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Syringin alleviates ovalbumin-induced lung inflammation in BALB/c mice asthma model via NF-κB signaling pathway.

Abstract
Asthma is an allergic chronic inflammatory disease of the pulmonary airways, characterized by the infiltration of white blood cells and release of inflammatory cytokines of complex pathways linked to its pathogenesis. Syringin extracted from various medicinal plants has been used extensively for the treatment of inflammatory diseases. Hence, this study was conducted to further explore the protective effects of the syringin in ovalbumin (OVA) induced-asthma mice model. OVA-sensitized BALB mice were treated intraperitonealy with three doses (25, 50 and 100 mg/kg) of the syringin which was validated by the alteration in the immunoglobulin E (IgE) levels, cytokines levels, histopathological evaluation inflammatory cell count, lung weight, nitrite (NO) levels, oxidative stress biomarkers and gene markers. The treatment of syringin intensely reduced the increased IgE, inflammatory cytokines, WBC count and restored the antioxidant stress markers OVA stimulated animals. In addition, a significant reduction in inflammation and mucus production was evidenced in histopathological analysis which was further validated by suppression NF-κB pathway activation by syringin. These results suggest that syringin may improve asthma symptoms in OVA-induced mice by modulating NF-κB pathway activation.
AuthorsRui Dai, Manman Niu, Ningling Wang, Yan Wang
JournalEnvironmental toxicology (Environ Toxicol) Vol. 36 Issue 3 Pg. 433-444 (Mar 2021) ISSN: 1522-7278 [Electronic] United States
PMID33146439 (Publication Type: Journal Article)
Copyright© 2020 Wiley Periodicals LLC.
Chemical References
  • Anti-Asthmatic Agents
  • Cytokines
  • Glucosides
  • NF-kappa B
  • Phenylpropionates
  • Ovalbumin
  • syringin
Topics
  • Animals
  • Anti-Asthmatic Agents (pharmacology)
  • Asthma (pathology)
  • Cytokines (metabolism)
  • Disease Models, Animal
  • Female
  • Glucosides (pharmacology)
  • Inflammation (pathology)
  • Lung (drug effects)
  • Mice
  • Mice, Inbred BALB C
  • NF-kappa B (metabolism)
  • Ovalbumin (adverse effects)
  • Phenylpropionates (pharmacology)
  • Pneumonia (drug therapy)
  • Signal Transduction (drug effects)

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