We can't find the internet
Attempting to reconnect
Something went wrong!
Hang in there while we get back on track
Physiological stress response of the Wistar albino rats orally exposed to polystyrene nanoparticles
Summary
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.
Sign in to start a discussion.
More Papers Like This
Nanoplastics-induced oxidative stress, antioxidant defense, and physiological response in exposed Wistar albino rats
Researchers orally exposed Wistar rats to polystyrene nanoplastics at multiple doses for five weeks and observed dose-dependent increases in oxidative stress. The study found significant alterations in liver and kidney function markers, disrupted energy metabolism, and changes in antioxidant enzyme activity, suggesting that nanoplastic exposure may affect multiple organ systems in mammals.
Screening for polystyrene nanoparticle toxicity on kidneys of adult male albino rats using histopathological, biochemical, and molecular examination results
Researchers found that oral exposure to polystyrene nanoparticles caused significant kidney damage in rats, including oxidative stress, impaired renal function, and tissue alterations that worsened with increasing dose, demonstrating their nephrotoxic potential.
In vivo impact assessment of orally administered polystyrene nanoplastics: biodistribution, toxicity, and inflammatory response in mice
Researchers orally administered polystyrene nanoplastics to mice for two weeks and tracked their distribution and biological effects. The nanoplastics accumulated primarily in the intestine, kidneys, and liver, triggering significant inflammatory responses and oxidative stress in these organs despite no visible tissue damage. The study provides evidence that even short-term oral exposure to nanoplastics can cause meaningful inflammatory changes in multiple organ systems.
Acute Toxicity Assessment of Orally Administered Microplastic Particles in Adult Male Wistar Rats
Researchers gave adult male rats a single oral dose of microplastics made from PET water bottles and found that even this one-time exposure altered markers of liver, heart, and kidney function. Higher doses also reduced food intake and increased signs of oxidative stress, which is cell damage caused by harmful molecules. This study suggests that even brief microplastic exposure could trigger early changes in organ function, raising questions about the cumulative effect of daily human exposure through food and water.
Thyroid endocrine status and biochemical stress responses in adult male Wistar rats chronically exposed to pristine polystyrene nanoplastics
Adult male rats were given daily oral doses of polystyrene nanoplastics for five weeks, causing dose-dependent reductions in thyroid hormone levels (T3, T4, FT3, FT4) and increases in TSH, along with elevated oxidative stress markers. The study provides evidence that chronic nanoplastic ingestion disrupts the thyroid endocrine system in a mammalian model.