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1.
J Appl Toxicol ; 36(10): 1364-73, 2016 10.
Artigo em Inglês | MEDLINE | ID: mdl-27225715

RESUMO

Titanium dioxide nanoparticles (TiO2 -NPs) have been widely used in many applications. Owing to their nanoscale size, interactions between cells and NPs have been expansively investigated. With the health concerns raised regarding the adverse effects of these interactions, closer examination of whether TiO2 -NPs can induce toxicity towards human cells is greatly needed. Therefore, in this study, we investigated the cytotoxicity of TiO2 -NPs towards human blood cells (peripheral blood mononuclear cells [PBMCs]) in serum-free medium, for which there is little information regarding the cytotoxic effects of TiO2 -NPs. Our results provide evidence that PBMCs treated with TiO2 -NPs (at concentrations ≥25 µg ml(-1) ) for 24 h significantly reduced cell viability and significantly increased production of toxic mediators such as reactive oxygen species and inflammatory response cytokines such as interleukin-6 and tumor necrosis factor-α (P < 0.05). Cell apoptosis induction also occurred at these concentrations. Significant expressions of cyclooxygenase-2 and interleukin-1ß were also observed in PBMCs treated with TiO2 -NPs at concentrations ≥125 µg ml(-1) . Our data presented here clearly indicate that the concentration of TiO2 -NPs (at size ~26.4 ± 1.2 nm) applied to human blood cells has a strong impact on cytotoxic induction. Copyright © 2016 John Wiley & Sons, Ltd.


Assuntos
Apoptose/efeitos dos fármacos , Interleucina-6/biossíntese , Leucócitos Mononucleares/efeitos dos fármacos , Nanopartículas/toxicidade , Titânio/toxicidade , Fator de Necrose Tumoral alfa/biossíntese , Permeabilidade da Membrana Celular/efeitos dos fármacos , Sobrevivência Celular/efeitos dos fármacos , Meios de Cultura Livres de Soro , Ciclo-Oxigenase 2/genética , Relação Dose-Resposta a Droga , Humanos , Interleucina-1beta/genética , Interleucina-6/imunologia , Leucócitos Mononucleares/imunologia , Leucócitos Mononucleares/patologia , Nanopartículas/química , Espécies Reativas de Oxigênio/metabolismo , Titânio/química , Fator de Necrose Tumoral alfa/imunologia
2.
Aquat Toxicol ; 224: 105517, 2020 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-32485496

RESUMO

Temperature affects physiological processes in organisms and the toxicity of chemicals. The widespread industrial use of ZnO causes contamination in aquatic ecosystems. This study aimed to investigate the chronic toxicity of ZnO at different temperatures using Daphnia magna as a model organism. The chronic toxicity of five different concentrations of ZnO was assessed at 23 °C and 28 °C. The results showed that higher concentrations of ZnO inhibited growth, production of first clutch eggs and juvenile accumulation at both 23 °C and 28 °C. Growth rate, numbers of first clutch eggs and juvenile accumulation were lower at 28 °C than at 23 °C. We also observed the levels of malondialdehyde (MDA) and superoxide dismutase (SOD) activity. At higher concentrations of ZnO, oxidative stress was induced leading to increase MDA level and decrease SOD activity at 28 °C. These findings indicated that high temperature and high concentration of ZnO inhibited the activity of enzymatic proteins. Nonetheless, among all treatments, the accumulation of zinc in D. magna was not significantly different. Our results suggested that both ZnO and higher temperature induced oxidative stress in D. magna. As a result, MDA concentration increased, SOD activity changed and the growth and reproduction of D. magna was adversely affected.


Assuntos
Daphnia/efeitos dos fármacos , Temperatura Alta , Características de História de Vida , Estresse Oxidativo/efeitos dos fármacos , Poluentes Químicos da Água/toxicidade , Óxido de Zinco/toxicidade , Animais , Daphnia/crescimento & desenvolvimento , Daphnia/metabolismo , Ecossistema , Temperatura Alta/efeitos adversos , Malondialdeído/metabolismo , Reprodução/efeitos dos fármacos
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