Estrogen and cytokines production - The possible cause of gender differences in neurological diseases

被引:102
作者
Czlonkowska, A
Ciesielska, A
Gromadzka, G
Kurkowska-Jastrzebska, I
机构
[1] Inst Psychiat & Neurol, Dept Neurol 2, PL-02957 Warsaw, Poland
[2] Med Univ Warsaw, Dept Expt & Clin Pharmacol, Warsaw, Poland
关键词
estrogen; cytokines; neurological diseases;
D O I
10.2174/1381612053381693
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Naturally occurring sexual dimorphism has been implicated in the risk, progression and recovery front numerous neurological disorders. These include head injury, multiple sclerosis (MS), stroke, and neurodegenerative diseases (Parkinson's disease (PD), Alzheimer's disease (AD) or amyotrophic lateral sclerosis (ALS). Accumulating evidence suggests that observed differences between men and women could result from estrogen's wide range of effects within the mammalian central nervous system (CNS), with it's neuroprotective effect being one of the most important. It seems possible that neuroprotective activity of estrogen could be partially a result of it's anti-inflammatory action. It has been well established that inflammation plays an important role in the etiopathogenesis and manifestation of brain pathological changes. In this regard, an important role has been Suggested for pro-inflammatory cytokines produced by activated glial cells, neurons and immune cells that invade brain tissue. Within the CNS, cytokines stimulate inflammatory processes that may impair blood-brain barrier permeability as well as promote apoptosis of neurons, oligodendrocytes and induce myelin damage. Given that estrogen may modulate cytokine expression, coupled with the fact that gender differences of cytokine production are apparent in animal models of PD and MS, suggests an important connection between hormonal-cytokine link in neurodegeneration. Indeed, while MS patients and mice subjected to experimental autoimmune encephalomyelitis (EAE) display gender specific alterations of IFN-gamma and IL-12, variations of TNF and IL-6 were associated with PD. Also in case of more acute neurodegenerative conditions, such as stroke, the effect of IL-6 gene G-174C polymorphism was different in males and females. Given that our understanding of the role of estrogen on cytokine production and accompanying CNS pathological conditions is limited, the present reviews aims to present some of our recent findings in this area and further evaluate the evidence that may be relevant to the design of new hormonal anti-inflammatory treatment strategies for neurodegenerative diseases.
引用
收藏
页码:1017 / 1030
页数:14
相关论文
共 134 条
[1]   Gender-linked brain injury in experimental stroke [J].
Alkayed, NJ ;
Harukuni, I ;
Kimes, AS ;
London, ED ;
Traystman, RJ ;
Hurn, PD .
STROKE, 1998, 29 (01) :159-165
[2]   Inflammation in central nervous system injury [J].
Allan, SM ;
Rothwell, NJ .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2003, 358 (1438) :1669-1677
[3]   GENETIC-CONTROL OF THE CD4/CD8 T-CELL RATIO IN HUMANS [J].
AMADORI, A ;
ZAMARCHI, R ;
DESILVESTRO, G ;
FORZA, G ;
CAVATTON, G ;
DANIELI, GA ;
CLEMENTI, M ;
CHIECOBIANCHI, L .
NATURE MEDICINE, 1995, 1 (12) :1279-1283
[4]   Estradiol repression of tumor necrosis factor-α transcription requires estrogen receptor activation function-2 and is enhanced by coactivators [J].
An, JP ;
Ribeiro, RCJ ;
Webb, P ;
Gustafsson, JÅ ;
Kushner, PJ ;
Baxter, JD ;
Leitman, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (26) :15161-15166
[5]   THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION [J].
ANGEL, P ;
KARIN, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) :129-157
[6]   Immunotherapy for multiple sclerosis: From theory to practice [J].
Antel, JP ;
Becher, B ;
Owens, T .
NATURE MEDICINE, 1996, 2 (10) :1074-1075
[7]   DIHYDROTESTOSTERONE EXERTS A DEPRESSIVE INFLUENCE ON THE PRODUCTION OF INTERLEUKIN-4 (IL-4), IL-5, AND GAMMA-INTERFERON, BUT NOT IL-2 BY ACTIVATED MURINE T-CELLS [J].
ARANEO, BA ;
DOWELL, T ;
DIEGEL, M ;
DAYNES, RA .
BLOOD, 1991, 78 (03) :688-699
[8]  
Azcoitia I, 1999, J NEUROSCI RES, V58, P815, DOI 10.1002/(SICI)1097-4547(19991215)58:6<815::AID-JNR8>3.0.CO
[9]  
2-R
[10]   Tumor necrosis factor-alpha - A mediator of focal ischemic brain injury [J].
Barone, FC ;
Arvin, B ;
White, RF ;
Miller, A ;
Webb, CL ;
Willette, RN ;
Lysko, PG ;
Feuerstein, GZ .
STROKE, 1997, 28 (06) :1233-1244