aging is a normal and inevitable cellular physiological process, however, in current days, individual or environmental factors are contributors to early aging, thus generating an impaired healthspan. barker, in an ecologic psychology context mentioned that "the environment always exerts influences in the individual". if we adapt this to the toxicological sphere, daily we are exposed to many agents, whether intentional (drug's abuse) or in a non-intentional manner (environmental or occupational), that induce countless toxic effects to the organism (influence). toluene is a major solvent used in industry of paints, gasoline and adhesives, therefore, workers are the non-intentional target public. however, toluene is also a psychoactive substance and epidemiologic data have shown its abuse as the third mostly consumed in comparison to others drugs there are many studies reporting the short-term effects of toluene, nevertheless, long-term effects after end of exposure are scarce. based on that, the aim of our work was to investigate the long-term impact of airborne exposure to toluene using caenorhabditis elegans. we used two strains:
n2 wild type and mutant
pe255 feIs5 [
sur-5p::luciferase::GFP +
rol-6(
su1006)] to measure atp levels. approximately 100 nematodes at
l4 stage were exposed to toluene in a vapor chamber for 24h, mimetizing two scenarios of exposure: scenario 1 (mean conc. 792 ppm) and scenario 2 (mean conc. 1,094 ppm). the experiments were conducted 1, 48 and 96 hours after exposure. lipofuscin autofluorescence was measured as an aging bioindicator, neurobehaviors (head trashes, velocity and path length) to assess healthspan, and atp levels as mitochondrial function endpoint. we observed that worms exposed to both scenarios of exposure have shown increase of cellular lipofuscin accumulation, and that exposed worms demonstrated a progressive reduction of mobility in a significant manner. these findings corroborated with a decrease of mitochondrial functionality, demonstrated by atp levels reduction. here we demonstrate that toluene-induced early cellular aging can occur associate to accentuated motor loss that could be explained by a mitochondrial dysfunction, thus impacting on healthspan reduction. the literature supports this discovery, once long-term exposures either intentionally or occupationally are harmful to humans, however, here we observed that even long periods after withdrawal the toluene effects remain.