2011Chinese Heart JournalRequires access

Protective effects of salidroside on lipopolysaccharide-induced injury in RAW264.7 cells

Pengtao Zhao

Open publisher page 0 citations

Abstract

AIM: To explore the protective effects and the underlying mechanism of salidroside(SDS) on lipopolysaccharide(LPS)-induced inflammation in murine macrophage RAW264.7 cells.METHODS: Cells were divided randomly into eight groups: control group(A group),LPS group(B group),SDS 5 group(C group),SDS 5+LPS group(D group),SDS 10 group(E group),SDS 10+LPS group(F group),SDS 20 group(G group) and SDS 20+LPS group(H group).After cells were stimulated with LPS(1 μg/ml) for 6 h in the presence or absence of 0-20 μg/ml SDS for 1 h,activation of nuclear factor kappa B(NF-κB) was detected and analyzed by Western blotting.Supernatant was then used for determination of TNF-α,IL-6,and IL-10 levels by ELISA and lactate dehydrogenase(LDH) activity with corresponding detection kit according to the manufacturer' s instructions.Cells were stimulated with LPS(1 μg/ml) for 24 h in the presence or absence of 0-20 μg/ml SDS for 1 h,and cell viability was measured using the MTT assay.RESULTS: MTT assay showed that 1 μg/ml LPS reduced cell viability,but SDS concentration-dependently reversed LPS-induced reduction of cell viability.Western blotting showed that SDS markedly inhibited the activation of NF-κB in LPS-treated cells.SDS concentration-dependently reduced LPS-induced TNF-α,IL-6,and LDH content and increased IL-10 content.CONCLUSION: Salidroside plays an important role in anti-inflammation of murine macrophage RAW264.7 cells induced by LPS.Protection may be correlated with inhibition of inflammatory factors through NF-κB signal pathway and the balance between pro-and anti-inflammatory systems.

About this research paper

What this paper is about

AIM: To explore the protective effects and the underlying mechanism of salidroside(SDS) on lipopolysaccharide(LPS)-induced inflammation in murine macrophage RAW264.7 cells.METHODS: Cells were divided randomly into eight groups: control group(A group),LPS group(B group),SDS 5 group(C group),SDS 5+LPS group(D group),SDS 10 group(E group),SDS 10+LPS group(F group),SDS 20 group(G group) and SDS 20+LPS group(H group).After cells were stimulated with LPS(1 μg/ml) for 6 h in the presence or absence of 0-20 μg/ml SDS for 1 h,activation of nuclear factor kappa B(NF-κB) was detected and analyzed by Western blotting.Supernatant was then used for determination of TNF-α,IL-6,and IL-10 levels by ELISA and lactate dehydrogenase(LDH) activity with corresponding detection kit according to the manufacturer' s instructions.Cells were stimulated with LPS(1 μg/ml) for 24 h in the presence or absence of 0-20 μg/ml SDS for 1 h,and cell viability was measured using the MTT assay.RESULTS: MTT assay showed that 1 μg/ml LPS reduced cell viability,but SDS concentration-dependently reversed LPS-induced reduction of cell viability.Western blotting showed that SDS markedly inhibited the activation of NF-κB in LPS-treated cells.SDS concentration-dependently reduced LPS-induced TNF-α,IL-6,and LDH content and increased IL-10 content.CONCLUSION: Salidroside plays an important role in anti-inflammation of murine macrophage RAW264.7 cells induced by LPS.Protection may be correlated with inhibition of inflammatory factors through NF-κB signal pathway and the balance between pro-and anti-inflammatory systems.

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

AIM: To explore the protective effects and the underlying mechanism of salidroside(SDS) on lipopolysaccharide(LPS)-induced inflammation in murine macrophage RAW264.7 cells.METHODS: Cells were divided randomly into eight groups: control group(A group),LPS group(B group),SDS 5 group(C group),SDS 5+LPS group(D group),SDS 10 group(E group),SDS 10+LPS group(F group),SDS 20 group(G group) and SDS 20+LPS group(H group).After cells were stimulated with LPS(1 μg/ml) for 6 h in the presence or absence of 0-20 μg/ml SDS for 1 h,activation of nuclear factor kappa B(NF-κB) was detected and analyzed by Western blotting.Supernatant was then used for determination of TNF-α,IL-6,and IL-10 levels by ELISA and lactate dehydrogenase(LDH) activity with corresponding detection kit according to the manufacturer' s instructions.Cells were stimulated with LPS(1 μg/ml) for 24 h in the presence or absence of 0-20 μg/ml SDS for 1 h,and cell viability was measured using the MTT assay.RESULTS: MTT assay showed that 1 μg/ml LPS reduced cell viability,but SDS concentration-dependently reversed LPS-induced reduction of cell viability.Western blotting showed that SDS markedly inhibited the activation of NF-κB in LPS-treated cells.SDS concentration-dependently reduced LPS-induced TNF-α,IL-6,and LDH content and increased IL-10 content.CONCLUSION: Salidroside plays an important role in anti-inflammation of murine macrophage RAW264.7 cells induced by LPS.Protection may be correlated with inhibition of inflammatory factors through NF-κB signal pathway and the balance between pro-and anti-inflammatory systems.

Key concepts: Salidroside, Lipopolysaccharide, Viability assay, Lactate dehydrogenase, Chemistry, Blot, Molecular biology, MTT assay

Related papers

Back to paper searchBrowse research topicsOriginal source
Protective effects of salidroside on lipopolysaccharide-induced injury in RAW264.7 cells — Research Paper | ScholarLens