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1. 辽宁中医药大学
2. 辽宁省肿瘤医院
3. 广东省佛山市顺德区伍仲珮纪念医院
纸质出版日期:2018
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董佳梓, 魏云涛, 许环宇, 等. 电针“足三里”对慢性疲劳综合征大鼠骨骼肌腺苷酸活化蛋白激酶/过氧化物酶体增殖物活化受体γ共激活因子α信号通路基因表达的影响[J]. 针刺研究, 2018,43(6):335-340.
DONG Jia-zi, WEI Yun-tao, XU Huan-yu, et al. Electroacupuncture of “Zusanli”(ST 36) Raises Muscular Force by Adjusting AMPK/PGC-1α Signaling in Rats with Chronic Fatigue Syndrome[J]. Acupuncture research, 2018, 43(6): 335-340.
董佳梓, 魏云涛, 许环宇, 等. 电针“足三里”对慢性疲劳综合征大鼠骨骼肌腺苷酸活化蛋白激酶/过氧化物酶体增殖物活化受体γ共激活因子α信号通路基因表达的影响[J]. 针刺研究, 2018,43(6):335-340. DOI: 10.13702/j.1000-0607.171010.
DONG Jia-zi, WEI Yun-tao, XU Huan-yu, et al. Electroacupuncture of “Zusanli”(ST 36) Raises Muscular Force by Adjusting AMPK/PGC-1α Signaling in Rats with Chronic Fatigue Syndrome[J]. Acupuncture research, 2018, 43(6): 335-340. DOI: 10.13702/j.1000-0607.171010.
目的:基于腺苷酸活化蛋白激酶(AMPK)/过氧化物酶体增殖物活化受体γ共激活因子α(PGC-1α)信号通路
观察针刺"足三里"对慢性疲劳综合征(CFS)大鼠骨骼肌细胞线粒体氧化应激的影响
阐释针刺"足三里"防治CFS的部分作用机制。方法:SD大鼠随机分为正常对照组、模型组、足三里组、非经非穴组
每组10只。采用多因素造模法复制CFS模型。足三里组电针双侧"足三里"
非经非穴组电针双侧非经非穴
每日1次
每次20min
持续10d。检测造模前后、治疗后大鼠抓力变化;Western blot法检测大鼠骨骼肌三磷酸腺苷(ATP)合酶、AMPK、磷酸化AMPK(p-AMPK)、沉默信息调节因子2相关酶Ⅰ(SIRT 1)以及PGC-1α蛋白的表达;荧光定量PCR技术检测大鼠骨骼肌ATP合酶、SIRT 1以及PGC-1αmRNA的表达。结果:造模后
模型组、足三里组、非经非穴组大鼠抓力较正常对照组明显下降(P<0.05)
治疗后足三里组大鼠抓力较模型组明显升高(P<0.05)。与正常对照组比较
模型组大鼠骨骼肌ATP合酶蛋白表达、ATP合酶mRNA表达明显下调(P<0.05
P<0.01)
p-AMPK/AMPK差异无统计学意义(P>0.05)
SIRT 1蛋白表达明显升高(P<0.01)
PGC-1α蛋白及mRNA的表达明显降低(P<0.01)。与模型组相比
足三里组大鼠骨骼肌ATP合酶mRNA表达明显上调(P<0.01)
p-AMPK/AMPK上调(P<0.05)
SIRT 1蛋白及mRNA、PGC-1α蛋白及mRNA的表达明显上调(P<0.01)。结论:针刺"足三里"可使CFS大鼠骨骼肌AMPK表达明显增加
提高SIRT 1的表达
进一步直接或间接激活PGC-1α
提高线粒体的ATP合成
改善机体线粒体氧化应激反应
维持机体能量代谢
从而起到对CFS的治疗作用。
Objective To observe the effect of electroacupuncture(EA)of"Zusanli"(ST 36)on mitochondrial oxidative stress of skeletal muscle in rats with chronic fatigue syndrome(CFS)based on adenosine 5′-monophosphate(AMP)-activated protein kinase(AMPK)/peroxlsome proliferator-activated receptor-γcoactivator-1α(PGC-1α )signaling
in order to reveal its mechanism underlying improvement of CFS.Methods Forty SD rats were randomly divided into normal control
CFS model
EA-Zusanli(ST 36)and EA-non-acupoint groups(n=10 rats in each group).The CFS model was established by forced exhausted load-bearing swimming(twice daily)
chronic constraint(1 h)and sleep deprivation(20 h/day)for 14 days.Following modeling
EA(2 Hz/100 Hz
2 V)was applied to bilateral Zusanli(ST 36)or non-acupoint(about 10-15 mm superior to the bilateral Iliac creast and about 20 mm lateral to the posterior median line)for 20 min
once a day for 10 days.The expression levels of ATP synthase
AMPK
phosphorylated(p)-AMPK
silent mating type information regulation 2 homolog-1(SIRT 1)and PGC-1α proteins
and ATP synthase
SIRT 1 and PGC-1α mRNAs of the quadriceps femoris muscle were detected by Western blot and fluorescence quantitative PCR
respectively.The rats' grabbing force was detected by using agrabbing-force detector.Results Compared with the normal group
the grabbing force
and the expression levels of ATP synthase and PGC-1α proteins and mRNAs were significantly decreased(P<0.05
P<0.01)
while the expression of SIRT 1 protein was significantly up-regulated(P<0.05)in the CFS model group.Following EA intervention
the grabbing force and the expression levels of ATP synthase mRNA
SIRT 1 and PGC-1α proteins and mRNAs
and p-AMPK/AMPK were significantly up-regulated in the EA-Zusanli(ST 36)group(P<0.05
P<0.01).Conclusion EA of ST 36 can raise the grabbing force of CFS rats
which may be related to its effects in up-regulating the expression of ATP synthase mRNA
SIRT 1 and PGC-1α proteins and mRNAs
and p-AMPK/AMPK to reduce mitochondrial oxidative stress reaction and in increasing ATP synthesis.
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