Home      About this journal      Authors      Editors      Readers      Archive      Contact us
Investigating the effect of total paeony glycoside on airway inflammation in mice with neutrophilic asthma based on the AMPK/Sirt1 pathway
Hits 537  Download times 249  Received:January 25, 2025  
View Full Text  View/Add Comment  Download reader
DOI   10.11656/j.issn.1672-1519.2025.06.16
Key Words   total paeony glycoside;AMPK/Sirt1 pathway;neutrophils;asthma;airway inflammation
Author NameAffiliationE-mail
WU Linlin Department of Respiratory Medicine, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital Zhengzhou Children's Hospital, Zhengzhou 450053, China  
SUN Xiaomin Department of Respiratory Medicine, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital Zhengzhou Children's Hospital, Zhengzhou 450053, China 13513892805@163.com 
YAN Xingyu Department of Respiratory Medicine, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital Zhengzhou Children's Hospital, Zhengzhou 450053, China  
HUANG Han Department of Respiratory Medicine, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital Zhengzhou Children's Hospital, Zhengzhou 450053, China  
Abstract
    [Objective] To investigate the effect of total paeony glycoside(TPG) on airway inflammation in mice with neutrophilic asthma based on the adenosine monophosphate-activated protein kinase(AMPK)/silent information regulator 1(Sirt1) pathway. [Methods] Asthmatic mice were prepared by nasal instillation of ovalbumin sensitization solution. The mice were randomly grouped into sensitization group,TPG low-dose(TPG-low,150 mg/kg TPG) group,TPG high-dose(TPG-high,300 mg/kg TPG) group,dexamethasone(4 mg/kg) group,and TPG-high+inhibitor(15 mg/kg) group. Subsequently,nebulization challenge was performed. Mice in the control group were injected with normal saline into the nasal cavity and challenged with atomized normal saline. After 1 hour,airway resistance was analyzed. Bronchoalveolar lavage fluid(BALF) was collected,and cells were classified and counted. The levels of inflammatory cytokines interleukin(IL)-6,tumor necrosis factor-α(TNF-α),and IL-17 in BALF were analyzed. The lung tissue was isolated,and the pathology of lung tissue,changes in airway mucus,AMPK phosphorylation(p-AMPK)/AMPK,and Sirt1 protein expression were detected. [Results] Compared with the control group,the expiratory pause,number of inflammatory cells such as neutrophils,the levels of IL-6,IL-17,TNF-α,inflammatory score,and PAS staining score increased in the sensitization group,while the expression of p-AMPK/AMPK and Sirt1 decreased(P<0.05). Compared with the sensitization group,the expiratory pause,number of inflammatory cells such as neutrophils,levels of IL-6,IL-17,TNF-α,inflammatory score,and PAS staining score decreased in the TPG-low group,TPG-high group,and dexamethasone group,while the expression of p-AMPK/AMPK and Sirt1 increased(P<0.05),and significant differences were observed among TPG groups(P<0.05). Compared with the TPG-high group,the expiratory pause,number of inflammatory cells such as neutrophils,the levels of IL-6,IL-17,TNF-α,inflammatory score,and PAS staining score increased in the TPG-high+inhibitor group,while the expression of p-AMPK/AMPK and Sirt1 decreased(P<0.05). [Conclusion] TPG alleviates airway inflammation in mice with neutrophilic asthma by upregulating the AMPK/Sirt1 pathway.

You are the 4020885 visitor.

Copyright @ 2007
Address: 10 Boyanghu Road, West District of Tuanbo New City, Jinghai District, Tianjin 301617, China  Postcode:
Tel:  Fax:  E-mail:
Beijing E-Tiller Co., Ltd.