Paeoniflorin ameliorates schistosomiasis liver fibrosis through regulating IL-13 and its signalling molecules in mice

被引:33
作者
Li, Xiaoyue [1 ,2 ,3 ,4 ]
Shen, Jilong [1 ,2 ,3 ,4 ]
Zhong, Zhengrong [1 ,2 ,3 ,4 ]
Peng, Jun [5 ]
Wen, Huiqin [1 ,3 ,4 ]
Li, Jing [1 ,3 ,4 ]
Luo, Qingli [1 ,3 ,4 ]
Wei, Wei [2 ]
机构
[1] Anhui Med Univ, Prov Lab Zoonoses, Hefei, Peoples R China
[2] Anhui Med Univ, Inst Clin Pharmacol, Hefei, Peoples R China
[3] Anhui Med Univ, Key Lab Microbiol & Parasitol Anhui, Hefei, Peoples R China
[4] Minist Educ China, Key Lab Gene Resource Utilizat Severe Dis, Hefei, Peoples R China
[5] Anhui Med Univ, Hosp Qing, Dept Pathol, Hefei, Anhui, Peoples R China
关键词
paeoniflorin; schistosomiasis; liver fibrosis; hepatic stellate cell; IL-13; suppressor of cytokine signalling-1; STAT6; HEPATIC STELLATE CELLS; COLLAGEN PRODUCTION; PAEONIA-LACTIFLORA; INTERLEUKIN-13; CYTOKINE; MANSONI; TRANSCRIPTION; INFLAMMATION; EXPRESSION; SOCS-1;
D O I
10.1017/S003118201000003X
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Treatment of liver fibrosis associated with Schistosoma japonicum ova-induced granulomas remains a challenging proposition. Paeoniflorin (PAE, C22H28O11) has anti-inflammatory, anti-allergic, and immunoregulatory effects and it is commonly used in Chinese Herbal prescriptions to treat hepatic disorders. The present study was carried out to investigate the effects of PAE on hepatic fibrosis of mice infected with S. japonicum and to explore its possible mechanism. Upon pathological examination of PAE-treated mice, the size of egg granuloma, fibrosis scores, the concentration of IL-13 and hydroxyproline in liver were significantly reduced compared with the model mice. In the primary culture of hepatic stellate cell (HSCs), PAE inhibited IL-13-induced collagen synthesis. These results suggested that PAE might alleviate the hepatic granulomas and fibrosis caused by S. japonicum and the inhibitory effect of PAE on hepatic fibrosis might be associated with its ability to decrease the level of IL-13 and to interfere with the IL-13 signalling molecule in HSCs.
引用
收藏
页码:1213 / 1225
页数:13
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