Protective effect and mechanism of ginsenoside Rg1 on H2O2 induced hippocampal neurons aging due to down-regulate NOX2 mediated NLRP1 inflammasome activation in vitro  

作　　者：Tan-zhen XU Ya-li CHEN Xiao-yan SHEN Ling-Ling SUN Bi-qiong ZHANG Da-ke HUANG Wei-zu LI 

机构地区：[1]Department of Pharmacology [2] Key Laboratory of Anti-inflammatory andlmmunopharmacology, Ministry of Education [2]Synthetic Laboratory of Basic Medicine College, Anhui Medical University, Hefei 230032, China

出　　处：《中国药理学与毒理学杂志》2018年第4期321-321,共1页Chinese Journal of Pharmacology and Toxicology

基　　金：supported by National Natural Science Foundation of China(81671384;81371329)

摘　　要：OBJECTIVE To explore the protective effects and mechanisms of Ginsenoside Rg1(Rg1) on H_2O_2-induced hippocampal neurons aging in vitro.METHODS The primary culture hippo.campal neurons(7 d) were randomly placed into six groups:normal control group,H_2O_2(200 μM) treat.ment group,and H_2O_2+Rg1(1,5 and 10μM) groups.The neurons were with Rg1(1,5 and 10 μmol·L^(-1))for 6 h.H_2O_2(200 μmol · L-1) was added to the medium and incubate for 18 h.The Dihydroethidium(DHE) staining was performed for ROS production assessment.The LDH release and Hoechst 33258 were performed to examine the neuronal damage and apoptosis.The immunoblot was used to deter.mine the expression of β-Gal,NOX2,p22 phox,p47 phox,NLRP-1,ASC and Caspase-1 in hippocampal neurons.The ELISA was performed to detect the levels of IL-1β and IL-18 released in the supernatant in hippocampal neurons.RESULTS Rg1(5 and 10 μmol·L^(-1)) significantly reduced the ROS production,attenuated H_2O_2-induced neuronal damage and apoptosis(P<0.05,P<0.01).The immunoblot results showed that Rg1(5 and 10 μmol·L^(-1)) treatment significantly decreased the expression of β-Gal,NOX2,p22 phox,p47 phox,NLRP-1,ASC and Caspase-1 in hippocampal neurons(P<0.05,P<0.01).Additionally,Rg1(5 and 10 μmol·L^(-1)) treatment significantly decreased IL-1β and IL-18 release in the supernatant.CONCLUSION The protective effect of Rg1 in H_2O_2-induced hippocampal neurons aging may be due to inhibit NOX2-NLRP1 activation.OBJECTIVE To explore the protective effects and mechanisms of Ginsenoside Rg1（Rg1） on H2O2-induced hippocampal neurons aging in vitro.METHODS The primary culture hippo.campal neurons（7 d） were randomly placed into six groups：normal control group,H2O2（200 μM） treat.ment group,and H2O2＋Rg1（1,5 and 10μM） groups.The neurons were with Rg1（1,5 and 10 μmol·L（-1））for 6 h.H2O2（200 μmol · L-1） was added to the medium and incubate for 18 h.The Dihydroethidium（DHE） staining was performed for ROS production assessment.The LDH release and Hoechst 33258 were performed to examine the neuronal damage and apoptosis.The immunoblot was used to deter.mine the expression of β-Gal,NOX2,p22 phox,p47 phox,NLRP-1,ASC and Caspase-1 in hippocampal neurons.The ELISA was performed to detect the levels of IL-1β and IL-18 released in the supernatant in hippocampal neurons.RESULTS Rg1（5 and 10 μmol·L（-1）） significantly reduced the ROS production,attenuated H2O2-induced neuronal damage and apoptosis（P〈0.05,P〈0.01）.The immunoblot results showed that Rg1（5 and 10 μmol·L（-1）） treatment significantly decreased the expression of β-Gal,NOX2,p22 phox,p47 phox,NLRP-1,ASC and Caspase-1 in hippocampal neurons（P〈0.05,P〈0.01）.Additionally,Rg1（5 and 10 μmol·L（-1）） treatment significantly decreased IL-1β and IL-18 release in the supernatant.CONCLUSION The protective effect of Rg1 in H2O2-induced hippocampal neurons aging may be due to inhibit NOX2-NLRP1 activation.

关 键 词：人参皂甙 海马神经体 治疗方法 临床分析 

分 类 号：R285.5[医药卫生—中药学]