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The protective effect of hydrogen sulfide on systemic sclerosis associated skin and lung fibrosis in mice model

BACKGROUD: Systemic sclerosis (SSc) caused fibrosis can be fatal and it still lack of effective treatment. Hydrogen sulfide (H(2)S) appears to be an attractive therapeutic candidates. This study aimed to investigate the protective effect of H(2)S on SSc-associated skin and lung fibrosis. METHODS: We...

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Detalles Bibliográficos
Autores principales: Wang, Zhi, Yin, Xiaoya, Gao, Luyan, Feng, Sheng, Song, Kai, Li, Lingyun, Lu, Ying, Shen, Huaying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4947075/
https://www.ncbi.nlm.nih.gov/pubmed/27468384
http://dx.doi.org/10.1186/s40064-016-2774-4
Descripción
Sumario:BACKGROUD: Systemic sclerosis (SSc) caused fibrosis can be fatal and it still lack of effective treatment. Hydrogen sulfide (H(2)S) appears to be an attractive therapeutic candidates. This study aimed to investigate the protective effect of H(2)S on SSc-associated skin and lung fibrosis. METHODS: We developed a model of SSc by subcutaneous injecting BLM to female C3H mice. The mice received daily subcutaneous injections of NaHS (56 and 112 μg/kg), an H(2)S donor. On days 7, 28, and 42, the mice were killed and blood samples were collected to measure the plasma H(2)S concentration, the skin and lung tissues was harvested for microscopic examination, immunohistochemistry and quantify biological parameters (hydroxyproline content, RT-qPCR and Western blot). RESULTS: In model group, the dermis of skin tissues at different time points gradually thickened, collagen deposition increased. The lung tissues presented pathological changes such as obvious inflammatory cell infiltration, increased collagen deposition and the plasma H(2)S concentrations points significantly decreased. Administration of NaHS markedly decreased the biomarkers of fibrosis such as α-smooth muscle actin, collagen-I, collagen-III, fibronectin, transforming growth factor-β1, Smad2/3 phosphorylation and inflammation including the marker protein of monocyte/macrophage and monocyte chemoattractant protein-1 in the lung. Compared to the low dose group, the expression in the high dose group have decreased trend, but the difference was not significant. CONCLUSION: We demonstrate the beneficial effects of H(2)S on SSc-associated skin and lung fibrosis. H(2)S may be a potential therapy against this intractable disease.