Multiple sclerosis: Neuroprotective alliance of estrogen-progesterone and gender

被引:62
作者
Kipp, Markus [1 ,2 ]
Amor, Sandra [2 ,3 ]
Krauth, Raphael [1 ]
Beyer, Cordian [1 ]
机构
[1] Rhein Westfal TH Aachen, Inst Neuroanat, D-52074 Aachen, Germany
[2] Vrije Univ Amsterdam Med Ctr, Dept Pathol, Amsterdam, Netherlands
[3] Queen Mary Univ London, Blizard Inst Cell & Mol Sci, Ctr Neurosci, Neuroimmunol Unit,Barts & London Sch Med & Dent, London, England
关键词
Estrogen; Progesterone; Oligodendrocyte; Multiple sclerosis; Inflammation; Neuroprotection; Myelin; Axon; Remyelination; CENTRAL-NERVOUS-SYSTEM; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; STEROID-HORMONE RECEPTORS; FIBROBLAST-GROWTH-FACTOR; TRAUMATIC BRAIN-INJURY; MOUSE MIDBRAIN NEURONS; MYELIN BASIC-PROTEIN; NEONATAL-RAT-BRAIN; INDUCED CELL-DEATH; SPINAL-CORD;
D O I
10.1016/j.yfrne.2012.01.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The potential of 17 beta-estradiol and progesterone as neuroprotective factors is well-recognized. Persuasive data comes from in vitro and animal models reflecting a wide range of CNS disorders. These studies have endeavored to translate findings into human therapies. Nonetheless, few human studies show promising results. Evidence for neuroprotection was obtained in multiple sclerosis (MS) patients. This chronic inflammatory and demyelinating disease shows a female-to-male gender prevalence and disturbances in sex steroid production. In MS-related animal models, steroids ameliorate symptoms and protect from demyelination and neuronal damage. Both hormones operate in dampening central and brain-intrinsic immune responses and regulating local growth factor supply, oligodendrocyte and astrocyte function. This complex modulation of cell physiology and system stabilization requires the gamut of steroid-dependent signaling pathways. The identification of molecular and cellular targets of sex steroids and the understanding of cell-cell interactions in the pathogenesis will offer promise of novel therapy strategies. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 16
页数:16
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