TY - JOUR
T1 - Antioxidants protect against dopamine-induced metallothionein-III (GIF) mRNA expression in mouse glial cell line (VR-2g)
AU - Sogawa, Chiharu
AU - Miyazaki, Ikuko
AU - Sogawa, Norio
AU - Asanuma, Masato
AU - Ogawa, Norio
AU - Furuta, Hiroaki
N1 - Funding Information:
This study was supported in part by Grants-in-Aid for Comprehensive Research on Aging and Health from the Japanese Ministry of Health and Welfare, and Grants-in-Aid from the Japanese Ministry of Education, Science, Sports and Culture.
PY - 2000/1/24
Y1 - 2000/1/24
N2 - Metallothionein (MT)-III, originally discovered as a growth inhibitory factor (GIF), is a brain specific isomer of MTs and is markedly reduced in the brain of patients with Alzheimer's disease (AD) or other neurodegenerative diseases. We analyzed the level and regulation of mRNA expression of MT-III in immortalized fetal mouse brain glial cells (VR-2g) by reverse transcriptase-polymerase chain reaction (RT-PCR). We have recently reported that dopamine (DA) increases the expression of MT-III mRNA in vitro. In this study, we investigated the mechanism of such increase by examining the effects of DA agonists (SKF38393 or bromocriptine) and DA antagonists (SCH23390 or sulpiride) on the expression of MT-III mRNA. MT-III mRNA did not change by either agonist and DA-increased MT-III mRNA was not inhibited by either antagonist. These results suggested that the induction of MT-III mRNA by DA was not mediated by stimulation of DA receptors. On the other hand, DA-induced MT-III mRNA expression was strongly inhibited by the addition of antioxidants (glutathione, vitamin E or ascorbic acid), indicating that DA-enhanced MT-III mRNA was mediated by reactive oxygen species. Our results suggest that oxidative stress may be one of the principle factors that modulate MT-III mRNA expression. Copyright (C) 2000 Elsevier Science B.V.
AB - Metallothionein (MT)-III, originally discovered as a growth inhibitory factor (GIF), is a brain specific isomer of MTs and is markedly reduced in the brain of patients with Alzheimer's disease (AD) or other neurodegenerative diseases. We analyzed the level and regulation of mRNA expression of MT-III in immortalized fetal mouse brain glial cells (VR-2g) by reverse transcriptase-polymerase chain reaction (RT-PCR). We have recently reported that dopamine (DA) increases the expression of MT-III mRNA in vitro. In this study, we investigated the mechanism of such increase by examining the effects of DA agonists (SKF38393 or bromocriptine) and DA antagonists (SCH23390 or sulpiride) on the expression of MT-III mRNA. MT-III mRNA did not change by either agonist and DA-increased MT-III mRNA was not inhibited by either antagonist. These results suggested that the induction of MT-III mRNA by DA was not mediated by stimulation of DA receptors. On the other hand, DA-induced MT-III mRNA expression was strongly inhibited by the addition of antioxidants (glutathione, vitamin E or ascorbic acid), indicating that DA-enhanced MT-III mRNA was mediated by reactive oxygen species. Our results suggest that oxidative stress may be one of the principle factors that modulate MT-III mRNA expression. Copyright (C) 2000 Elsevier Science B.V.
KW - Antioxidant
KW - Dopamine
KW - Dopamine receptor
KW - Glial cell
KW - Growth inhibitory factor (GIF)
KW - Metallothionein-III
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U2 - 10.1016/S0006-8993(99)02284-2
DO - 10.1016/S0006-8993(99)02284-2
M3 - Article
C2 - 10640628
AN - SCOPUS:0033987764
SN - 0006-8993
VL - 853
SP - 310
EP - 316
JO - Molecular Brain Research
JF - Molecular Brain Research
IS - 2
ER -