Chang L-Y, Wan H-C, Lai Y-L, Kuo Y-F, Liu T-Y, Chen Y-T, Hung S-L
Department of Dentistry, National Yang-Ming University, No. 155 Sec. 2 Li-Nong Street, Pei-Tou, Taipei, Taiwan.
J Periodontal Res. 2009 Apr;44(2):175-83. doi: 10.1111/j.1600-0765.2008.01104.x. Epub 2008 Oct 7.
Cytokines represent a central role in inflammatory tissue destruction and regulate the immune responses that may govern the progression of periodontal diseases. This study investigated the effects of areca nut extracts on the expression of inflammatory cytokines, tumor necrosis factor-alpha, interleukin-1beta, interleukin-6 and interleukin-8 in peripheral blood mononuclear cells. The role of oxidative stress of areca nut extracts was also examined using curcumin.
The expression of cytokines in peripheral blood mononuclear cells treated with extracts of ripe areca nut or extracts of tender areca nut was analyzed using enzyme-linked immunosorbent assay and reverse transcription-polymerase chain reaction.
Both extracts of ripe areca nut (< or = 40 microg/mL) and extracts of tender areca nut significantly enhanced the production of tumor necrosis factor-alpha and interleukin-1beta in peripheral blood mononuclear cells in a dose-dependent and time-dependent manner. The kinetics of mRNA expression of both cytokines was also enhanced by areca nut extracts. The stimulatory effects of areca nut extracts on the secretion of tumor necrosis factor-alpha, interleukin-1beta, interleukin-6 and interleukin-8 and on the mRNA expression of tumor necrosis factor-alpha, interleukin-1beta and interleukin-6 at 4 h of incubation were reduced by curcumin (20-50 microm). However, the level of interleukin-8 transcripts was not affected by curcumin. Moreover, interleukin-1beta induction by extracts of tender areca nut, but not by extracts of ripe areca nut, was weakened by 10 microm curcumin. The inhibitory effects of curcumin may vary with different cytokines and with different areca nut extract treatments.
The complex cytokine profile induced by areca nut extracts-treated peripheral blood mononuclear cells implied the possibility of enhanced local inflammation and altered immune functions by the areca chewing habit. The inhibitory effects of curcumin on cytokine expression suggested that oxidative stress might be involved in areca nut extracts-associated immune alteration.
细胞因子在炎症性组织破坏中起核心作用,并调节可能控制牙周疾病进展的免疫反应。本研究调查了槟榔提取物对外周血单核细胞中炎性细胞因子、肿瘤坏死因子-α、白细胞介素-1β、白细胞介素-6和白细胞介素-8表达的影响。还使用姜黄素检测了槟榔提取物的氧化应激作用。
采用酶联免疫吸附测定法和逆转录-聚合酶链反应分析成熟槟榔提取物或嫩槟榔提取物处理的外周血单核细胞中细胞因子的表达。
成熟槟榔提取物(≤40μg/mL)和嫩槟榔提取物均以剂量和时间依赖性方式显著增强外周血单核细胞中肿瘤坏死因子-α和白细胞介素-1β的产生。槟榔提取物也增强了这两种细胞因子mRNA表达的动力学。姜黄素(20 - 50μmol)可降低槟榔提取物在孵育4小时时对肿瘤坏死因子-α、白细胞介素-1β、白细胞介素-6和白细胞介素-8分泌以及对肿瘤坏死因子-α、白细胞介素-1β和白细胞介素-6 mRNA表达的刺激作用。然而,白细胞介素-8转录水平不受姜黄素影响。此外,10μmol姜黄素可减弱嫩槟榔提取物而非成熟槟榔提取物诱导的白细胞介素-1β。姜黄素的抑制作用可能因不同细胞因子和不同槟榔提取物处理而有所不同。
槟榔提取物处理的外周血单核细胞诱导的复杂细胞因子谱表明,嚼槟榔习惯可能会增强局部炎症并改变免疫功能。姜黄素对细胞因子表达的抑制作用表明氧化应激可能参与了槟榔提取物相关的免疫改变。