Cited by 55NF-κB Signaling PathwaysRespiratory Support and MechanismsNatural Compounds in Disease Treatment

Asiaticoside attenuates lipopolysaccharide-induced acute lung injury via down-regulation of NF-κB signaling pathway

Qiu, Jiaming, Yu, Lijun, Zhang, Xingxing, Wu, Qianchao, Wang, Di, Wang, Xiuzhi, Xia, Cheng, Feng, Haihua·2015·International Immunopharmacology

Abstract

Asiaticoside (AS), a triterpene glycoside isolated from Centella asiatica, has been shown to possess potent anti-inflammatory activity. However, the detailed molecular mechanisms of AS on lipopolysaccharide (LPS)-induced acute lung injury (ALI) model in mice are scanty. The purpose of this study was to evaluate the effect of AS on LPS-induced mouse ALI via down-regulation of NF-κB signaling pathway. We investigated the efficacy of AS on cytokine levels induced by LPS in bronchoalveolar lavage fluid (BALF) and RAW 264.7 cells. The production of cytokine (TNF-α and IL-6) was measured by enzyme-linked immunosorbent assay (ELISA). The lung wet-to-dry weight ratios were measured in LPS-challenged mice, and lung histopathologic changes observed via paraffin section were assessed. To further study the mechanism of AS protective effects on ALI, the activation of NF-κB p65 subunit and the degradation of IκBα were tested by western blot assay. We found that AS treatment at 15, 30 or 45mg/kg dose-dependently attenuated LPS-induced pulmonary inflammation by reducing inflammatory infiltration, histopathological changes, descended cytokine production, and pulmonary edema initiated by LPS. Furthermore, our results suggested that AS suppressed inflammatory responses in LPS-induced ALI through inhibition of the phosphorylation of NF-κB p65 subunit and the degradation of its inhibitor IκBα, and might be a new preventive agent of ALI in the clinical setting.

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Crossref · 10.1016/j.intimp.2015.03.022

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  • Asiaticoside dose-dependently reduces LPS-induced pulmonary inflammation by inhibiting inflammatory infiltration, histopathological changes, cytokine production and LPS-induced pulmonary oedema via down-regulation of NF-κB signalling pathway.

    “Asiaticoside has been studied to dose‐dependently reduce LPS‐induced pulmonary inflammation by inhibiting inflammatory infiltration, histopathological changes, cytokine production and LPS‐induced pulmonary oedema via down‐regulation of the NF‐κB signalling pathway.”

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Authors
Qiu, J., Yu, L., Zhang, X., Wu, Q., Wang, D., Wang, X., Xia, C., & Feng, H.
Affiliations
  • Jilin University (CN)
  • Inner Mongolia University for Nationalities (CN)
  • Heilongjiang Bayi Agricultural University (CN)
Corresponding author
  • Xia, Cheng
  • Feng, Haihua
Venue
International Immunopharmacology
Publisher
Elsevier BV
Published
2015-05
Volume
26
Issue
1
Pages
181-187
ISSN
1567-5769 (ISSN-L)
OpenAlex
W2039879861
Cited by
55
References
0
Citations by year
2025: 6 · 2024: 7 · 2023: 6 · 2022: 5 · 2021: 6 · 2020: 7 · 2019: 7 · 2018: 2 · 2017: 5 · 2016: 4
FWCI
1.21
Type
journal article
Language
en
Open access
closed
Locations
  • International Immunopharmacology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Nature Science Foundation of China (31372478, 31172172)
  • Key Laboratory Open Foundation of Animal Medicine of Heilongjiang Bayi Agricaltural University (AMKL2012007)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › NF-κB Signaling Pathways
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Respiratory Support and Mechanisms
  • Health Sciences › Medicine › Complementary and alternative medicine › Natural Compounds in Disease Treatment
Keywords
asiaticoside, Centella asiatica, acute lung injury, lipopolysaccharide, NF-κB signaling, NF-κB p65, IκBα degradation, anti-inflammatory activity, TNF-α, interleukin-6, lung inflammation, pulmonary edema, RAW 264.7 macrophages
MeSH terms
Animals, Anti-Inflammatory Agents, Cell Line, Disease Models, Animal, Lipopolysaccharides, Macrophages, Male, Mice, Inbred BALB C, Triterpenes, Signal Transduction, Down-Regulation, Cytokines, Transcription Factor RelA, Acute Lung Injury

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