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首页> 外文期刊>Journal of Periodontology >Effect of avocado and soybean unsaponifiables on gelatinase A (MMP-2), stromelysin 1 (MMP-3), and tissue inhibitors of matrix metalloproteinase (TIMP- 1 and TIMP-2) secretion by human fibroblasts in culture.
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Effect of avocado and soybean unsaponifiables on gelatinase A (MMP-2), stromelysin 1 (MMP-3), and tissue inhibitors of matrix metalloproteinase (TIMP- 1 and TIMP-2) secretion by human fibroblasts in culture.

机译:鳄梨和大豆不皂化物对培养物中人成纤维细胞分泌的明胶酶A(MMP-2),溶血素1(MMP-3)和基质金属蛋白酶组织抑制剂(TIMP-1和TIMP-2)的影响。

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BACKGROUND: In inflamed periodontal tissues, gingival fibroblasts are able to express matrix metalloproteinases (MMPs) and their natural inhibitors, tissue inhibitors of matrix metalloproteinases (TIMPs). They can also respond to growth factors and cytokines. In this study, the in vitro effects of avocado and soybean unsaponifiable residues (ASU), their fractions (avocado unsaponifiable [ASF] or soy unsaponifiable [SSF]) on MMP-2 and MMP-3, and the activity and secretion of their inhibitors TIMP-1 and TIMP-2 were investigated using cultured human gingival fibroblasts. METHODS: Gingival fibroblasts were cultured for 72 hours with ASU, ASF, and SSF at concentrations of 0. 1, 0.5, 2.5, 5, and 10 microg/ml of culture medium, after pretreatment or no pretreatment for 1 hour with interleukin-1beta (IL-1beta). MMP-2 and MMP-3 were detected and quantified in the culture media after zymography and image analysis. TIMP-1, TIMP-2, MMP-2, and MMP-3 were also evidenced by dot blotting and quantified by image analysis. RESULTS: In the absence of IL-1beta, a slight decrease in the secretion of MMP-2 was observed with lower doses of ASU, ASF, and SSF. The decrease of MMP-3 secretion was clearly marked with all fractions especially at low concentrations (0.1 and 2.5 microg/ml). A slight decrease in TIMP-2 secretion was seen for low doses of ASU, ASF, and SSF, while a small increase was seen at higher concentrations. Concerning TIMP-1, no significant variation was observed in culture medium for low concentrations, and a decrease was noted for 5 and 10 microg/ml of ASU, ASF, and SSF. As anticipated, IL-1beta induced a marked release of MMP-2, MMP-3, and TIMP-1, but no variation for TIMP-2 was seen. ASU, ASF, and SSF reversed the IL-1beta effect on gingival fibroblasts for MMP-2 and MMP-3, particularly with doses varying from 0.1 to 2.5 microg/ml and for TIMP-1, particularly with doses varying from 2.5 to 10 microg/ml. CONCLUSIONS: These findings suggest a potential role for avocado and soy unsaponifiable extracts to prevent the deleterious effects of IL-1beta that occur during periodontal diseases.
机译:背景:在发炎的牙周组织中,牙龈成纤维细胞能够表达基质金属蛋白酶(MMP)及其天然抑制剂,基质金属蛋白酶的组织抑制剂(TIMP)。它们还可以对生长因子和细胞因子作出反应。在这项研究中,鳄梨和大豆不可皂化残留物(ASU),其级分(鳄梨不可皂化[ASF]或大豆不可皂化[SSF])对MMP-2和MMP-3的体外作用及其抑制剂的活性和分泌使用培养的人类牙龈成纤维细胞研究了TIMP-1和TIMP-2。方法:牙龈成纤维细胞在ASU,ASF和SSF浓度分别为0、1、0.5、2.5、5和10 microg / ml的培养基中培养72小时,用白介素-1β预处理或不进行预处理1小时(IL-1beta)。经过酶谱分析和图像分析后,在培养基中检测并定量了MMP-2和MMP-3。 TIMP-1,TIMP-2,MMP-2和MMP-3也可以通过斑点印迹法得到证明,并通过图像分析进行定量。结果:在没有IL-1beta的情况下,观察到较低剂量的ASU,ASF和SSF可使MMP-2的分泌略有减少。所有组分均明显标记出MMP-3分泌的减少,尤其是在低浓度(0.1和2.5 microg / ml)下。对于低剂量的ASU,ASF和SSF,发现TIMP-2分泌略有减少,而在较高浓度下,观察到少量增加。关于TIMP-1,在低浓度的培养基中没有观察到明显的变化,ASU,ASF和SSF的浓度分别为5和10微克/毫升。如预期的那样,IL-1β诱导了MMP-2,MMP-3和TIMP-1的明显释放,但未见TIMP-2的变化。 ASU,ASF和SSF逆转了MMP-2和MMP-3对牙龈成纤维细胞的IL-1beta效应,尤其是剂量范围从0.1到2.5 microg / ml和TIMP-1,尤其是剂量范围从2.5到10 microg /毫升。结论:这些发现表明鳄梨和大豆不皂化提取物具有预防牙周疾病期间发生的IL-1β有害作用的潜在作用。

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