml;TXB2(164.68±11.90)vs(190.16±16.86)pg/ml;血小板聚集率(37.04±4.99)vs(47.21±5.42)%;均
P<0.05]。结论“高脂饮食+球囊损伤”增加了新西兰兔血小板的活化和聚集,在术后24小时达到高峰,阿托伐他汀治疗显著抑
制了血管损伤后急性期血小板的活化和聚集水平,且与药物剂量有关。

Abstract: Objective To investigate the effect of atorvastatin on platelet aggregation and activation in the acute phase following
balloon-induced carotid artery injury in rabbits fed cholesterol-enriched diet. Methods Thirty rabbits were randomly divided
into 5 equal groups, namely control group, high-cholesterol group, model group, low-dose (5 mg/kg daily) atorvastatin group,
and high-dose (10 mg/kg daily) atorvastatin group. Platelet aggregation rate was measured in the rabbits by turbidimetric
platelet aggregometry, and the changes of serum P-selectin and thromboxane B2 (TXB2) levels were detected with
enzyme-linked immunosorbent assay (ELISA). Results Compared with those in the control group, serum P-selectin level
increased significantly (P<0.01) but platelet aggregation rate and TXB2 level exhibited no obvious changes in high-cholesterol
group. After carotid artery balloon injury, P-selectin and TXB2 levels and platelet aggregation significantly increased in
cholesterol-fed rabbits, reaching the peak level at 24 h after the injury (P<0.01). Compared with the model group, low-dose
atorvastatin treatment significantly decreased P-selectin and TXB2 levels and inhibited platelet aggregation in cholesterol-fed
rabbits following carotid artery balloon injury (P<0.01), and such effects of atorvastatin were more prominent at a higher daily
dose of 10 mg/kg (P<0.05). Conclusions Carotid artery balloon injury in rabbits fed cholesterol-enriched diet can induce
platelet activation and aggregation, which reaches the peak level at 24 h after balloon injury and can be dose-dependently
inhibited by atorvastatin in the acute phase following the injury.