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首页> 外文期刊>African Journal of Biotechnology >The effect of chronic periodontitis on serum levels of matrix metalloproteinase-2 (MMP-2), tissue inhibitor of metalloproteinase-1 (TIMP-1), interleukin-12 (IL-12) and granulocytemacrophage colony-stimulating factor (GM-CSF)
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The effect of chronic periodontitis on serum levels of matrix metalloproteinase-2 (MMP-2), tissue inhibitor of metalloproteinase-1 (TIMP-1), interleukin-12 (IL-12) and granulocytemacrophage colony-stimulating factor (GM-CSF)

机译:慢性牙周炎对血清基质金属蛋白酶2(MMP-2),金属蛋白酶1组织抑制剂(TIMP-1),白介素12(IL-12)和粒细胞巨噬细胞集落刺激因子(GM-CSF)的影响

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A complex network of chemokines and pro- and anti-inflammatory mediators is involved in the initiation and progression of chronic periodontitis. Matrix metalloproteinases (MMPs), the main enzymes responsible for matrix degradation, are important for periodontal tissue destruction, but their activity can be inhibited by tissue inhibitors of metalloproteinases (TIMPs). Interleukin-12 (IL-12) and granulocyte-macrophage colony-stimulating factor (GM-CSF) have been shown to be involved in inflammatory and autoimmune diseases. Until now, no studies have reported on serum levels of MMP-2 and GM-CSF in chronic periodontitis patients and periodontally healthy subjects. Therefore, the aim of the present study was to determine the serum levels of MMP-2, TIMP-1, IL-12 and GM-CSF in chronic periodontitis patients, compared with periodontally healthy subjects. The test group of the study comprised 40 chronic periodontitis patients, whereas the control group included 108 periodontally healthy individuals. Blood samples were collected from all participants and examined using?enzyme-linked immunosorbent assay?(ELISA) analysis. Clinical periodontal parameters (bleeding on probing, clinical attachment level and probing pocket depth) and the serum levels of MMP-2, TIMP-1, IL-12 and GM-CSF were statistically significantly higher in the test group than in the conptrol group. These results may indicate that MMP-2, TIMP-1, IL-12 and GM-CSF could be involved in the initiation and progression of chronic periodontitis.
机译:趋化因子,促炎和抗炎介质的复杂网络参与了慢性牙周炎的发生和发展。基质金属蛋白酶(MMPs)是负责基质降解的主要酶,对牙周组织破坏很重要,但是它们的活性可以被组织金属蛋白酶(TIMPs)抑制剂抑制。白介素12(IL-12)和粒细胞巨噬细胞集落刺激因子(GM-CSF)已被证明与炎症和自身免疫性疾病有关。迄今为止,尚未有关于慢性牙周炎患者和牙周健康受试者的MMP-2和GM-CSF血清水平的研究报告。因此,本研究的目的是确定与牙周健康受试者相比,慢性牙周炎患者的MMP-2,TIMP-1,IL-12和GM-CSF的血清水平。该研究的测试组包括40位慢性牙周炎患者,而对照组则包括108位牙周健康个体。收集所有参与者的血样,并使用“酶联免疫吸附测定”(ELISA)分析。试验组的临床牙周参数(探查出血,临床附着水平和探查囊袋深度)以及MMP-2,TIMP-1,IL-12和GM-CSF的血清水平在统计学上显着高于对照药物。这些结果可能表明MMP-2,TIMP-1,IL-12和GM-CSF可能参与了慢性牙周炎的发生和发展。

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