Hormones, genes and the structure of sexual arousal

被引:16
作者
Frohlich, J
Ogawa, S
Morgan, M
Burton, L
Pfaff, D
机构
[1] Rockefeller Univ, Neurobiol & Behav Lab, New York, NY 10021 USA
[2] Fordham Univ, Dept Psychol, Bronx, NY 10458 USA
关键词
estrogenic hormones; sexual arousal; stimuli;
D O I
10.1016/S0166-4328(99)00079-0
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
Despite the inherent difficulty of connecting individual genes with integrated mammalian behaviors, it has been determined that a series of genes are turned on by estrogenic hormones acting in forebrain. Their products are, in turn, facilitatory for female reproductive behaviors such as lordosis. The causal routes by which two genes contribute to the control of lordosis behavior, the classical estrogen receptor gene (ER-alpha) and a thyroid hormone (TH) receptor gene (TR-beta), have been delineated. Beyond the mechanisms underlying the expression of concrete, specific natural behaviors, lies the question of sexual motivation. Required as an intervening variable to explain fluctuations in natural behaviors in the face of constant stimuli? motivational states have both general and specific features. Most theoretical and experimental approaches toward the general aspects of motivation have depended heavily on concepts of 'arousal.' Sexual arousal is likely to depend both on very general, broadly distributed neuronal influences and on specific affiliative and sexual tendencies. Is 'general arousal' a monolithic, undifferentiated process? In no way can a review at this time settle such issues, but the reasons behind six new experimental approaches to these questions are described. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:5 / 27
页数:23
相关论文
共 212 条
[31]   IMPLEMENTING TRANSGENIC AND EMBRYONIC STEM-CELL TECHNOLOGY TO STUDY GENE-EXPRESSION, CELL-CELL INTERACTIONS AND GENE-FUNCTION [J].
CAMPER, SA ;
SAUNDERS, TL ;
KENDALL, SK ;
KERI, RA ;
SEASHOLTZ, AF ;
GORDON, DF ;
BIRKMEIER, TS ;
KEEGAN, CE ;
KAROLYI, IJ ;
ROLLER, ML ;
BURROWS, HL ;
SAMUELSON, LC .
BIOLOGY OF REPRODUCTION, 1995, 52 (02) :246-257
[32]   EFFECTS OF INTERRUPTION OF LIMBIC SYSTEM PATHWAYS ON DIFFERENT MEASURES OF ACTIVITY [J].
CAPOBIANCO, S ;
HAMILTON, LW .
PHYSIOLOGY & BEHAVIOR, 1976, 17 (01) :65-72
[33]  
CHALMERS DT, 1995, J NEUROSCI, V15, P6340
[34]   PROLACTIN STIMULATES DOPAMINE RELEASE FROM MALE BUT NOT FROM FEMALE RAT STRIATAL TISSUE SUPER-FUSED INVITRO [J].
CHEN, YF ;
RAMIREZ, VD .
ENDOCRINOLOGY, 1982, 111 (05) :1740-1742
[35]   DELAYED-NON-MATCH-TO-SAMPLE PERFORMANCE IN THE RADIAL ARM MAZE - EFFECTS OF DOPAMINERGIC AND GABAERGIC AGENTS [J].
CHROBAK, JJ ;
NAPIER, TC .
PSYCHOPHARMACOLOGY, 1992, 108 (1-2) :72-78
[36]   SELECTIVE NEUROTOXIN LESIONS OF THE LATERAL SEPTUM - CHANGES IN SOCIAL AND AGGRESSIVE BEHAVIORS [J].
CLARKE, A ;
FILE, SE .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1982, 17 (04) :623-628
[37]   ANATOMICAL ANALYSIS OF THE INVOLVEMENT OF MESOLIMBOCORTICAL DOPAMINE IN THE LOCOMOTOR STIMULANT ACTIONS OF D-AMPHETAMINE AND APOMORPHINE [J].
CLARKE, PBS ;
JAKUBOVIC, A ;
FIBIGER, HC .
PSYCHOPHARMACOLOGY, 1988, 96 (04) :511-520
[38]   REACTIONS TO NOVELTY AND STIMULUS-CHANGE INDUCED RESPONSE DECREMENT [J].
CLAUS, HJ ;
BINDRA, D .
CANADIAN JOURNAL OF PSYCHOLOGY, 1960, 14 (02) :101-110
[39]   GENETIC-DIFFERENCES IN LOCOMOTOR ACTIVATION IN MICE [J].
CRABBE, JC .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1986, 25 (01) :289-292
[40]   Progress in antisense oligonucleotide therapeutic [J].
Crooke, ST ;
Bennett, CF .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1996, 36 :107-129