Zhen Lei, Fan De-sheng, Zhang Yan, Cao Xin-ming, Wang Li-ming
Department of Periodontology, Shanghai Stomatological Disease Center, Shanghai 200001, China.
Department of Pathology, Shanghai Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China.
Acta Pharmacol Sin. 2015 Feb;36(2):221-8. doi: 10.1038/aps.2014.131. Epub 2014 Dec 22.
To investigate the therapeutic effects of resveratrol (RSV) on periodontitis in diabetic mice and to explore the underlying mechanisms in vitro.
Experimental periodontitis was induced in db/db mice by ligature application of porphyromonas gingivalis. The mice were treated with RSV (20 mg/kg, p.o.) daily for 4 weeks. Alveolar bone loss, proinflammatory cytokines and TLR4 expression in the gingival tissue were measured. Cultured gingival epithelial cells (GECs) were used for in vitro studies. The transcriptional activity of TLR4 downstream signaling was analyzed using Western blotting.
RSV administration significantly decreased the blood glucose levels, and ameliorated alveolar bone loss in db/db mice with experimental periodontitis. RSV administration also suppressed the high levels of IL-1β, IL-6, IL-8, TNF-α, and TLR4 in gingival tissue of the mice. In the GECs incubated in high glucose medium, TLR4 expression was substantially upregulated, which was partly blocked in the presence of RSV. Lipopolysaccharides markedly increased the expression and secretion of IL-1β, IL-6, IL-8, and TNF-α in the GECs cultured in high glucose medium, which was also partly blocked in the presence of RSV. Furthermore, RSV significantly suppressed the phosphorylation of TLR4 downstream factors NF-κB p65, p38MAPK, and STAT3.
RSV exerts protective effects against experimental periodontitis in db/db mice via negative regulation of TLR4 signaling.
研究白藜芦醇(RSV)对糖尿病小鼠牙周炎的治疗作用,并在体外探讨其潜在机制。
通过结扎牙龈卟啉单胞菌诱导db/db小鼠发生实验性牙周炎。小鼠每日口服RSV(20mg/kg),持续4周。检测牙槽骨吸收、牙龈组织中促炎细胞因子和TLR4表达。使用培养的牙龈上皮细胞(GECs)进行体外研究。采用蛋白质印迹法分析TLR4下游信号的转录活性。
给予RSV可显著降低db/db实验性牙周炎小鼠的血糖水平,并改善牙槽骨吸收。给予RSV还可抑制小鼠牙龈组织中高水平的IL-1β、IL-6、IL-8、TNF-α和TLR4。在高糖培养基中培养的GECs中,TLR4表达显著上调,在RSV存在的情况下部分受到抑制。脂多糖显著增加高糖培养基中培养的GECs中IL-1β、IL-6、IL-8和TNF-α的表达和分泌,在RSV存在的情况下也部分受到抑制。此外,RSV显著抑制TLR4下游因子NF-κB p65、p38MAPK和STAT3的磷酸化。
RSV通过对TLR4信号的负调控对db/db小鼠实验性牙周炎发挥保护作用。