Diaphragmatic dysfunction in sepsis due to severe acute pancreatitis complicated by intra-abdominal hypertension

• Published in: Journal of international medical research 2018-04, Vol.46 (4), p.1349-1357
• Main Authors: Liao, Wei-Chao, Chen, Yan-Hong, Li, Hang-Yang, Wang, Ting-Ting, Lan, Peng, Pan, Kong-Han, Ge, Hui-Qing, Xie, Qiang-min, Zhou, Jian-Cang
• Format: Article
• Language: English
• Subjects: Hypertension; Oxidative stress; Pancreatitis; Reactive oxygen species; Research Reports; Rodents; Sepsis
• ISSN: 0300-0605; 1473-2300
• DOI: 10.1177/0300060517747163

Objective This study aimed to examine the mechanism of diaphragmatic dysfunction in sepsis due to severe acute pancreatitis (SAP) with intra-abdominal hypertension (IAH) in a rat model. Methods The rats were assigned at random to four groups: (1) control (n = 5), (2) SAP (n = 5), (3) SAP+IAH (n = 5), and (4) SAP+IAH+SS-31 (n = 5). Length and force output of the diaphragm were analysed in vivo. Histopathological examinations were performed by haematoxylin–eosin. Oxidative stress levels related to protease in diaphragmatic mitochondria were detected with a colorimetric technique. Results In the septic rat model due to SAP complicated by IAH, myofibres were increased. Muscle contractile function was significantly lower in the SAP+IAH group compared with the SAP and control groups. Glutathione peroxidase and superoxide dismutase levels were significantly lower and malondialdehyde levels were higher in the SAP and SAP+IAH groups compared with the control group. Notably, SS-31 could reverse atrophy of myofibres in SAP+IAH rats, as well as contractile dysfunction and mitochondrial dysfunction in the diaphragm. Conclusions Diaphragmatic structure and biomechanics are altered in septic rats due to SAP and IAH. This finding is mainly due to an increase in release of mitochondrial reactive oxygen species.