Molecular docking study and antireabsorptive activity of a semi-synthetic coumarin derivative from Platymiscium floribundum in the ligature-induced periodontitis in rats: the involvement of heme oxygenase-1
Autor: | Maria Elisabete Amaral de Moraes, Marcos Carlos de Mattos, Vicente de Paulo Teixeira Pinto, Paula Goes, João Alison de Moraes Silveira, Mary Anne Sousa Lima, Jordânia M. O. Freire, Hellíada Vasconcelos Chaves, Helyson Lucas Bezerra Braz, Bruna Rocha De Oliveira, Antônia Torres Ávila Pimenta, Karuza Maria Alves Pereira, José Jackson do N. Costa, Ana Larissa de Queiroz França, Mirna Marques Bezerra, A. M. L. R. Portela, Luzia Herminia Teixeira De Sousa, Roberta Jeane Bezerra Jorge |
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Rok vydání: | 2021 |
Předmět: |
Antioxidant
medicine.medical_treatment Interleukin-1beta Phytochemicals Alveolar Bone Loss Pharmacology Bone resorption Coumarins medicine Animals Periodontitis General Dentistry Dental alveolus biology Tumor Necrosis Factor-alpha Chemistry Fabaceae medicine.disease Rats Molecular Docking Simulation Heme oxygenase Mechanism of action Catalase Heme Oxygenase (Decyclizing) Toxicity biology.protein medicine.symptom Heme Oxygenase-1 |
Zdroj: | Clinical Oral Investigations. 26:1701-1711 |
ISSN: | 1436-3771 1432-6981 |
Popis: | This study aimed to evaluate the anti-resorptive activity of a semi-synthetic coumarin derivative from Platymiscium floribundum, named 6,7-dimethoxy-3-nitrocoumarin. Molecular docking studies were performed to test the binding performance of the derivative against targets associated with alveolar bone loss (TNF-α, IL-1β, and catalase) and a target considered an antioxidant defense (HO-1) during periodontitis. Periodontitis was induced by placing a nylon ligature around the second molars. The rats received for 11 days 6,7-dimethoxy-3-nitrocoumarin (0.01, 0.1, or 1 mg/kg) or vehicle. We investigated by RT-qPCR analysis (TNF-α, IL-1β, and HO-1 mRNA expression levels) and by colorimetric assay (catalase activity) the mechanism of action mediated by 6,7-dimethoxy-3-nitrocoumarin. The in vivo toxicity of 6,7-dimethoxy-3-nitrocoumarin was evaluated. 6,7-Dimethoxy-3-nitrocoumarin (0.1 or 1 mg/kg) reduced alveolar bone loss (1.05 ± 0.24), when compared to vehicle-treated group (3.05 ± 0.30). The interactions of 6,7-dimethoxy-3-nitrocoumarin and the four targets (TNF-α, IL-1β, catalase, and HO-1) showed firm bonds above 6.0 kcal/mol. 6,7-dimethoxy-3-nitrocoumarin (1 mg/kg) lowered mRNA expression levels of TNF-α (2.33 ± 0.56) and IL-1β (19.87 ± 2.9), while it increased both the mRNA expression levels of HO-1 (43.40 ± 1.05) and the catalase activity (46.42 ± 4.59), when compared to vehicle-treated group (46.29 ± 8.43; 37.83 ± 4.38; 1.58 ± 0.11; 8.93 ± 1.86, respectively). The animals did not show any signs of toxicity. 6,7-Dimethoxy-3-nitrocoumarin decreased inflammatory bone loss in the ligature-induced periodontitis in rats, and the activation of the HO-1 pathway may contribute, at least partially, to its protective effects by reducing TNF-α and IL-1β mRNA levels and increasing catalase activity. 6,7-Dimethoxy-3-nitrocumarin could be used as an adjunct to subgingival instrumentation during active and supportive periodontal treatment. |
Databáze: | OpenAIRE |
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