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重庆医科大学中医药学院
纸质出版日期:2018
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邱丽, 唐成林, 黄思琴, 等. 电针对急性痛风性关节炎大鼠滑膜巨噬细胞M 1/M 2极化分型的影响[J]. 针刺研究, 2018,43(12):767-772.
QIU Li, TANG Cheng-lin, HUANG Si-qin, et al. Effect of Electroacupuncture on Synovial M 1/M 2 Macrophage Polarization in Rats with Acute Gouty Arthritis[J]. Acupuncture research, 2018, 43(12): 767-772.
邱丽, 唐成林, 黄思琴, 等. 电针对急性痛风性关节炎大鼠滑膜巨噬细胞M 1/M 2极化分型的影响[J]. 针刺研究, 2018,43(12):767-772. DOI: 10.13702/j.1000-0607.180498.
QIU Li, TANG Cheng-lin, HUANG Si-qin, et al. Effect of Electroacupuncture on Synovial M 1/M 2 Macrophage Polarization in Rats with Acute Gouty Arthritis[J]. Acupuncture research, 2018, 43(12): 767-772. DOI: 10.13702/j.1000-0607.180498.
目的:观察电针对激活腺苷酸活化蛋白激酶(AMPK)以及对巨噬细胞从M 1促炎表型转换为M2抗炎表型的影响
探讨电针治疗急性痛风性关节炎的机制。方法:Wistar大鼠随机分为空白组、模型组、秋水仙碱组、电针组
每组15只。大鼠左膝关节注射0.2mL尿酸钠晶体(MSU)混悬液制备急性痛风性关节炎模型。秋水仙碱组予秋水仙碱0.3 mg·kg-1·d-1灌胃;电针组电针左侧"足三里""三阴交"
刺激10min
每日1次
连续7d。HE染色观察大鼠膝关节滑膜组织的病理形态;Western blot法检测大鼠膝关节滑膜组织磷酸化AMPK(p-AMPK)α蛋白表达水平;实时荧光定量PCR法检测大鼠膝关节滑膜组织中精氨酸酶-1(Arginase-1)、一氧化氮合酶(NOS)2、NOD样受体蛋白(NLRP)3、白细胞介素-1β(IL-1β)mRNA相对表达量。结果:与空白组比较
模型组滑膜组织炎性浸润程度重
炎性细胞增多
p-AMPKα表达水平显著降低(P<0.01)
Arginase-1、NOS 2、IL-1β和NLRP 3mRNA表达水平显著升高(P<0.01)。与模型组比较
秋水仙碱组滑膜组织炎性浸润程度较轻
炎性细胞较少
电针组次之;秋水仙碱组和电针组NOS 2、IL-1β和NLRP 3mRNA表达水平显著降低(P<0.05
P<0.01);秋水仙碱组和电针组p-AMPKα蛋白和Arginase-1mRNA表达水平显著升高(P<0.01
P<0.05)。与秋水仙碱组比较
电针组Arginase-1mRNA表达水平显著减低(P<0.05)。结论:电针治疗急性痛风性关节炎可能与激活AMPK来上调Arginase-1的表达
下调NOS 2、IL-1β、NLRP 3的表达
促进巨噬细胞从M 1促炎表型转换为M 2抗炎表型
进而抑制MSU晶体诱导的炎性反应有关。
Objective To explore the effect of electroacupuncture(EA)on the expression of synovial AMP-activated protein kinase(AMPK)proteinα
arginase-1 mRNA
nitric oxide synthase 2(NOS 2)mRNA
NOD-like receptor protein 3(NLRP 3)mRNA
and interleukin-1β(IL-1β)mRNA in acute gouty arthritis(AGA)rats
so as to explore its mechanisms underlying improvement of AGA via M 1/M 2 macrophage polarization.Methods Male Wistar rats were randomly divided into normal control
model
medication(colchicine)and EA groups(n=15 rats in each group).The AGA model was established by injection of sodium urate crystal(MSU)suspension(0.2 mL)into the articular cavity of the left knee.The rats of the normal control group received articular injection of normal saline(0.2 mL)of the left knee
and those of the medication group were treated by gavage of the colchicine(0.3 mg·kg-1·d-1)once daily for 7 days.EA(2 Hz/10 Hz
1.0 mA)was applied to"Zusanli"(ST 36)and"Sanyinjiao"(SP 6)of the left hind limb for 10 min
once daily for 7 days.The inflammatory conditions of the synovial membrane tissue of the left knee joint were observed by H.E.staining.The expression levels of phosphorylated AMPKα(p-AMPKα)protein
and arginase-1(a maker of M 2 macrophages)mRNA
NOS 2(a maker of M 1 macrophages)mRNA
NLRP 3 mRNA
and IL-1βmRNA in the knee joint synovial tissue were detected by Western blot and quantitative real-time PCR
respectively.Results Compared with the normal group
the inflammatory cell infiltration of the synovial tissue was more severe
the expression of p-AMPKαprotein was significantly decreased(P<0.01)
and the expression levels of arginase-1
NOS 2
IL-1βand NLRP 3 mRNAs were considerably increased in the model group(P<0.01).The expression levels of p-AMPKαprotein and arginase-1 mRNA were significantly up-regulated
and those of NOS 2
IL-1βand NLRP 3 mRNAs obviously down-regulated in both EA and medication groups relevant to the model group(P<0.01
P<0.05)
suggesting an increase of M 2 macrophage and a decrease of M 1 macrophage activity after EA.No significant differences were found between the EA and medication groups in up-regulating p-AMPKαexpression and in down-regulating NOS 2
IL-1βand NLRP 3 mRNA expression(P>0.05)
except higher up-regulation of arginase-1 mRNA in the medication group(P<0.05).Conclusion EA intervention can up-regulate the expression of arginase-1 mRNA and p-AMPKαprotein
and down-regulate the expression of NOS 2
IL-1βand NLRP 3 mRNAs in synovial tissues in AGA rats
which may contribute to its anti-inflammatory effect by promoting conversion of macrophages from M 1 pro-inflammatory phenotype to M 2 anti-inflammatory phenotype.
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