Differential cytotoxic responses of PC12 cells chronically exposed to psychostimulants or to hydrogen peroxide

被引:31
作者
Cunha-Oliveira, T
Rego, AC
Morgadinho, MT
Macedo, T
Oliveira, CR [1 ]
机构
[1] Univ Coimbra, Fac Med, Ctr Neurosci & Cell Biol, P-3004504 Coimbra, Portugal
[2] Univ Coimbra, Fac Med, Inst Biochem, P-3004504 Coimbra, Portugal
[3] Univ Coimbra, Fac Med, Inst Pharmacol & Expt Therapeut, P-3004504 Coimbra, Portugal
关键词
amphetamine; cocaine; drug abuse; neurotoxicity; oxidative stress;
D O I
10.1016/j.tox.2005.08.022
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Repeated abuse of stimulant drugs, cocaine and amphetamine, is associated with extraneuronal dopamine accumulation in specific brain areas. Dopamine may be cytotoxic through the generation of reactive oxygen species, namely hydrogen peroxide (H2O2), resulting from dopamine oxidative metabolism. In this work, we studied the cytotoxicity in PC12 cells (a dopaminergic neuronal model) chronically and/or acutely exposed to cocaine or amphetamine, as compared to H2O2 exposure. Chronic cocaine treatment induced sensitization to acute cocaine insult and increased cocaine-evoked accumulation of extracellular dopamine, although no changes in dihydroxyphenylacetic acid (DOPAC) levels were observed. Moreover, dopamine was depleted in cells chronically exposed to amphetamine and acute amphetamine toxicity persisted in these cells, indicating that dopamine was not involved in amphetamine cytotoxicity. PC12 cells chronically treated with H2O2 were totally resistant to acute H2O2, but not to acute cocaine or amphetamine exposure, suggesting that the toxicity induced by these stimulant drugs is unrelated to adaptation to oxidative stress. Interestingly, chronic cocaine treatment largely, but not completely, protected the cells against a H2O2 challenge, whilst a decrement in intracellular ATP was observed. This study shows that chronic treatment of PC 12 cells with cocaine or H2O2 modifies the cytotoxic response to an acute exposure to these agents. (C) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:54 / 62
页数:9
相关论文
共 42 条
[11]  
HYSLOP PA, 1988, J BIOL CHEM, V263, P1665
[12]   EFFECTS OF NERVE GROWTH-FACTOR ON CATALASE AND GLUTATHIONE-PEROXIDASE IN A HYDROGEN PEROXIDE-RESISTANT PHEOCHROMOCYTOMA SUBCLONE [J].
JACKSON, GR ;
SAMPATH, D ;
WERRBACHPEREZ, K ;
PEREZPOLO, JR .
BRAIN RESEARCH, 1994, 634 (01) :69-76
[13]   Possible role of NF-κB in Bcl-XL protection against hydrogen peroxide-induced PC12 cell death [J].
Jang, JH ;
Surh, YJ .
REDOX REPORT, 2004, 9 (06) :343-348
[14]   Neurotoxicity of amphetamine derivatives is mediated by caspase pathway activation in rat cerebellar granule cells [J].
Jiménez, A ;
Jordà, EG ;
Verdaguer, E ;
Pubill, D ;
Sureda, FX ;
Canudas, AM ;
Escubedo, E ;
Camarasa, J ;
Camins, A ;
Pallàs, M .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2004, 196 (02) :223-234
[15]   Dopamine-induced apoptosis is mediated by oxidative stress and is enhanced by cyanide in differentiated PC12 cells [J].
Jones, DC ;
Gunasekar, PG ;
Borowitz, JL ;
Isom, GE .
JOURNAL OF NEUROCHEMISTRY, 2000, 74 (06) :2296-2304
[16]   Amphetamine regulation of dopamine transport - Combined measurements of transporter currents and transporter imaging support the endocytosis of an active carrier [J].
Kahlig, KM ;
Javitch, JA ;
Galli, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (10) :8966-8975
[17]   Regulation of dopamine transporter function and plasma membrane expression by dopamine, amphetamine, and cocaine [J].
Kahlig, KM ;
Galli, A .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2003, 479 (1-3) :153-158
[18]   Amphetamine induces dopamine efflux through a dopamine transporter channel [J].
Kahlig, KM ;
Binda, F ;
Khoshbouei, H ;
Blakely, RD ;
McMahon, DG ;
Javitch, JA ;
Galli, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (09) :3495-3500
[19]  
Kim DK, 2001, J CELL SCI, V114, P4329
[20]   NF-κB mediates the adaptation of human U937 cells to hydrogen peroxide [J].
Kim, DK ;
Cho, ES ;
Lee, BR ;
Um, HD .
FREE RADICAL BIOLOGY AND MEDICINE, 2001, 30 (05) :563-571