Influence of melatonin associated with the Bio-Gide® membrane on osteoblast activity: an in vitro Study.

Eliene A Oliveira, Karen L Dalla-Costa, Fabiana Mg França, Kamila R Kantovitz, Daiane C Peruzzo
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引用次数: 2

Abstract

Melatonin (MLT) is a hormone responsible for regulating several physiological processes. It has been shown that MLT can be an important mediator in bone formation and stimulation, promoting osteoblast differentiation. In clinical practice, in tissue regeneration procedures, it is necessary to use membranes or barriers, associated with biomaterials, or not. The aim of this in vitro study was to assess the effect of melatonin on the activity of osteoblastic cells, associated, or not, with a resorbable collagen membrane (Bio-Gideä). For this, mice-derived pre-osteoblastic cells MC3T3 obtained from the ATCC (American Type Culture Collection) were used. Cultured cells were subject to the following treatments: MLT with a concentration of 1mM, a Bio-Gideä membrane and a membrane associated with MLT (Bio-Gideä + MLT). Proliferation and cell viability assays and protein lysate (ELISA test) quantification for the BMP-2 protein were carried out, in periods of 72 hours, 7 days and 10 days. After analyzing the data (one-way ANOVA, alpha=5%) it was observed that when MLT was used in isolation, there was an increase in cell proliferation and viability in osteoblastic cells (p<0.05). But, when MLT was associated with resorbable membranes, there was an inverse behavior, both in terms of proliferation and viability (p<0.05). In the case of the ELISA test, no secretion of BMP-2 was detected in any of the analyzed groups. It is concluded that MLT has a stimulatory effect on osteoblasts, but, when associated with Bio-Gideä resorbable membranes, it does not show any viable action in osteoblastic cell stimulation.

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与Bio-Gide®膜相关的褪黑激素对成骨细胞活性的影响:一项体外研究
褪黑激素(MLT)是一种负责调节几个生理过程的激素。研究表明,MLT是骨形成和刺激的重要介质,促进成骨细胞分化。在临床实践中,在组织再生过程中,是否有必要使用与生物材料相关的膜或屏障。这项体外研究的目的是评估褪黑素对成骨细胞活性的影响,是否与可吸收胶原膜相关(Bio-Gideä)。为此,使用从ATCC (American Type Culture Collection)获得的小鼠来源的成骨前细胞MC3T3。培养的细胞接受以下处理:浓度为1mM的MLT, Bio-Gideä膜和MLT相关膜(Bio-Gideä + MLT)。分别在72小时、7天和10天进行BMP-2蛋白的增殖、细胞活力测定和蛋白裂解物(ELISA)定量检测。在分析数据(单因素方差分析,α =5%)后,观察到当分离使用MLT时,成骨细胞的细胞增殖和活力增加(p
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