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Effect of low power laser irradiation on cultured fibroblast cells.

Research Project

Project/Area Number 07672200
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Surgical dentistry
Research InstitutionSchool of Dentistry, Aichi-Gakuin University

Principal Investigator

YOSHIDA Kenji  First Department of Oral and Maxillofacial Surgery, School of Dentistry, Aichi-Gakuin University.Associate prof., 歯学部・口腔外科学第1講座, 助教授 (40183701)

Co-Investigator(Kenkyū-buntansha) KANEKO Michio  First Department of Oral and Maxillofacial Surgery, School of Dentistry, Aichi-G, 歯学部・口腔外科学第1講座, 講師 (20261026)
KATO Mugio  First Department of Oral and Maxillofacial Surgery, School of Dentistry, Aichi-G, 歯学部・口腔外科学第1講座, 講師 (30214406)
Project Period (FY) 1995 – 1997
Project Status Completed (Fiscal Year 1997)
Budget Amount *help
¥2,300,000 (Direct Cost: ¥2,300,000)
Fiscal Year 1997: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1996: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 1995: ¥900,000 (Direct Cost: ¥900,000)
KeywordsLow Power Laser / Cultured Fibroblast Cells / Cell Proliferation / TIMP-1 / TIMP-2
Research Abstract

The present study showed that the biological effects on the cultured human gingival cells irradiated by two different wave length low-power lasers. Ana a control was set up in the non-irradiation group.
Results : Mitogen activity was increased by both wave length laser irradiations when the He-Ne watt density was 18.72 mW/cm^2, and the joule density was 5.62 J/cm^2, and when the Ga/Al/As diode watt density was 1.12 mWcm^2, and the joule density was 0.33 J/cm^2. The cell proliferation was increased under a 10% TIMP-1 and TIMP-2 free FCS+D-MEM condition. 48 hours after He-Ne irradiation and 24 hours after Ga-Al-As diode irradiation, there were significant differences. At that time, when TIMP-1 and TIMP-2 secretions in condition medium were measured with EIA,TIMP-1 secretion had significantly increased after 24 hours from irradiation with both lasers together with the He-Ne laser group and Ga-Al As diode laser group. But TIMP-2 detection was impossible by EIA.In the same culture conditions, when the Ga-Al-As diode laser was used to irradiate Gin-1 cells and the RT-PCR method was used to detect mRNA expression, an obvious difference in the TIMP-1 mRNA expression was found at 2 hours post-irradiation. But no difference in TIMP-2 mRNA expression was noted.
These results suggest that low-power lasers of appropriate irradiation accelerate human gingival fibroblast cell growth, and may promote acceleration of wound healing.

Report

(4 results)
  • 1997 Annual Research Report   Final Research Report Summary
  • 1996 Annual Research Report
  • 1995 Annual Research Report
  • Research Products

    (3 results)

All Other

All Publications (3 results)

  • [Publications] 山田 鉄郎: "低出力レーザー照射がヒト正常歯肉線維芽(Gin-1)細胞に及ぼす影響" 愛知学院大学歯学会誌. 36巻1号. 1-11 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Tetsuo, Yamada: "Effect of low power laser irradiation on human gingival fibroblasts." Aichi-Gakuin J.Dent.Sci.36. 1-11 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] 山田鉄郎: "低出力レーザー照射がヒト正常歯肉線維芽(Gin-1)細胞に及ぼす影響" 愛知学院大学歯学会誌. 36巻1号. 1-11 (1998)

    • Related Report
      1997 Annual Research Report

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Published: 1995-04-01   Modified: 2016-04-21  

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