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Quercetin ameliorates advanced glycation end product-induced wound healing impairment and inflammaging in human gingival fibroblasts.
Huang, Chao-Yen; Ng, Min Yee; Lin, Taichen; Liao, Yi-Wen; Huang, Wei-Shiuan; Hsieh, Chang-Wei; Yu, Cheng-Chia; Chen, Chun-Jung.
Afiliación
  • Huang CY; Institute of Oral Sciences, Chung Shan Medical University, Taichung, Taiwan.
  • Ng MY; Department of Emergency Medicine, Chung Shan Medical University Hospital, Taichung, Taiwan.
  • Lin T; School of Medicine, Chung Shan Medical University, Taichung, Taiwan.
  • Liao YW; School of Dentistry, Chung Shan Medical University, Taichung, Taiwan.
  • Huang WS; School of Dentistry, Chung Shan Medical University, Taichung, Taiwan.
  • Hsieh CW; Department of Dentistry, Chung Shan Medical University Hospital, Taichung, Taiwan.
  • Yu CC; Institute of Oral Sciences, Chung Shan Medical University, Taichung, Taiwan.
  • Chen CJ; Department of Medical Research, Chung Shan Medical University Hospital, Taichung, Taiwan.
J Dent Sci ; 19(1): 268-275, 2024 Jan.
Article en En | MEDLINE | ID: mdl-38303825
ABSTRACT
Background/

purpose:

Diabetes mellitus (DM) and periodontal disease are both prevalent and chronic inflammatory disorders that have significant health impact. Many studies have pointed out that advanced glycation end-products (AGEs) in DM induces inflammaging, which is a pre-aging and hyperinflammatory condition, and it has been linked to a greater likelihood in developing periodontitis. Inflammaging in DM has been shown to be driven by AGEs-induced cell senescence, inflammatory cytokines, and oxidative stress, resulting in the degradation of periodontium. Quercetin has shown abilities to decrease inflammation and oxidative stress in a variety of tissues, however, the effect in diabetic periodontitis remains uncertain. Thus, the aim of this study was to investigate its impacts on inflammaging in diabetic periodontitis. Materials and

methods:

We examined cell proliferation in human gingival fibroblasts (HGF), wound healing, IL-6 and IL-8 secretions, cellular senescence expression, and the formation of reactive oxygen species (ROS) in response to AGE stimulation with and without Quercetin intervention. Following that, we looked into NF-κß activity to see if Quercetin mediate its effects via this pro-inflammatory signaling.

Results:

Quercetin at 20 µM and below did not have any impact on HGFs' cell proliferation rate. Quercetin intervention improved the AGEs-impaired wound healing, in addition to the attenuation of AGEs-induced ROS in a dose-dependent pattern. Moreover, Quercetin therapy dose-dependently inhibited AGEs-induced cell senescence activity along with its senescence associated secretion phenotype (SASP) secretions such as IL-6 and IL-8. Western blot analysis indicated that Quercetin was able to reverse the phosphorylation of p65 and Iκß in AGEs-stimulated HGFs, demonstrating it can modulate NF-κß pathway.

Conclusion:

Accumulation of AGEs can elicit inflammaging in HGFs, as seen by increased pro-inflammatory cytokines, cell senescence expression and oxidative stress. The results proposed that Quercetin is able to ameliorate inflammaging in diabetic periodontitis and improve wound healing via the suppression of NF-κß pathway and hence, may be a promising approach for treatment of diabetes-associated periodontitis.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Dent Sci Año: 2024 Tipo del documento: Article País de afiliación: Taiwán Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Dent Sci Año: 2024 Tipo del documento: Article País de afiliación: Taiwán Pais de publicación: Países Bajos