Abdominal paracentesis drainage ameliorates myocardial injury in severe experimental pancreatitis rats through suppressing oxidative stress

被引:0
作者
Yi Wen [1 ]
Hong-Yu Sun [1 ]
Zhen Tan [1 ]
Ruo-Hong Liu [1 ]
Shang-Qing Huang [1 ]
Guang-Yu Chen [1 ]
Hao Qi [2 ]
Li-Jun Tang [1 ]
机构
[1] Department of General Surgery and Pancreatic Injury and Repair Key Laboratory of Sichuan Province, The General Hospital of Western Theater Command (Chengdu Military General Hospital)
[2] Department of Dermatology, The Air Force Hospital of Western Theater Command
基金
中国国家自然科学基金;
关键词
Abdominal paracentesis drainage; Severe acute pancreatitis; Myocardial injury; High mobility group box 1; Nicotinamide adenine dinucleotide phosphate oxidase; Oxidative stress;
D O I
暂无
中图分类号
R576 [胰腺疾病]; R542.2 [心肌疾病];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Abdominal paracentesis drainage(APD) is a safe and effective strategy for severe acute pancreatitis(SAP) patients. However, the effects of APD treatment on SAPassociated cardiac injury remain unknown.AIM To investigate the protective effects of APD on SAP-associated cardiac injury and the underlying mechanisms.METHODS SAP was induced by 5% sodium taurocholate retrograde injection in SpragueDawley rats. APD was performed by inserting a drainage tube with a vacuum ball into the lower right abdomen of the rats immediately after SAP induction.Morphological staining, serum amylase and inflammatory mediators, serum and ascites high mobility group box(HMGB) 1, cardiac-related enzymes indexes and cardiac function, oxidative stress markers and apoptosis and associated proteins were assessed in the myocardium in SAP rats. Nicotinamide adenine dinucleotide phosphate oxidase activity and mRNA and protein expression were also examined.RESULTS APD treatment improved cardiac morphological changes, inhibited cardiac dysfunction, decreased cardiac enzymes and reduced cardiomyocyte apoptosis,proapoptotic Bax and cleaved caspase-3 protein levels. APD significantly decreased serum levels of HMGB1, inhibited nicotinamide adenine dinucleotide phosphate oxidase expression and ultimately alleviated cardiac oxidative injury.Furthermore, the activation of cardiac nicotinamide adenine dinucleotide phosphate oxidase by pancreatitis-associated ascitic fluid intraperitoneal injection was effectively inhibited by adding anti-HMGB1 neutralizing antibody in rats with mild acute pancreatitis.CONCLUSION APD treatment could exert cardioprotective effects on SAP-associated cardiac injury through suppressing HMGB1-mediated oxidative stress, which may be a novel mechanism behind the effectiveness of APD on SAP.
引用
收藏
页码:35 / 54
页数:20
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