A preliminary evaluation of quercetin-mediated osteogenic gene expression in lipopolysaccharide-treated human periodontal ligament cells: an in vitro study.

IF 2.5 Q2 DENTISTRY, ORAL SURGERY & MEDICINE
Srishta Radhakrishnan, Prem Blaisie Rajula M, P L Ravi Shankar, Merita S, V Kalaivani, Rahila C
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Abstract

Aim: This study aimed to evaluate the effect of quercetin on osteogenic gene expression in lipopolysaccharide (LPS) stimulated human periodontal ligament cells (hPDLCs) under in vitro conditions.

Materials and methods: hPDLCs were cultured with LPS for 24 hours to simulate an inflammatory microenvironment. Following this pre-stimulation, cells were treated with quercetin at concentrations of 2.5 µM, 5 µM, and 10 µM for up to 14 days. No further exposure to LPS was performed during the subsequent culture period. The mRNA expression levels of osteogenic markers, osteopontin (OPN) and osteocalcin (OCN), were assessed on day 14 using Quantitative Real-Time PCR (RT-qPCR). Statistical analysis was performed using Welch's one-way ANOVA with Holm-adjusted post hoc comparisons.

Results: LPS stimulation significantly suppressed the expression of both OPN and OCN compared with the control group. However, quercetin treatment restored and dose-dependently increased the expression of these markers, with the greatest effect observed at 10 µM. At this concentration, OPN and OCN expression levels reached 5.80 ± 0.26 and 6.62 ± 0.30, respectively, relative to the control. A consistent dose-dependent upregulation was observed for both markers, indicating restoration of osteogenic gene expression.

Conclusion: Quercetin modulates the expression of osteogenic markers, including OPN and OCN, in LPS-stimulated hPDLCs under in vitro conditions. These findings suggest a potential modulatory role for quercetin in influencing osteogenic gene expression. However, additional in vitro functional assays and in vivo studies are necessary to establish its role in periodontal regeneration.

脂多糖处理人牙周韧带细胞中槲皮素介导的成骨基因表达的初步评价:一项体外研究。
目的:探讨槲皮素对脂多糖(LPS)刺激的人牙周韧带细胞成骨基因表达的影响。材料和方法:用LPS培养hpdlc 24小时,模拟炎症微环境。在这种预刺激之后,细胞被浓度为2.5µM、5µM和10µM的槲皮素处理长达14天。在随后的培养期间,没有进一步暴露于LPS。第14天采用实时荧光定量PCR (RT-qPCR)检测成骨标志物骨桥蛋白(OPN)和骨钙素(OCN) mRNA表达水平。统计分析采用Welch的单因素方差分析和holm校正后的事后比较。结果:与对照组相比,LPS刺激显著抑制了OPN和OCN的表达。然而,槲皮素处理恢复并剂量依赖性地增加了这些标志物的表达,在10µM时观察到的效果最大。在此浓度下,与对照组相比,OPN和OCN的表达量分别达到5.80±0.26和6.62±0.30。观察到两种标记物均呈剂量依赖性上调,表明成骨基因表达恢复。结论:槲皮素在体外条件下可调节lps刺激hpdlc中OPN、OCN等成骨标志物的表达。这些发现提示槲皮素在影响成骨基因表达方面具有潜在的调节作用。然而,额外的体外功能分析和体内研究是必要的,以确定其在牙周再生中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BDJ Open
BDJ Open Dentistry-Dentistry (all)
CiteScore
3.70
自引率
3.30%
发文量
34
审稿时长
30 weeks
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