Kim-Park Wan K, Allam Eman S, Palasuk Jadesada, Kowolik Michael, Park Kichuel K, Windsor L Jack
Department of Periodontology, Indiana University School of Dentistry, Indianapolis, IN, USA.
Department of Oral Biology, Indiana University School of Dentistry, Indianapolis, IN, USA; Oral and Dental Research Division, National Research Centre, Cairo, Egypt.
J Tradit Complement Med. 2015 Apr 29;6(4):343-346. doi: 10.1016/j.jtcme.2015.02.002. eCollection 2016 Oct.
Green tea (; lǜ chá) extracts have been shown to possess anti-oxidant and anti-inflammatory effects in various cell types. Green tea extract (GTX) has been shown to significantly inhibit the activity of collagenase-3 (matrix metalloproteinase-13 (MMP-13)) . MMPs, such as MMP-9, are known to be involved in many inflammatory diseases including periodontal disease. GTX and a major catechin, epigallocatechin-gallate (EGCG), were examined for their ability to inhibit purified MMP-9 activity and its release from stimulated neutrophils. Methanol extract of Green tea and commercially purchased EGCG (>95 % purity) were tested for their ability to inhibit MMP-9 activity and/or its release from neutrophils using a β-casein cleavage assay and gelatin zymography, respectively. Statistical analysis was performed by Student's t-test. GTX and EGCG at 0.1% (w/v) completely inhibited the activity of MMP-9. In addition, GTX and EGCG (0.1 %) significantly inhibited (p < 0.001) the release of MMP-9 from formyl-Met-Leu-Phe (FMLP)-stimulated human neutrophils by 62.01% ± 6.717 and 79.63% ± 1.308, respectively. The inhibitory effects of GTX and EGCG occurred in unstimulated neutrophils (52.42% ± 3.443 and 62.33% ± 5.809, respectively). When the inhibitory effect of EGCG was further characterized, it significantly inhibited the release of MMP-9 from the FMLP-stimulated human neutrophils in a dose-dependent manner. The effects of GTX and EGCG on MMPs could be extrapolated to clinical/ studies for the development of oral care products to prevent or treat chronic inflammatory diseases including periodontal diseases.
绿茶提取物已被证明在多种细胞类型中具有抗氧化和抗炎作用。绿茶提取物(GTX)已被证明能显著抑制胶原酶-3(基质金属蛋白酶-13(MMP-13))的活性。基质金属蛋白酶,如MMP-9,已知参与包括牙周病在内的许多炎症性疾病。研究了GTX和一种主要儿茶素表没食子儿茶素没食子酸酯(EGCG)抑制纯化的MMP-9活性及其从刺激的中性粒细胞中释放的能力。分别使用β-酪蛋白裂解试验和明胶酶谱法检测绿茶甲醇提取物和市售EGCG(纯度>95%)抑制MMP-9活性和/或其从中性粒细胞中释放的能力。采用学生t检验进行统计分析。0.1%(w/v)的GTX和EGCG完全抑制了MMP-9的活性。此外,GTX和EGCG(0.1%)显著抑制(p<0.001)甲酰甲硫氨酰亮氨酰苯丙氨酸(FMLP)刺激的人中性粒细胞释放MMP-9,分别为62.01%±6.717和79.63%±1.308。GTX和EGCG对未刺激的中性粒细胞也有抑制作用(分别为52.42%±3.443和62.33%±5.809)。当进一步研究EGCG的抑制作用时,发现它以剂量依赖的方式显著抑制FMLP刺激的人中性粒细胞释放MMP-9。GTX和EGCG对基质金属蛋白酶的作用可外推至临床/研究,以开发预防或治疗包括牙周病在内的慢性炎症性疾病的口腔护理产品。