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Aluminium oxide nanoparticles compromise spatial learning and memory performance in rats

Authors :
M'rad, Imen
Jeljeli, Mustapha
Rihane, Naima
hilber, pascal
Sakly, Mohsen
Amara, Salem
Laboratoire de Physiologie Intégrée [Bizerte, Tunisia]
Faculté des Sciences de Bizerte [Université de Carthage]
Université de Carthage - University of Carthage-Université de Carthage - University of Carthage
Université de Carthage - University of Carthage
Laboratoire Bio-PeroxIL. Biochimie du Peroxysome, Inflammation et Métabolisme Lipidique (Bio-PeroxIL)
Université de Bourgogne (UB)
Centre de Recherches sur les Fonctionnements et Dysfonctionnements Psychologiques (CRFDP)
Université de Rouen Normandie (UNIROUEN)
Normandie Université (NU)-Normandie Université (NU)-Institut de Recherche Interdisciplinaire Homme et Société (IRIHS)
Normandie Université (NU)-Normandie Université (NU)-Université de Rouen Normandie (UNIROUEN)
Normandie Université (NU)
Laboratoire de Physiologie Intégrée
Physiologie Intégrée
Institut de Recherche Interdisciplinaire Homme et Société (IRIHS)
Source :
EXCLI Journal, EXCLI Journal, 2018, 17, pp.200-210. ⟨10.17179/excli2017-1050⟩
Publication Year :
2018
Publisher :
Technische Universität Dortmund, 2018.

Abstract

Recently, the biosafety and potential influences of nanoparticles on central nervous system have received more attention. In the present study, we assessed the effect of aluminium oxide nanoparticles (Al2O3-NPs) on spatial cognition. Male Wistar rats were intravenously administered Al2O3-NP suspension (20 mg/kg body weight/day) for four consecutive days, after which they were assessed. The results indicated that Al2O3-NPs impaired spatial learning and memory ability. An increment in malondialdehyde levels with a concomitant decrease in superoxide dismutase activity confirmed the induction of oxidative stress in the hippocampus. Additionally, our findings showed that exposure to Al2O3-NPs resulted in decreased acetylcholinesterase activity in the hippocampus. Fur- thermore, Al2O3-NPs enhanced aluminium (Al) accumulation and disrupted mineral element homoeostasis in the hippocampus. However, they did not change the morphology of the hippocampus. Our results show a connection among oxidative stress, disruption of mineral element homoeostasis, and Al accumulation in the hippocampus, which leads to spatial memory deficit in rats treated with Al2O3-NPs.<br />EXCLI Journal;Vol. 17 2018

Details

Language :
English
Database :
OpenAIRE
Journal :
EXCLI Journal, EXCLI Journal, 2018, 17, pp.200-210. ⟨10.17179/excli2017-1050⟩
Accession number :
edsair.doi.dedup.....bf3029e539a2405360777cfdc7e3141c
Full Text :
https://doi.org/10.17877/de290r-18916