4.7 Article

Nanoplastics-induced oxidative stress, antioxidant defense, and physiological response in exposed Wistar albino rats

Journal

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
Volume 29, Issue 8, Pages 11332-11344

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s11356-021-15920-0

Keywords

Polystyrene nanoplastics; Rat; Bioaccumulation; Serum biomarkers; Oxidative stress

Funding

  1. Ahvaz Jundishapur University of Medical Sciences, Khuzestan, Iran [33011376]

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This study found that exposure to polystyrene nanoplastics can lead to oxidative stress and physiological changes in male rats, including an increase in reactive oxygen species, alterations in antioxidant responses, and changes in biochemical parameters. The results suggest possible neurobehavioral effects, dysfunctions in energy metabolism, and kidney dysfunction associated with exposure conditions. Further research with a larger sample size is needed to validate these findings.
Nowadays, plastic pollution and in particular nano(micro)plastics is considered as an issue of global concern in environmental samples. The present work was conducted to clarify the oxidative stress of polystyrene nanoplastics (PS-NPs) exposure and physiological response of male Wistar rats. Animals were treated orally with PS-NPs at four doses (1, 3, 6, and10 mg/kg-day) for 5 weeks. Results demonstrated the accumulation of PS-NPs through whole body scanning and also a dose-dependent increase in the production of reactive oxygen species (ROS). Alterations in antioxidant responses including serum levels of catalase (CAT) and total glutathione content were noticed, but not superoxide dismutase (SOD), pointing towards the perturbation of redox state induced by exposure conditions. 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. 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 may be the potential modes 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 consequences of NPs which might induce effects such as oxidative stress relating to the induction of antioxidant enzymes, the results warrant additional research with a larger sample size.

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