电针对帕金森病小鼠Nrf2/NLRP3/Caspase-1通路介导的细胞焦亡的影响OACSTPCD
Effect of electroacupuncture on Nrf2/NLRP3/Caspase-1 pathway mediated-pyroptosis in mice with Parkinson's disease
目的:观察电针对帕金森病(PD)小鼠黑质中核转录因子E2相关因子2(Nrf2)/NOD样受体家族蛋白3(NLRP3)/半胱氨酸蛋白酶-1(Caspase-1)通路的影响,探讨其神经保护机制.方法:将40只C57BL/6雄性小鼠随机分为正常组、模型组、假电针组、电针组,每组10只.采用鱼藤酮灌胃4周建立PD小鼠模型.电针组于"风府"和双侧"太冲""足三里"给予电针刺激,每日1次,连续2周;假电针组于同样穴位浅刺至皮下,连接电针仪后不通电,其余操作均同电针组.采用敞箱实验观察各组小鼠的行为学变化,酶联免疫吸附法检测小鼠血清中白细胞介素(IL)-1β和IL-18含量,免疫组织化学法检测小鼠黑质中酪氨酸羟化酶(TH)阳性表达,实时荧光定量PCR法检测小鼠黑质中Nrf2、NLRP3、Caspase-1、消皮素D(GSDMD)、IL-1β和IL-18 mRNA表达水平,Western blot法检测小鼠黑质中Nrf2、NLRP3、Caspase-1 和GSDMD蛋白表达水平.结果:与正常组比较,模型组小鼠行为学评分升高(P<0.01),自主运动的总时间缩短、总路程减少、平均速度降低(P<0.01),血清IL-1β和IL-18含量增加(P<0.01),黑质中TH阳性表达减少(P<0.01),Nrf2 mRNA和蛋白表达降低(P<0.01),NLRP3、Caspase-1、GSDMD mRNA和蛋白表达水平及IL-1β、IL-18 mRNA表达水平均升高(P<0.01).与模型组、假电针组比较,电针组小鼠行为学评分降低(P<0.01),自主运动的总时间延长、总路程增加、平均速度升高(P<0.01),血清IL-1β和IL-18 含量减少(P<0.01,P<0.05),黑质中TH阳性表达增加(P<0.01),Nrf2 mRNA和蛋白表达水平升高(P<0.01,P<0.05),NLRP3、Caspase-1、GSDMD mRNA和蛋白表达水平及IL-1β、IL-18 mRNA表达水平均降低(P<0.01).与模型组比较,假电针组小鼠上述各项指标差异均无统计学意义.结论:电针"风府""太冲"和"足三里"可改善PD小鼠运动障碍,减少黑质多巴胺神经元的丢失,抑制神经炎性反应,其作用机制可能与调控Nrf2/NLRP3/Caspase-1通路介导的细胞焦亡相关.
Objective To observe the effect of electroacupuncture(EA)on nuclear transcription factor E2 re-lated factor 2(Nrf2)/NOD-like receptor family pyrin domain-containing protein 3(NLRP3)/cysteine aspartic acid specific protease-1(Caspase-1)pathway in the substantia nigra(SN)of mice with Parkinson's disease(PD),so as to explore the neuroprotective mechanism of EA.Methods Forty C57BL/6 male mice were randomly divided into 4 groups,namely,control,PD model,EA and sham-EA groups,with 10 mice in each group.The PD mouse model was estab-lished by gavage of rotenone for 4 weeks.Mice in the EA group were given EA stimulation(1 mA,2 Hz)at"Fengfu"(GV36),bilateral"Taichong"(LR3)and"Zusanli"(ST36)for 30 min,once daily for 2 consecutive weeks.And mice in the sham-EA group were given acupuncture at the subcutaneous areas of the same acupoints without EA stimulation.The open-field test was used for assessment of mouse behavior.The levels of interleukin-1β(IL-1β)and interleukin-18(IL-18)in the serum were detected by enzyme-linked immunosorbent assay.The positive expression of tyrosine hy-droxylase(TH)in SN was determined by immunohistochemistry.The mRNA expression levels of Nrf2,NLRP3,Caspase-1,gasdermin D(GSDMD),IL-1β,IL-18 and the protein expression levels of Nrf2,NLRP3,Caspase-1 and GSDMD in the SN were detected by quantitative real-time PCR and Western blot,separately.Results After modeling,compared with the control group,the behavioral score was increased(P<0.01),the total exercise time,the total dis-tance and the average speed were decreased(P<0.01),and the positive expression of TH and the mRNA and protein expression levels of Nrf2 in the SN were decreased(P<0.01),while the contents of IL-1β and IL-18 in serum,the mRNA and protein expression levels of NLRP3,Caspase-1 and GSDMD and the mRNA expression levels of IL-1β and IL-18 in the SN were up-regulated(P<0.01)in the PD model group.Following EA intervention,the behavioral score was decreased(P<0.01),the total exercise time,total distance and average speed were increased(P<0.01),the posi-tive expression of TH and the mRNA and protein expressions of Nrf2 in SN were up-regulated(P<0.01,P<0.05),while the contents of IL-1β and IL-18 in serum,the mRNA and protein expression levels of NLRP3,Caspase-1 and GSDMD as well as the mRNA expression levels of IL-1β and IL-18 in the SN were down-regulated(P<0.01,P<0.05)in the EA group relative to the PD model and sham-EA groups.There were no significant differences in the above indicators be-tween the PD model and sham-EA groups.Conclusion EA stimulation of GV36,LR3 and ST36 can improve motor deficits,reduce the loss of dopamine neurons in the SN,and inhibit neuroinflammatory responses in mice with PD,which may be related to its effects in regulating the Nrf2/NLRP3/Caspase-1 pathway mediated pyroptosis.
张小蕾;胡梦妮;荣臻;李亚楠;汪瑶;马骏
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,武汉 430060
帕金森病电针细胞焦亡神经炎性反应核转录因子E2相关因子2NOD样受体家族蛋白3半胱氨酸蛋白酶-1
Parkinson's diseaseElectroacupuncturePyroptosisNeuroinflammationNuclear transcription factor E2 related factor 2NOD-like receptor family pyrin domain-containing protein 3Cysteine aspartic acid specific protease-1
《针刺研究》 2024 (001)
15-22 / 8
国家自然科学基金项目(No.81473788、81403456)
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