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亚急性二氧化硅纳米颗粒暴露导致大鼠海马区氧化应激和炎症,同时破坏胆碱能系统和行为功能。

Subacute silica nanoparticle exposure induced oxidative stress and inflammation in rat hippocampus combined with disruption of cholinergic system and behavioral functions.

机构信息

Laboratory of Toxicology-Microbiology and Environmental Health (17ES06), Faculty of Sciences of Sfax, University of Sfax, BP1171, 3000 Sfax, Tunisia.

Laboratory of Toxicology-Microbiology and Environmental Health (17ES06), Faculty of Sciences of Sfax, University of Sfax, BP1171, 3000 Sfax, Tunisia; Neurochemistry and Neuroimmunology Research Group, Department of Psychiatry and Psychotherapy, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Hauptstrasse 5, 79104 Freiburg, Germany.

出版信息

NanoImpact. 2021 Oct;24:100358. doi: 10.1016/j.impact.2021.100358. Epub 2021 Sep 25.

Abstract

Increasing environmental exposure to silica nanoparticles (SiNPs) and limited neurotoxicity studies pose a challenge for safety evaluation and management of these materials. This study aimed to explore the adverse effects and underlying mechanisms of subacute exposure to SiNPs by the intraperitoneal route on hippocampus function in rats. Data showed that SiNPs induced a significant increase in oxidative/nitrosative stress markers including reactive oxygen species (ROS), malondialdehyde (MDA), protein oxidation (PCO) and nitrite (NO) production accompanied by reduced antioxidant enzyme activity (catalase, superoxide dismutase, and glutathione peroxidase) and decreased glutathione (GSH). Phenotypically, SiNPs exhibited spatial learning and memory impairment in the Morris water maze (MWM) test, a decrease of the discrimination index in the novel object recognition test (NORT) and higher anxiety-like behavior. SiNPs affected the cholinergic system as reflected by reduced acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) activity. In addition, SiNPs significantly increased mRNA expression level of genes related to inflammation (TNF-α, IL-1β, IL-6, and COX-2) and decreased mRNA expression level of genes related to cholinergic system including choline acetyltransferase (ChAT), vesicular acetylcholine transporter (VAChT), AChE, muscarinic acetylcholine receptor M1 (m1AChR) and nicotinic acetylcholine receptors (nAChR). Histopathological results further showed an alteration in the hippocampus of treated animals associated with marked vacuolation in different hippocampus areas. These findings provide new insights into the molecular mechanism of SiNPs-induced hippocampal alterations leading to impairment of cognitive and behavioral functions, and implicating oxidative stress and inflammation in the hippocampus, as well as disruption of cholinergic system.

摘要

日益增加的环境暴露于硅纳米颗粒(SiNPs)和有限的神经毒性研究对这些材料的安全性评估和管理提出了挑战。本研究旨在通过腹腔途径探索亚急性暴露于 SiNPs 对大鼠海马功能的不良影响和潜在机制。数据显示,SiNPs 诱导氧化/硝化应激标志物显著增加,包括活性氧(ROS)、丙二醛(MDA)、蛋白质氧化(PCO)和亚硝酸盐(NO)的产生,同时抗氧化酶活性(过氧化氢酶、超氧化物歧化酶和谷胱甘肽过氧化物酶)降低,谷胱甘肽(GSH)减少。表型上,SiNPs 在 Morris 水迷宫(MWM)测试中表现出空间学习和记忆障碍,新颖物体识别测试(NORT)中的辨别指数降低,焦虑样行为增加。SiNPs 影响胆碱能系统,表现为乙酰胆碱酯酶(AChE)和丁酰胆碱酯酶(BChE)活性降低。此外,SiNPs 显著增加与炎症相关的基因(TNF-α、IL-1β、IL-6 和 COX-2)的 mRNA 表达水平,并降低与胆碱能系统相关的基因(包括胆碱乙酰转移酶(ChAT)、囊泡乙酰胆碱转运体(VAChT)、AChE、毒蕈碱乙酰胆碱受体 M1(m1AChR)和烟碱型乙酰胆碱受体(nAChR))的 mRNA 表达水平。组织病理学结果进一步显示,处理动物的海马发生改变,不同海马区域出现明显空泡化。这些发现为 SiNPs 诱导的海马改变导致认知和行为功能障碍的分子机制提供了新的见解,并提示氧化应激和炎症在海马中以及胆碱能系统的破坏。

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