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1. 湖北中医药大学针灸骨伤学院/针灸治未病湖北省协同创新中心
2. 湖北省中医院针灸科
纸质出版日期:2018
移动端阅览
陈茜, 王华, 梁凤霞, 等. “标本配穴”电针对慢性心肌缺血大鼠心电保护效应及代谢组学的影响[J]. 针刺研究, 2018,43(11):698-704.
CHEN Qian, WANG Hua, LIANG Feng-xia, et al. Protective Effect and Metabonomics Research of“Biao-Ben Acupoint Combination”Electroacupuncture in Chronic Myocardial Ischemia Model Rats[J]. Acupuncture research, 2018, 43(11): 698-704.
陈茜, 王华, 梁凤霞, 等. “标本配穴”电针对慢性心肌缺血大鼠心电保护效应及代谢组学的影响[J]. 针刺研究, 2018,43(11):698-704. DOI: 10.13702/j.1000-0607.170379.
CHEN Qian, WANG Hua, LIANG Feng-xia, et al. Protective Effect and Metabonomics Research of“Biao-Ben Acupoint Combination”Electroacupuncture in Chronic Myocardial Ischemia Model Rats[J]. Acupuncture research, 2018, 43(11): 698-704. DOI: 10.13702/j.1000-0607.170379.
目的:观察"标本配穴"电针对慢性心肌缺血大鼠心电图ST段振幅、心肌组织及血清标志代谢物的影响
探讨"标本配穴"电针对慢性心肌缺血大鼠心电活动的保护效应及可能调控的代谢途径。方法:将45只Wistar雄性大鼠随机分为空白组、模型组、电针组
每组15只。连续7d皮下注射盐酸异丙肾上腺素(5mg/kg)制备慢性心肌缺血大鼠模型。电针组大鼠自造模之日起予电针干预"内关""足三里""关元"
疏密波
频率2Hz/100Hz
电流强度1mA
每次10min
每日1次
连续21d。分别于造模前、造模后、干预后对大鼠进行心电图检测
HE染色法观察心肌组织结构变化
核磁共振质谱技术检测代谢物信息
利用偏最小二乘分析(PLS-DA)判别大鼠血清代谢组学的特点及其生物标记物。结果:在造模后
模型组、电针组大鼠心电图ST段振幅均高于正常组(P<0.01)
且电针组低于模型组(P<0.01);干预后电针组大鼠心电图ST段振幅较造模后降低(P<0.05)
明显低于模型组大鼠心电图ST段振幅(P<0.01)。与空白组比较
模型组大鼠心肌组织结构破坏明显
出现坏死、水肿等变化;与模型组比较
电针组心肌组织结构损伤程度明显减轻。PLS-DA得分图横坐标上空白组和电针组轮廓接近
葡萄糖、乳酸、肌酸、乙酸、3-羟基丁酸是潜在的代谢差异生物学标志物质(VIP>1)。结论:"标本配穴"电针干预可以预防或降低缺血对大鼠心肌造成的损伤
其可能主要通过糖、脂代谢及能量代谢来对心肌缺血大鼠进行调控。
Objective To observe the effect of electroacupuncture(EA)on ischemic electrocardiogram(ECG)
histopathological changes and serum metabolite profile in chronic myocardial ischemia(CMI)rats
so as to reveal its mechanisms underlying protecting ischemic myocardium.Methods A total of 45 male Wistar rats were randomly divided into normal control
CMI model and EA groups
with 15 rats being in each group.The rats in the control group received subcutaneous injection of 0.9%normal saline(5 mg·mg
(-1)
·d(-1)·d
(-1)
for 7 days)
and those in the model and EA groups received subcutaneous injection of isopropylarterenol hydrochloride(5 mg·mg(-1)
for 7 days)
and those in the model and EA groups received subcutaneous injection of isopropylarterenol hydrochloride(5 mg·mg
(-1)
·d(-1)·d
(-1)
for 7 days)to establish CMI model.EA(2 Hz/100 Hz
1 mA)was applied to bilateral"Zusanli"(ST 36)
"Guanyuan"(CV 4)and"Neiguan"(PC 6)for 10 min
once daily for 21 days.The ECG-ST segment of the standard limb lead II was used for evaluating the severity of myocardial ischemia
and the histopathological changes of myocardium were observed under microscope after H.E.staining.The profile of serum metabolites was analyzed by nuclear magnetic resonance mass spectrometry combined with principal component analysis(PCA)and partial least squares discriminant analysis(PLS-DA)in 21 rats(n=7 in each group).Results After modeling
the amplitude of ECG-ST was significantly increased in comparison with the normal control group(P
<
0.01)
suggesting a successful establishment of CMI model.H.E.stain showed an apparent injury of the myocardial tissue as interstitial edema
vasodilatation and hemorrhage
infiltration of inflammatory cells
unclear veins
and increased intercellular space
etc.with irregularly arranged myocardial cells being dissolved
ruptured and necrotic
and with obvious edema
blurred shape
uneven staining
karyopyknosis
and glass-like lesions.After EA intervention
the amplitude of ECG-ST in the EA group was evidently lower than that of the model group(P
<
0.01)
and the severity of the myocardial injury was relatively milder relevant to the model group
suggesting an alleviation of the injured myocardium.In the PLS-DA score plot
the normal control group and the EA group outline were close to each other
and Glucose
Lactate
Creatine
Acetate
3-Hydroybutyrate might be the potential metabolic differential biomarkers(VIP
>
1).The PLS-DA analysis revealed deviations in 51 differential biomarkers in serum
among which
Glucose
Lactate
Creatine
Acetate and 3-Hydroybutyrate may contribute to the effect of EA in improving CMI.Conclusion EA stimulation of acupoints can ameliorate ischemic myocardial injury in CMI rats
which may be related to its effect in regulating serum sugar
lipid metabolism and energy metabolism.
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