Anti-inflammatory effect of diterpenes-enriched fractions from Pterodon polygalaeflorus through inhibition of macrophage migration and cytokine production
Autor: | Kátia Costa de Carvalho Sabino, Maria da Graça Justo, Leosvaldo S. M. Velozo, Nathalia Regina F Leal, Mariana Vieira Vigliano, Fabiana A Pinto, Marsen Garcia Pinto Coelho, Thayane V de Sousa |
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Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Cell Survival medicine.medical_treatment Anti-Inflammatory Agents Lipopolysaccharide Receptors Nitric Oxide Synthase Type II Pharmaceutical Science Flow cytometry Mice 03 medical and health sciences chemistry.chemical_compound Geranylgeraniol Cell Movement In vivo medicine Animals MTT assay Viability assay Pharmacology medicine.diagnostic_test Plant Extracts Macrophages Fabaceae Cell migration Molecular biology In vitro 030104 developmental biology Cytokine chemistry Fruit Cytokines Diterpenes |
Zdroj: | Journal of Pharmacy and Pharmacology. 70:808-820 |
ISSN: | 2042-7158 0022-3573 |
DOI: | 10.1111/jphp.12889 |
Popis: | Objectives To evaluate the anti-inflammatory potential of Pterodon polygalaeflorus hexane extract (HE) and its fractions on macrophage migration in vitro and in vivo. Methods Hexane extract from P. polygalaeflorus fruits was fractionated and yielded four fractions. RAW 264.7 cells were treated with samples to evaluate cell viability (MTT assay), cell migration (wound healing and transwell assays), CD14 expression (flow cytometry), iNOS and cytokine mRNA expression (RT-qPCR), NO (Griess reaction) and cytokine (ELISA) production. In vivo migration was evaluated on the thioglycollate-induced peritonitis model. Qualitative analysis was performed by GC-MS. Key findings All fractions inhibited the NO production by LPS-stimulated RAW 264.7 cells. Fr3 and Fr4 presented the lowest IC50 values. The expressions of iNOS and IL-1β, TNF-α and IL-10 cytokines were inhibited by Fr3 and Fr4, whereas the CD14 expression was only inhibited by Fr3. All the samples inhibited RAW 264.7 migration in the wound healing and transwell assays. Fr3 and Fr4 reduced the migration of Mac-1+Gr-1− cells to the peritoneum and presented in their compositions: 6α-hydroxy-7β-acetoxyvouacapan-17β-oate, methyl 6α,7β-dihydroxyvouacapan-17β-oate, methyl 6α-acetoxy-7β-hydroxyvouacapan-17β-oate, geranylgeraniol and 14,15-epoxy-geranylgeraniol. Conclusions The anti-inflammatory effects of Fr3 and Fr4 involve inhibition of cell migration, iNOS expression and NO production, cytokine expression (mRNA and proteins) and CD14 expression (Fr3). |
Databáze: | OpenAIRE |
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