Relief of gouty arthritis in rats by total saponins from Dioscorea nipponica Makino through suppression of neutrophil extracellular trap formation via the PI3K/AKT/mTOR axis

Exp Ther Med. 2023 Aug 2;26(3):447. doi: 10.3892/etm.2023.12146. eCollection 2023 Sep.

Abstract

Gouty arthritis (GA) is an inflammatory disorder that is associated with elevated serum levels of uric acid. Total saponins from Dioscorea nipponica Makino (TSDN) are a natural component that ameliorates inflammation while also decreasing uric acid levels. The aim of the present study was to unravel the mechanism of TSDN in gouty rats in regard to regulation of the formation of neutrophil extracellular traps (NETs) via the PI3K/AKT/mTOR axis. A total of 40 Wistar rats were divided into 4 groups: normal, model, TSDN and rapamycin groups. Reverse-transcription-quantitative PCR (RT-qPCR) and western blot analysis were used to assess the mRNA and protein expression levels of the PI3K/AKT/mTOR axis. The formation of NETs was detected by immunohistochemical and immunofluorescent methods. ELISA was used to measure the levels of IL-1β and TNF-α. RT-qPCR and western blotting demonstrated that TSDN compromised the mRNA and protein expression levels of activated protein kinase (AMPK) and mTOR, as well as the mRNA expression levels of AKT and PTEN. Furthermore, it increased the protein expression levels of phosphorylated (p-) PI3K, p-AKT and p-AMPK. Immunohistochemical and immunofluorescent analyses revealed that TSDN decreased the protein expression levels of neutrophil elastase, proteinase 3, cathepsin G, lactoferrin and myeloperoxidase, as well as the number of citrullinated histone 3+ cells. TSDN also reduced the release of IL-1β and TNF-α. Overall, the anti-inflammatory action of TSDN in gouty rats may be realized by suppressing the formation of NETs by regulating the PI3K/AKT/mTOR axis.

Keywords: Dioscorea nipponica Makino; PI3K/AKT/mTOR; gouty arthritis; inflammation; neutrophil extracellular traps.

Grants and funding

Funding: The present study was supported by the Joint Guidance Project of Heilongjiang Natural Science Foundation (grant no. LH2021H099), the Start Fund of Postdoctoral Research in Heilongjiang (grant no. LRB146914), the Outstanding Youth Development Fund of Heilongjiang University of Chinese Medicine (grant no. 2019JC06), the Project of Heilongjiang Administration of Traditional Chinese Medicine (grant no. ZHY202094), the Graduate Innovative Scientific Research Project of Heilongjiang University of Chinese Medicine (grant no. 2020yjscx057) and the Natural Science Foundation of Heilongjiang (key project; grant no. ZD2020H006).