» Articles » PMID: 24448416

SiO2 Nanoparticles Change Colour Preference and Cause Parkinson's-like Behaviour in Zebrafish

Overview
Journal Sci Rep
Specialty Science
Date 2014 Jan 23
PMID 24448416
Citations 29
Authors
Affiliations
Soon will be listed here.
Abstract

With advances in the development of various disciplines, there is a need to decipher bio-behavioural mechanisms via interdisciplinary means. Here, we present an interdisciplinary study of the role of silica nanoparticles (SiO2-NPs) in disturbing the neural behaviours of zebrafish and a possible physiological mechanism for this phenomenon. We used adult zebrafish as an animal model to evaluate the roles of size (15-nm and 50-nm) and concentration (300 μg/mL and 1000 μg/mL) in SiO2-NP neurotoxicity via behavioural and physiological analyses. With the aid of video tracking and data mining, we detected changes in behavioural phenotypes. We found that compared with 50-nm nanosilica, 15-nm SiO2-NPs produced greater significant changes in advanced cognitive neurobehavioural patterns (colour preference) and caused potentially Parkinson's disease-like behaviour. Analyses at the tissue, cell and molecular levels corroborated the behavioural results, demonstrating that nanosilica acted on the retina and dopaminergic (DA) neurons to change colour preference and to cause potentially Parkinson's disease-like behaviour.

Citing Articles

Advancing Central Nervous System Drug Delivery with Microtubule-Dependent Transcytosis of Novel Aqueous Compounds.

Zhang M, Zhong S, An L, Xiang P, Hu N, Huang W Biomater Res. 2024; 28:0051.

PMID: 39050687 PMC: 11268840. DOI: 10.34133/bmr.0051.


Assessing Drug Administration Techniques in Zebrafish Models of Neurological Disease.

Chaoul V, Dib E, Bedran J, Khoury C, Shmoury O, Harb F Int J Mol Sci. 2023; 24(19).

PMID: 37834345 PMC: 10573323. DOI: 10.3390/ijms241914898.


VDAC1 Protein Regulation of Oxidative Damage and Mitochondrial Dysfunction-Mediated Cytotoxicity by Silica Nanoparticles in SH-SY5Y Cells.

Ning X, Li X, Ma K, Pang H, Tian T, Hao H Mol Neurobiol. 2023; 60(11):6542-6555.

PMID: 37458989 DOI: 10.1007/s12035-023-03491-9.


Silica Nanoparticles Promote α-Synuclein Aggregation and Parkinson's Disease Pathology.

Yuan X, Yang Y, Xia D, Meng L, He M, Liu C Front Neurosci. 2022; 15:807988.

PMID: 35095403 PMC: 8792744. DOI: 10.3389/fnins.2021.807988.


A perspective on persistent toxicants in veterans and amyotrophic lateral sclerosis: identifying exposures determining higher ALS risk.

Re D, Yan B, Calderon-Garciduenas L, Andrew A, Tischbein M, Stommel E J Neurol. 2022; 269(5):2359-2377.

PMID: 34973105 PMC: 9021134. DOI: 10.1007/s00415-021-10928-5.


References
1.
Nornes S, Newman M, Wells S, Verdile G, Martins R, Lardelli M . Independent and cooperative action of Psen2 with Psen1 in zebrafish embryos. Exp Cell Res. 2009; 315(16):2791-801. DOI: 10.1016/j.yexcr.2009.06.023. View

2.
Newman M, Tucker B, Nornes S, Ward A, Lardelli M . Altering presenilin gene activity in zebrafish embryos causes changes in expression of genes with potential involvement in Alzheimer's disease pathogenesis. J Alzheimers Dis. 2009; 16(1):133-47. DOI: 10.3233/JAD-2009-0945. View

3.
Kashiwada S . Distribution of nanoparticles in the see-through medaka (Oryzias latipes). Environ Health Perspect. 2006; 114(11):1697-702. PMC: 1665399. DOI: 10.1289/ehp.9209. View

4.
Slowing I, Trewyn B, Lin V . Mesoporous silica nanoparticles for intracellular delivery of membrane-impermeable proteins. J Am Chem Soc. 2007; 129(28):8845-9. DOI: 10.1021/ja0719780. View

5.
Shannon W, Culverhouse R, Duncan J . Analyzing microarray data using cluster analysis. Pharmacogenomics. 2003; 4(1):41-52. DOI: 10.1517/phgs.4.1.41.22581. View