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Protection against arsenic trioxide-induced autophagic cell death in U118 human glioma cells by use of lipoic acid.
Type
article
Resource
Food and Chemical Toxicology.(45):1027-1038.
Date Issued
2007
Author(s)
何元順
Tain-Junn Cheng
Ying-Jan Wang
Wei-Wan Kao
Rong-Jane Chen
Yuan-Soon Ho
Subjects
醫學檢驗暨生物技術學系
期刊論文
Abstract
Arsenic is an environmental toxicant found naturally in ground water. Epidemiological studies have suggested a correlation between
chronic arsenic exposure and potential brain tissue damage in clinical case and animal experiments. Lipoic acid (LA) is a thiol-compound
naturally occurring in plants and animals, which is thought to be a strong antioxidant and possess neuroprotective effects. The objective
of this study was to determine if the AS2O3-induced glial cell toxicity could be prevented by LA. The human malignant glioma cell
(U118) was selected as a research model. By using acridine orange staining and flow cytometry analysis, we found that autophagic,
but not apoptotic, cell death was significantly induced by AS2O3 in U118 cells, and that AS2O3-mediated autophagic cell death was
nearly completely attenuated by LA. Down-regulation of p53 and Bax proteins and the up-regulation of Bcl-2 and HSP-70 proteins were
observed by western blot in AS2O3-mediated autophagic cell death. Our results implied that LA completely inhibited U118 cells autophagic
cell death induced by AS2O3. We suggested that LA may emerge as a useful protective agent against arsenic-induced glial cell
toxicity and reversing arsenic-induced damage in human brain.
chronic arsenic exposure and potential brain tissue damage in clinical case and animal experiments. Lipoic acid (LA) is a thiol-compound
naturally occurring in plants and animals, which is thought to be a strong antioxidant and possess neuroprotective effects. The objective
of this study was to determine if the AS2O3-induced glial cell toxicity could be prevented by LA. The human malignant glioma cell
(U118) was selected as a research model. By using acridine orange staining and flow cytometry analysis, we found that autophagic,
but not apoptotic, cell death was significantly induced by AS2O3 in U118 cells, and that AS2O3-mediated autophagic cell death was
nearly completely attenuated by LA. Down-regulation of p53 and Bax proteins and the up-regulation of Bcl-2 and HSP-70 proteins were
observed by western blot in AS2O3-mediated autophagic cell death. Our results implied that LA completely inhibited U118 cells autophagic
cell death induced by AS2O3. We suggested that LA may emerge as a useful protective agent against arsenic-induced glial cell
toxicity and reversing arsenic-induced damage in human brain.
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