Estrogen as a neuroprotectant in stroke

被引:325
作者
Hurn, PD
Macrae, IM
机构
[1] Johns Hopkins Univ, Sch Med, Dept Anesthesiol & Crit Care Med, Baltimore, MD 21205 USA
[2] Univ Glasgow, Wellcome Surg Inst, Glasgow, Lanark, Scotland
关键词
estrogen; stroke; cerebral ischemia; reproductive steroids; neuroprotection;
D O I
10.1097/00004647-200004000-00001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Recent evidence suggests that reproductive steroids are important players in shaping stroke outcome and cerebrovascular pathophysiologic features. Although women are at lower risk for stroke than men, this native protection is lost in the postmenopausal years. Therefore, aging women sustain a large burden for stroke, contrary to a popular misconception that cancer is the main killer of women. Further, the value of hormone replacement therapy in stroke prevention or in improving outcome remains controversial. Estrogen has been the best studied of the sex steroids in both laboratory and clinical settings and is considered increasingly to be an endogenous neuroprotective agent. A growing number of studies demonstrate that exogenous estradiol reduces tissue damage resulting from experimental ischemic stroke in both sexes. This new concept suggests that dissecting interactions between estrogen and cerebral ischemia will yield novel insights into generalized cellular mechanisms of injury. Less is known about estrogen's undesirable effects in brain, for example, the potential for increasing seizure susceptibility and migraine. This review summarizes gender-specific aspects of clinical and experimental stroke and results of estrogen treatment on outcome in animal models of cerebral ischemia, and briefly discusses potential vascular and parenchymal mechanisms by which estrogen salvages brain.
引用
收藏
页码:631 / 652
页数:22
相关论文
共 247 条
[51]   The vascular protective effects of estrogen [J].
Farhat, MY ;
Lavigne, MC ;
Ramwell, PW .
FASEB JOURNAL, 1996, 10 (05) :615-624
[52]   Role of astroglia and insulin-like growth factor-I in gonadal hormone-dependent synaptic plasticity [J].
FernandezGalaz, MC ;
Morschl, E ;
Chowen, JA ;
TorresAleman, I ;
Naftolin, F ;
GarciaSegura, LM .
BRAIN RESEARCH BULLETIN, 1997, 44 (04) :525-531
[53]   DECREASED RISK OF STROKE AMONG POSTMENOPAUSAL HORMONE USERS - RESULTS FROM A NATIONAL COHORT [J].
FINUCANE, FF ;
MADANS, JH ;
BUSH, TL ;
WOLF, PH ;
KLEINMAN, JC .
ARCHIVES OF INTERNAL MEDICINE, 1993, 153 (01) :73-79
[54]   OVARIAN-STEROIDS INCREASE VERATRIDINE-INDUCED RELEASE OF AMINO-ACID NEUROTRANSMITTERS IN PREOPTIC AREA SYNAPTOSOMES [J].
FLEISCHMANN, A ;
MAKMAN, MH ;
ETGEN, AM .
BRAIN RESEARCH, 1990, 507 (01) :161-163
[55]   A COMPARATIVE STUDY OF CEREBRAL ATHEROSCLEROSIS IN MALES AND FEMALES [J].
FLORA, GC ;
BAKER, AB ;
LOEWENSON, RB ;
KLASSEN, AC .
CIRCULATION, 1968, 38 (05) :859-+
[56]   Mechanism of vascular smooth muscle relaxation by estrogen in depolarized rat and mouse aorta - Role of nuclear estrogen receptor and Ca2+ uptake [J].
Freay, AD ;
Curtis, SW ;
Korach, KS ;
Rubanyi, GM .
CIRCULATION RESEARCH, 1997, 81 (02) :242-248
[57]  
Funk J.L., 1991, DEMENTIA, V2, P268
[58]   ESTROGEN AND PROGESTERONE WITHDRAWAL INCREASES CEREBRAL VASOREACTIVITY TO SEROTONIN IN RABBIT BASILAR ARTERY [J].
FUTO, J ;
SHAY, J ;
BLOCK, S ;
HOLT, J ;
BEACH, M ;
MOSS, J .
LIFE SCIENCES, 1992, 50 (16) :1165-1172
[59]   Estradiol upregulates Bcl-2 expression in adult brain neurons [J].
Garcia-Segura, LM ;
Cardona-Gomez, P ;
Naftolin, F ;
Chowen, JA .
NEUROREPORT, 1998, 9 (04) :593-597
[60]  
Geary G. G., 1996, Society for Neuroscience Abstracts, V22, P910