Influence of neodymium-doped yttrium aluminum garnet laser exposure time on cytokine secretion in lipopolysaccharide-challenged rat peripheral blood mononuclear cells
Year: 2024
Type: article
Abstract: Multiple investigators have suggested that infrared laser energy facilitates hard and soft tissue wound healing through various mechanisms, including the suppression of inflammation. This study investigated the influence of neodymium-doped yttrium aluminum garnet (Nd:YAG) laser exposure time on pro-inflammatory cytokine/chemokine concentrations in lipopolysaccharide (LPS)-stimulated rat peripheral blood mononuclear cells (PBMCs). Cultured rat PBMCs were stimulated with various LPS concentrations (0, 10, 100, or 1000 ng/mL) and treated with Nd:YAG laser irradiation for 0 (control), 30, 45, or 60 s. For these experiments, the average power, pulse duration, and repetition rate remained constant at 5 W, 100 μs, and 20 Hz, respectively. Luminex magnetic microsphere immunoassays were used to compare the secretion of 27 inflammatory mediators from LPS-stimulated PBMCs in laser-irradiated versus control groups. Two-way analysis of variance was used to compare the main effects of laser exposure time and LPS concentration on cytokine/chemokine concentrations and evaluate the potential interaction between these factors. Four pro-inflammatory cytokines – tumor necrosis factor-α, macrophage inflammatory protein (MIP)-1α, MIP-2, and interferon gamma-induced protein-10 – exhibited a trend of reduced secretion in laser-irradiated cultures. The effect appeared more pronounced at longer exposure times (45 and 60 s). However, none of the 27 inflammatory mediators exhibited statistically significant reductions in concentrations in laser-irradiated cultures versus control cultures. These observations do not support a robust anti-inflammatory effect of Nd:YAG laser irradiation. Further studies should explore the potential impact of Nd:YAG laser irradiation on cytotoxicity and cellular growth kinetics and extend across a range of irradiation parameters and cell types.
Source: Global Translational Medicine
DOI: 10.36922/gtm.4433
Language: English
Subfield: Radiology, Nuclear Medicine and Imaging
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
OpenAlex ID: W4404490171