天津中医药大学第一附属医院
纸质出版:2019
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[1]王贤良,苏立硕,毛静远,王帅,赵国元,王聪.理气化痰活血方对冠状动脉微循环障碍模型大鼠血管内皮功能的影响[J].中医杂志,2019,60(21):1849-1853+1860.
WANG Xianliang, SU Lishuo, MAO Jingyuan, et al. Effect of Liqi Huatan Huoxue Formula(理气化痰活血方) on Vascular Endothelial Function in Coronary Artery Microcirculation Disorder Model Rats[J]. Journal of Traditional Chinese Medicine2019, 60(21): 1849-1853.
[1]王贤良,苏立硕,毛静远,王帅,赵国元,王聪.理气化痰活血方对冠状动脉微循环障碍模型大鼠血管内皮功能的影响[J].中医杂志,2019,60(21):1849-1853+1860. DOI: 10.13288/j.11-2166/r.2019.21.009.
WANG Xianliang, SU Lishuo, MAO Jingyuan, et al. Effect of Liqi Huatan Huoxue Formula(理气化痰活血方) on Vascular Endothelial Function in Coronary Artery Microcirculation Disorder Model Rats[J]. Journal of Traditional Chinese Medicine2019, 60(21): 1849-1853. DOI: 10.13288/j.11-2166/r.2019.21.009.
目的探讨理气化痰活血方对冠状动脉微循环障碍的影响及可能作用机制。方法健康雄性SD大鼠245只随机分为理气化痰活血方组、缬沙坦组、模型组各80只
空白组5只。除空白组外
其余3组均采用经心尖部向左心室注射月桂酸钠的方法建立大鼠冠状动脉微循环障碍模型。理气化痰活血方组及缬沙坦组术前1天及术后4周分别给予理气化痰活血方药(浓度2. 25 g/ml)、缬沙坦悬浊液(浓度8. 89 mg/ml)1 ml/100 g灌胃
模型组及空白组给予1 ml/100 g蒸馏水灌胃
均每日1次。实验期间观察各组大鼠死亡情况;理气化痰活血方组、缬沙坦组、模型组分别于术后1 h、24 h、1周、2周、3周、4周各时间点随机处死5只大鼠
空白组4周时处死
检测各组大鼠血清内皮素1 (ET-1)、一氧化氮(NO)、血管性血友病因子(vWF)浓度及心肌组织纤维介素(fgl 2) mRNA表达。结果模型组、理气化痰活血方组、缬沙坦组大鼠总计分别死亡44只、40只、42只
3组大鼠术中及术后死亡情况比较差异无统计学意义(P> 0. 05)。术后4周时
模型组大鼠较空白组血清ET-1浓度升高
v WF浓度降低(P <0. 01)
血清NO浓度和心肌组织fgl 2 mRNA表达差异无统计学意义(P> 0. 05)。与模型组同时间比较
理气化痰活血方组和缬沙坦组术后1 h、24 h、1周、2周、3周、4周血清ET-1浓度降低(P <0. 05或P <0. 01)。与模型组和缬沙坦组同时间比较
术后4周理气化痰活血方组血清NO浓度升高
vWF浓度降低(P <0. 05或P <0. 01)。术后2周、3周理气化痰活血方组心肌组织fgl 2 mRNA表达显著低于模型组(P <0. 01)。结论理气化痰活血方可能通过降低冠状动脉微循环障碍大鼠血清ET-1、vWF浓度及心肌组织fgl 2 mRNA表达
升高血清NO浓度
从而起到保护血管内皮功能的作用。
Objective To explore the possible mechanism of action of Liqi Huatan Huoxue Formula( 理气化痰活血方) in improving coronary microcirculation disturbance. Methods A total of 245 healthy male SD rats were randomly divided into a Liqi Huatan Huoxue Formula group
a valsartan group and a model group
with 80 rats in each group. In addition
a blank group was set with 5 rats. Except for the blank group
the other 3 groups were established a model of coronary microcirculation disorder by injecting sodium laurate into the left ventricle. The Liqi Huatan Huoxue Formula group and the valsartan group were given Liqi Huatan Huoxue Formula( concentration 2. 25 g/ml)and valsartan suspension( concentration 8. 89 mg/ml) 1 ml/100 g 1 day before operation and 4 weeks after operation.The model group and the blank group were given 1 ml/100 g of distilled water for gavage
once a day. During the experiment
the deaths of the rats in each group were observed. Five rats were randomly sacrificed at the time points of1 h
24 h
1 w
2 w
3 w and 4 w after the operation in the Liqi Huatan Huoxue Formula group
the valsartan group and the model group. The rats were sacrificed at 4 w in the blank group. The concentrations of serum endothelin-1( ET-1)
nitric oxide( NO)
von Willebrand factor( v WF) and myocardial tissue fibrin( fgl 2) mRNA were detected.Results There were 44 deaths
40 deaths
and 42 deaths respectively in the model group
Liqi Huatan Huoxue Formula group and the valsartan group. There was no statistically significant difference in the intraoperative and postoperative mortality among the 3 groups( P > 0. 05). At 4 w after operation
the concentration of serum ET-1 in the model group was higher than that in the blank group
and the concentration of vWF was decreased( P < 0. 01). There was no significant difference in serum NO concentration and fgl 2 mRNA expression between the 2 groups( P >0. 05). At the same time
compared with the model group
the serum ET-1 concentrations in the Liqi Huatan Huoxue Formula group and the valsartan group were decreased at 1 h
24 h
1 w
2 w
3 w
4 w( P < 0. 05 or P < 0. 01).Compared with the model group and the valsartan group
the serum NO concentration increased and the vWF concentration decreased( P < 0. 05 or P < 0. 01). The expression of fgl 2 mRNA in myocardial tissue at 2 w
3 w in the Liqi Huatan Huoxue Formula group was significantly lower than that of the model group( P < 0. 01). Conclusion Liqi Huatan Huoxue Formula may protect vascular endothelial function by reducing the concentration of ET-1 and vWF in serum and the expression of fgl 2 in myocardial tissue and increasing the concentration of NO in serum of rats with coronary microcirculation disturbance.
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