2013China Medical HeraldRequires access

The therapeutical effect and mechanism of acitretin in scleroderma mice model

Ping Zhou

Open publisher page 0 citations

Abstract

Objective To study the therapeutical effect of acitretin for systemic scleroderma(SSc) in the mouse model.Peripheral blood IL-17,IL-10,IL-6 and TGF-β1,which were Th17/Treg related factors were examined to explore the possible mechanism of acitretin.Methods 24 female BALB/c mice were randomly divided into control group,SSc group and acitretin group.SSc group and acitretin group were given subcutaneous injections of bleomycin for 4 weeks,and acitrein group were given acitretin 6 mg/(kg.d) orally for 4 weeks.4 weeks later,pathological changes of the skin and lung of the mice were detected.Enzyme-linked immunosorbent assay(ELISA) was used to measure the levels of IL-17,IL-10,IL-6 and TGF-β1 in the serum.Results Skin thickness,skin inflammation score,lung inflammation score of acitretin group were significantly lower than the SSc group [(140.25 ±20.24) μm vs(191.88±40.95) μm,(0.75± 0.01) scores vs(2.00±0.76) scores,(1.38±0.52) scores vs(2.00±0.92) scores,P 0.05).Serum IL-17,IL-6,IL-10 of acitretin group were significantly lower than the SSc group [(50.69 ±11.72) pg/mL vs(66.89±16.62) pg/mL,(85.77± 12.06) pg/mL vs(118.68±22.62) pg/mL,(57.65±21.74) pg/mL vs(131.07±22.52) pg/mL,P 0.05].Serum TGF-β1 levels of three groups showed no significant differences.Conclusion Acitretin significantly improves symptoms of skin and lungs in the scleroderma mice model,and its mechanism may related with Th17/Treg balance.

About this research paper

What this paper is about

Objective To study the therapeutical effect of acitretin for systemic scleroderma(SSc) in the mouse model.Peripheral blood IL-17,IL-10,IL-6 and TGF-β1,which were Th17/Treg related factors were examined to explore the possible mechanism of acitretin.Methods 24 female BALB/c mice were randomly divided into control group,SSc group and acitretin group.SSc group and acitretin group were given subcutaneous injections of bleomycin for 4 weeks,and acitrein group were given acitretin 6 mg/(kg.d) orally for 4 weeks.4 weeks later,pathological changes of the skin and lung of the mice were detected.Enzyme-linked immunosorbent assay(ELISA) was used to measure the levels of IL-17,IL-10,IL-6 and TGF-β1 in the serum.Results Skin thickness,skin inflammation score,lung inflammation score of acitretin group were significantly lower than the SSc group [(140.25 ±20.24) μm vs(191.88±40.95) μm,(0.75± 0.01) scores vs(2.00±0.76) scores,(1.38±0.52) scores vs(2.00±0.92) scores,P 0.05).Serum IL-17,IL-6,IL-10 of acitretin group were significantly lower than the SSc group [(50.69 ±11.72) pg/mL vs(66.89±16.62) pg/mL,(85.77± 12.06) pg/mL vs(118.68±22.62) pg/mL,(57.65±21.74) pg/mL vs(131.07±22.52) pg/mL,P 0.05].Serum TGF-β1 levels of three groups showed no significant differences.Conclusion Acitretin significantly improves symptoms of skin and lungs in the scleroderma mice model,and its mechanism may related with Th17/Treg balance.

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 study the therapeutical effect of acitretin for systemic scleroderma(SSc) in the mouse model.Peripheral blood IL-17,IL-10,IL-6 and TGF-β1,which were Th17/Treg related factors were examined to explore the possible mechanism of acitretin.Methods 24 female BALB/c mice were randomly divided into control group,SSc group and acitretin group.SSc group and acitretin group were given subcutaneous injections of bleomycin for 4 weeks,and acitrein group were given acitretin 6 mg/(kg.d) orally for 4 weeks.4 weeks later,pathological changes of the skin and lung of the mice were detected.Enzyme-linked immunosorbent assay(ELISA) was used to measure the levels of IL-17,IL-10,IL-6 and TGF-β1 in the serum.Results Skin thickness,skin inflammation score,lung inflammation score of acitretin group were significantly lower than the SSc group [(140.25 ±20.24) μm vs(191.88±40.95) μm,(0.75± 0.01) scores vs(2.00±0.76) scores,(1.38±0.52) scores vs(2.00±0.92) scores,P 0.05).Serum IL-17,IL-6,IL-10 of acitretin group were significantly lower than the SSc group [(50.69 ±11.72) pg/mL vs(66.89±16.62) pg/mL,(85.77± 12.06) pg/mL vs(118.68±22.62) pg/mL,(57.65±21.74) pg/mL vs(131.07±22.52) pg/mL,P 0.05].Serum TGF-β1 levels of three groups showed no significant differences.Conclusion Acitretin significantly improves symptoms of skin and lungs in the scleroderma mice model,and its mechanism may related with Th17/Treg balance.

Key concepts: Acitretin, Medicine, Scleroderma (fungus), Gastroenterology, Internal medicine, Bleomycin, Inflammation, Immunology

Related papers

Back to paper searchBrowse research topicsOriginal source
The therapeutical effect and mechanism of acitretin in scleroderma mice model — Research Paper | ScholarLens