[en] In rats, expression of the immediate early gene, c-fos observed in the brain following male copulatory behavior relates mostly to the detection of olfactory information originating from the female and to somatosensory feedback from the penis. However, quail, like most birds, are generally considered to have a relatively poorly developed sense of smell. Furthermore, quail have no intromittent organ (e.g., penis). It is therefore intriguing that expression of male copulatory behavior induces in quail and rats a similar pattern of c-fos expression in the medial preoptic area (mPOA), bed nucleus of the stria terminalis (BSTM) and parts of the amygdala. We analyzed here by immunocytochemistry Fos expression in the mPOA/BSTM/amygdala of male quail that had been allowed to copulate with a female during standardized tests. Before these tests, some of the males had either their nostrils plugged, or their cloacal area anesthetized, or both. A control group was not exposed to females. These manipulations did not affect frequencies of male sexual behavior and all birds exposed to a female copulated normally. In the mPOA, the increased Fos expression induced by copulation was not affected by the cloacal gland anesthesia but was markedly reduced in subjects deprived of olfactory input. Both manipulations affected copulation-induced Fos expression in the BSTM. No change in Fos expression was observed in the amygdala. Thus immediate early gene expression in the mPOA and BSTM of quail is modulated at least in part by olfactory cues and/or somatosensory stimuli originating from the cloacal gland. Future work should specify the nature of these stimuli and their function in the expression of avian male sexual behavior.
Taziaux, Mélanie ; Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Biologie de la différenciation sexuelle du cerveau
Keller, Matthieu
Ball, Gregory F
Balthazart, Jacques ; Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Biologie de la différenciation sexuelle du cerveau
Language :
English
Title :
Site-specific effects of anosmia and cloacal gland anesthesia on Fos expression induced in male quail brain by sexual behavior.
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Bibliography
Absil P., Riters L.V., and Balthazart J. Preoptic aromatase cells project to the mesencephalic central gray in the male Japanese quail (Coturnix japonica). Horm Behav 40 (2001) 369-383
Adkins E.K., and Adler N.T. Hormonal control of behavior in the Japanese quail. J Comp Physiol Psychol 81 (1972) 27-36
Adler N., and Bermant G. Sexual behavior of male rats: effects of reduced sensory feedback. J Comp Physiol Psychol 61 (1966) 240-243
Aronson L.R., and Cooper M.L. Olfactory deprivation and mating behavior in sexually experienced male cats. Behav Biol 11 (1974) 459-480
Aste N., Balthazart J., Absil P., Grossmann R., Mülhbauer E., Viglietti-Panzica C., et al. Anatomical and neurochemical definition of the nucleus of the stria terminalis in Japanese quail (Coturnix japonica). J Comp Neurol 396 (1998) 141-157
Ball G.F., and Balthazart J. Hormonal regulation of brain circuits mediating male sexual behavior in birds. Physiol Behav 83 (2004) 329-346
Ball G.F., Tlemçani O., and Balthazart J. Induction of the Zenk protein after sexual interactions in male Japanese quail. Neuroreport 8 (1997) 2965-2970
Balthazart J., and Absil P. Identification of catecholaminergic inputs to and outputs from aromatase-containing brain areas of the Japanese quail by tract tracing combined with tyrosine hydroxylase immunocytochemistry. J Comp Neurol 382 (1997) 401-428
Balthazart J., Absil P., Gerard M., Appeltants D., and Ball G.F. Appetitive and consummatory male sexual behavior in Japanese quail are differentially regulated by subregions of the preoptic medial nucleus. J Neurosci 18 (1998) 6512-6527
Balthazart J., and Ball G.F. The Japanese quail as a model system for the investigation of steroid-catecholamine interactions mediating appetitive and consummatory aspects of male sexual behavior. Annu Rev Sex Res 9 (1998) 96-176
Balthazart J., and Ball G.F. Topography in the preoptic region: differential regulation of appetitive and consummatory male sexual behaviors. Front Neuroendocrinol 28 (2007) 161-178
Balthazart J., Dupiereux V., Aste N., Viglietti-Panzica C., Barrese M., and Panzica G.C. Afferent and efferent connections of the sexually dimorphic medial preoptic nucleus of the male quail revealed by in vitro transport of DiI. Cell Tissue Res 276 (1994) 455-475
Balthazart J., and Schoffeniels E. Pheromones are involved in the control of sexual behaviour in birds. Naturwissenschaften 66 (1979) 55-56
Balthazart J., Schumacher M., and Ottinger M.A. Sexual differences in the Japanese quail: behavior, morphology and intracellular metabolism of testosterone. Gen Comp Endocrinol 51 (1983) 191-207
Balthazart J., and Surlemont C. Androgen and estrogen action in the preoptic area and activation of copulatory behavior in quail. Physiol Behav 48 (1990) 599-609
Balthazart J., and Surlemont C. Copulatory behavior is controlled by the sexually dimorphic nucleus of the quail POA. Brain Res Bull 25 (1990) 7-14
Balthazart J., Surlemont C., and Harada N. Aromatase as a cellular marker of testosterone action in the preoptic area. Physiol Behav 51 (1992) 395-409
Baum M.J., and Everitt B.J. Increased expression of c-fos in the medial preoptic area after mating in male rats: role of afferent inputs from the medial amygdala and midbrain central tegmental field. Neuroscience 50 (1992) 627-646
Baylé J.D., Ramade F., and Oliver J. Stereotaxic topography of the brain of the quail. J Physiol (Paris) 68 (1974) 219-241
Bingman V.P., Casini G., Nocjar C., and Jones T.J. Connections of the piriform cortex in homing pigeons (Columba livia) studied with fast blue and WGA-HRP. Brain Behav Evol 43 (1994) 206-218
Birkhead T.R., and Moller A.P. Sperm competition in birds (1992), Academic Press, San Diego, CA
Brennan P.A., and Zufall F. Pheromonal communication in vertebrates. Nature 444 (2006) 308-315
Briskie J.V., and Montgomerie R. Sexual selection and the intromittent organ of birds. J Avian Biol 28 (1997) 73-86
Charlier T.D., Ball G.F., and Balthazart J. Sexual behavior activates the expression of the immediate early genes c-fos and Zenk (egr-1) in catecholaminergic neurons of male Japanese quail. Neuroscience 131 (2005) 13-30
Claro F., Segovia S., Guilamon A., and Del Abril A. Lesions in the medial posterior region of the BST impair sexual behavior in sexually experienced and inexperienced male rats. Brain Res Bull 36 (1995) 1-10
Coolen L.M., Peters H.J., and Veening J.G. Distribution of Fos immunoreactivity following mating versus anogenital investigation in the male rat brain. Neuroscience 77 (1997) 1151-1161
Coolen L.M., Peters H.J.P.W., and Veening J.G. Anatomical interrelationships of the medial preoptic area and other brain regions activated following male sexual behavior: a combined Fos and tract-tracing study. J Comp Neurol 397 (1998) 421-435
D'Hondt E., Vermeiren J., Peeters K., Balthazart J., Tlemçani O., Ball G.F., et al. Validation of a new antiserum directed towards the synthetic c-terminus of the FOS protein in avian species: immunological, physiological and behavioral evidence. J Neurosci Methods 91 (1999) 31-45
del Hoyo J., Elliott A., and Sargatal J. Handbook of the birds of the world vol. 1 (1992), Lynx Edition, Barcelona
Devor M., and Murphy M.R. The effect of peripheral olfactory blockade on the social behavior of the male golden hamster. Behav Biol 9 (1973) 31-42
Dominguez J.M., and Hull E.M. Dopamine, the medial preoptic area, and male sexual behavior. Physiol Behav 86 (2005) 356-368
Domjan M. Going wild in the laboratory: learning about species-typical cues. In: Medin D. (Ed). The psychology of learning and motivation vol. 38 (1998), Academic Press, San Diego 155-186
Domjan M., and Hall S. Determinants of social proximity in Japanese quail (Coturnix coturnix japonica): male behavior. J Comp Psychol 100 (1986) 59-67
Domjan M., and Nash S. Stimulus control of social behaviour in male Japanese quail. Anim Behav 36 (1988) 1006-1015
Domjan M., O'Vary D., and Greene P. Conditioning of appetitive and consummatory sexual behavior in male Japanese quail. J Exp Anal Behav 50 (1988) 505-519
Dudley C.A., Chakravarty S., and Barnea A. Female odors lead to rapid activation of mitogen-activated protein kinase (MAPK) in neurons of the vomeronasal system. Brain Res 915 (2001) 32-46
Emery D.E., and Sachs B.D. Copulatory behavior in male rats with lesions in the bed nucleus of the stria terminalis. Physiol Behav 17 (1976) 803-806
Evrard H.C., and Balthazart J. The assessment of nociceptive and non-nociceptive skin sensitivity in the Japanese quail (Coturnix japonica). J Neurosci Methods 116 (2002) 135-146
Fujiwara K.T., Ashida K., Nishima H., Iba H., Miyajima N., Nishizawa M., et al. The chicken c-fos gene: cloning and nucleotide sequence analysis. J Virol 61 (1987) 4012-4018
Gagliardo A., Pecchia T., Savini M., Odetti F., Ioalè P., and Vallortigara G. Olfactory lateralization in homing pigeons: initial orientation of birds receiving a unilateral olfactory input. Eur J Neurosci 25 5 (2007) 1511-1516
Goldfoot D.A., Essock-Vitale S.M., Asa C.S., Thornton J.E., and Leshner A.I. Anosmia in male rhesus monkeys does not alter copulatory activity with cycling females. Science 199 (1978) 1095-1096
Hagelin J.C. Odors and chemical signaling. In: Jamieson B.G.M. (Ed). Reproductive biology and phylogeny of birds, Part B vol. 6B (2007), Science Publishers, Enfield (NH) Jersey, Plymouth 75-119
Hagelin J.C., and Jones I.L. Bird odors and other chemical substances: a defense mechanism or overlooked mode of intraspecific communication?. The Auk 124 (2007) 741-761
Hagelin J.C., Jones I.L., and Rasmussen L.E. A tangerine-scented social odour in a monogamous seabird. Proc R Soc Lond [Biol] 270 (2003) 1323-1329
Hart B.L., and Haugen C.M. Scent marking and sexual behavior maintained in anosmic male dogs. Commun Behav Biol 6 (1971) 131-135
Heimer L., and Larsson K. Mating behavior of male rats after olfactory bulb lesion. Physiol Behav 2 (1967) 207-209
Hull E.M., Meisel R.L., and Sachs B.D. Male sexual behavior. In: Pfaff D.W., Arnold A.P., Etgen A.M., Fahrbach S.E., and Rubin R.T. (Eds). Hormones brain and behavior vol. 2 (2002), Academic Press, San Diego, CA 1-137
Hutchison R.E. Hormonal differentiation of sexual behavior in Japanese quail. Horm Behav 11 (1978) 363-387
Jacob J., Balthazart J., and Schoffeniels E. Sex differences in the chemical composition of uropygial gland waxes in domestic ducks. Biochem Syst Ecol 7 (1979) 149-153
Jones R.B., and Gentle M.J. Olfaction and behavioral modification in domestic chicks (Gallus domesticus). Physiol Behav 34 (1985) 917-924
Keller M., Douhard Q., Baum M.J., and Bakker J. Sexual experience does not compensate for the disruptive effects of zinc sulfate-lesioning of the main olfactory epithelium on sexual behavior in male mice. Chem Senses 31 (2006) 753-762
Kelliher K.R., Baum M.J., and Meredith M. The ferret's vomeronasal organ and accessory olfactory bulb: effect of hormone manipulation in adult males and females. Anat Rec 263 (2001) 280-288
Keverne E.B. Importance of olfactory and vomeronasal systems for male sexual function. Physiol Behav 83 (2004) 177-187
Kuenzel W.J., and Masson M. A stereotaxic atlas of the brain of the chick (Gallus domesticus) (1988), The Johns Hopkins University Press, Baltimore
Larsson K. Impaired mating performances in male rats after anosmia induced peripherally or centrally. Brain Behav Evol 4 (1971) 463-471
Mandiyan V.S., Coats J.K., and Shah N.M. Deficits in sexual and aggressive behaviors in Cnga2 mutant mice. Nat Neurosci 8 (2005) 1660-1662
Marshall J.C. Biology and comparative physiology of birds (1961), Academic Press, New York
Meddle S.L., King V.M., Follett B.K., Wingfield J.C., Ramenofsky M., Foidart A., et al. Copulation activates Fos-like immunoreactivity in the male quail forebrain. Behav Brain Res 85 (1997) 143-159
Meisel R.L., and Sachs B.D. The physiology of male sexual behavior. In: Knobil E., and Neill J.D. (Eds). The physiology of reproduction. 2 ed. vol. 2 (1994), Raven Press, New York 3-105
Mello C.V., Vicario D.S., and Clayton D.F. Song presentation induces gene expression in the songbird forebrain. Proc Natl Acad Sci USA 89 (1992) 6818-6822
Michael R.P., and Keverne E.B. Pheromones in the communication of sexual status in primates. Nature 218 (1968) 746-749
Murphy A.Z., and Hoffman G.E. Distribution of gonadal steroid receptor-containing neurons in the preoptic-periaqueductal gray-brainstem pathway: a potential circuit for the initiation of male sexual behavior. J Comp Neurol 438 (2001) 191-212
Murphy M.R., and Schneider G.E. Olfactory bulb removal eliminates mating behavior in the male golden hamster. Science 167 (1970) 302-304
Panzica G.C., Viglietti-Panzica C., and Balthazart J. The sexually dimorphic medial preoptic nucleus of quail: a key brain area mediating steroid action on male sexual behavior. Front Neuroendocrinol 17 (1996) 51-125
Pfaus J.G., and Heeb M.M. Implications of immediate-early gene induction in the brain following sexual stimulation of female and male rodents. Brain Res Bull 44 (1997) 397-407
Pfeiffer C.A., and Johnston R.E. Hormonal and behavioral responses of male hamsters to females and female odors: roles of olfaction, the vomeronasal system, and sexual experience. Physiol Behav 55 (1994) 129-138
Porter R.H., Hepper P.G., Bouchot C., and Picard M. A simple method for testing odor detection and discrimination in chicks. Physiol Behav 67 (1999) 459-462
Porter R.H., Picard M., Arnould C., and Tallet C. Chemosensory deficits are associated with reduced weight gain in newly hatched chicks. Anim Res 51 (2002) 337-345
Porter R.H., Roelofsen R., Picard M., and Arnould C. The temporal development and sensory mediation of social discrimination in domestic chicks. Anim Behav 70 (2005) 359-364
Powers J.B., Newman S.W., and Bergondy M.L. MPOA and BNST lesions in male Syrian hamsters: differential effects on copulatory and chemoinvestigatory behaviors. Behav Brain Res 23 (1987) 181-195
Powers J.B., and Winans S.S. Sexual behavior in peripherally anosmic male hamsters. Physiol Behav 10 (1973) 361-368
Reiner A., and Karten H.J. Comparison of olfactory bulb projections in pigeons and turtles. Brain Behav Evol 27 (1985) 11-27
Reiner A., Perkel D.J., Bruce L.L., Butler A.B., Csillag A., Kuenzel W., et al. Revised nomenclature for avian telencephalon and some related brainstem nuclei. J Comp Neurol 473 (2004) 377-414
Rieke G.K., and Wenzel B.M. Forebrain projections of the pigeon olfactory bulb. J Morphol 158 (1978) 41-55
Rizvi T.A., Murphy A.Z., Ennis M., Behbehani M.M., and Shipley M.T. Medial preoptic area afferents to periaqueductal gray medullo-output neurons: a combined Fos and tract tracing study. J Neurosci 16 (1996) 333-344
Robertson G.S., Pfaus J.G., Atkinson L.J., Matsumura H., Phillips A.G., and Fibiger H.C. Sexual behavior increases c-fos expression in the forebrain of the male rat. Brain Res 564 (1991) 352-357
Rowe F.A., and Edwards D.A. Olfactory bulb removal: influences on the mating behavior of male mice. Physiol Behav 8 (1972) 37-41
Sachs B.D. Photoperiodic control of the cloacal gland of the Japanese quail. Science 157 (1967) 201-203
Sachs B.D., and Barfield R.J. Temporal patterning of sexual behavior in the male rat. J Comp Physiol Psychol 73 (1970) 359-364
Schumacher M., and Balthazart J. The postnatal demasculinization of sexual behavior in the Japanese quail. Horm Behav 18 (1984) 298-312
Seiwert C.M., and Adkins-Regan E. The foam production system of the male Japanese quail: characterization of structure and function. Brain Behav Evol 52 (1998) 61-80
Taziaux M., Cornil C.A., Dejace C., Arckens L., Ball G.F., and Balthazart J. Neuroanatomical specificity in the expression of the immediate early gene c-fos following expression of appetitive and consummatory male sexual behaviour in Japanese quail. Eur J Neurosci 23 (2006) 1869-1887
Tlemçani O., Ball G.F., D'Hondt E., Vandesande F., Sharp P.J., and Balthazart J. Fos induction in the Japanese quail brain after expression of appetitive and consummatory aspects of male sexual behavior. Brain Res Bull 52 (2000) 249-262
Valcourt R.J., and Sachs B.D. Penile reflexes and copulatory behavior in male rats following lesions in the bed nucleus of the stria terminalis. Brain Res Bull 4 (1979) 131-133
Veening J.G., and Coolen L.M. Neural activation following sexual behavior in the male and female rat brain. Behav Brain Res 92 (1998) 181-193
Winans S.S., and Powers J.B. Olfactory and vomeronasal deafferentation of male hamsters: histological and behavioral analyses. Brain Res 126 (1977) 325-344
Yoon H., Enquist L.W., and Dulac C. Olfactory inputs to hypothalamic neurons controlling reproduction and fertility. Cell 123 (2005) 669-682
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