Sex differences in partner preferences in humans and animals

被引:20
作者
Balthazart, Jacques [1 ]
机构
[1] Univ Liege, GIGA Neurosci, 15 Ave Hippocrate, B-4000 Liege, Belgium
关键词
sexual orientation; sexual partner preference; homosexuality; organizing effects of steroids; epigenetic controls; CONGENITAL ADRENAL-HYPERPLASIA; SEXUALLY DIMORPHIC NUCLEUS; MEDIAL PREOPTIC AREA; GENE-EXPRESSION; CHROMOSOME COMPLEMENT; ANTERIOR HYPOTHALAMUS; CLOACAL EXSTROPHY; ANDROGEN RECEPTOR; X-CHROMOSOME; MOUSE-BRAIN;
D O I
10.1098/rstb.2015.0118
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
A large number of morphological, physiological and behavioural traits are differentially expressed by males and females in all vertebrates including humans. These sex differences, sometimes, reflect the different hormonal environment of the adults, but they often remain present after subjects of both sexes are placed in the same endocrine conditions following gonadectomy associated or not with hormonal replacement therapy. They are then the result of combined influences of organizational actions of sex steroids acting early during development, or genetic differences between the sexes, or epigenetic mechanisms differentially affecting males and females. Sexual partner preference is a sexually differentiated behavioural trait that is clearly controlled in animals by the same type of mechanisms. This is also probably true in humans, even if critical experiments that would be needed to obtain scientific proof of this assertion are often impossible for pragmatic or ethical reasons. Clinical, epidemiological and correlative studies provide, however, converging evidence strongly suggesting, if not demonstrating, that endocrine, genetic and epigenetic mechanisms acting during the pre- or perinatal life control human sexual orientation, i.e. homosexuality versus heterosexuality. Whether they interact with postnatal psychosexual influences remains, however, unclear at present.
引用
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页数:11
相关论文
共 99 条
[1]   Neural, not gonadal, origin of brain sex differences in a gynandromorphic finch [J].
Agate, RJ ;
Grisham, W ;
Wade, J ;
Mann, S ;
Wingfield, J ;
Schanen, C ;
Palotie, A ;
Arnold, AP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (08) :4873-4878
[2]  
[Anonymous], HORMONES BRAIN AND B
[3]   The importance of having two X chromosomes [J].
Arnold, Arthur P. ;
Reue, Karen ;
Eghbali, Mansoureh ;
Vilain, Eric ;
Chen, Xuqi ;
Ghahramani, Negar ;
Itoh, Yuichiro ;
Li, Jingyuan ;
Link, Jenny C. ;
Ngun, Tuck ;
Williams-Burris, Shayna M. .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2016, 371 (1688)
[4]   Conceptual frameworks and mouse models for studying sex differences in physiology and disease: Why compensation changes the game [J].
Arnold, Arthur P. .
EXPERIMENTAL NEUROLOGY, 2014, 259 :2-9
[5]   The end of gonad-centric sex determination in mammals [J].
Arnold, Arthur P. .
TRENDS IN GENETICS, 2012, 28 (02) :55-61
[6]   What does the "four core genotypes" mouse model tell us about sex differences in the brain and other tissues? [J].
Arnold, Arthur P. ;
Chen, Xuqi .
FRONTIERS IN NEUROENDOCRINOLOGY, 2009, 30 (01) :1-9
[7]   Sex Determination: Why So Many Ways of Doing It? [J].
Bachtrog, Doris ;
Mank, Judith E. ;
Peichel, Catherine L. ;
Kirkpatrick, Mark ;
Otto, Sarah P. ;
Ashman, Tia-Lynn ;
Hahn, Matthew W. ;
Kitano, Jun ;
Mayrose, Itay ;
Ming, Ray ;
Perrin, Nicolas ;
Ross, Laura ;
Valenzuela, Nicole ;
Vamosi, Jana C. .
PLOS BIOLOGY, 2014, 12 (07) :1-13
[8]  
Bagemihl B., 1999, BIOLOGICAL EXUBERANC
[9]   Sexual partner preference requires a functional aromatase (Cyp19) gene in male mice [J].
Bakker, J ;
Honda, S ;
Harada, N ;
Balthazart, J .
HORMONES AND BEHAVIOR, 2002, 42 (02) :158-171
[10]   HORMONAL-REGULATION OF ADULT PARTNER PREFERENCE BEHAVIOR IN NEONATALLY ATD-TREATED MALE-RATS [J].
BAKKER, J ;
BRAND, T ;
VANOPHEMERT, J ;
SLOB, AK .
BEHAVIORAL NEUROSCIENCE, 1993, 107 (03) :480-487