Quercetin Preserves Oral Cavity Health by Mitigating Inflammation and Microbial Dysbiosis

Front Immunol. 2021 Nov 26:12:774273. doi: 10.3389/fimmu.2021.774273. eCollection 2021.

Abstract

Failure to attenuate inflammation coupled with consequent microbiota changes drives the development of bone-destructive periodontitis. Quercetin, a plant-derived polyphenolic flavonoid, has been linked with health benefits in both humans and animals. Using a systematic approach, we investigated the effect of orally delivered Quercetin on host inflammatory response, oral microbial composition and periodontal disease phenotype. In vivo, quercetin supplementation diminished gingival cytokine expression, inflammatory cell infiltrate and alveolar bone loss. Microbiome analyses revealed a healthier oral microbial composition in Quercetin-treated versus vehicle-treated group characterized by reduction in the number of pathogenic species including Enterococcus, Neisseria and Pseudomonas and increase in the number of non-pathogenic Streptococcus sp. and bacterial diversity. In vitro, Quercetin diminished inflammatory cytokine production through modulating NF-κB:A20 axis in human macrophages following challenge with oral bacteria and TLR agonists. Collectively, our findings reveal that Quercetin supplement instigates a balanced periodontal tissue homeostasis through limiting inflammation and fostering an oral cavity microenvironment conducive of symbiotic microbiota associated with health. This proof of concept study provides key evidence for translational studies to improve overall health.

Keywords: A20; IL-6; NF-κB; TNF; flavonoids; microbiome; periodontal diseases; toll-like receptor (TLR).

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alveolar Bone Loss / drug therapy
  • Alveolar Bone Loss / etiology
  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Antioxidants / pharmacology
  • Biomarkers
  • Cell Line
  • Cytokines / metabolism
  • Dysbiosis / drug therapy*
  • Gingiva / drug effects
  • Gingiva / microbiology
  • Humans
  • Immunohistochemistry
  • Inflammation Mediators / metabolism
  • Macrophages
  • Male
  • Mice
  • Microbiota / drug effects*
  • Models, Animal
  • Models, Biological
  • Mouth / drug effects*
  • Mouth / microbiology*
  • Periodontal Diseases / drug therapy
  • Periodontal Diseases / etiology
  • Periodontal Diseases / pathology
  • Quercetin / pharmacology*

Substances

  • Anti-Inflammatory Agents
  • Antioxidants
  • Biomarkers
  • Cytokines
  • Inflammation Mediators
  • Quercetin