Long-term safety of low-level laser therapy at different power densities and single or multiple applications to the bone marrow in mice

Photomed Laser Surg. 2013 Jun;31(6):269-73. doi: 10.1089/pho.2012.3395. Epub 2013 May 15.

Abstract

Objective: The purpose of this study was to determine the long-term safety effect of low-level laser therapy (LLLT) to the bone marrow (BM) in mice.

Background data: LLLT has been shown to have a photobiostimulatory effect on various cellular processes and on stem cells. It was recently shown that applying LLLT to BM in rats post-myocardial infarction caused a marked reduction of scar tissue formation in the heart.

Methods: Eighty-three mice were divided into five groups: control sham-treated and laser-treated at measured density of either 4, 10, 18, or 40 mW/cm(2) at the BM level. The laser was applied to the exposed flat medial part of the tibia 8 mm from the knee joint for 100 sec. Mice were monitored for 8 months and then killed, and histopathology was performed on various organs.

Results: No histological differences were observed in the liver, kidneys, brain or BM of the laser-treated mice as compared with the sham-treated, control mice. Moreover, no neoplasmic response in the tissues was observed in the laser-treated groups as compared with the control, sham-treated mice. There were no significant histopathological differences among the same organs under different laser treatment regimes in response to the BM-derived mesenchymal stem cell proliferation following LLLT to the BM.

Conclusions: LLLT applied multiple times either at the optimal dose (which induces photobiostimulation of stem cells in the BM), or at a higher dose (such as five times the optimal dose), does not cause histopathological changes or neoplasmic response in various organs in mice, as examined over a period of 8 months.

MeSH terms

  • Animals
  • Bone Marrow / radiation effects*
  • Dose-Response Relationship, Radiation
  • Kidney / radiation effects
  • Liver / radiation effects
  • Low-Level Light Therapy*
  • Mesenchymal Stem Cells / radiation effects
  • Mice
  • Mice, Inbred ICR
  • Stem Cells / radiation effects