Ferreira Adriana Nayme Segovia, Silveira Landulfo, Genovese Walter João, de Araújo Vera Cavalcante, Frigo Lúcio, de Mesquita Ricardo Alves, Guedes Eduardo
Group of Biomolecular Spectroscopy, Institute of Research and Development (IP&D), University of Vale do Paraíba (UNIVAP), São José dos Campos, Brazil.
Photomed Laser Surg. 2006 Jun;24(3):358-65. doi: 10.1089/pho.2006.24.358.
This study investigated the biomodulatory effect of the gallium- aluminum-arsenate laser (GaAlAs) in pulp cells on reactional dentinogenesis, and on the expression of collagen type III (Col III), tenascin (TN), and fibronectin (FN) in irradiated dental tissues and controls (not irradiated).
Several studies suggest a biomodulatory influence of low-intensity laser radiation in the inflammatory and reparative processes of biological tissues.
Sixteen human premolar teeth were selected (after extraction due to orthodontal reasons) and divided into irradiated and control groups. Black class V cavity preparations were accomplished in both groups. For the irradiated group, GaAlAs laser (670 nm, 50 mW) with an energy density of 4 J/cm2 was used. Soon after, the cavities were restored with a glass ionomer and the extractions made after 14 and 42 days.
Histological changes were observed by light microscopy; less intense inflammatory reaction in the irradiated group was found when compared to the controls. Only the irradiated group of 42 days exhibited an area associated with reactional dentinogenesis. After immunohistochemical analysis by the streptoavidin-biotin complex (SABC) method, the expression of Col III, TN, and FN was greater in the irradiated groups.
Our results suggest that a GaAlAs laser with energy density of 4 J/cm2 and wavelength of 670 nm caused biomodulation in pulp cells and expression of collagen, but not collagen of the extracellular matrix, after preparation of a cavity.
本研究调查了砷化镓铝激光(GaAlAs)对牙髓细胞反应性牙本质形成的生物调节作用,以及对受照射牙齿组织和对照组(未受照射)中III型胶原蛋白(Col III)、腱生蛋白(TN)和纤连蛋白(FN)表达的影响。
多项研究表明,低强度激光辐射对生物组织的炎症和修复过程具有生物调节作用。
选取16颗因正畸原因拔除的人类前磨牙,分为照射组和对照组。两组均制备V类黑色窝洞。对于照射组,使用能量密度为4 J/cm²的GaAlAs激光(670 nm,50 mW)。随后,用玻璃离子体修复窝洞,并在14天和42天后进行拔牙。
通过光学显微镜观察组织学变化;与对照组相比,照射组的炎症反应较轻。仅42天的照射组出现了与反应性牙本质形成相关的区域。采用链霉亲和素-生物素复合物(SABC)法进行免疫组织化学分析后,照射组中Col III、TN和FN的表达更高。
我们的结果表明,能量密度为4 J/cm²、波长为670 nm的GaAlAs激光在制备窝洞后对牙髓细胞产生了生物调节作用,并使胶原蛋白表达增加,但细胞外基质中的胶原蛋白未增加。