2012Zhongguo redai yixueRequires access

Inhibiting effect and basic mechanism of salvianolic acid B on mouse hepatoma hepa1-6 cell line

Ge WenHua

Open publisher page 0 citations

Abstract

Objectives To observe the inhibiting effect and basic mechanism of Salvianolic acid B on mouse hepatoma hepa1-6 cell line. Methods Hepa1-6 cell culture was taken as in vitro model.MTT method was used for testing the cytotoxicity effect of Salvianolic acid B on the hepatoma cell line.Hepatoma cell death style was tested with Annexin V method in flow cytometry.Apoptosis related genes were tested with realtime quantitative PCR assay. Results Salvianolic acid B have marked cytotoxic effect on the heap1-6 cell line in certain range of concentration.Its TC50 is 31.9ug/ml.The proportion of hepa1-6 cell apoptosis were between 27.58 and 74.26% when Salvianolic acid B was administrated in the concentration of 25-50ug/ml.The anti-apoptosis factor BCL-2 mRNA level was significantly decreased and pro-apoptosis factor Bax mRNA level was significantly elevated. Conclusion Salvianolic acid B can significantly inhibit the propagation of hepa1-6 cell line in vitro.The related mechanism is induction of cell apoptosis.

About this research paper

What this paper is about

Objectives To observe the inhibiting effect and basic mechanism of Salvianolic acid B on mouse hepatoma hepa1-6 cell line. Methods Hepa1-6 cell culture was taken as in vitro model.MTT method was used for testing the cytotoxicity effect of Salvianolic acid B on the hepatoma cell line.Hepatoma cell death style was tested with Annexin V method in flow cytometry.Apoptosis related genes were tested with realtime quantitative PCR assay. Results Salvianolic acid B have marked cytotoxic effect on the heap1-6 cell line in certain range of concentration.Its TC50 is 31.9ug/ml.The proportion of hepa1-6 cell apoptosis were between 27.58 and 74.26% when Salvianolic acid B was administrated in the concentration of 25-50ug/ml.The anti-apoptosis factor BCL-2 mRNA level was significantly decreased and pro-apoptosis factor Bax mRNA level was significantly elevated. Conclusion Salvianolic acid B can significantly inhibit the propagation of hepa1-6 cell line in vitro.The related mechanism is induction of cell apoptosis.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objectives To observe the inhibiting effect and basic mechanism of Salvianolic acid B on mouse hepatoma hepa1-6 cell line. Methods Hepa1-6 cell culture was taken as in vitro model.MTT method was used for testing the cytotoxicity effect of Salvianolic acid B on the hepatoma cell line.Hepatoma cell death style was tested with Annexin V method in flow cytometry.Apoptosis related genes were tested with realtime quantitative PCR assay. Results Salvianolic acid B have marked cytotoxic effect on the heap1-6 cell line in certain range of concentration.Its TC50 is 31.9ug/ml.The proportion of hepa1-6 cell apoptosis were between 27.58 and 74.26% when Salvianolic acid B was administrated in the concentration of 25-50ug/ml.The anti-apoptosis factor BCL-2 mRNA level was significantly decreased and pro-apoptosis factor Bax mRNA level was significantly elevated. Conclusion Salvianolic acid B can significantly inhibit the propagation of hepa1-6 cell line in vitro.The related mechanism is induction of cell apoptosis.

Key concepts: Apoptosis, Annexin, Cell culture, Flow cytometry, Cell, Cytotoxicity, In vitro, Molecular biology

Related papers

Back to paper searchBrowse research topicsOriginal source
Inhibiting effect and basic mechanism of salvianolic acid B on mouse hepatoma hepa1-6 cell line — Research Paper | ScholarLens