Abstract
Several studies performed in mammals and, more recently, in other vertebrates, demonstrated that sex differences in reproductive behavior as well as in neuronal circuitries involved in its control largely depend on steroid hormones. The perinatal exposure to gonadal steroids and the presence of the appropriate gonadal hormones in the adulthood are necessary for the full expression of sexual behaviour (for a complete list of references see Panzica et al., 1995). More recently, a new group of studies indicated that gonadal hormones can cause changes in brain morphology and functions in the adult brain also in regions which are not directly related to sexual functions (i.e. the regulation of cholinergic neurons by estradiol in the rat forebrain according to a sexually dimorphic pattern). Furthermore, other steroid hormones other than gonadal hormones are also effective on neural structures which do not belong to the traditional neuroendocrine brain targets (Luine and Harding, 1994). With aging, the gonads undergo anatomical, histological and vascular changes, and as a result of these changes all forms of circulating gonadal hormones decrease in both female and male. The magnitude of this decline is considerably dependent on individuals, age and health status (for a review see Timiras et al., 1995). As a consequence, alterations that occur in neuroendocrine systems during aging can provide new insights into the general problem of how steroid modulate neuronal circuitries throughout the life.
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References
Arendash, G.W. and Gorski, R.A. (1983). Effects of discrete lesions of the sexually dimorphic nucleus of the pre-optic area or other medial preoptic regions on the sexual behavior of male rats. Brain Res.Bull. 10, 147–154.
Arnold, A.P. (1990). The passerine bird song system as a model in neuroendocrine research. J.Exp.Zool. 4 (suppl), 22–30.
Arnold, A.P. and Schlinger, B.A. (1993). The puzzle of sexual differentiation of the brain and behavior in Zebra finches. Poultry Science Rev. 5, 3–13.
Aste, N., Panzica, G.C., Viglietti-Panzica, C., and Balthazart, J. (1991). Effects of in ovo estradiol benzoate treatments on sexual behavior and size of neurons in the sexually dimorphic medial preoptic nucleus of Japanese quail. Brain Res.Bull. 27. 713–720.
Aste, N., Panzica, G.C., Aimar, P., Viglietti-Panzica, C., Harada, N., Foidart, A., and Balthazart, J. (1994). Morphometric studies demonstrate that aromatase-immunoreactive cells are the main target of androgens and estrogens in the quail medial preoptic nucleus. Exp.Brain Res. 101, 241–252.
Aste, N., Panzica, G.C., Viglietti-Panzica, C., Absil, P., Balthazart, J., MĂĽhlbauer, E., and Grossmann, R. (1995). The vasotocin system of the nucleus of the stria terminalis in the Japanese quail. Soc.Neurosci.Abstr. 21. 357.
Aste, N., Mühlbauer, E., and Grossmann, R. (1996a). Distribution of AVT gene expressing neurons in the prosencephalon ofjapanese quail and chicken. Cell Tissue Res. 286, 365–373.
Aste, N., Viglietti-Panzica, C., Balthazart, J., and Panzica, G.C. (1996b). Influence of gonadal hormones on peptidergic pathways of the quail brain. Poultry and Avian Biology Reviews 6, 275.
Aste, N., Viglietti-Panzica, C., Mühlbauer, E., Grossmann, R., and Panzica, G.C. (1996c). Sexual dimorphism of vasotocinergic structures in quail nucleus of stria terminalis. Italian J.Anatomy Embriol. 101, Suppl.1, 136–137.
Ball, G.F., Nock, B., McEwen, B.S., and Balthazart, J. (1989). Distribution of a,-adrenergic receptors in the brain of the Japanese quail as determined by quantitative autoradiography: implication for the control of sexually dimorphic reproductive processes. Brain Res. 491, 68–79.
Balthazart, J., Foidart, A., Surlemont, C., and Harada, N. (1990a). Preoptic Aromatase in Quail: Behavioral, Biochemical and lmmunocytochemical Studies. In Hormones, Brain and Behaviour in Vertebrates. Vol.2. Behavioural activation in males and females–Social interactions and reproductive endocrinology. Comp. Physiol. Vol. 9 (ed Balthazart, J. ) pp. 45–62. Karger, Basel, New York
Balthazart, J., Foidart, A., Surlemont, C., Vockel, A., and Harada, N. (1990b). Distribution of aromatase in the brain of the Japanese quail, ring dove, and zebra finch: an immunocytochemical study. J.Comp.Neurol. 301, 276–288.
Balthazart, J. and Surlemont, C. (1990). Copulatory behavior is controlled by the sexually dimorphic nucleus of the quail preoptic area. Brain Res.Bull. 25, 7–14.
Balthazart, J., Foidart, A., Surlemont, C., and Harada, N. (1991). Neuroanatomical specificity in the co-localization of aromatase and estrogen receptors. J.Neurobiol. 22, 143–157.
Balthazart, J., Surlemont, C., and Harada, N. (1992). Aromatase as a cellular marker of testosterone action in the preoptic area. Physiol.Behay. 51, 395–409.
Balthazart, J. (1993). Brain aromatase and reproductive function. In Local.systems in reproduction (eds Magness, R.R. and Naftolin, F. ) pp. 13–31. Raven Press, New York
Balthazart, J., and Foidart, A. (1993). Neural bases of behavioral sex differences in quail. In The development of sex differences and similarities in behavior (ed Haug, M. ) pp. 51–75. Kluwer Acad.Publ., Amsterdam.
Balthazart, J., Dupiereux, V., Aste, N., Viglietti-Panzica, C., Barrese, M., and Panzica, G.C. (1994). Afferent and efferent connections of the sexually dimorphic medial preoptic nucleus of the male quail revealed by in vitro transport of Dil. Cell Tissue Res. 276, 455–475.
Balthazart, J., Absil, P., Viglietti-Panzica, C., and Panzica, G.C. (1997). Vasotocinergic innervation of areas containing aromatase-immunoreactive cells in the quail forebrain. J.Neurobiol. (in press)
Breedlove, S.M. (1992). Sexual dimorphism in the vertebrate nervous system. J.Neurosci. 12, 4133–4142.
Brody, H. (1992). The aging brain. Acta Neurol.Scand. 85, 40–44.
Castagna, C., Absil, P., and Balthazart, J. (1996). Central effects of vasotocin on appetitive and consummatory sexual behavior in male quail. Soc.Neurosci.Abstr. 22, 2068.
Celotti, F., Melcangi, R.C., and Martini, L. (1992). The 5a-reductase in the brain: molecular aspects and relation to brain function. Front.Neuroendocrinol. 13, 163–215.
Chambers, K.C., Thornton, J.E., and Roselli, C.E. (1991). Age-related deficits in brain androgen binding and metabolism, testosterone, and sexual behavior of male rats. Neurobiol.Aging 12, 123–130.
De Jonge, F.H., Louwerse, A.L., Ooms, M.P., Evers, P., Endert, E., and Van De Poll, N.E. (1990). Lesions of the SDN-POA inhibit sexual behavior of male Wistar rats. Brain Res.Bull. 23, 483–492.
De Vries, G.J. (1990). Sex differences in neurotransmitter systems. J.Neuroendocrinol. 2, 1–13.
De Vries, G.J., Al Shamma, H.A., and Zhou, L. (1994). The sexually dimorphic vasopressin innervation of the brain as a model for steroid modulation of neuropeptide transmission. In Hormonal restructuring of the adult brain. Basic and clinical perspectives. Ann. New York Acad.Sciences. Vol. 743 (eds Luine, V.N. and Harding, C.F. ) pp. 95–120. New York Acad.Sciences, New York
Dellovade, T.L., Rissman, E.F., Thompson, N., Harada, N., and Ottinger, M.A. (1995). Co-localization of aromatase enzyme and estrogen receptor immunoreactivity in the preoptic area during reproductive aging. Brain Res. 674, 181–187.
Doman, W.A. and Malsbury, C.W. (1989). Neuropeptides and male sexual behavior. Neurosci.Biobehay.Rev. 13, 1–15.
Dorsa, D.M., Smith, E.R., and Davidson, J.M. (1984). Immunoreactive [3-endorphin and LHRH levels in the brains of aged male rats with impaired sex behavior. Neurobiol.Aging 5, 115–120.
Fink, G., Rosie, R., Sheward, W.J., Thomson, E., and Wilson, H. (1991). Steroid Control of Central Neuronal Interactions and Function. J.Steroid Biochem.Mol.Biol. 40, 123–132.
Fliers, E., De Vries, G.J., and Swaab, D.F. (1985). Changes with aging in the vasopressin and oxytocin innervation of the rat brain. Brain Res. 348, 1–8.
Goudsmit, E., Fliers, E., and Swaab, D.F. (1988). Testosterone supplementation restores vasopressin innervation in the senescent rat brain. Brain Res. 473, 306–313.
Gruenewald, D.A. and Matsumoto, A.M. (1991). Age-related decreases in serum gonadotropin levels and gonadotropin-releasing hormone expression in the medial preoptic area of the male rat are dependent upon testicular feddback. Endocrinol. 129, 2442–2450.
Jurkevich, A., Barth, S.W., Aste, N., Panzica, G.C., and Grossmann, R. (1996a). Intracerebral sex differences in the vasotocin system in birds: possible implication on behavioral and autonomic functions. Horm.Behay. (in press)
Jurkevich, A., Barth, S.W., and Grossmann, R. (1996b). Sexual dimorphism of arg-vasotocin gene expressing neurons in the telencephalon and dorsal diencephalon of the domestic fowl. An immunocytochemical and in situ hybridization study. Cell Tissue Res. 287, 69–77.
Kawata, M. (1995). Roles of steroid hormones and their receptors in structural organization in the nervous system. Neurosci.Res. 24, 1–46.
Le Vay, S. (1991). A Difference in Hypothalamic Structure Between Heterosexual and Homosexual Men. Science 253, 1034–1037.
Luine, V.N., and Harding, C.F. (1994). Hormonal restructuring of the adult brain: Basic and clinical perspectives. Annals New York Academy of Sciences. Vol. 743, New York Acad.Sci., New York.
McCarthy, M.M., Schlenker, E.H., and Pfaff, D.W. (1993). Enduring consequences of neonatal treatment with antisense oligodeoxynucleotides to estrogen receptor messenger ribonucleic acid on sexual differentiation of rat brain. Endocrinol. 133, 433–439.
McEwen, B.S., Davis, P., Parson, B., and Pfaff, D.W. (1979). The brain: target for steroid hormone action. Ann.Rev.Neurosci. 2, 65–112.
McEwen, B.S. (1991). Steroid affect neural activity by acting on the membrane and the genome. Trends Pharmacol.Sci. 12, 141–147.
Meisel, R.L., and Sachs, B.D. (1994). The physiology of male sexual behavior. In The Physiology of reproduction (eds Knobil, E. and Neill, J.D. ) pp. 3–105. Raven Press, New York.
Ottinger, M.A. and Balthazart, J. (1986). Altered endocrine and behavioral responses with reproductive aging in the male Japanese quail. Horm.Behay. 20, 83–94.
Ottinger, M.A. (1992). Altered neuroendocrine mechanisms during reproductive aging. Poultry Science Rev. 4, 235–248.
Ottinger, M.A., Nisbet, I.C.T., and Finch, C.E. (1995). Aging and reproduction: Comparative endocrinology of the Common Tern and Japanese quail. Am.Zool. 35, 299–306.
Ottinger, M.A., Thompson, N., Viglietti-Panzica, C., and Panzica, G.C. (1997). Neuroendocrine regulation of GnRH and behavior during aging in birds. Brain Res.Bull. (in press)
Panzica, G.C., Viglietti-Panzica, C., Calcagni, M., Anselmetti, G.C., Schumacher, M., and Balthazart, J. (1987). Sexual differentiation and hormonal control of the sexually dimorphic medial preoptic nucleus in quail. Brain Res. 416, 59–68.
Panzica, G.C., Viglietti-Panzica, C., Sanchez, F., Sante, P., and Balthazart, J. (1991). Effects of testosterone on a selected neuronal population within the preoptic sexually dimorphic nucleus of the Japanese quail. J.Comp.Neurol. 303, 443–456.
Panzica, G.C., Aste, N., Viglietti-Panzica, C., and Fasolo, A. (1992). Neuronal circuits controlling quail sexual behavior. Chemical neuroanatomy of the septo-preoptic region. Poultry Science Rev. 4, 249–259.
Panzica, G.C., Aste, N., Dellovade, T.L., Rissman, E.F., Foidart, A., Balthazart, J., and Ottinger, M.A. (1994). Aromatase-containing cells of the medial preoptic nucleus respond differentially to testosterone in young and aged male quail. Ann.Endocrinol. 55, 37.
Panzica, G.C., Aste, N., Viglietti-Panzica, C., and Ottinger, M.A. (1995). Structural sex differences in the brain: Influence of gonadal steroids and behavioral correlates. J.Endocrinol.lnvest. 18, 232–252.
Panzica, G.C., Castagna, C., Aste, N., Viglietti Panzica, C., and Balthazart, J. (1996a). Testosterone effects on the neuronal ultrastructure in the medial preoptic nucleus of male Japanese quail. Brain Res.Bull. 39, 281–292.
Panzica, G.C., Garcia-Ojeda, E., Viglietti Panzica, C., Thompson, N.E., and Ottinger, M.A. (1996b). Testosterone effects on vasotocinergic innervation of sexually dimorphic medial preoptic nucleus and lateral septum during aging in male quail. Brain Res. 712, 190–198.
Panzica, G.C., Viglietti-Panzica, C., and Balthazart, J. (1996e). The sexually dimorphic medial preoptic nucleus of quail: a key brain area mediating steroid action on male sexual behavior. Front.Neuroendocrinol. 17, 1–75.
Pfaff, D.W., Schwartz-Giblin, S., McCarthy, M.M., and Kow, L.M. (1994). Cellular and molecular mechanisms of female reproductive behaviors. In The physiology of reproduction (eds Knowbil, E. and Neill, J.D. ) pp. 107–220. Raven Press, New York
Ramirez, V.D., Zheng, J., and Siddique, K.M. (1996). Membrane receptors for estrogen, progesterone, and testosterone in teh rat brain: fantasy or reality? Cell.Mol.Neurobiol. 16, 175–198.
Roselli, C.E. and Resko, J.A. (1993). Aromatase activity in the rat brain: hormonal regulation and sex differences. J. Steroid Biochem.Mol.Biol. 44, 499–508.
Schumacher, M. and Balthazart, J. (1986). Testosterone-induced brain aromatase is sexually dimorphic. Brain Res. 370. 285–293.
Schumacher, M. (1990). Rapid membrane effects of steroid hormones: an emerging concept in neuroendocrinology. Trends in Neuroscience 13, 359–362.
Swaab, D.F., Gooren, L.J.G., and Hofman, M.A. (1992). The human hypothalamus in relation to gender and sexual orientation. In The human hypothalamus in health and disease. Progress in brain research, vol. 93 (eds Swaab, D.F., Hofman, M.A., Mirmiran, M., Ravid, R., and Van Leeuwen, F.W. ) pp. 205–215. Elsevier, Amsterdam
Taylor, G., Bardgett, M., Farr, S., Humphrey, W., Womack, S., and Weiss, J. (1996). Aging of the brain-testicular axis: reproductive systems of healthy old male rats with or without endocrine stimulation. Proc.Soc.Exp.Biol.Med. 211, 69–75.
Timiras, P.S. (1996). Hormones and aging, (UnPub).
Tobet, S.A., and Fox, T.O. (1992). Sex differences in neuronal morphology influenced hormonally throughout life. In Handbook of Behavioral Neurobiology, Vol. 11: Sexual differentiation (eds Gerall, A.A., Moltz, H., and Ward, I.L. ) pp. 41–83. Plenum Press, New York.
Viglietti-Panzica, C. (1986). Immunohistochemical study of the distribution of vasotocin reacting neurons in avian diencephalon. J.Himforsch. 27, 559–566.
Viglietti-Panzica, C., Panzica, G.C., Fiori, M.G., Calcagni, M., Anselmetti, G.C., and Balthazart, J. (1986). A sexually dimorphic nucleus in the quail preoptic area. Neurosci.Lett. 64, 129–134.
Viglietti-Panzica, C. and Panzica, G.C. (1991). Peptidergic neurons in the avian brain. Ann.Sci.Nat.Zool., Paris 12, 137–155.
Viglietti-Panzica, C., Anselmetti, G.C., Balthazart, J., Aste, N., and Panzica, G.C. (1992). Vasotocinergic innervation of the septal region in the Japanese quail: sexual differences and the influence of testosterone. Cell Tissue Res. 267, 261–265.
Viglietti-Panzica, C., Aste, N., Balthazart, J., and Panzica, G.C. (1994). Vasotocinergic innervation of sexually dimorphic medial preoptic nucleus of the male Japanese quail: influence of testosterone. Brain Res. 657, 171–184.
Viglietti-Panzica, C., Garcia-Ojeda, E., Aste, N., Panzica, G.C., Thompson, N., and Ottinger, M.A. (1996). The vasotocin system in the quail brain: changes with age. Soc.Neurosci.Abstr. 22, 1890.
Witkin, J.W. (1989). Aging changes in synaptology of luteinizing hormone-releasing hormone neurons in male rat preoptic area. Neuroendocrinology 49, 344–348.
Yahr, R. and Gregory, J.E. (1993). The medial and lateral cell groups of the sexually dimorphic area of the gerbil hypothalamus are essential for male sex behavior and act via separate pathways. Brain Res. 631, 287–296.
Zhou, J.N., Hofman, M.A., Gooren, L.J.G., and Swaab, D.F. (1995). A sex difference in the human brain and its relation to transsexuality. Nature 378, 68–70.
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Panzica, G.C., GarcĂa-Ojeda, E., Viglietti-Panzica, C., Aste, N., Ottinger, M.A. (1997). Role of Testosterone in the Activation of Sexual Behavior and Neuronal Circuitries in the Senescent Brain. In: Filogamo, G., Vernadakis, A., Gremo, F., Privat, A.M., Timiras, P.S. (eds) Brain Plasticity. Advances in Experimental Medicine and Biology, vol 429. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-9551-6_20
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