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1. 湖南中医药大学针灸推拿学院
2. 厦门大学化学化工学院
3. 厦门理工学院体育系
纸质出版日期:2018
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唐雅妮, 谭成富, 刘薇薇, 等. 基于核磁共振氢谱技术研究电针“内关”穴对心肌缺血再灌注损伤大鼠血清及心肌组织代谢物的影响[J]. 针刺研究, 2018,43(3):152-162.
TANG Ya-ni, TAN Cheng-fu, LIU Wei-wei, et al. Effect of Electroacupuncture at “Neiguan” (PC 6)on Serum and Myocardial Metabolites in Rats with Myocardial Ischemia Reperfusion Injury Based on Nuclear Magnetic Resonance Spectroscopy[J]. Acupuncture research, 2018, 43(3): 152-162.
唐雅妮, 谭成富, 刘薇薇, 等. 基于核磁共振氢谱技术研究电针“内关”穴对心肌缺血再灌注损伤大鼠血清及心肌组织代谢物的影响[J]. 针刺研究, 2018,43(3):152-162. DOI: 10.13702/j.1000-0607.170436.
TANG Ya-ni, TAN Cheng-fu, LIU Wei-wei, et al. Effect of Electroacupuncture at “Neiguan” (PC 6)on Serum and Myocardial Metabolites in Rats with Myocardial Ischemia Reperfusion Injury Based on Nuclear Magnetic Resonance Spectroscopy[J]. Acupuncture research, 2018, 43(3): 152-162. DOI: 10.13702/j.1000-0607.170436.
目的:基于核磁共振氢谱(1 H NMR)研究电针"内关"穴对心肌缺血再灌注损伤(MIRI)大鼠血清和心肌组织代谢物的影响
探讨电针"内关"穴对MIRI大鼠代谢模式的影响。方法:30只SD雄性大鼠随机分为对照组、模型组、电针组。对照组:不予电针
仅用鼠板束缚大鼠
每次20min
每日1次
持续7d;模型组予心肌缺血再灌注造模:至第7天后结扎冠状动脉左前降支40 min后恢复血流60 min;电针组(频率10Hz/50Hz
脉冲宽度0.5ms
强度1mA):每日电针双侧"内关"穴1次
时间20min
持续7d
于第7天电针后造模。造模结束后
收集3组大鼠的血清和心肌组织。利用1 H NMR进行代谢物检测并利用多元统计方法主成分分析(PCA)、正交偏最小二乘分析(OPLS-DA)进行模式识别。结果:与对照组相比
模型组大鼠血清的亮氨酸、异亮氨酸、缬氨酸、3-羟基丁酸、乳酸、丙氨酸、赖氨酸、醋酸盐、N-乙酰糖蛋白、丙酮、乙酰乙酸、琥珀酸、谷氨酰胺、多不饱和脂肪酸、肌酸、甘油磷酸胆碱、甘氨酸均浓度下降
低密度脂蛋白/极低密度脂蛋白、葡萄糖浓度上升;其中除丙酮、乙酰乙酸和多不饱和脂肪酸外
低密度脂蛋白/极低密度脂蛋白在电针后下降到接近对照组水平
其它代谢物浓度均在电针后上升到接近对照组水平
电针组大鼠血清的代谢模式更接近对照组。与对照组相比
模型组大鼠心肌组织的乳酸、丙氨酸、赖氨酸、谷氨酸、谷氨酰胺、天冬氨酸、甘油磷酸胆碱、肌酸、牛磺酸、甘氨酸、苏氨酸、腺苷一磷酸、烟酰胺腺嘌呤二核苷酸浓度下降
葡萄糖浓度明显上升;其中肌酸、甘油磷酸胆碱、烟酰胺腺嘌呤二核苷酸浓度在电针后上升
葡萄糖浓度在电针后下降;此外
电针组大鼠心肌组织苏氨酸、腺苷一磷酸浓度较模型组进一步下降;电针组大鼠心肌的代谢模式虽然有向对照组偏移的趋势
但与对照组差异还是较大。结论:电针"内关"穴可调节MIRI大鼠糖代谢、脂肪酸代谢、氨基酸代谢及能量代谢
对心肌具有一定的保护作用
但其具体的代谢通路及机制需要进一步研究。
Objective We have repeatedly demonstrated that electroacupuncture(EA)of"Neiguan"(PC 6)can improve myocardial ischemia in rats.The present study was designed to investigate the metabolomic profile of peripheral blood serum and myocardium involving EA-induced improvement of myocardial ischemia-reperfusion injury(MIRI)in rats by using nuclear magnetic resonance spectroscopy.Methods Thirty male SD rats were equally randomized into blank control
model and EA groups.Rats of the control group were only banded for 20 min
once a day for 7 days.The MIRI model was established by occlusion of the anterior descending branch of the left coronary artery for 40 min
followed by reperfusion for 60 min
and rats of the model group were banded as those in the control group.EA(10 Hz/50 Hz
1 mA)was applied to bilateral PC 6 for 20 min
once daily for 7 days.The blood samples and left ventricular myocardial tissues were collected for assaying the profiles of differential metabolites using 1 H nuclear magnetic resonance(1 H NMR)spectroscopy and multivariate statistical analysis such as the principal components analysis(PCA)
partial least squares-discriminant analysis(PLS-DA)and orthogonal PLS-DA(O-PLS-DA)with SIMCA-P software 12.0.Results A total of 19 differential metabolites(17 down-regulated
2 up-regulated)in the serum and 14 differential metabolites(13 down-regulated and 1 up-regulated)in the ischemic left myocardium were identified after MIRI.Of the 19 serum differential metabolites
amino acids(leucine
isoleucine
valine
alanine
lysine
glycine
glutamine)
3-hydroxy butyric acid(3-HB)
lactic acid
acetate
N-acetyl glycoprotein(NAc)
acetone
acetoacetate
succinate
polyunsaturated fatty acids(PUFA)
creatine
glycerophosphocholine(GPC)were down-regulated;while low density lipoprotein(LDL)
LDL/very low density lipoprotein(LDL/VLDL)and glucose obviously up-regulated.Of the 14 myocardial differential metabolites
amino acids(alanine
lysine
glutamate
glutamine
aspartate
taurine
glycine
threonine)
GPC
creatine
lactic acid
adenosine monophosphate(AMP)
nicotinamide adenine dinucleotide(NAD+)were significantly decreased
and glucose was up-regulated.Following EA treatment
most of the decreased serum differential metabolites except acetone
acetoacetate and PUFA
and the increased serum LDL
LDL/VLDL and glucose recovered
basically close to the control level;and the decreased myocardial creatine
GPC and NAD+ were also apparently up-regulated and the increased myocardial glucose was down-regulated.But
myocardial threonine and AMP still presented a decreasing state.Although the pattern of myocardial differential metabolites of the EA group had a trend to be close to the control group
the significant difference still existed
while the metabolic pattern of serum metabolites in the EA group was close to that of the control group.Conclusion EA stimulation of PC 6 can regulate serum or/and myocardial metabolites as amino acids
carbohydrates
lipids
etc.in MIRI rats
of which both serum and myocardial creatine
GPC and glucose may be jointly confer a favorable potential for EA-induced improvement of MIRI.
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