کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5637865 | 1583270 | 2017 | 9 صفحه PDF | دانلود رایگان |

- The polyphenol velutin is not cytotoxic to either RAW 264.7 or differentiated osteoclasts.
- The polyphenol velutin downregulates osteoclastogenesis (cell differentiation).
- The polyphenol velutin inhibits HIF-1α through NF-ÆB pathway.
ObjectivesHypoxia-inducible factor-1α (HIF-1α) has been implicated in periodontal tissue inflammation and possibly in osteoclast differentiation, while polyphenols are known to be anti-inflammatory natural compounds that are capable of regulating the NF-κB protein complex pathway. The objective of this study was to investigate cytotoxicity and HIF-1α expression through the NF-κB pathway by polyphenol velutin (Euterpe oleracea Mart.), found in the pulp of acai fruit, during inflammatory RAW 264.7 differentiation.DesignRAW 264.7 mouse monocyte macrophage cells were stimulated with RANKL (30 ng/mL) and Porphyromonas gingivalis lipopolysaccharide (1 μg/mL). Cells were treated with various concentrations of velutin (0.5-2 μM) to check for viability, morphology, osteoclast differentiation, and HIF-1α expression (Western blot).ResultsAlamar blue cell viability assay showed no toxicity to RAW cells with the use of velutin in all concentrations tested (p > 0.05). Velutin did not induce cell apoptosis based on caspase 3/7 assay (p > 0.05). Fluorescence images stained by DAPI showed no alteration in the morphology of RAW cell nuclei (p > 0.05) treated with velutin. TRAP assays demonstrated a dose-dependent reduction in osteoclast formation by velutin when compared with control (p < 0.05). Velutin showed a reduction in HIF-1α expression related to IκB phosphorylation when compared with control (p < 0.001).ConclusionsAt the tested concentrations, velutin was not cytotoxic to RAW 264.7 and differentiated cells. Velutin reduced osteoclast differentiation and downregulated HIF-1α through the NF-κB pathway.
Journal: Archives of Oral Biology - Volume 83, November 2017, Pages 348-356