Abstract
The most important welding processes used are the Gas Metal Arc (GMA) welding, the Tungsten Inert Gas (TIG) welding, and the Manual Metal Arc (MMA) welding processes. The goal of our investigation was to monitor the distribution of iron (Fe), manganese (Mn), calcium (Ca) and magnesium (Mg) in the lung, spleen, liver, and kidney of mice after inhalation exposure of different welding methods using different steel base materials. The treatment groups were the following: MMA-mild steel, MMA-molybdenum-manganese (MoMn) alloy, TIG-mild steel, and TIG-stainless steel. The samples were taken 24- and 96 hours after the treatments.Most importantly, it was found that the Mn concentration in the lung’ samples of the MMA-mild steel and the MMA-MoMn groups was increased extremely at both sampling times and in the spleen’ samples also. In the TIG groups, the rise of the Mn concentration was only considerable in the lungs and spleens at 24h, and emerged concentration was found in the liver in 96h samples. Histopathology demonstrated emerged siderin content in the spleens of the treated animals and in siderin filled macrophages in the lungs mostly in all treated groups. Traces of high-level glycogen retention was found in the MMA groups at both sampling times. Similar glycogen retention in TIG-Ms and TIG stainless group’s liver samples and emerged number of vacuoles, especially in the hepatocytes of the TIG-stainless steel 96h group were also found.The mentioned results raise the consequence that there is a considerable difference in the kinetics of the Mn distribution between the MMA- and the TIG-fume treated groups. Hence, the result suggests that manganese has a particle-size dependent toxico-kinetics property. The anomaly of the glycogen metabolism indicates the systemic effect of the welding fumes. Also, the numerous vacuoles mentioned above show a possible liver-specific adverse effect of some components of the TIG-stainless steel welding fumes.
Mild steel and stainless steel welding fumes elicit pro‐inflammatory and pro‐oxidant effects in first trimester trophoblast cells
