The effects of paeoniflorin injection on soluble triggering receptor expressed on myeloid-1 (sTREM-1) levels in severe septic rats.
10.4196/kjpp.2016.20.6.565
- Author:
Xiao Rong LIU
1
;
Jie XU
;
Yi Min WANG
;
Ming Suo JI
;
Fu Shan LIU
Author Information
1. ICU, Tianjin TEDA Hospital, Tianjin 300457, China. xrliu1234@163.com
- Publication Type:Original Article
- Keywords:
Dysfunction syndrome;
Endotoxin;
Paeoniflorin;
Sepsis;
Soluble TREM-1;
Xuebijing
- MeSH:
Animals;
Aspartate Aminotransferases;
Creatine;
Enzyme-Linked Immunosorbent Assay;
Hematologic Tests;
Inflammation;
Intestinal Mucosa;
Intestine, Small;
Kidney;
Leukocyte Count;
Liver;
Lung;
Models, Animal;
Multiple Organ Failure;
Plasma;
Platelet Count;
Rats*;
Rats, Wistar;
Sepsis;
Stomach
- From:The Korean Journal of Physiology and Pharmacology
2016;20(6):565-571
- CountryRepublic of Korea
- Language:English
-
Abstract:
Paeoniflorin (PAE) is the most abundant compound in Xuebijing injection widely used to treat sepsis. We aimed to investigate effect of PAE on expression of soluble triggering receptor expressed on myeloid cells-1 (sTREM-1) in a rat model of sepsis. Wistar rats were divided into Normal, Model, and PAE groups (n=20 each). Endotoxin was administrated at 5 mg/ml/kg in Model and PAE rats to establish rat sepsis model. 1 h after endotoxin administration, PAE was administrated at 4 ml/kg in PAE group once per day for 3 days. Routine blood tests and biochemical indexes were assessed, including aspartate aminotransferase (AST) and creatine kinase-MB (CK-MB). The plasma sTREM-1 level was measured using quantitative ELISA. At the end of experiment, the small intestine, liver, kidney and lung were subjected to pathological examinations. A rat model of sepsis-induced multiple organ dysfunction syndrome (MODS) was established successfully with endotoxin administration (5 mg/ml/kg), evidenced by histo-pathological examinations, routine blood tests and biochemical indexes: platelet count decreased and white blood cell count increased (p<0.05), CK-MB and AST increased (p<0.05). PAE treatment significantly reduced the plasma levels of AST, CK-MB, and sTREM-1, compared to Model group (p<0.05). Meanwhile, sepsis-induced damages in the liver, lung, stomach and intestinal mucosa were also markedly ameliorated by PAE treatment. PAE demonstrated a significantly protective effect in a rat model of sepsis by decreasing plasma sTREM-1 level, reducing inflammation, preventing MODS and protecting organ functions.
