Chronic fluoxetine suppresses circulating estrogen and the enhanced spatial learning of estrogen-treated ovariectomized rats

被引:36
作者
Taylor, GT
Farr, S
Klinga, K
Weiss, J
机构
[1] Univ Missouri, Behav Neurosci Grp, St Louis, MO 63121 USA
[2] St Louis Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[3] Univ Frauenklin, Abt Gynaekol Endokrinol & Fertilitatsstoerungen, D-6900 Heidelberg, Germany
[4] Univ Heidelberg, Zentrum Mol Biol, D-6900 Heidelberg, Germany
关键词
estrogen; SSRI; fluoxetine; serotonin; spatial memory;
D O I
10.1016/j.psyneuen.2004.03.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We are interested in developing animal models to evaluate cognitive processes as influenced by the interplay of steroidal hormones and drugs commonly used in psychotherapy. Two experiments with female rats were conducted to evaluate the interaction of estrogen with the serotonin specific reuptake inhibitor (SSRI) fluoxetine on spatial learning and memory and on the endocrine system. In experiment 1, estrogen (50 mug estradiol benzoate/kg body weight) was administered SC to young adult, ovariectomized (OVX) rats either alone or in combination with fluoxetine (2 mg/kg SC). After a month, the groups were compared with appropriate OVX and gonadally intact controls on trials to criterion in a hole board spatial memory task using massed training trials. Experiment 2 was a dose-response study of the influence of fluoxetine (0.5-5 mg/kg) on circulating estrogen in OVX, estrogen treated females. Results were that the OVX females administered estrogen only reached the learning criterion significantly faster than the other groups. All other groups, including the estrogen + fluoxetine animals, performed no better than the controls. Combining fluoxetine with estrogen also lowered circulating estrogen titers, with the least estrogen reductions being in the group receiving the highest dosage of fluoxetine. No differences among groups were found on measures of activity in an open field or for anxiety in a plus maze. Conclusions were that administration of estrogen improved spatial learning and memory in OVX rats, whereas concurrent fluoxetine exposure suppressed the levels of estrogen in circulation and eliminated the gains in spatial performance obtained from chronic estrogen exposure. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1241 / 1249
页数:9
相关论文
共 52 条
[11]   Repeated blockade of mineralocorticoid receptors, but not of glucocorticoid receptors impairs food rewarded spatial learning [J].
Douma, BRK ;
Korte, SM ;
Buwalda, B ;
la Fleur, SE ;
Bohus, B ;
Luiten, PGM .
PSYCHONEUROENDOCRINOLOGY, 1998, 23 (01) :33-44
[12]   Modulation of memory processing in the cingulate cortex of mice [J].
Farr, SA ;
Uezu, K ;
Creonte, TA ;
Flood, JF ;
Morley, JE .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2000, 65 (03) :363-368
[13]   EFFECT OF OVARIAN-STEROIDS ON FOOTSHOCK AVOIDANCE-LEARNING AND RETENTION IN FEMALE MICE [J].
FARR, SA ;
FLOOD, JF ;
SCHERRER, JF ;
KAISER, FE ;
TAYLOR, GT ;
MORLEY, JE .
PHYSIOLOGY & BEHAVIOR, 1995, 58 (04) :715-723
[14]   Sex steroid control of mood, mental state and memory [J].
Fink, G ;
Sumner, BEH ;
McQueen, JK ;
Wilson, H ;
Rosie, R .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 1998, 25 (10) :764-775
[15]   FLUOXETINE ENHANCES MEMORY PROCESSING IN MICE [J].
FLOOD, JF ;
CHERKIN, A .
PSYCHOPHARMACOLOGY, 1987, 93 (01) :36-43
[16]  
Freeman Marc E., 1994, P613
[17]   ESTRUS-ASSOCIATED DECREMENTS IN A WATER MAZE TASK ARE LIMITED TO ACQUISITION [J].
FRYE, CA .
PHYSIOLOGY & BEHAVIOR, 1995, 57 (01) :5-14
[18]   Estrogen replacement enhances acquisition of a spatial memory task and reduces deficits associated with hippocampal muscarinic receptor inhibition [J].
Gibbs, RB .
HORMONES AND BEHAVIOR, 1999, 36 (03) :222-233
[19]   Selective serotonin reuptake inhibitors directly alter activity of neurosteroidogenic enzymes [J].
Griffin, LD ;
Mellon, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (23) :13512-13517
[20]   Cytochrome P450 enzymes: Interpretation of their interactions with selective serotonin reuptake inhibitors .2. [J].
Harvey, AT ;
Preskorn, SH .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 1996, 16 (05) :345-355