Journal Article

Sapidolide A alleviates acetaminophen-induced acute liver injury by inhibiting NLRP3 inflammasome activation in macrophages

Zhou, Qian, Weng, Qin-jie, Wang, Jia-jia, Wang, Jin-cheng, Yang, Bo, Shi, Qi, Qiu, Yue-ping, Lou, Da-yong, He, Qiao-jun, Zhou, Li-qin, Zhang, Lu-lu

2022

Overview

Macrophages play a critical role in the pathogenesis of acetaminophen (APAP)-induced liver injury (AILI), a major cause of acute liver failure or even death. Sapidolide A (SA) is a sesquiterpene lactone extracted from Baccaurea ramiflora Lour., a folk medicine used in China to treat inflammatory diseases. In this study, we investigated whether SA exerted protective effects on macrophages, thus alleviated the secondary hepatocyte damage in an AILI. We showed that SA (5–20 μM) suppressed the phosphorylated activation of NF-κB in a dose-dependent manner, thereby inhibiting the expression and activation of the NOD-like receptor protein 3 (NLRP3) inflammasome and pyroptosis in LPS/ATP-treated mouse bone marrow-derived primary macrophages (BMDMs). In human hepatic cell line L02 co-cultured with BMDMs, SA (10 μM) protected macrophages from the pyroptosis induced by APAP-damaged L02 cells. Moreover, SA treatment reduced the secondary liver cell damage aggravated by the conditioned medium (CM) taken from LPS/ATP-treated macrophages. The in vivo assessments conducted on mice pretreated with SA (25, 50 mg/kg, ip) then with a single dose of APAP (400 mg/kg, ip) showed that SA significantly alleviated inflammatory responses of AILI by inhibiting the expression and activation of the NLRP3 inflammasome. In general, the results reported herein revealed that SA exerts anti-inflammatory effects by regulating NLRP3 inflammasome activation in macrophages, which suggests that SA has great a potential for use in the treatment of AILI patients.

• Publisher: Springer Nature Singapore,Nature Publishing Group
• Subject: Acetaminophen / Adenosine Triphosphate - metabolism / Analgesics / Animals / Biomedical and Life Sciences / Biomedicine / Bone marrow / Cell activation / Drug overdose / Hepatocytes / Humans / Immunology / Inflammasomes / Inflammasomes - metabolism / Inflammatory diseases / Internal Medicine / Lipopolysaccharides / Lipopolysaccharides - pharmacology / Liver / Liver - metabolism / Liver diseases / Liver failure / Macrophages / Macrophages - metabolism / Medical Microbiology / Mice / Mice, Inbred C57BL / NF-κB protein / NLR Family, Pyrin Domain-Containing 3 Protein - metabolism / NLR Proteins - metabolism / Pharmacology/Toxicology / Pyroptosis / Traditional medicine / Vaccine