2012•Journal of New Chinese MedicineRequires access

Effect of Shenmai Injection on Chondrocyte Proliferation Induced by Interleukin-1 Beta in Rabbits

Zhiqian Jiang

Open publisher page 0 citations

Abstract

Objective:To observe the effect of Shenmai Injection on chondrocyte proliferation induced by interleukin-1 beta in rabbits.Methods:The degenerated chondrocyte model was induced established by IL-1 beta inducing rabbit chondrocyte in vitro.The model cells were divided into the blank group,the model group,1% Shenmai group,5% Shenmai group and 10% of Shenmai group.The blank group was cultured by DMEM with 10% fetal bovine serum,and the model group was cultured by DMEM with 10ng/mL IL-1 beta.Shenmai groups of 1%,5% and 10% were cultured by DMEM with 10ng/mL IL-1 beta for 24h firstly,and then was culture DMEM with Shenmai injection of 1%,5%,10% respectively in culture medium.Chondrocyte proliferation was detected by MTT assay.Results:Absorbance(OD) value in the model group was decreased(P 0.01compared with that in the blank group).It refered that IL-1β can inhibits chondrocyte proliferation to establish the degenerated chondrocyte model.The differences of absorbance(OD) value among all Shenmai groups and the model group were significant differences(P 0.01).It refered that Shenmai injections of different concentration can obviously promote the degenerated chondrocyte proliferation,the proliferation effect being positively correlated with the concentration.Conclusion:Shenmai injection can obviously promote the chondrocyte proliferation induced by IL-1β in rabbits,which might be the mechanism of Shenmai injection to prevent and treat joint degeneration.

About this research paper

What this paper is about

Objective:To observe the effect of Shenmai Injection on chondrocyte proliferation induced by interleukin-1 beta in rabbits.Methods:The degenerated chondrocyte model was induced established by IL-1 beta inducing rabbit chondrocyte in vitro.The model cells were divided into the blank group,the model group,1% Shenmai group,5% Shenmai group and 10% of Shenmai group.The blank group was cultured by DMEM with 10% fetal bovine serum,and the model group was cultured by DMEM with 10ng/mL IL-1 beta.Shenmai groups of 1%,5% and 10% were cultured by DMEM with 10ng/mL IL-1 beta for 24h firstly,and then was culture DMEM with Shenmai injection of 1%,5%,10% respectively in culture medium.Chondrocyte proliferation was detected by MTT assay.Results:Absorbance(OD) value in the model group was decreased(P 0.01compared with that in the blank group).It refered that IL-1β can inhibits chondrocyte proliferation to establish the degenerated chondrocyte model.The differences of absorbance(OD) value among all Shenmai groups and the model group were significant differences(P 0.01).It refered that Shenmai injections of different concentration can obviously promote the degenerated chondrocyte proliferation,the proliferation effect being positively correlated with the concentration.Conclusion:Shenmai injection can obviously promote the chondrocyte proliferation induced by IL-1β in rabbits,which might be the mechanism of Shenmai injection to prevent and treat joint degeneration.

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

Objective:To observe the effect of Shenmai Injection on chondrocyte proliferation induced by interleukin-1 beta in rabbits.Methods:The degenerated chondrocyte model was induced established by IL-1 beta inducing rabbit chondrocyte in vitro.The model cells were divided into the blank group,the model group,1% Shenmai group,5% Shenmai group and 10% of Shenmai group.The blank group was cultured by DMEM with 10% fetal bovine serum,and the model group was cultured by DMEM with 10ng/mL IL-1 beta.Shenmai groups of 1%,5% and 10% were cultured by DMEM with 10ng/mL IL-1 beta for 24h firstly,and then was culture DMEM with Shenmai injection of 1%,5%,10% respectively in culture medium.Chondrocyte proliferation was detected by MTT assay.Results:Absorbance(OD) value in the model group was decreased(P 0.01compared with that in the blank group).It refered that IL-1β can inhibits chondrocyte proliferation to establish the degenerated chondrocyte model.The differences of absorbance(OD) value among all Shenmai groups and the model group were significant differences(P 0.01).It refered that Shenmai injections of different concentration can obviously promote the degenerated chondrocyte proliferation,the proliferation effect being positively correlated with the concentration.Conclusion:Shenmai injection can obviously promote the chondrocyte proliferation induced by IL-1β in rabbits,which might be the mechanism of Shenmai injection to prevent and treat joint degeneration.

Key concepts: Chondrocyte, Medicine, Interleukin, In vitro, Andrology, BETA (programming language), Interleukin 1β, Endocrinology

Related papers

Back to paper searchBrowse research topicsOriginal source
Effect of Shenmai Injection on Chondrocyte Proliferation Induced by Interleukin-1 Beta in Rabbits — Research Paper | ScholarLens