2012Zhongguo yaolixue tongbaoRequires access

The effect of H168 on hepatic stellate cell apoptosis and its possible mechanism

Shizhong Zheng

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Abstract

Aim To observe the effect of H168 on HSC apoptosis and its possible mechanism.Methods LDH kit was used to detect the effect of H168 on LDH activity;MTT was used to detect the effect of drug on HSC-T6 proliferation;apoptosis was measured by using flow cytometry(FCM) analysis with Annexin-Ⅴ/PI dual staining for apoptotic cell ratio;Western blot was used to detect the protein expression of Bcl-2、Bax and Caspase-3.Results No obvious cytotoxic effect was found when the final concentration of H168 was less than 150 μmol·L-1;MTT found that H168 could inhibit HSC-T6 proliferation at the concentration of 10 μmol·L-1 and 25 μmol·L-1;FCM detection found H168 promoted apoptosis of HSC in a dose-dependent manner;Western blot results showed that H168 could promote HSC-T6 apoptosis by promoting Bax/Bcl-2 and Caspase-3 protein expression.Conclusion H168 has the function of promoting the apoptosis of HSC-T6 by promoting Bax/Bcl-2 and Caspase-3 protein expression.

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Aim To observe the effect of H168 on HSC apoptosis and its possible mechanism.Methods LDH kit was used to detect the effect of H168 on LDH activity;MTT was used to detect the effect of drug on HSC-T6 proliferation;apoptosis was measured by using flow cytometry(FCM) analysis with Annexin-Ⅴ/PI dual staining for apoptotic cell ratio;Western blot was used to detect the protein expression of Bcl-2、Bax and Caspase-3.Results No obvious cytotoxic effect was found when the final concentration of H168 was less than 150 μmol·L-1;MTT found that H168 could inhibit HSC-T6 proliferation at the concentration of 10 μmol·L-1 and 25 μmol·L-1;FCM detection found H168 promoted apoptosis of HSC in a dose-dependent manner;Western blot results showed that H168 could promote HSC-T6 apoptosis by promoting Bax/Bcl-2 and Caspase-3 protein expression.Conclusion H168 has the function of promoting the apoptosis of HSC-T6 by promoting Bax/Bcl-2 and Caspase-3 protein expression.

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Available abstract

Aim To observe the effect of H168 on HSC apoptosis and its possible mechanism.Methods LDH kit was used to detect the effect of H168 on LDH activity;MTT was used to detect the effect of drug on HSC-T6 proliferation;apoptosis was measured by using flow cytometry(FCM) analysis with Annexin-Ⅴ/PI dual staining for apoptotic cell ratio;Western blot was used to detect the protein expression of Bcl-2、Bax and Caspase-3.Results No obvious cytotoxic effect was found when the final concentration of H168 was less than 150 μmol·L-1;MTT found that H168 could inhibit HSC-T6 proliferation at the concentration of 10 μmol·L-1 and 25 μmol·L-1;FCM detection found H168 promoted apoptosis of HSC in a dose-dependent manner;Western blot results showed that H168 could promote HSC-T6 apoptosis by promoting Bax/Bcl-2 and Caspase-3 protein expression.Conclusion H168 has the function of promoting the apoptosis of HSC-T6 by promoting Bax/Bcl-2 and Caspase-3 protein expression.

Key concepts: Apoptosis, Annexin, Western blot, Flow cytometry, Molecular biology, MTT assay, Pi, Hepatic stellate cell

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