Alogliptin alleviates liver fibrosis via suppression of activated hepatic stellate cell
文献类型:期刊论文
作者 | Zhang, Hanyan1; Sun, Dandan2; Wang, Guanzhen2; Cui, Shichao2; Field, Robert A.3; Li, Jia2; Zang, Yi2 |
刊名 | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS |
出版日期 | 2019-04-02 |
卷号 | 511期号:2页码:387-393 |
ISSN号 | 0006-291X |
关键词 | DPP4 Alogliptin Liver fibrosis Hepatic stellate cell |
DOI | 10.1016/j.bbrc.2019.02.065 |
通讯作者 | Li, Jia(jli@simm.ac.cn) ; Zang, Yi(yzang@simm.ac.cn) |
英文摘要 | Liver fibrosis occurs in most types of chronic liver diseases. The understanding of the pathogenesis of liver fibrosis has grown considerably, but the effective treatments are still lacking. Alogliptin, a classical Dipeptidyl peptidase-4 (DPP4) inhibitor with great effects on type 2 diabetes, has shown the potential to protect liver, but its effects on the progression of liver fibrosis have not been clarified. Herein, we explored the anti-fibrosis effects of alogliptin. In vitro, we demonstrated that alogliptin suppressed the activation of LX-2 upon transforming growth factor-beta (TGF-beta) challenge. In vivo, chronic treatment with alogliptin alleviated hepatic steatosis and protected from the liver injury in ob/ob mice, which delayed the progression of liver fibrosis. Furthermore, alogliptin significantly relieved the hepatic fibrosis in CCI4-induced liver fibrosis mouse model. In conclusion, our results demonstrate that negatively modulation of alogliptin on hepatic stellate cell (HSC) activation might contribute to liver fibrosis alleviation. Our research provides the potential possibility of alogliptin on the application for liver fibrosis therapy and suggests that DPP4 may be a novel target for liver fibrosis therapy. (C) 2019 Elsevier Inc. All rights reserved. |
WOS关键词 | DIPEPTIDYL PEPTIDASE-4 INHIBITOR ; PATHOGENESIS ; REGENERATION ; NAFLD ; DPP4 |
资助项目 | National Natural Science Foundation of China[31871414] ; National Natural Science Foundation of China[81673489] ; Science and Technology Commission of Shanghai Municipality[16430724100] ; K. C. Wong Education Foundation |
WOS研究方向 | Biochemistry & Molecular Biology ; Biophysics |
语种 | 英语 |
出版者 | ACADEMIC PRESS INC ELSEVIER SCIENCE |
WOS记录号 | WOS:000461404700029 |
源URL | [http://119.78.100.183/handle/2S10ELR8/290365] |
专题 | 新药研究国家重点实验室 |
通讯作者 | Li, Jia; Zang, Yi |
作者单位 | 1.Nanchang Univ, Sch Pharm, 461 Bayi Rd, Nanchang 330006, Jiangxi, Peoples R China 2.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Natl Ctr Drug Screening, Shanghai 201203, Peoples R China 3.John Innes Ctr, Dept Biol Chem, Norwich Res Pk, Norwich NR4 7UH, Norfolk, England |
推荐引用方式 GB/T 7714 | Zhang, Hanyan,Sun, Dandan,Wang, Guanzhen,et al. Alogliptin alleviates liver fibrosis via suppression of activated hepatic stellate cell[J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,2019,511(2):387-393. |
APA | Zhang, Hanyan.,Sun, Dandan.,Wang, Guanzhen.,Cui, Shichao.,Field, Robert A..,...&Zang, Yi.(2019).Alogliptin alleviates liver fibrosis via suppression of activated hepatic stellate cell.BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,511(2),387-393. |
MLA | Zhang, Hanyan,et al."Alogliptin alleviates liver fibrosis via suppression of activated hepatic stellate cell".BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 511.2(2019):387-393. |
入库方式: OAI收割
来源:上海药物研究所
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