Posttraining androgens' enhancement of cognitive performance is temporally distinct from androgens' increases in affective behavior

被引:80
作者
Frye, Cheryl A. [1 ]
Lacey, Elizabeth H. [1 ]
机构
[1] SUNY Albany, Albany, NY 12222 USA
基金
美国国家科学基金会;
关键词
Testosterone; Androgen; Conditioned Place Preference; Estrous Cycle; Spatial Ability;
D O I
10.3758/CABN.1.2.172
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Steroid hormone-induced variations in spatial learning and memory tasks have been reported. In this study, androgens' effects in various cognitive and affective tasks were investigated in order to determine whether any observed differences in cognitive performance could be due to affective changes produced by the hormones. Ovariectomized rats (N = 72) received 0.0, 3.0, or 7.5 mg/kg subcutaneously, of testosterone (T), dihydrotestosterone (DHT), or 5 alpha-androstane-3 alpha,17 beta-diol (3 alpha-Diol) suspended in 10% ethanol/sesame oil v/v. For the cognitive tasks (Y maze, inhibitory avoidance, and object recognition), subjects were injected after training trials. For the affective tasks (open field, elevated plus maze, and tailflick), subjects were injected 1 or 24 h before testing. Posttraining injections that produced physiological concentrations of androgens - T, DHT, and 3 alpha-Diol - 1 h later increased the percentage of correct choices in the Y maze, the latencies to cross to the shock-associated side of the inhibitory avoidance chamber, and percentage of time exploring novel objects 24 h later, when androgen levels were no longer increased. Administration of T, DHT, and 3 alpha-Diol also increased the number of entries into the center squares of a brightly lit open field, open-arm time in the elevated plus maze, and tailflick latencies 1 but not 24 h following administration. These findings suggest that these androgens, when administered following training, can enhance cognitive performance in the tasks investigated 24 h later when androgen levels nadir, but overt changes in the affective behaviors examined occurred at the time of physiological concentrations 1 h but not 24 h following androgen administration. These findings suggest posttraining androgens can enhance consolidation and cognitive performance, independent of their anxiolytic actions.
引用
收藏
页码:172 / 182
页数:11
相关论文
共 87 条
[21]   THE RESPONSE TO ANALGESIA TESTING IS AFFECTED BY GONADAL-STEROIDS IN THE RAT [J].
FORMAN, LJ ;
TINGLE, V ;
ESTILOW, S ;
CATER, J .
LIFE SCIENCES, 1989, 45 (05) :447-454
[22]  
Frye C. A., PSYCHONEURO IN PRESS
[23]  
Frye C. A, 2001, TESTOSTERONE M UNPUB
[24]   PROGESTERONE METABOLITES, EFFECTIVE AT THE GABA(A) RECEPTOR COMPLEX, ATTENUATE PAIN SENSITIVITY IN RATS [J].
FRYE, CA ;
DUNCAN, JE .
BRAIN RESEARCH, 1994, 643 (1-2) :194-203
[25]   Behavioral effects of 3 alpha-androstanediol .1. Modulation of sexual receptivity and promotion of GABA-stimulated chloride flux [J].
Frye, CA ;
VanKeuren, KR ;
Erskine, MS .
BEHAVIOURAL BRAIN RESEARCH, 1996, 79 (1-2) :109-118
[26]   HORMONAL MILIEU AFFECTS TAILFLICK LATENCY IN FEMALE RATS AND MAY BE ATTENUATED BY ACCESS TO SUCROSE [J].
FRYE, CA ;
BOCK, BC ;
KANAREK, RB .
PHYSIOLOGY & BEHAVIOR, 1992, 52 (04) :699-706
[27]   Analgesic effects of the neurosteroid 3 alpha-androstanediol [J].
Frye, CA ;
VanKeuren, KR ;
Rao, PN ;
Erskine, MS .
BRAIN RESEARCH, 1996, 709 (01) :1-9
[28]   The neurosteroids DHEA and DHEAS may influence cognitive performance by altering affective state [J].
Frye, CA ;
Lacey, EH .
PHYSIOLOGY & BEHAVIOR, 1999, 66 (01) :85-92
[29]   Androgenic neurosteroids: Anti-seizure effects in an animal model of epilepsy [J].
Frye, CA ;
Reed, TAW .
PSYCHONEUROENDOCRINOLOGY, 1998, 23 (04) :385-399
[30]  
Frye CA, 1996, BEHAV NEUROSCI, V110, P603