Organizational effects of estrogens on brain vasotocin and sexual behavior in quail

被引:0
作者
Panzica, GC
Castagna, C
Viglietti-Panzica, C
Russo, C
Tlemçani, O
Balthazart, J
机构
[1] Univ Liege, Biochem Lab, Res Grp Behav Neuroendocrinol, B-4020 Liege, Belgium
[2] Univ Turin, Dept Anat Pharmacol & Forens Med, I-10126 Turin, Italy
来源
JOURNAL OF NEUROBIOLOGY | 1998年 / 37卷 / 04期
关键词
preoptic area; bed nucleus of the stria terminalis; lateral septum; sexual differentiation; copulatory behavior; Japanese quail;
D O I
10.1002/(SICI)1097-4695(199812)37:4<684::AID-NEU15>3.0.CO;2-U
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Reproductive behavior is sexually differentiated in quail: The male-typical copulatory behavior is never observed in females even after treatment with high doses of testosterone (T). This sex difference in behavioral responsiveness to T is organized during the embryonic period by the exposure of female embryo to estrogens. We showed recently that the sexually dimorphic medial preoptic nucleus (POM), a structure that plays a key role in the activation of male copulatory behavior, is innervated by a dense steroid-sensitive network of vasotocin-immunoreactive (VT-ir) fibers in male quail. This innervation is almost completely absent in the female POM and is not induced by a chronic treatment with T, suggesting that this neurochemical difference could be organizational in nature. This idea was tested by injecting fertilized quail eggs of both sexes on day 9 of incubation with either estradiol benzoate (EB) (25 mu g, a treatment that suppresses the capacity to show copulatory behavior in adulthood) or the aromatase inhibitor R76713 (10 mu g, a treatment that makes adult females behaviorally responsive to T), or with the solvents as a control (C). At 3 weeks posthatch, all subjects were gonadectomized and later implanted with Silastic capsules filled with T. Two weeks later, all birds were perfused and brain sections were processed for VT immunocytochemistry. Despite the similarity of the adult endocrine conditions of the subjects (all were gonadectomized and treated with T Silastic implants providing the same plasma level of steroid to all subjects), major qualitative differences were observed in the density of VT-ir structures in the POM of the different groups. Dense immunoreactive structures (fibers and a few cells) were observed in the POM of C males but not females; EB males had completely lost this immunoreactivity (and lost the capacity to display copulatory behavior); and, conversely, R76713 females displayed a male-typical VT-ir system in the nucleus (and also high levels of copulatory behavior). Similar changes in immunoreactivity were seen in the nucleus of the stria terminalis and in the lateral septum (VT-ir fibers only in this case) but not in the magnocellular vasotocinergic system. These neurochemical changes closely parallel the effects of the embryonic treatments on male copulatory behavior. The vasotocinergic system of the POM can therefore be considered an accurate marker of the sexual differentiation of brain circuits mediating this behavior. (C) 1998 John Wiley & Sons, Inc.
引用
收藏
页码:684 / 699
页数:16
相关论文
共 50 条
[31]   Low dose effects of bisphenol A on sexual differentiation of the brain and behavior in rats [J].
Kubo, K ;
Arai, O ;
Omura, M ;
Watanabe, R ;
Ogata, R ;
Aou, S .
NEUROSCIENCE RESEARCH, 2003, 45 (03) :345-356
[32]   7α-Hydroxypregnenolone regulates diurnal changes in sexual behavior of male quail [J].
Ogura, Yuki ;
Haraguchi, Shogo ;
Nagino, Koki ;
Ishikawa, Kei ;
Fukahori, Yoko ;
Tsutsui, Kazuyoshi .
GENERAL AND COMPARATIVE ENDOCRINOLOGY, 2016, 227 :130-135
[33]   Sexual behavior in Japanese quail as a test end point for endocrine disruption:: Effects of in Ovo exposure to ethinylestradiol and diethylstilbestrol [J].
Halldin, K ;
Berg, C ;
Brandt, I ;
Brunström, B .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1999, 107 (11) :861-866
[34]   Rapid changes in brain aromatase activity in the female quail brain following expression of sexual behaviour [J].
de Bournonville, C. ;
Ball, G. F. ;
Balthazart, J. ;
Cornil, C. A. .
JOURNAL OF NEUROENDOCRINOLOGY, 2017, 29 (11)
[35]   Effects of sex steroids on aromatase mRNA expression in the male and female quail brain [J].
Voigt, Cornelia ;
Ball, Gregory F. ;
Balthazart, Jacques .
GENERAL AND COMPARATIVE ENDOCRINOLOGY, 2011, 170 (01) :180-188
[36]   Estrogens, Brain, and Behavior: Lessons from Knockout Mouse Models [J].
Hill, Rachel A. ;
Boon, Wah Chin .
SEMINARS IN REPRODUCTIVE MEDICINE, 2009, 27 (03) :218-228
[37]   Maternal effects in quail and zebra finches: Behavior and hormones [J].
Adkins-Regan, Elizabeth ;
Banerjee, Sunayana B. ;
Correa, Stephanie M. ;
Schweitzer, Cecile .
GENERAL AND COMPARATIVE ENDOCRINOLOGY, 2013, 190 :34-41
[38]   Effects of tryptophan and probiotic supplementation on growth and behavior in quail [J].
Yildirim, A. ;
Kraimi, N. ;
Constantin, P. ;
Mercerand, F. ;
Leterrier, C. .
POULTRY SCIENCE, 2020, 99 (11) :5206-5213
[39]   Key role of estrogen receptor β in the organization of brain and behavior of the Japanese quail [J].
Court, Lucas ;
Vandries, Laura ;
Balthazart, Jacques ;
Cornil, Charlotte A. .
HORMONES AND BEHAVIOR, 2020, 125
[40]   Hormonal regulation of brain circuits mediating male sexual behavior in birds [J].
Ball, GF ;
Balthazart, J .
PHYSIOLOGY & BEHAVIOR, 2004, 83 (02) :329-346