2014•Chinese Journal of Gastroenterology and HepatologyRequires access

Influence of hydrogen sulfide in p38MAPK signaling pathway on rat hepatic stellate cell apoptosis

Xu Guang Xi

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Abstract

Objective To investigate the influence of hydrogen sulfide in p38 MAPK signaling pathway on rat hepatic stellate cells(HSC) apoptosis and the changes of phospho-P38,Caspase-3 protein. Methods Control group(HSC-T6 plus 10% fetal bovine serum containing DMEM medium),Dimethyl sulfoxide group(DMSO was added based on control group,final concentration for 0. 1%),Sodium Hydrosulfide group(Sodium Hydrosulfide was added based on control group,final concentration for 50 μmol/L),SB group(SB203580 was added based on Dimethyl sulfoxide group,final concentration for 75 μmol/L),SB with Sodium Hydrosulfide group were set up in this study. The apoptotic rate was detected by Hoechst 33342,the expression of phosphorylated p38MAPK(P-p38MAPK) and Caspase-3 protein level were determined by Western blotting. Results Compared with control group,the apoptotic rate of HSC-T6 cells in SB203580 group and SB with Sodium Hydrosulfide group was increased(P 0. 05),the levels of P-p38 and Caspase-3positive expression in SB with Sodium Hydrosulfide group were significantly increased(P 0. 01); Compared with SB with Sodium Hydrosulfide group,the apoptotic rate of HSC-T6 cells in SB group and SB with Sodium Hydrosulfide group was increased(P 0. 01),the expression of P-p38 MAPK protein was decreased(P 0. 01); the level of Caspase-3positive expression in SB with Sodium Hydrosulfide group was more than SB group(P 0. 05). Conclusion Hydrogen sulfide could enhance the expression of p38 MAPK and Caspase-3 protein and make SB203580 induced HSC-T6 cells apoptosis,the mechanism of action could be related to phosphorylation of p38 MAPK and activation of Caspase-3.

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Objective To investigate the influence of hydrogen sulfide in p38 MAPK signaling pathway on rat hepatic stellate cells(HSC) apoptosis and the changes of phospho-P38,Caspase-3 protein. Methods Control group(HSC-T6 plus 10% fetal bovine serum containing DMEM medium),Dimethyl sulfoxide group(DMSO was added based on control group,final concentration for 0. 1%),Sodium Hydrosulfide group(Sodium Hydrosulfide was added based on control group,final concentration for 50 μmol/L),SB group(SB203580 was added based on Dimethyl sulfoxide group,final concentration for 75 μmol/L),SB with Sodium Hydrosulfide group were set up in this study. The apoptotic rate was detected by Hoechst 33342,the expression of phosphorylated p38MAPK(P-p38MAPK) and Caspase-3 protein level were determined by Western blotting. Results Compared with control group,the apoptotic rate of HSC-T6 cells in SB203580 group and SB with Sodium Hydrosulfide group was increased(P 0. 05),the levels of P-p38 and Caspase-3positive expression in SB with Sodium Hydrosulfide group were significantly increased(P 0. 01); Compared with SB with Sodium Hydrosulfide group,the apoptotic rate of HSC-T6 cells in SB group and SB with Sodium Hydrosulfide group was increased(P 0. 01),the expression of P-p38 MAPK protein was decreased(P 0. 01); the level of Caspase-3positive expression in SB with Sodium Hydrosulfide group was more than SB group(P 0. 05). Conclusion Hydrogen sulfide could enhance the expression of p38 MAPK and Caspase-3 protein and make SB203580 induced HSC-T6 cells apoptosis,the mechanism of action could be related to phosphorylation of p38 MAPK and activation of Caspase-3.

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Available abstract

Objective To investigate the influence of hydrogen sulfide in p38 MAPK signaling pathway on rat hepatic stellate cells(HSC) apoptosis and the changes of phospho-P38,Caspase-3 protein. Methods Control group(HSC-T6 plus 10% fetal bovine serum containing DMEM medium),Dimethyl sulfoxide group(DMSO was added based on control group,final concentration for 0. 1%),Sodium Hydrosulfide group(Sodium Hydrosulfide was added based on control group,final concentration for 50 μmol/L),SB group(SB203580 was added based on Dimethyl sulfoxide group,final concentration for 75 μmol/L),SB with Sodium Hydrosulfide group were set up in this study. The apoptotic rate was detected by Hoechst 33342,the expression of phosphorylated p38MAPK(P-p38MAPK) and Caspase-3 protein level were determined by Western blotting. Results Compared with control group,the apoptotic rate of HSC-T6 cells in SB203580 group and SB with Sodium Hydrosulfide group was increased(P 0. 05),the levels of P-p38 and Caspase-3positive expression in SB with Sodium Hydrosulfide group were significantly increased(P 0. 01); Compared with SB with Sodium Hydrosulfide group,the apoptotic rate of HSC-T6 cells in SB group and SB with Sodium Hydrosulfide group was increased(P 0. 01),the expression of P-p38 MAPK protein was decreased(P 0. 01); the level of Caspase-3positive expression in SB with Sodium Hydrosulfide group was more than SB group(P 0. 05). Conclusion Hydrogen sulfide could enhance the expression of p38 MAPK and Caspase-3 protein and make SB203580 induced HSC-T6 cells apoptosis,the mechanism of action could be related to phosphorylation of p38 MAPK and activation of Caspase-3.

Key concepts: Sodium hydrosulfide, Hepatic stellate cell, Apoptosis, p38 mitogen-activated protein kinases, Chemistry, Dimethyl sulfoxide, Sodium, Signal transduction

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