Molecular mechanism of artesunate attenuates the release of proinflammatory cytokines from macrophages
10.12092/j.issn.1009-2501.2023.09.002
- Author:
Mengling LIAO
1
;
Yan WANG
1
;
Jing LUO
1
;
Nuoyan WANG
1
;
Ling HUA
1
;
Yu ZHANG
1
;
Fei DENG
1
;
Yue YUAN
1
;
Jun ZHOU
1
;
Hong ZHOU
1
Author Information
1. Key Laboratory of Basic Pharmacology of Ministry of Education, Joint International Research Laboratory of Ethnomedicine of Ministry of Education, Zunyi Medical University
- Publication Type:Journal Article
- Keywords:
artesunate;
inflammation;
LPS;
macrophages;
PI3KIII
- From:
Chinese Journal of Clinical Pharmacology and Therapeutics
2023;28(9):969-978
- CountryChina
- Language:Chinese
-
Abstract:
AIM: Lipopolysaccharide (LPS) on the cell membrane of gram negative bacteria is closely related to the occurrence and development of severe acute pancreatitis (SAP). Local and systemic monocyte / macrophages play an important role in the inflammatory process of SAP. Artesunate (AS) was reported to protect rats with severe acute pancreatitis by reducing the release of proinflammatory cytokines. This study further explored the molecular mechanism of anti-inflammatory effect of AS. METHODS: The release of proinflammatory cytokines in the supernatant were studied by enzyme-linked immunosorbent assay. Then, the mRNA expressions of PI3K-III and its key molecules in signaling pathway were detected by real-time quantitative PCR. Finally, the phosphorylation levels of PI3KIII were detected by Western blot. RESULTS: AS could significantly inhibit the release of proinflammatory cytokines from mouse macrophage induced by LPS. Autophagy inhibitor 3-methyladenine (3-MA) could significantly inhibit the release of TNF-α from mouse macrophages induced by LPS; LPS significantly increased the mRNA expression of PI3KIII and its key molecules in mouse peritoneal macrophages (PMs). Finally, AS could significantly inhibit the increase of PI3K-III phosphorylation induced by LPS in PMs. CONCLUSION: The anti-inflammatory mechanism of AS is closely related to the inhibition of PI3K-III phosphorylation.
