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Physiological stress response of the Wistar albino rats orally exposed to polystyrene nanoparticles
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Rats given oral doses of polystyrene nanoparticles for five weeks showed dose-dependent increases in oxidative stress markers and changes in liver and kidney enzyme levels. The findings suggest that ingested nanoplastics can cause biochemical stress in mammals, providing data relevant to assessing human health risks.
Abstract Background Few studies have examined nano-sized plastic particulates (NPs) exposure in relation to oxidative stress and biochemical responses in rodents, commonly used for toxicity evaluations on which to base risk assessment for humans.Methods Here we explored possible oxidative stress and biochemical responses of five weeks oral exposure to polystyrene (PS) nanoparticles (1, 3, 6 and 10 mg/kg body weight per day) in male rats. We used variance analysis and variance explained statistic eta-squared (𝜂 2 ) to estimate the strength of relationships worked out. The whole body scanning further provided insight into the bio-distribution of nanoplastics upon oral exposure.Results Results demonstrated the accumulation of PS-NPs through whole body and also a dose-dependent increase in the production of reactive oxygen species (ROS). Significant alterations in antioxidant responses including serum levels of catalase, superoxide dismutase (SOD), and total glutathione content were noticed, pointing towards a perturbation of redox state induced by the exposure conditions. Acetylcholinesterase level in highest dose group was about 40 percent lower than those in control group. Biochemical parameters viz. glucose, cortisol, lipase, lactate, lactate dehydrogenase (LDH), alkaline phosphatase, gamma-glutamyl transpeptidase (GGT), triglycerides, and urea showed a significant increase, while total protein, albumin and globulin levels showed an appreciable decline.Conclusion The pattern of associations noticed with AChE activity and biochemical responses in our study suggests the possibility that a neurobehavioral effect or dysfunctions in energy metabolism, or both, may be the potential mode of action, possibly through stress response as well as liver function. Perturbations of creatinine and uric acid levels are indeed plausible biological explanations for the association with kidney dysfunction. Although we provided a new scientific clue for exploring the biological effects of plastics nanoparticles, the results warrant additional research with a larger sample size. The suggested potential mechanisms also remains to be investigated.
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