Neuroprotective actions of sex steroids in Parkinson's disease

被引:203
作者
Bourque, Melanie [1 ,2 ]
Dluzen, Dean E. [3 ]
Di Paolo, Therese [1 ,2 ]
机构
[1] Univ Laval, Med Ctr, CHUL, Mol Endocrinol & Genom Res Ctr, Quebec City, PQ G1V 4G2, Canada
[2] Univ Laval, Fac Pharm, Quebec City, PQ G1K 7P4, Canada
[3] Northeastern Ohio Univ Coll Med & Pharm, Coll Med, Dept Anat, Rootstown, OH 44272 USA
基金
加拿大健康研究院;
关键词
Estrogen; Progesterone; Androgens; Neuroprotection; Sex difference; Parkinson's disease; Akt; MAPK/ERK; MPTP; Methamphetamine; ACTIVATED PROTEIN-KINASE; INDUCED DOPAMINE DEPLETION; ESTROGEN-RECEPTOR-ALPHA; INDUCED CELL-DEATH; METHAMPHETAMINE-INDUCED NEUROTOXICITY; GLYCOGEN-SYNTHASE KINASE-3-BETA; MONOAMINE TRANSPORTER VMAT2; REGULATES BCL-2 EXPRESSION; MPTP-INDUCED NEUROTOXICITY; NMDA-INDUCED TOXICITY;
D O I
10.1016/j.yfrne.2009.04.014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The sex difference in Parkinson's disease, with a higher susceptibility in men, suggests a modulatory effect of sex steroids in the brain. Numerous studies highlight that sex steroids have neuroprotective properties against various brain injuries. This paper reviews the protective effects of sex hormones, particularly estradiol, progesterone and androgens, in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) animal model of Parkinson's disease as compared to methamphetamine toxicity. The molecular mechanisms underlying beneficial actions of sex steroids on the brain have been investigated showing steroid, dose, timing and duration specificities and presently focus is on the dopamine signaling pathways, the next frontier. Both genomic and non-genomic actions of estrogen converge to promote survival factors and show sex differences. Neuroprotection by estrogen involves activation of signaling molecules such as the phosphatidylinositol-3 kinase/Akt and the mitogen-activated protein kinase pathways. Interaction with growth factors, such as insulin-like growth factor 1, also contributes to protective actions of estrogen. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:142 / 157
页数:16
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