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[Protective effects of oxymatrine against H2O2-induced damage in L02 cells].
Han, Yan-Zhong; Zhou, Yong-Feng; Sang, Xiu-Xiu; Liu, Hui-Min; Cui, He-Rong; Meng, Ya-Kun; Li, Guang-Quan; He, Lan-Zhi; Yin, Ping; Wang, Jia-Bo; Bai, Zhao-Fang; Xiao, Xiao-He.
Afiliação
  • Han YZ; Chengde Medical college, Chengde 067000, China.
  • Zhou YF; China Military Institute of Chinese Medicine, 302 Military Hospital, Beijing 100039, China.
  • Sang XX; China Military Institute of Chinese Medicine, 302 Military Hospital, Beijing 100039, China.
  • Liu HM; Chengde Medical college, Chengde 067000, China.
  • Cui HR; China Military Institute of Chinese Medicine, 302 Military Hospital, Beijing 100039, China.
  • Meng YK; Chengde Medical college, Chengde 067000, China.
  • Li GQ; China Military Institute of Chinese Medicine, 302 Military Hospital, Beijing 100039, China.
  • He LZ; China Military Institute of Chinese Medicine, 302 Military Hospital, Beijing 100039, China.
  • Yin P; China Military Institute of Chinese Medicine, 302 Military Hospital, Beijing 100039, China.
  • Wang JB; China Military Institute of Chinese Medicine, 302 Military Hospital, Beijing 100039, China.
  • Bai ZF; China Military Institute of Chinese Medicine, 302 Military Hospital, Beijing 100039, China.
  • Xiao XH; China Military Institute of Chinese Medicine, 302 Military Hospital, Beijing 100039, China.
Zhongguo Zhong Yao Za Zhi ; 41(7): 1302-1307, 2016 Apr.
Article em Zh | MEDLINE | ID: mdl-28879747
ABSTRACT
To investigate the protective effects of oxymatrine (OMT) against H2O2-induced damage in L02 cells and research the mechanism,L02 cells were used as the research object. The oxidative stress model of L02 was established by hydrogen peroxide (H2O2). CCK-8 was used to detect the cell activation of L02 cells treated by different OMT. FCM (flow cytometry) assay was used to evaluate the cell proliferation of L02 cells treated by OMT. The apoptosis of L02 cells was detected using Annexin-V/7-AAD apoptosis detection kit. The level of ROS was detected by DCFH-DA fluorescence probe. The GSH-PX and SOD were detected by micro plate and colorimetric method. Results showed that when the concentration of OMT is between 6.25 and 100 mg•L⁻¹, it could promote the production of NADPH and strengthen the activity of GSH-PX and SOD to get rid of the ROS to protect the L02 cell from the apoptosis of L02 cell induced by H2O2.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Quinolizinas / Estresse Oxidativo / Substâncias Protetoras / Alcaloides / Peróxido de Hidrogênio Limite: Humans Idioma: Zh Revista: Zhongguo Zhong Yao Za Zhi Assunto da revista: FARMACOLOGIA / TERAPIAS COMPLEMENTARES Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Quinolizinas / Estresse Oxidativo / Substâncias Protetoras / Alcaloides / Peróxido de Hidrogênio Limite: Humans Idioma: Zh Revista: Zhongguo Zhong Yao Za Zhi Assunto da revista: FARMACOLOGIA / TERAPIAS COMPLEMENTARES Ano de publicação: 2016 Tipo de documento: Article País de afiliação: China