4.7 Article

Exposure to dibutyl phthalate adsorbed to multi-walled carbon nanotubes causes neurotoxicity in mice by inducing the release of BDNF

期刊

SCIENCE OF THE TOTAL ENVIRONMENT
卷 852, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.scitotenv.2022.158319

关键词

Dibutyl phthalate; Multi-walled carbon nanotubes; The combined exposure; Neurotoxicity; Brain-derived neurotrophic factor

资金

  1. National Natural Science Foundation of China [32170508, 31772471]

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This study investigates whether dibutyl phthalate (DBP), an environmental hormone disruptor, mediated by multi-walled carbon nanotubes (MWCNTs), can more easily cross the blood-brain barrier and whether it has neurotoxic effects on brain cells. The results demonstrate that MWCNTs adsorbed with DBP can induce the release of BDNF, accelerate the apoptosis of neurons, reduce the number of nerve cells, activate microglia, leading to neuroinflammation and nervous system toxicity.
Multi-walled carbon nanotubes (MWCNTs) and dibutyl phthalate (DBP) exist extensively in the environment, and they are easy to form compound pollution through pi-pi interactions in the environment. We investigate whether DBP, an environmental hormone disruptor, mediated by CNTs can more easily cross the blood-brain barrier, and whether DBP entering the brain has neurotoxic effects on the cells in the brain. Experimental subjects were 40 male Kunming (KM) mice randomly divided into 4 groups: the control group; the MWCNTs group; the DBP group; and the MWCNTs+DBP group. The mice were exposed via tail intravenous injection once every 3 days for 21 days, following which toxicology studies were carried out. The results of behavioral experiments showed that the mice in the com-bined exposure group (MWCNTs+DBP) exhibited spatial learning and memory impairment, and anxiety-like behav-ior. Staining of hippocampal sections of mouse brain tissue showed that, in the CA1, CA2, and DG areas, the number of neurons decreased, the nucleus was pyknotic, the cell body was atrophied, and levels of the microglia marker Iba-1 increased. By proteomic KEGG analysis, we found that the DEPs were mainly those related to neurodegenerative dis-eases. Immunohistochemistry in the hippocampus indicated that the level of brain-derived neurotrophic factor (BDNF) in the DG region was significantly increased. RT-PCR results revealed that the expression levels of P53, caspase3, and Bax genes related to apoptosis were up-regulated. The experimental results demonstrated that the mechanism of the combined-exposure injury to neurons in the hippocampus of mice may be that MWCNTs with adsorbed DBP can induce the release of BDNF, accelerate the apoptosis of neurons, and reduce the number of nerve cells, which activates microglia, causing neuroinflammation and nervous system toxicity.

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