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Protective effects of HTD4010, a Reg3α/PAP-derived peptide, in mouse model of acute pancreatitis via toll-like receptor 4 pathway.

Authors :
Wu, Jingyi
Ma, Xiaojie
Chen, Weiwei
Yang, Na
Gao, Lin
Mao, Wenjian
Yang, Jing
Yang, Qi
Dong, Jie
Tong, Zhihui
Li, Baiqiang
Lu, Guotao
Li, Weiqin
Source :
Biochemical & Biophysical Research Communications. May2019, Vol. 512 Issue 4, p670-677. 8p.
Publication Year :
2019

Abstract

Acute pancreatitis (AP) is one of the most common digestive tract diseases, but effective drug therapy is still lack. Regenerating gene protein 3α (Reg3α) administration significantly reduced the severity of AP in mice. HTD4010 is a new 15 amino acid long synthetic peptide and its biological activities are similar to Reg3α. This study aimed to explore whether HTD4010 could protect pancreatic acinar cells against necrosis and decrease the inflammatory response in AP, and thus to explore underlying mechanisms. It was shown that administration of HTD4010 alleviated significantly the severity of biliary AP (BAP), characterized as less degree of pancreatic histological damage and acinar cell injury (both apoptosis and necroptosis), lower levels of serum amylase and pro-inflammatory cytokines. Moreover, HTD4010 down-regulated the expression of toll-like receptor 4 (TLR4) protein, and TLR4 deficiency eliminated the protective effect of HTD4010 on BAP in mice. In conclusion, these results showed that HTD4010 could alleviate the severity of pancreatitis, reduce the acinar cells necrosis and inflammatory response possibly by TLR4 signaling pathway in AP. • HTD4010 is a new 15 amino acid long synthetic peptide. • HTD4010 reduced the inflammatory response and acinar cells necrosis in BAP mice. • HTD4010 could alleviate the severity of AP by TLR4 signaling pathway. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0006291X
Volume :
512
Issue :
4
Database :
Academic Search Index
Journal :
Biochemical & Biophysical Research Communications
Publication Type :
Academic Journal
Accession number :
136352147
Full Text :
https://doi.org/10.1016/j.bbrc.2019.03.107