The PKCδ-Nrf2-ARE signalling pathway may be involved in oxidative stress in arsenic-induced liver damage in rats

被引:48
作者
Hu, Yong [1 ]
Yu, Chun [1 ]
Yao, Maolin [1 ]
Wang, Lei [1 ]
Liang, Bing [1 ]
Zhang, Bixia [2 ]
Huang, Xiaoxin [2 ]
Zhang, Aihua [1 ]
机构
[1] Guizhou Med Univ, Key Lab Environm Pollut Monitoring & Dis Control, Minist Educ, Dept Toxicol,Sch Publ Hlth, Guiyang 550025, Guizhou, Peoples R China
[2] PLA, Hosp 44, Guiyang 550025, Guizhou, Peoples R China
关键词
Arsenic poisoning; Liver damage; Oxidative stress; PKC delta; Nrf2; ARE; MESSENGER-RNA; NRF2; EXPRESSION; CELLS; ACTIVATION; TOXICITY; EXPOSURE; MUSCLE; MICE;
D O I
10.1016/j.etap.2018.05.012
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Arsenic poisoning is a worldwide endemic disease that affects thousands of people. Growing evidence from animal, cell, and human studies indicates that arsenic has deleterious effects on the liver. Oxidative stress is considered the primary mechanism for arsenic toxicity in liver damage. However, the mechanisms remain unclear. In light of this fact, the main objective of this study was to investigate the effects of the protein kinase C delta-nuclear factor E2-related factor 2-antioxidant response element (PKC delta-Nrf2-ARE) signalling pathway on oxidative stress in liver damage. In the present study, we used a model of liver damage induced by coal-burning arsenic in rats, which was set up by our research group. The oxidative stress index and the transcription and protein expression levels of PKC delta, Nrf2, Keap1, SOD1, and GPx1 were detected, and then their correlation analyses were carried out. The results demonstrated that coal-burning arsenic can cause oxidative stress liver damage in rats, which may be related to the PKC delta-Nrf2-ARE signalling pathway. This study may provide a new pathway for studies of the mechanisms of arsenism.
引用
收藏
页码:79 / 87
页数:9
相关论文
共 28 条
[1]   Alveolar socket healing: what can we learn? [J].
Araujo, Mauricio G. ;
Silva, Cleverson O. ;
Misawa, Monica ;
Sukekava, Flavia .
PERIODONTOLOGY 2000, 2015, 68 (01) :122-134
[2]   The effects of melatonin on liver functions in arsenic-induced liver damage [J].
Bali, Ilhan ;
Bilir, Bulent ;
Emir, Seyfi ;
Turan, Filiz ;
Yilmaz, Ahsen ;
Gokkus, Tuba ;
Aydin, Murat .
TURKISH JOURNAL OF SURGERY, 2016, 32 (04) :233-237
[3]  
Bastien D., 2007, SIGNAL TRANSDUCTION, P198
[4]  
Calyniuk B., 2016, Annales Academiae Medicae Silesiensis-Slaski Uniwersytet Medyczny w Katowicach, V70, P224, DOI [10.18794/aams/65697, DOI 10.18794/AAMS/65697]
[5]   Pomegranate protects against arsenic-induced p53-dependent ROS-mediated inflammation and apoptosis in liver cells [J].
Choudhury, Sreetama ;
Ghosh, Sayan ;
Mukherjee, Sudeshna ;
Gupta, Payal ;
Bhattacharya, Saurav ;
Adhikary, Arghya ;
Chattopadhyay, Sreya .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2016, 38 :25-40
[6]  
Chung Jin-Yong, 2014, J Prev Med Public Health, V47, P253, DOI 10.3961/jpmph.14.036
[7]   KEAP1-NRF2 signalling and autophagy in protection against oxidative and reductive proteotoxicity [J].
Dodson, Matthew ;
Redmann, Matthew ;
Rajasekaran, Namakkal S. ;
Darley-Usmar, Victor ;
Zhang, Jianhua .
BIOCHEMICAL JOURNAL, 2015, 469 :347-355
[8]   Protein disulfide isomerase overexpression in vascular smooth muscle cells induces spontaneous preemptive NADPH oxidase activation and Nox1 mRNA expression: Effects of nitrosothiol exposure [J].
Fernandes, Denise C. ;
Manoel, Ana Heloisa O. ;
Wosniak, Joao, Jr. ;
Laurindo, Francisco R. .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2009, 484 (02) :197-204
[9]   Delayed Correlation of mRNA and Protein Expression in Rapamycin-treated Cells and a Role for Ggc1 in Cellular Sensitivity to Rapamycin [J].
Fournier, Marjorie L. ;
Paulson, Ariel ;
Pavelka, Norman ;
Mosley, Amber L. ;
Gaudenz, Karin ;
Bradford, William D. ;
Glynn, Earl ;
Li, Hua ;
Sardiu, Mihaela E. ;
Fleharty, Brian ;
Seidel, Christopher ;
Florens, Laurence ;
Washburn, Michael P. .
MOLECULAR & CELLULAR PROTEOMICS, 2010, 9 (02) :271-284
[10]   Brief intense interval exercise activates AMPK and p38 MAPK signaling and increases the expression of PGC-1α in human skeletal muscle [J].
Gibala, Martin J. ;
Mcgee, Sean L. ;
Garnham, Andrew P. ;
Howlett, Kirsten F. ;
Snow, Rodney J. ;
Hargreaves, Mark .
JOURNAL OF APPLIED PHYSIOLOGY, 2009, 106 (03) :929-934