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1.
Chemosphere ; 324: 138292, 2023 May.
Artigo em Inglês | MEDLINE | ID: mdl-36870618

RESUMO

Soil contamination by microplastics (MPs) has gained widespread attention, whose fate may be influenced by land use types. The effects of land use types and the intensity of human activities on the distribution and sources of soil MPs at the watershed scale are unclear. In this study, 62 surface soil sites in representing five land use types (urban, tea garden, dryland, paddy field and woodland) and 8 freshwater sediment sites were investigated in the Lihe River watershed. MPs were detected in all samples, and the average abundance of soil and sediments was 401.85 ± 214.02 and 222.13 ± 54.66 items/kg, respectively. The soil MPs abundance followed the sequence: urban > paddy field > dryland > tea garden > woodland. Soil MP distribution and MP communities were significant different (p < 0.05) among land use types. The similarity of MP community highly correlated with geographic distance, and woodlands and freshwater sediments may be a potential fate for MPs in the Lihe River watershed. Soil clay, pH, and bulk density significantly correlated with MP abundance and fragment shape (p < 0.05). The positive correlation between population density, Total- Point of Interest (POI) and MP diversity indicates the importance of intensity of human activities in exacerbating soil MP pollution (p < 0.001). Plastic waste sources accounted for 65.12%, 58.60%, 48.15% and 25.35% of MPs in urban, tea garden, dryland and paddy field soils, respectively. Differences in the intensity of agricultural activities and cropping patterns were associated with different percentages of mulching film sources in the three types of agricultural soils. This study provides new ideas for the quantitative analysis of soil MP sources in different land use types.


Assuntos
Microplásticos , Poluentes Químicos da Água , Humanos , Microplásticos/análise , Plásticos , Solo , Rios , Poluentes Químicos da Água/análise , Monitoramento Ambiental , China , Chá
2.
J Cell Physiol ; 237(8): 3292-3304, 2022 08.
Artigo em Inglês | MEDLINE | ID: mdl-35616291

RESUMO

Bisphenol A (BPA) in the environment can have deleterious effects on humans and animals. BPA can exert nephrotoxicity by inducing oxidative stress. Selenium (Se) deficiency can specifically impair kidney tissues and additionally show a synergistic effect on the toxicity of several environmental chemicals. However, the toxic effects of BPA on the chicken kidney and whether Se deficiency produces synergistic effects on the toxicity of BPA remain poorly understood. Herein, we established BPA exposure models and Se deficiency model in vivo and in vitro, and described the discovery path of BPA aggravation on apoptosis and necroptosis in Se-deficient chicken kidneys via regulation of oxidative stress and phosphatidylinositol 3-kinase/threonine kinase (PI3K/AKT) signaling pathway. We found that BPA exposure increased reactive oxygen species and malondialdehyde levels, reduced activities of catalase, GPx, and superoxide dismutase, downregulated PI3K and AKT expressions, activated Bcl/Bax-Caspase 9-Caspase 3, and receptor-interacting protein kinase 1/mixed lineage kinase domain-like protein signaling pathways, resulting in apoptosis and necroptosis in the chicken kidney. In addition, Se deficiency significantly promoted the expression of renal apoptosis and necroptosis in BPA-exposed chicken kidneys. Altogether, our results showed that BPA aggravates apoptosis and necroptosis in Se-deficient chicken kidneys via regulation of oxidative stress and PI3K/AKT signaling pathway. Our findings elucidate the mechanism of BPA nephrotoxicity and Se deficiency exacerbation toxicity in chickens and will provide great significance for the protection of the ecological environment and animal health.


Assuntos
Compostos Benzidrílicos , Rim , Fenóis , Selênio , Animais , Apoptose , Compostos Benzidrílicos/toxicidade , Galinhas/metabolismo , Rim/efeitos dos fármacos , Rim/patologia , Necroptose , Estresse Oxidativo , Fenóis/toxicidade , Fosfatidilinositol 3-Quinases/metabolismo , Proteínas Proto-Oncogênicas c-akt/metabolismo , Selênio/deficiência
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