Diabetes aggravates acute pancreatitis possibly via activation of NLRP3 inflammasome in db/db mice

被引:3
|
作者
Gao, Lin [1 ]
Lu, Guo-Tao [1 ,2 ]
Lu, Ying-Ying [3 ]
Xiao, Wei-Ming [2 ]
Mao, Wen-Jian [1 ]
Tong, Zhi-Hui [1 ]
Yang, Na [1 ]
Li, Bai-Qia Ng [1 ]
Yang, Qi [1 ]
Ding, Yan-Bing [2 ]
Li, Wei-Qin [1 ,3 ]
机构
[1] Nanjing Univ, Med Sch, Jinling Hosp, Dept Gen Surg,SICU, 305 Zhongshan East Rd, Nanjing 210002, Jiangsu, Peoples R China
[2] Yangzhou Univ, Affiliated Hosp, Dept Gastroenterol, 386 Hanjiang Media Rd, Yangzhou 225000, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Jiling Hosp, Dept Gen Surg, Nanjing 211166, Jiangsu, Peoples R China
来源
AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH | 2018年 / 10卷 / 07期
基金
中国国家自然科学基金;
关键词
Type; 2; diabetes; acute pancreatitis; NLRP3; inflammasome; db/db mice; susceptibility; METABOLIC SYNDROME; MELLITUS; RISK; ASSOCIATION; MANAGEMENT; ENDOCRINE; EXOCRINE; OBESITY;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Clinical studies have confirmed that patients with diabetes had an elevated risk of acute pancreatitis (AP) and diabetes was associated with increased severity and mortality in patients with AP. However, these studies failed to prove a cause-and-effect relationship between diabetes and AP. In the present study, we for the first time have evaluated the effects of diabetes on AP by adopting a type 2 diabetes animal model db/db mice and investigated the possible underlying mechanisms. The results showed that in comparison to wide type (WT) mice, db/db mice showed exacerbated pancreatic and pulmonary injuries, elevated serum amylase and lipase levels, increased myeloperoxidase (MPO) expressions in pancreatic and pulmonary tissues as well as increased apoptotic acinar cells after AP induction. Furthermore, we observed that NLRP3 inflammasome in pancreatic tissues was remarkably activated in db/db mice compared with WT mice. In addition, we also found that diabetes could increase the susceptibility of mice to AP. Taken together, our results indicated that diabetes could predispose and aggravate the disease severity of AP potentially via promoting the activation of NLRP3 inflammasome pathway.
引用
收藏
页码:2015 / 2025
页数:11
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