Yoshida Ayaka, Shiotsu-Ogura Yukako, Wada-Takahashi Satoko, Takahashi Shun-suke, Toyama Toshizo, Yoshino Fumihiko
Division of Photomedical Dentistry, Department of Oral Science, Graduate School of Dentistry, Kanagawa Dental University, 82 Inaoka-cho, Yokosuka, Kanagawa 238-8580, Japan.
Division of Dentistry of Circulation Control, Department of Oral Science, Graduate School of Dentistry, Kanagawa Dental University, 82 Inaoka-cho, Yokosuka, Kanagawa 238-8580, Japan.
J Photochem Photobiol B. 2015 Oct;151:48-53. doi: 10.1016/j.jphotobiol.2015.07.001. Epub 2015 Jul 3.
It has been reported that oxidative stress with reactive oxygen species (ROS) generation is induced by blue light irradiation to a living body. Only limited research has been reported in dental field on the dangers of blue light, mostly focusing on cytotoxicity associated with heat injury of dental pulp. We thus performed an in vivo study on oral tissue exposed to blue light. ROS generated upon blue light irradiation of flavin adenine dinucleotide were measured by electron spin resonance spectroscopy. After blue light irradiation, the palatal gingiva of Wistar rats were isolated. Collected samples were subjected to biochemical analysis of lipid peroxidation and glutathione. Singlet oxygen was generated by blue light irradiation, but was significantly quenched in an N-acetyl-L-cysteine (NAC) concentration-dependent manner. Blue light significantly accelerated oxidative stress and increased the oxidized glutathione levels in gingival tissue. These effects were also inhibited by NAC pre-administration. The results suggest that blue light irradiation at clinical levels of tooth bleaching treatment may enhance lipid peroxidation by the induction of oxidative stress and the consumption of a significant amount of intracellular glutathione. In addition, NAC might be an effective supplement for the protection of oral tissues against blue light irradiation-induced oxidative damage.
据报道,蓝光照射活体可诱导产生具有活性氧(ROS)的氧化应激。在牙科领域,关于蓝光危害的研究报道有限,主要集中在与牙髓热损伤相关的细胞毒性方面。因此,我们对暴露于蓝光下的口腔组织进行了一项体内研究。通过电子自旋共振光谱法测量黄素腺嘌呤二核苷酸经蓝光照射后产生的ROS。蓝光照射后,分离出Wistar大鼠的腭部牙龈。对收集的样本进行脂质过氧化和谷胱甘肽的生化分析。蓝光照射产生单线态氧,但在N - 乙酰 - L - 半胱氨酸(NAC)浓度依赖性方式下被显著淬灭。蓝光显著加速氧化应激并增加牙龈组织中氧化型谷胱甘肽水平。NAC预先给药也可抑制这些作用。结果表明,牙齿漂白治疗临床水平的蓝光照射可能通过诱导氧化应激和消耗大量细胞内谷胱甘肽来增强脂质过氧化。此外,NAC可能是保护口腔组织免受蓝光照射诱导的氧化损伤的有效补充剂。