期刊论文详细信息
Bratislava Medical Journal
Mitochondrial toxicity of aluminium nanoparticles in comparison to its ionic form on isolated rat brain mitochondria
article
M. Arab-Nozari1  E. Zamani3  A. Latifi1  F. Shaki1 
[1] Pharmaceutical Science Research Center, Hemoglobinopathy Institute, Mazandaran University of Medical Sciences;Department of Toxicology and Pharmacology, Faculty of Pharmacy, Mazandaran University of Medical Sciences;Department of Toxicology and Pharmacology, Faculty of Pharmacy, Guilan University of Medical Sciences
关键词: aluminium;    nanoparticle;    isolated brain mitochondria;    toxicity;    oxidative stress;   
DOI  :  10.4149/BLL_2019_083
学科分类:医学(综合)
来源: AEPress, s.r.o.
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【 摘 要 】

OBJECTIVES: The aim of this study was to evaluate the toxic effect of AlNPs on rat brain mitochondria and compare it with that of aluminium’s ionic form. METHODS: Mitochondria were isolated from rat brain. Isolated mitochondria were treated with normal saline (Control) and different concentrations of aluminium ions (AlIs) and AlNPs (50, 100 and 200 μM). Then, the effect of AlNPs on electron transport chain complexes as well as various endpoints such as mitochondrial oxidative damage (reactive oxygen species, lipid peroxidation, glutathione, and protein carbonyl) and mitochondrial function were assessed. Also, apoptosis was evaluated by cytochrome c release, mitochondrial membrane potential and swelling. RESULTS: When compared to the control group, the exposure to AlNPs showed a marked elevation in oxidative stress markers and inhibition of complex III which was accompanied by disturbance in mitochondrial function. Also, AlNPs induced a significant collapse of mitochondrial membrane potential, mitochondrial swelling, and cytochrome c release. CONCLUSIONS: The comparison of mitochondrial toxicity markers between both forms of aluminium revealed that the toxic effect of AlNPs on isolated brain mitochondria was substantially greater than that that caused by AlIs, which can probably be ascribed to its higher reactivity (Tab. 1, Fig. 8, Ref. 45).

【 授权许可】

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