Low Level Laser Therapy (LLLT) Effects of He-Ne Laser with Different Irradiation Conditions on Proliferation in Various Cultured Cells
-
- Yoshitaka YATAGAI
- Department of Operative Dentistry, School of Dentistry, Aichi Gakuin University
-
- Dai SHIMIZU
- Department of Surgery, School of Dentistry, Aichi Gakuin University
-
- Yoshihiko SUGITA
- Department of Pathology, School of Dentistry, Aichi Gakuin University
-
- Shuji NOMOTO
- Department of Surgery, School of Dentistry, Aichi Gakuin University
-
- Morioki FUJITANI
- Department of Operative Dentistry, School of Dentistry, Aichi Gakuin University
-
- Akira SENDA
- Department of Operative Dentistry, School of Dentistry, Aichi Gakuin University
Bibliographic Information
- Other Title
-
- 種々の照射条件でHe-Neレーザー照射した各種培養細胞の増殖活性におけるLow Level Laser Therapy (LLLT) 効果
Abstract
<p> Purpose: Our previous studies have shown the potential effect of He-Ne laser irradiation on the proliferation activity of cancers. This study investigated the effects of He-Ne Laser irradiation with various irradiation conditions on proliferation in cultured human gingival fibroblasts and cultured human oral squamous cell carcinomas.</p><p> Materials and Methods: The HGF-1 cell, which is a fibroblast cell line, and the H157 cell and H314 cell, which are oral squamous cell carcinomas, were used as cultured cells. The cells were irradiated with low-energy He-Ne laser with the following three different power and duration combinations: L1: 1.38 J/cm2, 10 min, L2: 5.75 J/cm2, 42 min, and L3: 5.75 J/cm2, 10 min. L1 and L2 were irradiated at a distance of 20.2 mm; L3 was irradiated with the tip contacting at the bottom. Various cells were incubated in 24-multiwell plastic culture dishes with Dulbecco’s modified Eagle medium (D-MEM) containing 10% fetal bovine serum. After the laser irradiation, cell numbers were determined at 0, 3, 6, 12, 24, 36, 48, 72 and 120 hours, and the proliferation was examined using WST-8.</p><p> Results: In the case of L1, regarding initial growth compared with that in the non-irradiated control, HGF-1 and H314 showed enhanced proliferation by the He-Ne laser irradiation. In the case of L2, we demonstrated that the He-Ne laser used in the present study has a potential suppressive effect on HGF-1, H157 and H314. In the case of L3, cell proliferation was significantly higher in HGF-1 and H157 on initial growth and on H314 on late growth.</p><p> Conclusion: The present study showed that irradiation conditions are most important for the LLLT effects of He-Ne laser, and that He-Ne laser irradiation may contribute to the proliferation of various cultured cells. However, the degree of proliferation differs depending on the optimal condition of the cell.</p>
Journal
-
- The Japanese Journal of Conservative Dentistry
-
The Japanese Journal of Conservative Dentistry 59 (6), 509-515, 2016
The Japanese Society of Conservative Dentistry
- Tweet
Details 詳細情報について
-
- CRID
- 1390282680497623040
-
- NII Article ID
- 130005239845
-
- ISSN
- 21880808
- 03872343
-
- Text Lang
- ja
-
- Data Source
-
- JaLC
- CiNii Articles
- KAKEN
-
- Abstract License Flag
- Disallowed