Quercetin ameliorates advanced glycation end product-induced wound healing impairment and inflammaging in human gingival fibroblasts
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...
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description | 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.
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-κβ activity to see if Quercetin mediate its effects via this pro-inflammatory signaling.
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 Iκβ in AGEs-stimulated HGFs, demonstrating it can modulate NF-κβ pathway.
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-κβ pathway and hence, may be a promising approach for treatment of diabetes-associated periodontitis. |
doi_str_mv | 10.1016/j.jds.2023.04.014 |
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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-κβ activity to see if Quercetin mediate its effects via this pro-inflammatory signaling.
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 Iκβ in AGEs-stimulated HGFs, demonstrating it can modulate NF-κβ pathway.
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-κβ pathway and hence, may be a promising approach for treatment of diabetes-associated periodontitis.</description><identifier>ISSN: 1991-7902</identifier><identifier>EISSN: 2213-8862</identifier><identifier>DOI: 10.1016/j.jds.2023.04.014</identifier><identifier>PMID: 38303825</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Advanced glycation end products ; Original ; Periodontitis ; Quercetin</subject><ispartof>Journal of dental sciences, 2024-01, Vol.19 (1), p.268-275</ispartof><rights>2023 Association for Dental Sciences of the Republic of China</rights><rights>2023 Association for Dental Sciences of the Republic of China. Publishing services by Elsevier B.V.</rights><rights>2023 Association for Dental Sciences of the Republic of China. Publishing services by Elsevier B.V. 2023 Association for Dental Sciences of the Republic of China</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c452t-83afcc94ac731036d518bc31a341ec3b51a0ba6cba90911b3be4d3d6be27e9393</citedby><cites>FETCH-LOGICAL-c452t-83afcc94ac731036d518bc31a341ec3b51a0ba6cba90911b3be4d3d6be27e9393</cites><orcidid>0000-0002-8575-4180 ; 0000-0003-2056-6290 ; 0000-0002-0533-9762</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10829550/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jds.2023.04.014$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,3548,27923,27924,45994,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38303825$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Chao-Yen</creatorcontrib><creatorcontrib>Ng, Min Yee</creatorcontrib><creatorcontrib>Lin, Taichen</creatorcontrib><creatorcontrib>Liao, Yi-Wen</creatorcontrib><creatorcontrib>Huang, Wei-Shiuan</creatorcontrib><creatorcontrib>Hsieh, Chang-Wei</creatorcontrib><creatorcontrib>Yu, Cheng-Chia</creatorcontrib><creatorcontrib>Chen, Chun-Jung</creatorcontrib><title>Quercetin ameliorates advanced glycation end product-induced wound healing impairment and inflammaging in human gingival fibroblasts</title><title>Journal of dental sciences</title><addtitle>J Dent Sci</addtitle><description>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.
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-κβ activity to see if Quercetin mediate its effects via this pro-inflammatory signaling.
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 Iκβ in AGEs-stimulated HGFs, demonstrating it can modulate NF-κβ pathway.
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-κβ pathway and hence, may be a promising approach for treatment of diabetes-associated periodontitis.</description><subject>Advanced glycation end products</subject><subject>Original</subject><subject>Periodontitis</subject><subject>Quercetin</subject><issn>1991-7902</issn><issn>2213-8862</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kc9u1DAQxi1URJfSB-CC_AIJ_pNkY3GoqqoFpEoICc7W2J7sepXYKzvZqncevF62VHDhNPJ8831j-0fIe85qznj3cVfvXK4FE7JmTc1484qshOCy6vtOnJEVV4pXa8XEOXmb846xrpdd-4acy14y2Yt2RX59XzBZnH2gMOHoY4IZMwV3gGDR0c34aGH2MVAMju5TdIudKx9KKepDXEp3izD6sKF-2oNPE4aZQmn7MIwwTbD5rQW6XSYI9HjyBxjp4E2KZoQ853fk9QBjxsvnekF-3t3-uPlS3X_7_PXm-r6yTSvmqpcwWKsasGvJmexcy3tjJQfZcLTStByYgc4aUExxbqTBxknXGRRrVFLJC3J1yt0vZkJny00TjHqf_ATpUUfw-l8l-K3exIPmrBeqbVlJ4KcEm2LOCYcXM2f6yETvdGGij0w0a3RhUjwf_t764vgDoQx8Og1gefvBY9LZejx-v09oZ-2i_0_8Ey9Folc</recordid><startdate>20240101</startdate><enddate>20240101</enddate><creator>Huang, Chao-Yen</creator><creator>Ng, Min Yee</creator><creator>Lin, Taichen</creator><creator>Liao, Yi-Wen</creator><creator>Huang, Wei-Shiuan</creator><creator>Hsieh, Chang-Wei</creator><creator>Yu, Cheng-Chia</creator><creator>Chen, Chun-Jung</creator><general>Elsevier B.V</general><general>Association for Dental Sciences of the Republic of China</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8575-4180</orcidid><orcidid>https://orcid.org/0000-0003-2056-6290</orcidid><orcidid>https://orcid.org/0000-0002-0533-9762</orcidid></search><sort><creationdate>20240101</creationdate><title>Quercetin ameliorates advanced glycation end product-induced wound healing impairment and inflammaging in human gingival fibroblasts</title><author>Huang, Chao-Yen ; Ng, Min Yee ; Lin, Taichen ; Liao, Yi-Wen ; Huang, Wei-Shiuan ; Hsieh, Chang-Wei ; Yu, Cheng-Chia ; Chen, Chun-Jung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c452t-83afcc94ac731036d518bc31a341ec3b51a0ba6cba90911b3be4d3d6be27e9393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Advanced glycation end products</topic><topic>Original</topic><topic>Periodontitis</topic><topic>Quercetin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Chao-Yen</creatorcontrib><creatorcontrib>Ng, Min Yee</creatorcontrib><creatorcontrib>Lin, Taichen</creatorcontrib><creatorcontrib>Liao, Yi-Wen</creatorcontrib><creatorcontrib>Huang, Wei-Shiuan</creatorcontrib><creatorcontrib>Hsieh, Chang-Wei</creatorcontrib><creatorcontrib>Yu, Cheng-Chia</creatorcontrib><creatorcontrib>Chen, Chun-Jung</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of dental sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Chao-Yen</au><au>Ng, Min Yee</au><au>Lin, Taichen</au><au>Liao, Yi-Wen</au><au>Huang, Wei-Shiuan</au><au>Hsieh, Chang-Wei</au><au>Yu, Cheng-Chia</au><au>Chen, Chun-Jung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quercetin ameliorates advanced glycation end product-induced wound healing impairment and inflammaging in human gingival fibroblasts</atitle><jtitle>Journal of dental sciences</jtitle><addtitle>J Dent Sci</addtitle><date>2024-01-01</date><risdate>2024</risdate><volume>19</volume><issue>1</issue><spage>268</spage><epage>275</epage><pages>268-275</pages><issn>1991-7902</issn><eissn>2213-8862</eissn><abstract>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.
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-κβ activity to see if Quercetin mediate its effects via this pro-inflammatory signaling.
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 Iκβ in AGEs-stimulated HGFs, demonstrating it can modulate NF-κβ pathway.
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-κβ pathway and hence, may be a promising approach for treatment of diabetes-associated periodontitis.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>38303825</pmid><doi>10.1016/j.jds.2023.04.014</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-8575-4180</orcidid><orcidid>https://orcid.org/0000-0003-2056-6290</orcidid><orcidid>https://orcid.org/0000-0002-0533-9762</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Advanced glycation end products Original Periodontitis Quercetin |
title | Quercetin ameliorates advanced glycation end product-induced wound healing impairment and inflammaging in human gingival fibroblasts |
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