摘要
目的:探讨川芎嗪结构修饰产物Liguzinediol对阿霉素诱导的慢性心力衰竭(CHF)模型大鼠血流动力学的影响。方法:取SD大鼠腹腔注射2 mg/kg阿霉素复制CHF模型,将造模成功的大鼠采用随机数字表法分为生理盐水组、阳性对照组(去乙酰毛花苷注射液,0.022 5 mg/kg)和Liguzinediol低、中、高剂量组(5、10、20 mg/kg),每组8只,另取8只正常大鼠作为空白对照组(生理盐水)。各组大鼠单次静脉注射相应药物后,通过多道生理记录仪左心室插管记录左心室收缩内压(LVSP)、左心室最大压力上升/下降速度(±dp/dt_(max))、收缩压(SP)、舒张压(DP)、心率(HR)等血流动力学指标,记录时间分别为给药后1、5、10、20、40、60、90、120 min。结果:与空白对照组比较,生理盐水组大鼠的LVSP、+dp/dt_(max)、│-dp/dt_(max)│、SP、HR和给药后120 min的DP均明显降低(P<0.05)。与生理盐水组比较,Liguzinediol低剂量组大鼠给药后5~60 min的LVSP、40~90 min的+dp/dt_(max)、10~40 min的SP均明显升高(P<0.05或P<0.01);Liguzinediol中剂量组大鼠给药后5~90 min的LVSP、10~60 min的SP、10~60 min(20 min除外)的DP均明显升高(P<0.05或P<0.01);Liguzinediol高剂量组大鼠给药后1~120 min的LVSP、5~90 min的+dp/dt_(max)、5~60 min的│-dp/dt_(max)│和SP、40~60 min的DP均明显升高(P<0.05或P<0.01)。结论:单次静脉注射Liguzinediol能显著增强CHF模型大鼠的心肌收缩功能,进而控制或缓解其CHF。
OBJECTIVE:To investigate the effects of ligustrazine structural modification product Liguzinediol on hemodynamics in chronic heart failure(CHF)model rats induced by adriamycin.METHODS:SD rats were given intraperitoneal injection of adriamycin(2 mg/kg)to induce CHF model.Model rats were randomly divided into normal saline group,positive control group(Deacetyl tricyanidin injection,0.022 5 mg/kg)and Liguzinediol low-dose,medium-dose and high-dose groups(5,10,20 mg/kg),with 8 rats in each group.Other 8 normal rats were selected as blank control group(normal saline).Each group was given relevant medicine intravenously.The left ventricular systolic pressure(LVSP),maximal rate of rise or drop of left ventricular(±dp/dtmax),systolic pressure(SP),diastolic pressure(DP),heart rate(HR)and other hemodynamic indexes were recorded by multichannel physiological recorder at 1,5,10,20,40,60,90,120 min after medication.RESULTS:Compared with blank control group,LVSP,+dp/dtmax,│-dp/dtmax│,SP,HR and DP at 120 min after medication of normal saline group were decreased significantly(P<0.05).Compared with normal saline group,LVSP at 5-60 min after medication,+dp/dtmax at 40-90 min after medication,SP at 10-40 min after medication were increased significantly in Liguzinediol low-dose group(P<0.05 or P<0.01).LVSP at 5-90 min after medication,SP at 10-60 min after medication,DP at 10-60 min(except for 20 min)after medication were increased significantly in Liguzinediol medium-dose group(P<0.05 or P<0.01).LVSP at 1-120 min after medication,+dp/dtmax at 5-90 min after medication,│-dp/dtmax│,and SP at 5-60 min after medication,DP at 40-60 min after medication were increased significantly in Liguzinediol high-dose group(P<0.05 or P<0.01).CONCLUSIONS:Single intravenous injection of Liguzinediol can significantly enhance ventricular systolic function of CHF model rats so as to control or relieve CHF.
作者
李育
朱青
郭瑶
郭瑞
赵凤鸣
李伟
卞慧敏
LI Yu;ZHU Qing;GUO Yao;GUO Rui;ZHAO Fengming;LI Wei;BIAN Huimin(School of Medicine and Life Science,Nanjing University of TCM,Nanjing 210023,China;School of Pharmacy,Nanjing University of TCM,Nanjing 210023,China;Jiangsu Key Lab for Pharmacology and Safety Evaluation of Chinese Materia Medica,Nanjing 210023,China)
出处
《中国药房》
CAS
北大核心
2019年第1期15-20,共6页
China Pharmacy
基金
国家自然科学基金资助项目(No.81500310
81573304
8157130318)
江苏省中药资源产业化过程协调创新中心重点项目(No.ZDXM-2-1)
江苏高校"青蓝工程"资助项目