Estrogen counteracts ozone-induced oxidative stress and nigral neuronal death

被引:32
作者
Angoa-Perez, Mariana
Jiang, Hao
Rodriguez, Alba I.
Lemini, Cristina
Levine, Robert A. [1 ]
Rivas-Arancibia, Selva
机构
[1] Univ Nacl Autonoma Mexico, Fac Med, Dept Physiol, Mexico City 04510, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Fac Med, Dept Pharmacol, Mexico City 04510, DF, Mexico
[3] Henry Ford Hlth Syst, William T Gossett Neurol Labs, Detroit, MI USA
[4] Henry Ford Hlth Syst, Complementary & Integrat Med Program, Detroit, MI USA
关键词
estrogen; oxidative stress; ozone; substantia nigra; tyrosine hydroxylase;
D O I
10.1097/00001756-200604240-00014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Oxidative stress is implicated in the premature death of dopamine neurons in substantia nigra in Parkinson's disease. The incidence of Parkinson's disease is higher in men than in women, and estrogen may provide neuroprotection against oxidative damage,We examined the protective effects of estrogen on rat nigral death after chronic ozone inhalation. Ozone inhalation produced impaired nigral cell morphology and loss of dopamine neurons in ovariectornized rats. This was counteracted after 60 days of 17 beta-estradiol treatment, when blood levels were highest. These results indicate that ozone exposure may be a useful Parkinson's disease model and neuroprotection afforded by 17 beta-estradiol is dependent on the high levels achieved after its prolonged administration. (c) 2006 Lippincott Williams & Wilkins.
引用
收藏
页码:629 / 633
页数:5
相关论文
共 25 条
[1]   From clinical evidence to molecular mechanisms underlying neuroprotection afforded by estrogens [J].
Amantea, D ;
Russo, R ;
Bagetta, G ;
Corasaniti, MT .
PHARMACOLOGICAL RESEARCH, 2005, 52 (02) :119-132
[2]   Estradiol prevents kainic acid-induced neuronal loss in the rat dentate gyrus [J].
Azcoitia, I ;
Sierra, A ;
Garcia-Segura, LM .
NEUROREPORT, 1998, 9 (13) :3075-3079
[3]  
Bednarek-Tupikowska Grazyna, 2002, Ginekol Pol, V73, P61
[4]   Neuroprotection against oxidative stress by estrogens: Structure-activity relationship [J].
Behl, C ;
Skutella, T ;
Lezoualch, F ;
Post, A ;
Widmann, M ;
Newton, CJ ;
Holsboer, F .
MOLECULAR PHARMACOLOGY, 1997, 51 (04) :535-541
[5]   Ozone and short-term mortality in 95 US urban communities, 1987-2000 [J].
Bell, ML ;
McDermott, A ;
Zeger, SL ;
Samet, JM ;
Dominici, F .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 292 (19) :2372-2378
[6]   Redox imbalance [J].
Berg, D ;
Youdim, M ;
Riederer, P .
CELL AND TISSUE RESEARCH, 2004, 318 (01) :201-213
[7]   Effects of drospirenone/estrogen combinations on bone metabolism [J].
Christiansen, C .
CLIMACTERIC, 2005, 8 :35-41
[8]   Neuroprotective effects of estrogen upon the nigrostriatal dopaminergic system [J].
Dluzen, DE .
JOURNAL OF NEUROCYTOLOGY, 2000, 29 (5-6) :387-399
[9]   Oxidative stress to dopaminergic neurons as models of Parkinson's disease [J].
Gille, G ;
Hung, ST ;
Reichmann, H ;
Rausch, WD .
STRESS: CURRENT NEUROENDOCRINE AND GENETIC APPROACHES, 2004, 1018 :533-540
[10]   Dopamine cell morphology and glial cell hypertrophy and process branching in the nigrostriatal system after striatal 6-OHDA analyzed by specific sterological tools [J].
Gomide, VG ;
Bibancos, T ;
Chadi, G .
INTERNATIONAL JOURNAL OF NEUROSCIENCE, 2005, 115 (04) :557-582