Nareika A, Maldonado A, He L, Game B A, Slate E H, Sanders J J, London S D, Lopes-Virella M F, Huang Y
Division of Endocrinology, Diabetes and Medical Genetics, Department of Medicine, Medical University of South Carolina, Charleston, SC 29403, USA.
J Periodontal Res. 2007 Feb;42(1):31-8. doi: 10.1111/j.1600-0765.2006.00911.x.
It has been established that periodontal diseases are more prevalent and of greater severity in diabetic patients than in nondiabetic patients. Recent studies have underscored the role of monocytes and macrophages in periodontal tissue inflammation and destruction in diabetic patients. Although it has been shown that monocytes isolated from diabetic patients produce more inflammatory cytokines and that gingival crevicular fluid collected from diabetic patients contains higher levels of inflammatory cytokines than that obtained from nondiabetic patients, the underlying mechanisms are not well understood.
U937 histiocytes cultured in medium containing either normal (5 mM) or high (25 mM) glucose were treated with 100 ng/ml of lipopolysaccharide for 24h. After the treatment, cytokines in the medium and cytokine mRNA in the cells were quantified using enzyme-linked immunosorbet assay and real-time polymerase chain reaction, respectively.
In this study, we demonstrated that the pre-exposure of U937 histiocytes to high glucose concentrations markedly increased the lipopolysaccharide-induced secretion of pro-inflammatory cytokines and chemokines and the cellular inducible nitric oxide level compared with pre-exposure to normal glucose. Our data also showed that the increased secretion of cytokines was a result of increased mRNA expression. Furthermore, the effects of statin and peroxisome proliferators-activated receptor agonists on high glucose-enhanced secretion of cytokines were determined. The results showed that simvastatin, but not fenofibrate or pioglitazone, inhibited high glucose-enhanced cytokine release.
This study has shown that high glucose concentrations and lipopolysaccharide act synergistically to stimulate the secretion of inflammatory mediators, and that statin is capable of suppressing the high glucose-boosted proinflammatory response. This study therefore delineates a novel mechanism by which hyperglycemia enhances the inflammatory responses of macrophages and suggests that statin may be useful in the treatment of periodontal disease in diabetic patients.
已证实,糖尿病患者的牙周疾病比非糖尿病患者更为普遍且病情更严重。近期研究强调了单核细胞和巨噬细胞在糖尿病患者牙周组织炎症和破坏中的作用。尽管已表明从糖尿病患者分离出的单核细胞会产生更多炎症细胞因子,且从糖尿病患者收集的龈沟液中炎症细胞因子水平高于非糖尿病患者,但潜在机制尚未完全明确。
将在含有正常(5 mM)或高(25 mM)葡萄糖的培养基中培养的U937组织细胞用100 ng/ml脂多糖处理24小时。处理后,分别使用酶联免疫吸附测定法和实时聚合酶链反应对培养基中的细胞因子和细胞中的细胞因子mRNA进行定量。
在本研究中,我们证明,与预先暴露于正常葡萄糖相比,将U937组织细胞预先暴露于高葡萄糖浓度下会显著增加脂多糖诱导的促炎细胞因子和趋化因子的分泌以及细胞诱导型一氧化氮水平。我们的数据还表明,细胞因子分泌增加是mRNA表达增加的结果。此外,还确定了他汀类药物和过氧化物酶体增殖物激活受体激动剂对高葡萄糖增强的细胞因子分泌的影响。结果表明,辛伐他汀可抑制高葡萄糖增强的细胞因子释放,而非诺贝特或吡格列酮则无此作用。
本研究表明,高葡萄糖浓度和脂多糖协同作用以刺激炎症介质的分泌,且他汀类药物能够抑制高葡萄糖增强的促炎反应。因此,本研究阐明了高血糖增强巨噬细胞炎症反应的新机制,并表明他汀类药物可能有助于治疗糖尿病患者的牙周疾病。