Penehyclidine hydrochloride regulates angiopoietin 2/vascular endothelial cadherin (Ang2/VE-cadherin) pathway to alleviate LPS induced lung injury in rats.
- Author:
Fengyong YANG
1
;
Dongdong FANG
2
;
Binghan ZHANG
3
;
Yanjie SUN
2
;
Haifeng LIU
3
;
Yongjie QI
2
;
Guangchen WEI
3
Author Information
1. Jinan City People's Hospital EICU, Jinan Municipal Key Laboratory of Acute Lung Injury Medicine, Jinan Municipal Clinical Research Center of Critical Care Medicine, Jinan Clinical Medicine Research Program for Respiratory Disease Medicine, Jinan 271100, China. *Corresponding author, E-mail: yyfhjgn@163.com.
2. Jinan City People's Hospital EICU, Jinan Municipal Clinical Research Center of Critical Care Medicine, Jinan Clinical Medicine Research Program for Respiratory Disease Medicine, Jinan 271100, China.
3. Jinan City People's Hospital EICU, Jinan Municipal Key Laboratory of Acute Lung Injury Medicine, Jinan Municipal Clinical Research Center of Critical Care Medicine, Jinan Clinical Medicine Research Program for Respiratory Disease Medicine, Jinan 271100, China.
- Publication Type:Journal Article
- MeSH:
Rats;
Mice;
Animals;
Male;
Lipopolysaccharides/metabolism*;
Tumor Necrosis Factor-alpha/metabolism*;
Angiopoietin-2/pharmacology*;
Interleukin-6/metabolism*;
Rats, Sprague-Dawley;
Lung;
Acute Lung Injury/metabolism*;
Sepsis/metabolism*
- From:
Chinese Journal of Cellular and Molecular Immunology
2023;39(8):708-713
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the effect and mechanism of penehyclidine hydrochloride (PHCD) on vascular endothelial injury in septic rats. Methods Fifty male SD rats were randomly divided into control group, lipopolysaccharide (LPS) induced sepsis group (model group), low dose PHCD (0.3 mg/kg) group, medium dose PHCD (1.0 mg/kg) group and high dose PHCD (3.0 mg/kg) groups, ten mice for each group. Normal saline was injected into the tail vein of the control group, and 10 mg/kg lipopolysaccharide (LPS) was injected into the tail vein of the rats in other groups to prepare the sepsis rat models. After the models were successfully established, low, medium and high doses (0.3, 1.0, 3.0 mg/kg) of PHCD solution were injected into the tail vein of the rats of corresponding groups. Wet/dry mass ratio (W/D) of lung tissue of rats in each group was measured, and ELISA was used to assay interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), IL-6 content and rat plasma angiopoietin 2 (Ang2) content in bronchoalveolar lavage fluid (BALF). HE staining was used to observe the pathological changes of lung tissues. Immunohistochemical staining was used to observe the expression of Ang2 in the right lung tissues. Western blot analysis was performed to detect Ang2 and vascular endothelial cadherin (VE-cadherin) protein in lung tissues. Results Compared with the control group, the W/D ratio of the lung tissues of rats in the model group and the contents of IL-1β, IL-6 and TNF-α in BALF were significantly increased; the lung tissues showed obvious pathological damage, with up-regulation of Ang2 expression and down-regulation of VE-Cadherin expression. Compared with the model group, the W/D ratio of the lung tissues of rats in three PHCD treatment groups and the contents of IL-1β, IL-6 and TNF-α in BALF were significantly reduced; the pathological damage of lung tissue was significantly reduced, with down-regulation of Ang2 expression and up-regulation of VE-cadherin expression. Conclusion PHCD can reduce LPS-induced lung inflammation in rats with sepsis by regulating the Ang2/VE-Cadherin pathway, thereby improving vascular endothelial injury.
