家蚕
超氧化物歧化酶
中肠
摄入
脂质过氧化
过氧化氢酶
微塑料
活性氧
生物
化学
毒理
生物化学
氧化应激
幼虫
细胞生物学
生态学
基因
作者
Camilla Carla Parenti,Andrea Binelli,Silvia Caccia,Camilla Della Torre,Stefano Magni,G. Pirovano,Morena Casartelli
出处
期刊:Chemosphere
[Elsevier]
日期:2020-10-01
卷期号:257: 127203-127203
被引量:31
标识
DOI:10.1016/j.chemosphere.2020.127203
摘要
Information on the occurrence and effects of nanoplastics in ecosystems worldwide currently represent one of the main challenges from the ecotoxicological point of view. This is particularly true for terrestrial environments, in which nanoplastics are released directly by human activities or derive from the fragmentation of larger plastic items incorrectly disposed. Since insects can represent a target for these emerging contaminants in land-based community, the aim of this study was the evaluation of ingestion of 0.5 μm polystyrene nanoplastics and their effects in silkworm (Bombyx mori) larvae, a useful and well-studied insect model. The ingestion of nanoplastics, the possible infiltration in the tissues and organ accumulation were checked by confocal microscopy, while we evaluated the effects due to the administered nanoplastics through a multi-tier approach based on insect development and behaviour assessment, as endpoints at organism level, and the measurements of some biochemical responses associated with the imbalance of the redox status (superoxide dismutase, catalase, glutathione s-transferase, reactive oxygen species evaluation, lipid peroxidation) to investigate the cellular and molecular effects. We observed the presence of microplastics in the intestinal lumen, but also inside the larvae, specifically into the midgut epithelium, the Malpighian tubules and in the haemocytes. The behavioural observations revealed a significant (p < 0.05) increase of erratic movements and chemotaxis defects, potentially reflecting negative indirect effects on B. mori survival and fitness, while neither effect on insect development nor redox status imbalance were measured, with the exception of the significant (p < 0.05) inhibition of superoxide dismutase activity.
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