| Home  | About ScienceAsia  | Publication charge  | Advertise with us  | Subscription for printed version  | Contact us  
Editorial Board
Journal Policy
Instructions for Authors
Online submission
Author Login
Reviewer Login
Volume 51 Number 2
Volume 51 Number 1
Volume 50S Number 1
Volume 50 Number 6
Volume 50 Number 5
Volume 50 Number 4
Earlier issues
Volume 49 Number 3


Research articles

ScienceAsia 51 (2023): 1-10 |doi: 10.2306/scienceasia1513-1874.2023.028


Caspase-1 inhibitor VX-765 alleviates PM2.5-induced hepatic lipid metabolism disorder in mice


Sisi Qina, Lei Wub, Yongheng Wanga,c, Ning Lia, Changyu Qina, Shoufang Jianga, Jianfen Weid, Naijun Wud, Fuyuan Caoa,e,*, Shuang Lia,c,e,*

 
ABSTRACT:     Long-term exposure to PM2.5 is associated with hepatic lipid metabolism disorders, in which caspase-1 is involved, but the mechanism is not fully understood. This study focused on the role of the caspase-1 inhibitor VX-765. Along-term PM2.5 exposure model was constructed by concentrating ambient air particles. Mice were intraperitoneally administered with VX-765. The body weight, liver index, blood lipid, and hepatic disorder indices were measured. Hematoxylin and eosin staining, immunohistochemical staining, Western blot analysis, and real-time quantitative polymerase chain reaction were employed to assess histopathological changes and quantify the expression levels of target proteins and mRNAs. The results indicated that VX-765 could inhibit hepatic disorder, improve body weight and liver index, and regulate lipid metabolism by affecting the expression of key factors such as caspase-1, IL-1?, SREBP-1, PPAR-?, PPAR-?, and PDK4. In conclusion, caspase-1 inhibitors offer a novel approach for alleviating hepatic disorder caused by long-term PM2.5 exposure.

Download PDF

Downloads Views


a School of Public Health, North China University of Science and Technology, Hebei 063210 China
b School of Psychology and Mental health, North China University of Science and Technology, Hebei 063210 China
c Hebei Key Laboratory of Organ Fibrosis Research, North China University of Science and Technology, Hebei 063210 China
d Department of Endocrinology, North China University of Science and Technology Affiliated Hospital, Hebei 063210 China
e Animal Experimental Center, North China University of Science and Technology, Hebei 063210 China

* Corresponding author, E-mail: c-fuyuan@163.com, lishuangdwzx@ncst.edu.cn

Received 18 Jul 2024, Accepted 21 Feb 2025