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Anti-Inflammatory Properties of Yellow Passion Fruit Bagasse Extract and Its Potential Role in Periodontal Wound Healing In Vitro

ORCID
0000-0002-2756-5947
Affiliation
Department of Periodontology and Operative Dentistry, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany;(L.V.F.);(M.E.S.L.);(J.D.)
Nogueira, Andressa V. B.;
ORCID
0000-0003-2336-9946
Affiliation
Department of Periodontology and Operative Dentistry, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany;(L.V.F.);(M.E.S.L.);(J.D.)
Faria, Luan V.;
ORCID
0000-0003-4878-3174
Affiliation
Department of Periodontology and Operative Dentistry, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany;(L.V.F.);(M.E.S.L.);(J.D.)
Lopes, Maria Eduarda S.;
ORCID
0000-0001-7187-1012
Affiliation
Faculdade de Zootecnia e Engenharia de Alimentos (FZEA), Universidade de São Paulo (USP), Pirassununga 13635-900, SP, Brazil;
Viganó, Juliane;
ORCID
0000-0002-8182-7207
Affiliation
Faculty of Food Engineering, Department of Food Engineering, University of Campinas (UNICAMP), Campinas 13083-862, SP, Brazil;
Martínez, Julian;
ORCID
0000-0002-4619-2461
Affiliation
Department of Periodontology, School of Dental Medicine, University of Bern, 3010 Bern, Switzerland;
Eick, Sigrun;
ORCID
0000-0002-7082-9290
Affiliation
Department of Diagnosis and Surgery, School of Dentistry at Araraquara, São Paulo State University—UNESP, Araraquara 14801-385, SP, Brazil;
Cirelli, Joni A.;
ORCID
0000-0002-8808-8769
Affiliation
Department of Periodontology and Operative Dentistry, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany;(L.V.F.);(M.E.S.L.);(J.D.)
Deschner, James

Background/Objectives : Periodontal disease involves chronic immunoinflammatory processes and microbial dysbiosis, making phytochemicals with anti-inflammatory properties potential therapeutic agents. This study aimed to assess the modulatory effects of yellow passion fruit bagasse extract (PFBE) on periodontal cells under microbial condition. Methods : A human periodontal ligament (PDL) cell line was exposed to F. nucleatum ATCC 25586 to simulate a microbial environment in vitro in the presence and absence of PFBE containing three different concentrations (0.25, 0.50, and 1.00 µg/mL) of piceatannol. Pro-inflammatory markers (TNF-α, IL-8, CCL2), the antioxidant enzyme SOD2, and the protease marker MMP-1 were analyzed by real-time PCR. Protein levels were assessed via ELISA and NF-κB nuclear translocation by immunofluorescence. Cell viability was investigated using live/dead and alamarBlue assays, and in vitro wound healing was evaluated by an automated scratch assay. Results : PDL cells exposed to F. nucleatum significantly increased the gene and protein expression of all inflammatory markers. The stimulatory effects of F. nucleatum were significantly reduced when PDL cells were simultaneously exposed to PFBE. F. nucleatum triggered the NF-κB nuclear translocation while PFBE abrogated the F. nucleatum -stimulated NF-κB nuclear translocation at 60 min. Viability assays demonstrated that neither PFBE nor F. nucleatum were toxic or significantly affected PDL cell viability. In vitro wound closure was improved by the addition of PFBE to F. nucleatum . Conclusions : PFBE exhibited anti-inflammatory and anti-proteolytic effects while improving in vitro wound healing, suggesting a potential modulatory role of PFBE in periodontal disease prevention and treatment.

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