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Assessing the impact of low level laser therapy (LLLT) on biological systems: a review
Published in International Journal of Radiation Biology, 2019
Ruwaidah A. Mussttaf, David F. L. Jenkins, Awadhesh N. Jha
It has been reported that the photo-reactivating enzyme (DNA photolyase) distinguishes one type of DNA damage as its substrate (i.e. the cyclobutane-type pyrimidine dimer), and combines with these dimers in the dark (Smith 1991). However, when exposing the enzyme-substrate complex to visible light, the enzyme uses the absorbed energy of light to split the dimer to produce repaired (original) DNA. Mbene (2008) treated wounded human skin fibroblast cells by He-Ne laser with 5 J/cm2 and 16 J/cm2 doses. Irradiation with 5 J/cm2 and 16 J/cm2 showed insignificant change in DNA damage, as determined by alkaline comet assay, at 1 h when compared to their respective controls. However, a significant decrease in DNA damage at 24 h incubation due to the mechanism of DNA repair was shown (Mbene 2008).