Polyvinyl chloride (PVC) microplastics are emerging contaminants affecting biological wastewater treatment processes. So far, the toxicological investigation of PVC microplastics usually focused on the anaerobic and denitrifying bacteria. It seems that the primary lymphocytes isolated from peripheral blood are more sensitive than most other organ cell types in vitro; therefore, the aim of this study was to assess the cytotoxicity of PVC microplastic on human and fish blood lymphocytes as a useful ex vivo model for accelerated human toxicity studies. Using biochemical analyses, we showed human lymphocytes are more sensitive to toxic effects of PVC microplastic than fish lymphocytes. Our result showed that addition of PVC microplastic at 24, 48, and 96 μ g/ml for 3 h to human blood lymphocytes induced cytotoxicity. The PVC microplastic-induced cytotoxicity on human blood lymphocytes was associated with intracellular reactive oxygen species (ROS) formation, lysosomal membrane injury, mitochondrial membrane potential (MMP) collapse, depletion of glutathione, and lipid peroxidation. According to our results, PVC microplastic particles induce oxidative stress and organelle damage in human lymphocytes, while these significant alterations in toxicity parameters in PVC microplastic-treated fish lymphocytes were not observed. Finally, our findings suggest that human lymphocytes are more sensitive to PVC microplastic toxicity compared with fish lymphocytes.
Risperidone is an atypical antipsychotic drug used for the pharmacotherapy of
psychiatric disorders. Some reports indicate that risperidone is toxic to
various systems of the body, including the immune system. This study evaluated
the toxicity effect of risperidone on human blood lymphocytes. To achieve this
aim, lymphocytes were isolated using Ficoll paque plus. The results showed that
risperidone (12, 24 and 48 nM) causes toxicity in human blood
lymphocytes by increasing the level of intracellular reactive oxygen species
(ROS), damage to lysosomal membrane, the collapse of the mitochondrial membrane
potential (MMP), and increased extracellular oxidized glutathione (GSSG). Also,
exposure of human blood lymphocytes to risperidone is associated with a decrease
in intracellular glutathione (GSH) levels. Finally, it could be concluded that
oxidative stress is one of the mechanisms of risperidone-induced toxicity in
human blood lymphocytes.
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