Neuroprotective effects of estradiol in middle-aged female rats

被引:165
作者
Dubal, DB [1 ]
Wise, PM [1 ]
机构
[1] Univ Kentucky, Coll Med, Dept Physiol, Lexington, KY 40536 USA
关键词
D O I
10.1210/en.142.1.43
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Estrogen replacement therapy in postmenopausal women ameliorates cognitive dysfunction and decreases the risk and/or severity of neurodegenerative conditions such as Alzheimer's disease and stroke. Furthermore, estradiol exerts neuroprotective effects in a variety of in vitro and in vivo models of brain injury. We have previously shown that physiological levels of estradiol attenuate ischemic brain injury in young female rats. However, neurodegenerative events occur more frequently in elderly women who are chronically hypoestrogenic. Therefore, we investigated whether aging rats remain responsive to the neuroprotective actions of estradiol. Young (3-4 months) and middle-aged (9-12 months) rats were ovariectomized and treated for 1 week with estradiol before middle cerebral artery occlusion (MCAO). Regional cerebral blood flow was monitored in some animals at the time of injury. Brains were collected 24 h after MCAO and infarct volume was analyzed. Our data demonstrate that in both young and aging rats, low and high physiological doses of estradiol decrease ischemic injury by almost 50%, compared with oil-treated controls. Additionally, our data suggest that estradiol acts in both age groups via blood flow-independent mechanisms, as basal and postinjury blood flow was equivalent between estradiol- and oil-treated young and aging rats. These data demonstrate that replacement with physiological levels of estradiol protects against stroke-related injury in young and aging female rats and strongly suggest that older animals remain responsive to the protective actions of estradiol.
引用
收藏
页码:43 / 48
页数:6
相关论文
共 62 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]   Neuroprotective effects of female gonadal steroids in reproductively senescent female rats [J].
Alkayed, NJ ;
Murphy, SJ ;
Traystman, RJ ;
Hurn, PD .
STROKE, 2000, 31 (01) :161-167
[3]   Effect of age and sex on N-methyl-D-aspartate antagonist-induced neuronal necrosis in rats [J].
Auer, RN .
STROKE, 1996, 27 (04) :743-746
[4]  
BAUGHMAN VL, 1988, ANESTH ANALG, V67, P677
[5]   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
[6]   17-BETA ESTRADIOL PROTECTS NEURONS FROM OXIDATIVE STRESS-INDUCED CELL-DEATH IN-VITRO [J].
BEHL, C ;
WIDMANN, M ;
TRAPP, T ;
HOLSBOER, F .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 216 (02) :473-482
[7]   17 beta-estradiol enhances the outgrowth and survival of neocortical neurons in culture [J].
Brinton, RD ;
Tran, J ;
Proffitt, P ;
Montoya, M .
NEUROCHEMICAL RESEARCH, 1997, 22 (11) :1339-1351
[8]  
Canese R, 1998, MAGN RESON MATER PHY, V7, P28
[9]   Estrogen status affects sensitivity to focal cerebral ischemia in stroke-prone spontaneously hypertensive rats [J].
Carswell, HVO ;
Dominiczak, AF ;
Macrae, IM .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2000, 278 (01) :H290-H294
[10]   The effects of 17β-estradiol on ischemia-induced neuronal damage in the gerbil hippocampus [J].
Chen, J ;
Adachi, N ;
Liu, K ;
Arai, T .
NEUROSCIENCE, 1998, 87 (04) :817-822