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1. 山东中医药大学针灸推拿学院
2. 山东中医药大学附属医院治未病中心
3. 山东中医药大学附属医院针灸科
纸质出版日期:2019
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李洋, 于慧娟, 张昌云, 等. 电针“夹脊”穴预处理对心肌缺血再灌注损伤大鼠细胞色素P450信号通路蛋白表达的影响[J]. 针刺研究, 2019,44(4):248-252.
LI Yang, YU Hui-juan, ZHANG Chang-yun, et al. Effect of “Jiaji” (EX-B2)-electroacupuncture preconditioning on expression of myocardial cytochrome P450 enzyme in rats with acute myocardial ischemia-reperfusion injury[J]. Acupuncture research, 2019, 44(4): 248-252.
李洋, 于慧娟, 张昌云, 等. 电针“夹脊”穴预处理对心肌缺血再灌注损伤大鼠细胞色素P450信号通路蛋白表达的影响[J]. 针刺研究, 2019,44(4):248-252. DOI: 10.13702/j.1000-0607.180086.
LI Yang, YU Hui-juan, ZHANG Chang-yun, et al. Effect of “Jiaji” (EX-B2)-electroacupuncture preconditioning on expression of myocardial cytochrome P450 enzyme in rats with acute myocardial ischemia-reperfusion injury[J]. Acupuncture research, 2019, 44(4): 248-252. DOI: 10.13702/j.1000-0607.180086.
目的:观察电针"夹脊"穴预处理对心肌缺血再灌注损伤(MIRI)大鼠的心肌保护作用及对细胞色素P450(CYP450)信号通路蛋白表达的影响。方法:Wistar大鼠随机分为假手术组、模型组、夹脊组、内关组、阳陵泉组、曲池组
每组10只。采用左冠状动脉结扎法复制MIRI大鼠模型。各电针预处理组电针相应穴位
每次30min
每日1次
连续针刺7d。HE染色法观察各组大鼠心肌组织病理形态
透射电镜下观察心肌细胞超微结构
Western blot法检测心肌CYP450相关分子CYP1A1、CYP2B2、CYP2C11、CYP4A2蛋白的表达水平。结果:模型组缺血区心肌纤维肿胀、紊乱
可见局灶性坏死区
心肌间质有大量炎性细胞浸润。夹脊组和内关组均可见心肌纤维轻度肿胀
散见部分坏死
间质出血
与模型组比较
炎性细胞浸润明显减轻。透射电镜下可见模型组肌原纤维排列紊乱
线粒体结构模糊
肿胀、空泡化。夹脊组和内关组心肌纤维结构较清晰
线粒体数量和结构无明显异常。与假手术组比较
模型组心肌CYP1A1、CYP2B2蛋白表达水平均显著增高(P<0.05)。与模型组比较
夹脊组、内关组、阳陵泉组心肌CYP1A1、CYP4A2蛋白表达水平均显著降低(P<0.01)
夹脊组和内关组心肌CYP2B2、CYP2C11蛋白表达水平显著增高(P<0.01)。与夹脊组比较
曲池组心肌CYP1A1、CYP4A2蛋白表达水平显著升高(P<0.05)
CYP2B2、CYP2C11蛋白表达水平显著降低(P<0.05)。结论:电针"夹脊"穴和"内关"穴预处理均能够上调CYP450表氧化酶蛋白表达水平
下调CYP450ω-羟化酶蛋白表达水平
起到心肌保护作用。
Objective To investigate the effect of"Jiaji"(EX-B2)-electroacupuncture(EA)preconditioning on structural changes of myocardium and expression of cytochrome P450(CYP450)enzymes in acute myocardial ischemia-reperfusion injury(MIRI)rats.Methods Sixty male Wistar rats were randomly divided into sham operation
model
EX-B2
Neiguan(PC6)
Yanglingquan(GB34)and Quchi(LI11)groups(n=10 in each group).The MIRI model was established by occlusion of the descending anterior branch of the left coronary artery for 30 min
followed by reperfusion for 30 min.EA preconditioning(2 Hz/100 Hz
1 mA)was respectively applied to EX-B2
PC6
GB34
and LI11 for 30 min
once daily for 7 days.Morphological changes of myocardium were observed by H.E.staining.The ultrastructure of myocardial cells was observed by transmission electron microscope(TEM).The protein expression levels of myocardial CYP450(CYP1 A1
CYP2 B2
CYP2 C11 and CYP4 A2)were detected by Western blot.Results In MIRI rats
myocardial pathological changes as swollen
disorganized arrangement
and partially ruptured myocardial fibers with unclear limit and necrosis and infiltration of lots of inflammatory cells under microscope
and focal myofilament degeneration
dissolution and necrosis with interstitial edema
vague mitochondria with swelling and vacuolation
ruptured and disorganized arrangement of crests under TEM were found in the ischemic area
which was obviously milder in rats of both EX-B2 and PC6 groups.After modeling
the expression of myocardial CYP1 A1 and CYP2 B2 protein were significantly up-regulated in the model group relevant to the sham operation group(P<0.05).In EA preconditioning groups
the expression levels of CYP1 A1 and CYP4 A2 proteins in the EX-B2
PC6 and GB34 groups were obviously down-regulated(P<0.01)
and those of CYP2 B2 and CYP2 C11 proteins in both EX-B2 and PC6 groups were markedly up-regulated relevant to the model group(P<0.01).Compared with the EX-B2 group
the expression levels of CYP1 A1
CYP4 A2 proteins in the LI11 group were significantly up-regulated(P < 0.05)
and CYP2 B2
CYP2 C11 proteins were significantly down-regulated(P<0.05).No significant differences were found between the model and sham operation groups in the expression levels of myocardial CYP2 C11 and CYP4 A2 proteins
between the LI11 and model groups in the expression of CYP1 A1
CYP2 B2
CYP2 C11 and CYP4 A2
between the GB34 and model groups in the expression of CYP2 B2
CYP2 C11(all P>0.05).Conclusion EA preconditioning at EX-B2 and PC6 can suppress MIRI induced up-regulation of myocardial CYP450ω-hydroxylase CYP1 A1 and CYP4 A2 expression and further up-regulate the expression of myocardial epoxygenase CYP2 B2 and CYP2 C11 proteins in acute MIRI rats
thus playing a role in myocardial protection.
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