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[Protective effects of luteolin against acetaminophen-induced damage in L02 liver cells].
He, Lan-Zhi; Meng, Ya-Kun; Han, Yan-Zhong; Zhang, Zhen-Fang; Yin, Ping; Sang, Xiu-Xiu; Xiao, Xiao-He; Bai, Zhao-Fang.
Afiliación
  • He LZ; School of Pharmacy, Hunan University of Traditional Chinese Medicine, Changsha 410208, China.
  • Meng YK; China Military Institute of Chinese Medicine, 302 Military Hospital, Beijing 100039, China.
  • Han YZ; School of Pharmacy, Jiangxi University of Traditional Chinese Medicine, Nanchang 330004, China.
  • Zhang ZF; 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.
  • Sang XX; China Military Institute of Chinese Medicine, 302 Military Hospital, Beijing 100039, China.
  • Xiao XH; School of Pharmacy, Jiangxi University of Traditional Chinese Medicine, Nanchang 330004, China.
  • Bai ZF; China Military Institute of Chinese Medicine, 302 Military Hospital, Beijing 100039, China.
Zhongguo Zhong Yao Za Zhi ; 41(22): 4234-4239, 2016 Nov.
Article en Zh | MEDLINE | ID: mdl-28933094
This paper was aimed to investigate the protective effects of luteolin (Lut) against acetaminophen(APAP)-induced damage in L02 liver cells. CCK-8 was used to detect the cell activation of L02 cells treated by different Lut. The concentration and time of APAP induced L02 cell damage was screened. The effect of Lut on APAP induced apoptosis of L02 cells was detected by cell morphological observation, CCK-8 assay and flow cytometry. The contents of MDA, GSH and SOD activity in cell supernatant were detected by colorimetric assay. The expression of apoptosis-related genes Bax, Bcl-2 and caspase-3 was detected by RT-PCR. The results showed that Lut in 2.5-40 µmol•L⁻¹ range does not affect the activity of L02 cells; 12 mmol•L⁻¹ APAP incubated with L02 cell 12 h to establish damage model. Compared with the model group, the cell status of Lut group was significantly improved, the cell body was increased, the adherence ability was recovered, and the apoptosis rate was obviously decreased. MDA content decreased significantly (P<0.05, P<0.01), GSH and SOD activity significantly increased (P<0.05, P<0.01), at the same time, it could up-regulate expression of Bcl-2 mRNA and down-regulate the expression of Bax and caspase-3 mRNA. In conclusion,Lut has protective effect on APAP induced L02 cell injury, and its mechanism may be related to the reduction of oxidative stress and inhibition of apoptosis.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Sustancias Protectoras / Hepatocitos / Luteolina / Acetaminofén Límite: Humans Idioma: Zh Revista: Zhongguo Zhong Yao Za Zhi Asunto de la revista: FARMACOLOGIA / TERAPIAS COMPLEMENTARES Año: 2016 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Sustancias Protectoras / Hepatocitos / Luteolina / Acetaminofén Límite: Humans Idioma: Zh Revista: Zhongguo Zhong Yao Za Zhi Asunto de la revista: FARMACOLOGIA / TERAPIAS COMPLEMENTARES Año: 2016 Tipo del documento: Article País de afiliación: China