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Molecular Mechanisms of Steroid Hormone Actions in the Brain

  • Chapter
Hormones and Aggressive Behavior

Abstract

As evidenced by the diversity and comprehensiveness of the other chapters in this book, the hypothesis that endogenous and exogenous steroid hormones can have direct effects on neurons in specific regions of the brain that may in turn precipitate and/or regulate the expression of aggressive behaviors is now widely accepted, even though we still know surprisingly little about the molecular mechanisms of these hormone actions. This paucity of information is striking in view of the long history of experimental behavioral neuroendocrinology dating back for literally thousands of years, to when castration was first used to curb sexual and aggressive behaviors in man and other animals (see Luttge, 1971). Over a century ago, Berthold (1849/1944) was the first to report that castration and subsequent testis transplantation could reversibly inhibit sexual, aggressive, and crowing behaviors in roosters, thus setting the pattern for future studies on the endocrine bases of these and other behaviors in many species. The present chapter reviews recent literature on the molecular mechanisms of estrogen, progestin, androgen, and glucocorticoid hormone actions in the mammalian brain. Each of these classes of steroids has been shown to influence the display of agonistic behaviors in mammals. No attempt will be made to relate the biochemical and behavioral actions of these steroids, because this material is reviewed in other chapters in this book.

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References

  • Acs, A., Palkovits, M., & Stark, E. Changes of glutamic acid decarboxylase activity after dexameth-asone in selected areas of the rat brain. Neuroscience Letters, 1980, 19, 97–101.

    Article  PubMed  CAS  Google Scholar 

  • Adler, N. T., & Pfaff, D. W. (Eds.). Neurobiology of reproduction. Book in preparation, 1983.

    Google Scholar 

  • Alderson, L. M., Starr, M. S., & Baum, M. J. Effects of castration on dopamine metabolism in rat striatum and limbic forebrain. Society for Neuroscience Abstracts, 1979, 5, 1471.

    Google Scholar 

  • Allera, A., Rao, G. S., & Breuer, H. Specific interaction of corticosteroids with components of the cell membrane which are involved in the translocation of the hormone into the intravesicular space of purified rat liver plasma membrane vesicles. Journal of Steroid Biochemistry, 1980, 12, 259–266.

    Article  PubMed  CAS  Google Scholar 

  • Altman, J., & Bayer, S. A. Development of the diencephalon in the rat: I. Autoradiographic study of the time of origin and settling patterns of neurons of the hypothalamus. Journal of Comparative Neurology, 1978, 182, 945–972.

    Article  PubMed  CAS  Google Scholar 

  • Angelucci, L., Valeri, P., Palmery, M., Paracchioli, F. R., & Catalani, A. Brain glucocorticoid receptor: correlation of in vivo uptake of corticosterone with behavioral, endocrine and neurophamacol- ogical events. Advances in Biochemical Psychopharmacology, 1980, 21, 391–406.

    PubMed  CAS  Google Scholar 

  • Anton-Tay, F., Pelham, R. W., & Wurtman, R. J. Increased turnover of 3H-norepinephrine in rat brain following castration or treatment with ovine follicle-stimulating hormone. Endocrinology, 1969, 84, 1489–1492.

    Article  PubMed  CAS  Google Scholar 

  • Asai, M., Yu, W., & Leung, B. S. Cytoplasmic competitors of estrogen receptor at chromatin binding site. Endocrine Society Abstracts, 1979, 781.

    Google Scholar 

  • Azmitia, E. C., & McEwen, B. S. Corticosterone regulation of tryptophan hydroxylase in midbrain of the rat. Science, 1969, 166, 1274–1276.

    Article  PubMed  CAS  Google Scholar 

  • Azmitia, E. C., & McEwen, B. S. Adrenalcortical influence on rat brain tryptophan hydroxylase activity. Brain Research, 1974, 78, 291–302.

    Article  PubMed  CAS  Google Scholar 

  • Azmitia, E. C., & McEwen, B. S. Early response of rat brain tryptophan hydroxylase activity to cycloheximide, puromycin and corticosterone. Journal of Neurochemistry, 1976, 27, 773–778.

    Article  PubMed  CAS  Google Scholar 

  • Azmitia, E. C., Algeri, S., & Costa, E. In vivo conversion of 3H-L-tryptophan into 3H-serotonin in brain areas of adrenalectomized rats. Science, 1970, 169, 201–203.

    Article  PubMed  CAS  Google Scholar 

  • Ball, P., & Knuppen, R. Catecholoestrogens (2- and 4-hydroxyoestrogens)-Chemistry, biogenesis, metabolism, occurrence and physiological significance. Acta Endocrinologica, 1980, 93, Supple- mentum 232.

    Google Scholar 

  • Bapna, J., Neff, N. H., & Costa, E. A method for studying norepinephrine and serotonin metabolism in small regions of rat brain: Effect of ovariectomy on amine metabolism in anterior and posterior hypothalamus. Endocrinology, 1971, 89, 1345–1349.

    Article  PubMed  CAS  Google Scholar 

  • Beattie, C. W., & Soyka, L. F. Influence of progestational steroids in hypothalamic tyrosine hydroxylase activity in vitro. Endocrinology, 1973, 93, 1453–1455.

    Article  PubMed  CAS  Google Scholar 

  • Beattie, C. W., Rodgers, C. H., & Soyka, L. F. Influence of ovariectomy and ovarian steroids on hypothalamic tyrosine hydroxylase activity in the rat. Endocrinology, 1972, 91, 276–279.

    Article  PubMed  CAS  Google Scholar 

  • Beinfeld, M. C., & Packman, P. M. Estrogen induction of specific soluble proteins in the hypothalamus of the immature rat. Biochemical and Biophysical Research Communications, 1976, 73, 646–652.

    Article  PubMed  CAS  Google Scholar 

  • Bernard, B., & Paolino, R. Time dependent changes in brain biogenic amine dynamics following castration in male rats. Journal of Neurochemistry, 1974, 22, 951–956.

    Article  PubMed  CAS  Google Scholar 

  • Berthold, A. A. Transplantation der Hoden. Archiv för Anatomi, Physiologie und wissenschaftliche Medicin, 1849, 16, 42–46. (Trans, in Bulletin of the History of Medicine, 1944, 16, 399–401.)

    Google Scholar 

  • Beyer, C. Endocrine control of sexual behavior. New York: Raven Press, 1979.

    Google Scholar 

  • Biegon, A., Bercovitz, H., & Samuel, D. Serotonin receptor concentration during the estrous cycle of the rat. Brain Research, 1980, 187, 221–225.

    Article  PubMed  CAS  Google Scholar 

  • Birmingham, M. K., Stumpf, W. E., & Sar, M. Nuclear localization of aldosterone in rat brain cells assessed by autoradiography. Experientia, 1979, 35, 1240–1241.

    Article  PubMed  CAS  Google Scholar 

  • Biro, J. The effect of luteinizing hormone releasing hormone (LH-RH) and oestrogen on RNA synthesis in anterior pituitary and different brain regions of rats. Endokrinologie, 1978, 72, 285–290.

    PubMed  CAS  Google Scholar 

  • Bjorklund, A., Hakamson, R., Nobin, A., & Sjoberg, N. O. Increase in rabbit hypothalamic histidine decarboxylase activity after oophorectomy and thyroidectomy. Experientia, 1972, 28, 1232–1233.

    Article  PubMed  CAS  Google Scholar 

  • Blaustein, J. D., & Feder, H. H. Cytoplasmic progestin receptors in guinea pig brain: Characteristics and relationship to the induction of sexual behavior. Brain Research, 1979, 169, 481–497. (a)

    Article  PubMed  CAS  Google Scholar 

  • Blaustein, J. D., & Feder, H. H. Cytoplasmic progestin receptors in female guinea pig brain and their relationship to refractoriness in expression of female sexual behavior. Brain Research, 1979, 177, 489–498. (b)

    Article  PubMed  CAS  Google Scholar 

  • Blaustein, J. D., & Feder, H. H. Nuclear progestin receptors in guinea pig brain measured by an in vitro exchange assay after hormonal treatments that affect lordosis. Endocrinology, 1980, 106, 1061–1069.

    Article  PubMed  CAS  Google Scholar 

  • Blaustein, J. D., & Wade, G. N. Progestin binding by brain and pituitary cell nuclei and female rat sexual behavior. Brain Research, 1978, 140, 360–367.

    Article  PubMed  CAS  Google Scholar 

  • Brawer, J. R., & Naftolin, F. The effects of oestrogen on hypothalamic tissue. Sex Hormones and Behavior, 1979, 62, 19–40.

    CAS  Google Scholar 

  • Breuer, H., & Koster, G. Interaction between oestrogens and neurotransmitters at the hypophysial- hypothalamic level. Journal of Steroid Biochemistry, 1974, 5, 961–968.

    Article  CAS  Google Scholar 

  • Butte, J. C., Kakihana, R., & Noble, E. P. Circadian rhythm of corticosterone levels in rat brain. Journal of Endocrinology, 1976, 68, 235–239.

    Article  PubMed  CAS  Google Scholar 

  • Callard, G. V., Petro, Z., & Ryan, K. Conversion of androgen to estrogen and other steroids in the vertebrate brain. American Zoologist, 1978, 18, 511–523.

    CAS  Google Scholar 

  • Cardinali, D. P., & Gomez, E. Changes in hypothalamic noradrenaline, dopamine and serotonin uptake after estradiol administration to rats. Journal of Endocrinology, 1977, 73, 181–182.

    Article  PubMed  CAS  Google Scholar 

  • Carrillo, A. J. Estrogen receptors in the medial basal hypothalamus of the rat following complete hypothalamic deafferentation. Brain Research, 1980, 816, 157–164.

    Article  Google Scholar 

  • Carroll, B. J., Heath, B., & Jarrett, D. B. Corticosteroids in brain tissue. Endocrinology, 1975, 97, 290–300.

    Article  PubMed  CAS  Google Scholar 

  • Chamness, G. C., Jennings, A. W., & McGuire, W. L. Estrogen receptor binding to isolated nuclei. A nonsaturable process. Biochemistry, 1974, 13, 327–331.

    Article  PubMed  CAS  Google Scholar 

  • Chan, L., Means, A. R., & O’Malley, B. W. Steroid hormone regulation of specific gene expression. Vitamins and Hormones, 1978, 36, 259–295.

    Article  PubMed  CAS  Google Scholar 

  • Cheng, Y.-J., & Karavolas, H. J. Subcellular distribution and properties of progesterone (A4-ste- roid)5a-reductase in rat medial basal hypothalamus. Journal of Biological Chemistry, 1975, 250, 7997–8003.

    PubMed  CAS  Google Scholar 

  • Chiocchio, S. R., Negro-Vilar, A., & Tramezami, J. H. Acute changes in norepinephrine content in the median eminence induced by orchidectomy or testosterone replacement. Endocrinology, 1976, 99, 629–635.

    PubMed  CAS  Google Scholar 

  • Chytil, F., & Toft, D. O. Corticoid binding component in rat brain. Journal of Neurochemistry, 1972, 19, 2877–2880.

    Article  PubMed  CAS  Google Scholar 

  • Cidlowski, J. A., & Muldoon, T. G. Estrogenic regulation of cytoplasmic receptor populations in estrogen-responsive tissue of the rat. Endocrinology, 1974, 95, 1621–1629.

    Article  PubMed  CAS  Google Scholar 

  • Cidlowski, J. A., & Muldoon, T. G. Sex-related differences in the regulation of cytoplasmic estrogen receptor levels in responsive tissues of the rat. Endocrinology, 1976, 98, 833–841.

    Article  PubMed  CAS  Google Scholar 

  • Clark, C. R., & Nowell, N. W. Binding properties of testosterone receptors in the hypothalamic- preoptic area of the adult male mouse brain. Steroids, 1979, 33, 407–426.

    Article  PubMed  CAS  Google Scholar 

  • Clark, J. H., & Peck, E. J., Jr. Nuclear retention of receptor oestrogen complex and nuclear acceptor sites. Nature, 1976, 260, 635–637.

    Article  PubMed  CAS  Google Scholar 

  • Cornwell-Jones, C. A., & Marasco, E. M. Castration decreases olfactory bulb norepinephrine in male rats but not hamsters. Brain Research, 1980, 183, 377–382.

    Article  PubMed  CAS  Google Scholar 

  • Cramer, O. M., Parker, C. R., & Porter, J. C. Estrogen inhibition of dopamine release into hypophysial portal blood. Endocrinology, 1979, 104, 419–422. (a)

    Article  PubMed  CAS  Google Scholar 

  • Cramer, O. M., Parker, C. R., & Porter, J. C. Stimulation of dopamine release into hypophysial portal blood by administration of progesterone. Endocrinology, 1979, 105, 929–933. (b)

    Article  PubMed  CAS  Google Scholar 

  • Crowley, W. R., O’Donohue, T. L., & Jacobowitz, D. M. Changes in catecholamine content in discrete brain nuclei during the estrous cycle of the rat. Brain Research, 1978, 147, 315–326.

    Article  PubMed  CAS  Google Scholar 

  • Crowley, W. R., O’Donohue, T. L., Wachslicht, H., & Jacobowitz, D. M. Effects of estrogen and progesterone on plasma gonadotropins and on catecholamine levels and turnover in discrete brain regions of ovariectomized rats. Brain Research, 1978, 154, 345–357.

    Article  PubMed  CAS  Google Scholar 

  • Crowley, W. R., O’Donohue, T. L., Muth, E. A., & Jacobowitz, D. M. Effects of ovarian hormones on levels of luteinizing hormone in plasma and on serotonin concentrations in discrete brain nuclei. Brain Research Bulletin, 1979, 4, 571–574.

    Article  PubMed  CAS  Google Scholar 

  • Curtis, D. R., & Johnston, G. A. R. Amino acid transmitters in the mammalian central nervous system. Ergebnisse der Physiologie, 1974, 69, 97–188.

    CAS  Google Scholar 

  • Davies, I. J., Naftolin, F., Ryan, K. J., Fishman, J., & Siu, J. The affinity of catechol estrogens for estrogen receptors in the pituitary and anterior hypothalamus of the rat. Endocrinology, 1975, 97, 554–557.

    Article  PubMed  CAS  Google Scholar 

  • Debus, G., & Kehr, W. Catecholamine and 5-hydroxytryptamine synthesis and metabolism following intraventricular injection of dibutyryl cyclic AMP. Journal of Neural Transmission, 1979, 45, 195–206.

    Article  PubMed  CAS  Google Scholar 

  • Denari, J. H., & Rosner, J. M. Sexual steroid uptake in the alloxanized diabetic rat. Steroids and Lipids Research, 1972, 3, 151–155.

    PubMed  CAS  Google Scholar 

  • Dokas, L. A. Corticosterone and RNA metabolism in the rat hippocampus. Society for Neuroscience Abstracts, 1979, 5, 1498.

    Google Scholar 

  • Donoso, A. O. Induction of prolactin and luteinizing hormone release by histamine in male and female rats and the influence of brain transmitter antagonists. Journal of Endocrinology, 1978, 76, 193–202.

    Article  PubMed  CAS  Google Scholar 

  • Donoso, A. O., & Moyano, M. B. G. Adrenergic activity in hypothalamus and ovulation. Proceedings of the Society of Experimental Biology and Medicine, 1970, 135, 633–635.

    CAS  Google Scholar 

  • Donoso, A. O., Stefano, F. J. E., Biscardi, A. M., & Cukier, J. Effects of castration on hypothalamic catecholamines. American Journal of Physiology, 1967, 212, 737–739.

    PubMed  CAS  Google Scholar 

  • Dunn, A. J., Gildersleeve, N. B., & Gray, H. E. Mouse brain tyrosine hydroxylase and glutamic acid decarboxylase following treatment with adrenocorticotrophic hormone, vasopressin or corticosterone. Journal of Neurochemistry, 1978, 31, 977–982.

    Article  PubMed  CAS  Google Scholar 

  • Early, C. J., & Leonard, B. E. GABA and gonadal hormones. Brain Research, 1978, 155, 27–34.

    Article  Google Scholar 

  • Eaton, G. G., Goy, R. W., & Resko, J. A. Brain uptake and metabolism of estradiol benzoate and estrous behavior in ovariectomized guinea pigs. Hormones and Behavior, 1975, 6, 81–97.

    Article  PubMed  CAS  Google Scholar 

  • Edwards, E. M., & Rousseau, G. G. Effects of adrenalectomy and corticosteroids on three enzymes involved in amino acid metabolism in the brain of adult and newborn rats. Journal of Steroid Biochemistry, 1980, 13, 567–569.

    Article  PubMed  CAS  Google Scholar 

  • Eisenfeld, A. J. 3H-Estradiol: In vitro binding to macromolecules from rat hypothalamus, anterior pituitary and uterus. Endocrinology, 1970, 86, 1313–1318.

    Article  CAS  Google Scholar 

  • Enderly, C. A., & Wilson, C. A. The effect of ovarian steroids on the accumulation of 3H-labelled monoamines by hypothalamic tissue in vitro. Brain Research, 1974, 73, 321–331.

    Article  Google Scholar 

  • Engel, J., Ahlenius, S., Almgren, O., Carlsson, A., Larsson, K., & Sodersten, P. Effects of gonadec- tomy and hormone replacement on brain monoamine synthesis in male rats. Pharmacology, Biochemistry and Behavior, 1979, 10, 149–154.

    Article  CAS  Google Scholar 

  • Ermish, A., & Ruhle, H. -J. Autoradiographic demonstration of aldosterone-concentrating neuron populations in rat brain. Brain Research, 1978, 147, 154–158.

    Article  Google Scholar 

  • Etgen, A. M., Lee, K. S., & Lynch, G. Glucocorticoid modulation of specific protein metabolism in hippocampal slices maintained in vitro. Brain Research, 1979, 165, 37–45.

    Article  PubMed  CAS  Google Scholar 

  • Etgen, A. M., Martin, M., Gilbert, R.J., Lynch, G. Characterization of corticosterone-induced protein synthesis in hippocampal slices. Journal of Neurochemistry, 1980, 35, 598–602.

    Article  PubMed  CAS  Google Scholar 

  • Fahn, S. Regional distribution studies of GABA and other putative neurotransmitters and their enzymes. In E. Roberts, T. N. Chase, & D. B. Tower (Eds.), GABA in nervous system function. New York: Raven Press, 1976.

    Google Scholar 

  • Feder, H. H., Siegel, H., & Wade, G. N. Uptake of [6,7,-3H] estradiol-17β in ovariectomized rats, guinea pigs, and hamsters: Correlation with species differences in behavioral responsiveness to estradiol. Brain Research, 1974, 71, 93–103.

    Article  PubMed  CAS  Google Scholar 

  • Fekete, M. I., Stark, E., Herman, J. P., Palkovits, M., & Kanyicska, B. Catecholamine concentration of various brain nuclei of the rat as affected by ACTH and corticosterone. Neuroscience Letters, 1978, 10, 153–158.

    Article  PubMed  CAS  Google Scholar 

  • Fleischer-Lambropoulos, H., Sarkander, H.-I., & Brade, W. P. Effects of polyamines on amino acid incorporation into protein by cerebral and cerebellar as well as “neural” and “glial” nuclei of rat brain. Biochemical and Biophysical Research Communications, 1975, 63, 792–800.

    Article  PubMed  CAS  Google Scholar 

  • Florez-Lozano, J. A., Menendez-Patterson, A., & Marin, B. Sexual behavior of the pancreatectomized (95%) male hamster (Mesocricetus auratus). Physiology & Behavior, 1978, 20, 465–468.

    Article  CAS  Google Scholar 

  • Foreman, M. M., & Porter, J. C. Effects of catechol estrogens and catecholamines on hypothalamic and corpus striatal tyrosine hydroxylase activity. Journal of Neurochemistry, 1980, 34, 1175–1183.

    Article  PubMed  CAS  Google Scholar 

  • Foreman, M. M., Wickersham, E. W., & Anthony, A. Cytophotometric analysis of hypothalamic RNA fluctuations during the rat estrous cycle. Brain Research, 1977, 119, 471–475.

    Article  PubMed  CAS  Google Scholar 

  • Fox, T. O. Conversion of the hypothalamic estradiol receptor to the ‘nuclear’ form. Brain Research, 1977, 120, 580–583.

    Article  PubMed  CAS  Google Scholar 

  • Fox, T. O., & Johnston, C. Estradiol receptors from mouse brain and uterus: Binding to DNA. Brain Research, 1974, 77, 330–336.

    Article  PubMed  CAS  Google Scholar 

  • Franks, S., Ball, P., Naftolin, F., & Ruf, K. B. Effect of catechol oestrogens on induced ovulation in the immature rat. Journal of Endocrinology, 1980, 86, 263–268.

    Article  PubMed  CAS  Google Scholar 

  • Frohman, L. A., & Berelowitz, M. The physiological and pharmacological control of anterior pituitary hormone secretion. In C. B. Nemeroff & A. J. Dunn (Eds.), Peptides, hormones, and behavior: Molecular and behavioral neuroendocrinology. New York: Spectrum Publications, 1983.

    Google Scholar 

  • Ganong, W. F. The role of catecholamines and acetylcholine in the regulation of endocrine function. Life Sciences, 1974, 15, 1401–1414.

    Article  PubMed  CAS  Google Scholar 

  • Gentry, R. T., Wade, G. N., & Blaustein, J. D. Binding of [3H]estradiol by brain cell nuclei and female rat sexual behavior: Inhibition by experimental diabetes. Brain Research, 1977, 135, 135–146.

    Article  PubMed  CAS  Google Scholar 

  • Ginsburg, M., MacLusky, N. J., Morris, J. D., & Thomas, P. J. Physiological variation in abundance of oestrogen specific high-affinity binding sites in hypothalamus, pituitary and uterus of the rat. Journal of Endocrinology, 1975, 64, 443–449.

    Article  PubMed  CAS  Google Scholar 

  • Goertz, B. Effect of polamines on cell-free protein synthesizing systems from rat cerebral cortex, cerebellum and liver. Brain Research, 1979, 173, 125–135.

    Article  PubMed  CAS  Google Scholar 

  • Gordon, J. H., Nance, D. M., Wallis, C. J., & Gorski, R. A. Effects of estrogen on dopamine turnover, glutamic acid decarboxylase activity and lordosis behavior in septal lesioned female rats. Brain Research Bulletin, 1977, 2, 341–346.

    Article  PubMed  CAS  Google Scholar 

  • Gordon, J. H., Nance, D. M., Wallis, C. J., & Gorski, R. A. Effect of septal lesions and chronic estrogen treatment on dopamine, GABA and lordosis behavior in male rats. Brain Research Bulletin, 1979, 4, 85–89.

    Article  PubMed  CAS  Google Scholar 

  • Gorski, J., & Gannon, F. Current models of steroid hormone action: A critique. Annual Review of Physiology, 1976, 38, 425–450.

    Article  PubMed  CAS  Google Scholar 

  • Gray, H. E., Jasper, T. W., Luttge, W. G., Shukla, J. B., & Rennert, O. M. Estrogen increases hypothalamic and pituitary polyamine levels in ovariectomized rats. Journal of Neurochemistry, 1980, 34, 753–755.

    Article  PubMed  CAS  Google Scholar 

  • Green, A. R., & Curzon, G. Effects of hydrocortisone and immobilization on tryptophan metabolism in brain and liver of rats of different ages. Biochemical Pharmacology, 1975, 24, 713–716.

    Article  PubMed  CAS  Google Scholar 

  • Greenstein, B. D. An assay for RNA polymerase activity in rat brain nuclei-Effects of injection of oestradiol benzoate. Journal of Endocrinology, 1980, 85, 341–347.

    Article  PubMed  CAS  Google Scholar 

  • Grosser, B. I., & Axelrod, L. R. Conversion of cortisol to cortisol acetate, cortisone acetate and cortisone by the developing primate brain. Steroids, 1968, 11, 827–836.

    Article  PubMed  CAS  Google Scholar 

  • Grosser, B. I., Stevens, W., & Reed, D. J. Properties of corticosterone-binding macromolecules from rat brain cytosol. Brain Research, 1973, 57, 387–395.

    Article  PubMed  CAS  Google Scholar 

  • Gunaga, K. P., & Menon, K. M. J. Effect of catecholamines and ovarian hormones on cyclic AMP accumulation in rat hypothalamus. Biochemical and Biophysical Research Communications, 1973, 54, 440–448.

    Article  PubMed  CAS  Google Scholar 

  • Gunaga, K. P., Kawano, A., & Menon, K.M.J. In vivo effect of estradiol benzoate on the accumulation of adenosine 3’,5’-cyclic monophosphate in the rat hypothalamus. Neuroendocrinology, 1974, 16, 273–281.

    Article  CAS  Google Scholar 

  • Gustafsson, J. -A., Pousette, A., & Svensson, E. Sex-specific occurrence of androgen receptors in rat brain. Journal of Biological Chemistry, 1976, 251, 4047–4054.

    PubMed  CAS  Google Scholar 

  • Heritage, A. S., & Grant, L. D. 3H-Dihydrotestosterone in catecholamine neurons of rat brain stem. Anatomical Record, 1979, 193, 564.

    Google Scholar 

  • Heritage, A. S., Grant, L. D., & Stumpf, W. E. 3H-Estradiol in catecholamine neurons of rat brain stem: Combined localization by autoradiography and formaldehyde-induced fluorescence. Journal of Comparative Neurology, 1977, 176, 607–630.

    Article  PubMed  CAS  Google Scholar 

  • Heritage, A. S., Stumpf, W. E., Sar, M., & Grant, L. D. Brainstem catecholamine neurons are target sites for sex steroid hormones. Science, 1980, 207, 1377–1379.

    PubMed  CAS  Google Scholar 

  • Hill, M. J., Goddard, P., & Williams, R. E. O. Gut bacteria and aetiology of cancer of the breast. Lancet, 1971, 2, 472–473.

    Article  PubMed  CAS  Google Scholar 

  • Honma, K., & Wuttke, W. Norepinephrine and dopamine turnover rates in the medial preoptic area and medial-basal hypothalamus of the rat brain after various endocrinological manipulations. Endocrinology, 1980, 106, 1848–1853.

    Article  PubMed  CAS  Google Scholar 

  • Horowitz, S. B., & Moore, L. C. The nuclear permeability, intracellular distribution and diffusion of insulin in the amphibian oocyte. Journal of Cellular Biology, 1974, 60, 405–415.

    Article  CAS  Google Scholar 

  • Hruska, R. E., & Silbergeld, E. K. Increased dopamine receptor sensitivity after estrogen treatment. Society for Neuroscience Abstracts, 1979, 5, 236.

    Google Scholar 

  • Hyyppa, M. T., Cardinali, D. P., Baumgarten, H. G., & Wurtman, R. J. Rapid accumulation of H3- serotonin in brains of rats receiving intraperitoneal H3-tryptophan: Effects of 5,6-dihydroxy - tryptamine or female sex hormones. Journal of Neural Transmission, 1973, 34, 111–124.

    Article  PubMed  CAS  Google Scholar 

  • Inaba, M., & Kamata, K. Effect of estradiol-17’ and other steroids on noradrenaline and dopamine binding to synaptic membrane fragments of rat brain. Journal of Steroid Biochemistry, 1979, 11, 1491–1497.

    Article  PubMed  CAS  Google Scholar 

  • Iuvone, P. M., Morasco, J., & Dunn, A. J. Effects of corticosterone on the synthesis of [3H]catecholamines in the brains of CD-1 mice. Brain Research, 1977, 120, 571–576.

    Article  PubMed  CAS  Google Scholar 

  • Jasper, T. W. Polyamines in the normally developing male and female mouse brain. Unpublished doctoral dissertation, University of Florida, 1980.

    Google Scholar 

  • Jellink, P. H., Davis, P. G., Krey, L. C., Luine, V. N., Roy, E. J., & McEwen, B. S. Central and peripheral action of estradiol and catechol estrogens administered by continuous infusion. Endocrine Society Abstracts, 1979, 838.

    Google Scholar 

  • Jungblut, P. W., Kallweit, E., Sierralta, W., Truitt, A. J., & Wagner, R. K. The occurrence of steroidfree, ‘activated’ estrogen receptor in target cell nuclei. Hoppe-Seyler’s Zietschrift för Physiologische Chemie, 1978, 359, 1259–1268.

    Article  CAS  Google Scholar 

  • Jungblut, P. W., Hughes, A., Gaues, J., Kallweit, E., Marschler, I., Pari, F., Sierralta, W., Szendro, P. I., & Wagner, R. K. Mechanisms involved in the regulation of steroid receptor levels. Journal of Steroid Biochemistry, 1979, 11, 273–278.

    Article  PubMed  CAS  Google Scholar 

  • Kahwanago, I., Heinrichs, W. L. R., & Herrmann, W. L. Estradiol receptors in hypothalamus and anterior pituitary gland: Inhibition of estradiol binding by SH-group blocking agents and clom- iphene citrate. Endocrinology, 1970, 86, 1319–1326.

    Article  PubMed  CAS  Google Scholar 

  • Kaneyuki, T., Kohsaka, M., & Shohmori, T. Sex hormone metabolism in the brain-Influence of central acting drugs on 5-alpha-reduction in rat diencephalon. Endocrinologia Japonica, 1979, 26, 345–352.

    Article  PubMed  CAS  Google Scholar 

  • Kar, van de, L., Levine, J., & Van Orden, L. S. Serotonin in hypothalamic nuclei: Increased content after castration of male rats. Neuroendocrinology, 1978, 27, 186–192.

    Article  PubMed  Google Scholar 

  • Kato, J. The role of hypothalamic and hypophyseal 5a-dihydrotestosterone, estradiol and progesterone receptors in the mechanism of feedback action. Journal of Steroid Biochemistry, 1975, 6, 979–987.

    Article  PubMed  CAS  Google Scholar 

  • Kato, J. Cytosol and nuclear receptors for 5a-dihydrotestosterone and testosterone in the hypothalamus and hypophysis, and testosterone receptors isolated from neonatal female rat hypothalamus. Journal of Steroid Biochemistry, 1976, 7, 1179–1187.

    Article  PubMed  CAS  Google Scholar 

  • Kato, J., & Minaguchi, H. Cholinergic and adrenergic mechanisms in the female rat hypothalamus with special reference to reproductive functions. Gunma Symposium on Endocrinology, 1964, 1, 269–281.

    Google Scholar 

  • Kato, J., & Onouchi, T. Nuclear progesterone receptors and characterization of cytosol receptors in the rat hypothalamus and anterior hypophysis. Journal of Steroid Biochemistry, 1979, 11, 845–854.

    Article  PubMed  CAS  Google Scholar 

  • Kazama, N., & Longcope, C. In vivo studies of the metabolism of estrone and estradiol-17’ by the brain. Steroids, 1974, 23, 469–481.

    Article  PubMed  CAS  Google Scholar 

  • Kelly, M. J., Moss, R. L., & Dudley, C. A. The effects of ovariectomy on the responsiveness of preoptic-septal neurons to microelectrophoresed estrogen. Neuroendocrinology, 1978, 25, 204–211.

    Article  PubMed  CAS  Google Scholar 

  • Kendrick, K. M., & Drewett, R. F. Testosterone-sensitive neurons respond to oestradiol, but not to dihydrotestosterone. Nature, 1980, 286, 67–68.

    Article  PubMed  CAS  Google Scholar 

  • Kim, Y. S., Stumpf, W., Sar, M., & Martinez-Vargas, M. C. Estrogen and androgen target cells in the brain of fishes, reptiles and birds: Phylogeny and ontogeny. American Zoologist, 1978, 18, 425–434.

    CAS  Google Scholar 

  • Kiely, M. E. Effect of hypophysectomy, adrenalectomy and glucocorticoids on tryptophan accumulation by rat cerebral cortex slices. Research Communications in Psychology, Psychiatry and Behavior, 1980, 5, 49–60.

    CAS  Google Scholar 

  • Kizer, J. S., Palkovits, M., Zivin, J., Brownstein, M., Saavedra, J. M., & Kopin, J. J. The effect of endocrinological manipulations of tyrosine hydroxylase and dopamine-β-hydroxylase activities in individual hypothalamic nuclei of the adult male rat. Endocrinology, 1974, 95, 799–812.

    Article  PubMed  CAS  Google Scholar 

  • Kizer, J. S., Palkovits, M., Kopin, I. J., Saavedra, J. M., & Brownstein, M. J. Lack of effect of various endocrine manipulations on tryptophan hydroxylase activity of individual nuclei of the hypothalamus, limbic system and midbrain of the rat. Endocrinology, 1976, 98, 743–747.

    Article  PubMed  CAS  Google Scholar 

  • Kizer, J. S., Humm, J., Nicholson, G., Greeley, G., & Youngblood, W. The effect of castration, thyroidectomy and haloperidol upon the turnover rates of dopamine and norepinephrine and the kinetic properties of tyrosine hydroxylase in discrete hypothalamic nuclei of the male rat. Brain Research, 1978, 146, 95–107.

    Article  PubMed  CAS  Google Scholar 

  • de Kloet, E. R., & McEwen, B. S. Differences between cytosol receptor complexes with corticosterone and dexamethasone in hippocampal tissue from rat brain. Biochemica et Biophysica Acta, 1976, 421, 124–132.

    Google Scholar 

  • de Kloet, E. R., Wallach, G., & McEwen, B. S. Differences in corticosterone and dexamethasone binding to rat brain and pituitary. Endocrinology, 1975, 96, 598–609.

    Article  PubMed  Google Scholar 

  • Kobayashi, R. M., & Reed, K. C. Conversion of androgens to estrogens (aromatization) in discrete regions of the rat brain: Sexual differences and effects of castration. Society for Neuroscience Abstracts, 1977, 3, 1115.

    Google Scholar 

  • Kovacs, G. L., Telegdy, G., & Lissak, K. Dose-dependent action of corticosteroids on brain serotonin content and passive avoidance behavior. Hormones and Behavior, 1977, 8, 155–165.

    Article  PubMed  CAS  Google Scholar 

  • Krause, J. E., & Karavolas, H. J. Subcellular location of hypothalamic progesterone metabolizing enzymes and evidence for distinct NADH- and NADPH-linked 3a-hydroxysteroid oxidore- ductase activity. Journal of Steroid Biochemistry, 1980, 13, 271–280.

    Article  PubMed  CAS  Google Scholar 

  • Krey, L. C., Kamel, F., & McEwen, B. S. Parameters of neuroendocrine aromatization and estrogen receptor occupation in the male rat. Brain Research, 1980, 193, 277–283.

    Article  PubMed  CAS  Google Scholar 

  • Krieger, A., & Wuttke, W. Effects of ovariectomy and hyperprolactinemia on tyrosine hydroxylase and dopamine-β-hydroxylase activity in various limbic and hypothalamic structures. Brain Research, 1980, 193, 173–180.

    Article  PubMed  CAS  Google Scholar 

  • Kubli-Garfias, C., & Whalen, R. E. Induction of lordosis behavior in female rats by intravenous administration of progestins. Hormones and Behavior, 1977, 9, 380–386.

    Article  PubMed  CAS  Google Scholar 

  • Kueng, W., Wirz-Justice, A., Menzi, B., & Chappuis-Arndt, E. Regional brain variation of tryptophan monoamines, monoamine oxidase activity, plasma free tryptophan and total tryptophan during the estrous cycle of the rat. Neuroendocrinology, 1976, 21, 289–296.

    Article  PubMed  CAS  Google Scholar 

  • Kumakura, K., Hoffman, M., Cocchi, D., Trabucchi, M., Speno, P. F., & Muller, E. E. Long term effect of ovariectomy on dopamine stimulated adenylate cyclase in rat striatum and nucleus accumbens. Psychopharmacologia, 1979, 61, 13–16.

    Article  CAS  Google Scholar 

  • Kumar, S. A., Beach, T. A., & Dickerman, H. W. Specificity of oligodeoxynucleotide binding of mouse uterine cytosol estradiol receptors. Proceedings of the National Academy of Science (U.S.A.), 1980, 77, 3341–3345.

    Article  CAS  Google Scholar 

  • Ladisich, W. Effects of progesterone on regional 5-hydroxytryptamine metabolism in rat brain. Neuropharmacology, 1974, 13, 877–883.

    Article  PubMed  CAS  Google Scholar 

  • Landau, I. T., & Feder, H. H. Whole cell and nuclear uptake of [3H]estriol in neural and peripheral tissues of the ovariectomized guinea pig. Brain Research, 1977, 121, 190–195.

    Article  PubMed  CAS  Google Scholar 

  • Landau, I. T., & Feder, H. H. Uptake and metabolism of 3H-estrone in neural and peripheral tissue of gonadectomized adult and neonatal guinea pigs. Psychoneuroendocrinology, 1980, 5, 25–32.

    Article  PubMed  CAS  Google Scholar 

  • Lee, H., Davies, I. J., & Ryan, K. J. Progesterone receptor in the hypothalamic cytosol of female rats. Endocrinology, 1979, 104, 791–800.

    Article  PubMed  CAS  Google Scholar 

  • Levy, C., Mortel, R., Eychenne, B., Robel, P., & Baulieu, E. E. Unoccupied nuclear oestradiol- receptor sites in normal human endometrium. Biochemical Journal, 1980, 185, 733–738.

    PubMed  CAS  Google Scholar 

  • Lieberburg, I., & McEwen, B. S. Estradiol-17’ a metabolite of testosterone recovered in cell nuclei from limbic areas of adult male rat brains. Brain Research, 1975, 91, 171–174.

    Article  PubMed  CAS  Google Scholar 

  • Lieberburg, I., & McEwen, B. S. Brain cell nuclear retention of testosterone metabolites, 5a-dihy- drotestosterone and estradiol-17’ in adult rats. Endocrinology, 1977, 100, 588–597.

    Article  PubMed  CAS  Google Scholar 

  • Lieberburg, I., MacLusky, N. J., & McEwen, B. S. 5a-Dihydrotestosterone (DHT) receptors in rat brain and pituitary cell nuclei. Endocrinology, 1977, 100, 598–607.

    Article  PubMed  CAS  Google Scholar 

  • Linkie, D. M. Estrogen receptors in different target tissues: Similarities of form-dissimilarities of transformation. Endocrinology, 1977, 101, 1862–1870.

    Article  PubMed  CAS  Google Scholar 

  • Linkie, D. M., & Siiteri, P. K. A re-examination of the interaction of estradiol with target cell receptors. Journal of Steroid Biochemistry, 1978, 9, 1071–1078.

    Article  PubMed  CAS  Google Scholar 

  • Lippman, M., Bolan, G., Monaco, M., Pinkus, L., & Engel, L. Model systems for the study of estrogen action in tissue culture. Journal of Steroid Biochemistry, 1976, 7, 1045–1051.

    Article  PubMed  CAS  Google Scholar 

  • Little, M., Szendro, P., Hughes, A., & Jungblut, P. W. Biosynthesis and transformation of microsomal and cytosol estradiol receptors. Journal of Steroid Biochemistry, 1975, 6, 493–500.

    Article  PubMed  CAS  Google Scholar 

  • Lloyd, T., & Ebersole, B. J. Feedback inhibition of tyrosine hydroxylase from five regions of rat brain by 2-hydroxyestradiol and dihydroxyphenylalanine. Journal of Neurochemistry, 1980, 34, 726–731.

    Article  PubMed  CAS  Google Scholar 

  • Lloyd, T., Weisz, J., & Breakfield, X. O. The catechol estrogen, 2-hydroxyestradiol, inhibits catechol- O-methyltransferase activity in neuroblastoma cells. Journal of Neurochemistry, 1978, 31, 245–250.

    Article  PubMed  CAS  Google Scholar 

  • Loy, R., & Milner, T. A. Sexual dimorphism in extent of axonal sprouting in rat hippocampus. Science, 1980, 205, 1282–1284.

    Article  Google Scholar 

  • Luck, D. N. Comparison of the effects of oestrogen on macromolecular synthesis in the uterus and brain of the immature mouse. Journal of Reproduction and Fertility, 1975, 43, 359–362.

    Article  PubMed  CAS  Google Scholar 

  • Luine, V. N., & McEwen, B. S. Effect of oestradiol on turnover of type A monoamine oxidase in brain. Journal of Neurochemistry, 1911, 28, 1221–1227. (a)

    Article  Google Scholar 

  • Luine, V. N., & McEwen, B. S. Effects of an estrogen antagonist on enzyme activities and (3H)estradiol nuclear binding in uterus, pituitary and brain. Endocrinology, 1977, 100, 903–910. (b)

    Article  PubMed  CAS  Google Scholar 

  • Luine, V. N., Khylcheveskaya, R. I., & McEwen, B. S. Oestrogen effects on brain and pituitary enzyme activities. Journal of Neurochemistry, 1974, 23, 925–934.

    Article  PubMed  CAS  Google Scholar 

  • Luine, V. N., Khylcheveskaya, R. I., & McEwen, B. S. Effect of gonadal hormones on enzyme activities in brain and pituitary of male and female rats. Brain Research, 1975, 86, 283–292. (a)

    Article  PubMed  CAS  Google Scholar 

  • Luine, V. N., Khylcheveskaya, R. I., & McEwen, B. S. Effect of gonadal steroids on activities of monoamine oxidase and choline acetylase in rat brain. Brain Research, 1975, 86, 293–306. (b)

    Article  PubMed  CAS  Google Scholar 

  • Luine, V. N., McEwen, B. S., & Black, I. B. Effect of 17’-estradiol on hypothalamic tyrosine hydroxylase activity. Brain Research, 1977, 120, 188–192.

    Article  PubMed  CAS  Google Scholar 

  • Luine, V. N., MacLusky, N. J., & McEwen, B. S. Testosterone effects on enzymes in central and peripheral target sites in Tfm mutant mice. Society for Neuroscience Abstracts, 1979, 5, 1529.

    Google Scholar 

  • Luine, V. N., Park, D., Joh, T., Reis, D., & McEwen, B. S. Immunochemical demonstration of increased choline acetyltransferase concentration in rat preoptic area after estradiol administration. Brain Research, 1980, 191, 273–277.

    Article  PubMed  CAS  Google Scholar 

  • Lupo Di Prisco, C., Lucarini, N., & Dessi-Fulgheri, F. Testosterone aromatization in rat brain is modulated by social environment. Physiology & Behavior, 1978, 20, 345–348.

    Article  CAS  Google Scholar 

  • Luttge, W. G. The role of gonadal hormones in the sexual behavior of the rhesus monkey and human: A literature survey. Archives of Sexual Behavior, 1971, 1, 61–88.

    Article  CAS  Google Scholar 

  • Luttge, W. G. The estrous cycle of the rat: Effects on the accumulation of estrogenic metabolites in brain and peripheral tissues. Brain Research, 1972, 38, 315–325.

    Article  PubMed  CAS  Google Scholar 

  • Luttge, W. G. Endocrine control of mammalian male sexual behavior: An analysis of the potential role of testosterone metabolites. In C. Beyer (Ed.), Endocrine control of sexual behavior. New York: Raven Press, 1979.

    Google Scholar 

  • Luttge, W. G. Cerebral effects of gonadal steroid hormones. In C. B. Nemeroff & A. J. Dunn (Eds.), Peptides, Hormones and Behavior: Molecular and behavioral neuroendocrinology. New York: Spectrum Publications, 1983.

    Google Scholar 

  • Luttge, W. G., & Jasper, T. W. Studies on the possible role of 2-OH-estradiol in the control of sexual behavior in female rats. Life Sciences, 1977, 20, 419–426.

    Article  PubMed  CAS  Google Scholar 

  • Luttge, W. G., & Whalen, R. E. The accumulation, retention and interaction of oestradiol and oestrone in central neural and peripheral tissues of gonadectomized female rats. Journal of Endocrinology, 1972, 52, 379–395.

    Article  PubMed  CAS  Google Scholar 

  • Luttge, W. G., Gray, H. E., & Hughes, J. R. Regional and subcellular 3H-estradiol localization in selected brain regions and pituitary of female mice: Effects of unlabeled estradiol and various anti-hormones. Brain Research, 1976, 104, 273–281.

    Article  PubMed  CAS  Google Scholar 

  • Maas, J. W., & Mednieks, M. Hydrocortisone-mediated increase of norepinephrine uptake by brain slices. Science, 1971, 171, 178–179.

    Article  PubMed  CAS  Google Scholar 

  • MacLusky, N. J., & McEwen, B. S. Progestin receptors in rat brain: Distribution and properties of cytoplasmic progestin-binding sites. Endocrinology, 1980, 106, 192–202.

    Article  PubMed  CAS  Google Scholar 

  • MacLusky, N. J., Turner, B. B., & McEwen, B. S. Corticosteroid binding in rat brain and pituitary cytosols: Resolution of multiple binding components by polyacrylamide gel based isoelectric focusing. Brain Research, 1977, 130, 564–571.

    Article  PubMed  CAS  Google Scholar 

  • Mainwaring, W. I. P., Symes, E. K., & Higgins, S. J. Nuclear components responsible for the retention of steroid-receptor complexes, especially from the stand-point of the specificity of hormonal responses. Biochemical Journal, 1976, 156, 129–141.

    PubMed  CAS  Google Scholar 

  • Manak, R., Wertz, N., Slabaugh, M., Denari, H., Wang, J.-T., & Gorski, J. Purification and characterization of the estrogen-induced protein (IP) of the rat uterus. Molecular and Cellular Endocrinology, 1980, 17, 119–132.

    Article  PubMed  CAS  Google Scholar 

  • Martin, P. M., & Sheridan, P. J. Intracellular distribution of estrogen receptors-A function of preparation. Experientia, 1980, 36, 620–622.

    Article  PubMed  CAS  Google Scholar 

  • Matsumoto, A., & Arai, Y. Synaptogenic effect of estrogen on the hypothalamic arcuate nucleus of the adult female rat. Cell and Tissue Research, 1979, 198, 427–433.

    Article  PubMed  CAS  Google Scholar 

  • Matsumoto, A., & Arai, Y. Sexual dimorphism in wiring pattern in the hypothalamic arcuate nucleus and its modification by neonatal hormone environment. Brain Research, 1980, 190, 238–242.

    Article  PubMed  CAS  Google Scholar 

  • Mazurkiewicz-Kwilecki, I. M., & Prell, G. D. Brain histamine: Plasma corticosterone, spontaneous locomotor activity and temperature. Pharmacology, Biochemistry and Behavior, 1980, 12, 549–553.

    Article  CAS  Google Scholar 

  • McEwen, B. S., Magnus, C., & Wallach, G. Soluble corticosterone-binding macromolecules extracted from rat brain. Endocrinology, 1972, 90, 217–226.

    Article  PubMed  CAS  Google Scholar 

  • McEwen, B. S., Wallach, G., & Magnus, C. Corticosterone binding to hippocampus: Immediate and delayed influences of the absence of adrenal secretion. Brain Research, 1974, 70, 321–334.

    Article  PubMed  CAS  Google Scholar 

  • McGinnis, M. Y., Gordon, J. H., & Gorski, R. A. Time course and localization of the effects of estrogen on glutamic acid decarboxylase activity. Journal of Neurochemistry, 1980, 34, 785–792. (a)

    Article  PubMed  CAS  Google Scholar 

  • McGinnis, M. Y., Gordon, J. H., & Gorski, R. A. Influence of γ-aminobutyric acid on lordosis behavior and dopamine activity in estrogen primed spayed female rats. Brain Research, 1980, 184, 179–191. (b)

    Article  PubMed  CAS  Google Scholar 

  • Menendez-Patterson, A., Florez-Lozano, J. F., & Marin, B. Effects of ovariectomy on the oxidative metabolism of the central nervous system and adrenal glands in female hamster (Mesocricetus auratus). Experientia, 1979, 35, 349–350.

    Article  PubMed  CAS  Google Scholar 

  • Meyer, J. S., Luine, V. N., Khylcheveskaya, R. I., & McEwen, B. S. Glucocorticoids and hippocampal enzyme activity. Brain Research, 1979, 166, 172–175.

    Article  PubMed  CAS  Google Scholar 

  • Meyerson, B. J., & Eliasson, M. Pharmacological and hormonal control of reproductive behavior. In L. L. Iversen, S. D. Iversen, & S. H. Snyder (Eds.), (Vol. 8): Handbook of Psychopharmacology Drugs, transmitters, and behavior. New York: Plenum Press, 1977.

    Google Scholar 

  • Michal, E. K. Dexamethasone inhibits multi-unit activity in the rat hippocampus. Brain Research, 1974, 65, 180–183.

    Article  PubMed  CAS  Google Scholar 

  • Millard, S. A., Costa, E., & Gall, E. M. On the control of brain serotonin turnover by end product inhibition. Brain Research, 1972, 40, 545–551.

    Article  PubMed  CAS  Google Scholar 

  • Miller, A. L., Chaptal, C., McEwen, B. S., & Peck, E. J. Modulation of high affinity GABA uptake into hippocampal synaptosomes by glucocorticoids. Psychoneuroendocrinology, 1978, 3, 155–164.

    Article  PubMed  CAS  Google Scholar 

  • Mioduszewski, R., Grandison, L., & Meites, J. Stimulation of prolactin release in rats by GABA. Proceedings of the Society of Experimental Biology and Medicine, 1976, 151, 44–46.

    CAS  Google Scholar 

  • Mobley, P. L., & Sulser, F. Adrenal corticoids regulate sensitivity of noradrenaline receptor coupled adenylate cyclase in brain. Nature, 1980, 286, 608–609.

    Article  PubMed  CAS  Google Scholar 

  • Moguilevsky, J. A. Oxidative activity of different hypothalamic areas during sexual cycle in rats. Acta Physiologica Latino Americana, 1965, 15, 423–424.

    PubMed  CAS  Google Scholar 

  • Moguilevsky, J. A., Libertun, C., & Foglia, V. G. Metabolic sensitivity of different hypothalamic areas to luteinizing hormone (LH), follicle stimulating hormone (FSH), and testosterone. Neuroendocrinology, 1970, 6, 153–159. (a)

    Article  PubMed  CAS  Google Scholar 

  • Moguilevsky, J. A., Libertun, C., & Foglia, V. G. Oxidative metabolism of the hypothalamus in hypophysectomized-castrated rats. Experientia, 1970, 26, 421–422. (b)

    Article  PubMed  CAS  Google Scholar 

  • Moguilevsky, J. A., Kalbermann, L. E., Libertun, C., & Gomez, C. J. Effects of ovariectomy on the amino acid incorporation into proteins of anterior pituitary and hypothalamus of rats. Proceedings of the Society of Experimental Biology and Medicine, 1971, 136, 1115–1118.

    CAS  Google Scholar 

  • Moguilevsky, J. A., Schiaffini, O., Szwarcfarb, B., & Libertun, C. Metabolic evidences of the short feed back mechanism controlling LH and FSH secretion. Acta Endocrinologica Panamericana, 1971, 2, 177–186.

    Google Scholar 

  • Moguilewsky, M., & Raynaud, J.-P. Estrogen-sensitive progestin-binding sites in the female rat brain and pituitary. Brain Research, 1979, 164, 165–175. (a)

    Article  PubMed  CAS  Google Scholar 

  • Moguilewsky, M., & Raynaud, J.-P. The relevance of hypothalamic and hypophyseal progestin receptor regulation in the induction and inhibition of sexual behavior in the female rat. Endocrinology, 1979, 104, 516–522. (b)

    Article  Google Scholar 

  • Moguilewsky, M., & Raynaud, J.-P. Evidence for a specific mineralocorticoid receptor in rat pituitary and brain. Journal of Steroid Biochemistry, 1980, 12, 309–314.

    Article  PubMed  CAS  Google Scholar 

  • Monbon, M., Loras, B., Reboud, J. P., & Bertrand, J. Binding and metabolism of testosterone in the rat brain during sexual maturation: I. Macromolecular binding of androgens. Journal of Steroid Biochemistry, 1974, 5, 417–424.

    Article  PubMed  CAS  Google Scholar 

  • Moore, K. E., & Phillipson, O. T. Effects of dexamethasone on phenylethanolamine N-methyltrans- ferase and adrenaline in the brains and superior cervical ganglia of adult and neonatal rats. Journal of Neurochemistry, 1975, 25, 289–294.

    Article  PubMed  CAS  Google Scholar 

  • Morrell, J. I., & Pfaff, D. W. A neuroendocrine approach to brain function: Localization of sex steroid concentrating cells in vertebrate brains. American Zoologist, 1978, 18, 447–460.

    CAS  Google Scholar 

  • Mosebach, K.-O., & Peter, H.-G. Early influences of testosterone and 19-nortestosterone on the metabolism of L-histidine-14C in the brain of immature male rats. Acta Endocrinologica, 1971, Supplement 155, 28.

    Google Scholar 

  • Motta, M. The endocrine functions of the brain. New York: Raven Press, 1980.

    Google Scholar 

  • Moudgil, V. K., & Kanungo, M. S. Effect of age of the rat on induction of acetylcholinesterase of the brain by 17’-estradiol. Biochemica et Biophysica Acta, 1973, 329, 211–220.

    CAS  Google Scholar 

  • Munaro, N. I. The effect of ovarian steroids on hypothalamic 5-hydroxy-tryptamine neuronal activity. Neuroendocrinology, 1978, 26, 270–276.

    Article  PubMed  CAS  Google Scholar 

  • Murayama, A., Fukai, F., & Yamamoto, T. Disorganization and in vitro assembly of the constituents of the cytoplasmic estrogen receptor system of cow uterus. Journal of Biochemistry, 1980, 88, 1457–1466.

    PubMed  CAS  Google Scholar 

  • Muth, E. A., Crowley, W. R., & Jacobowitz, D. M. Effect of gonadal hormones on luteinizing hormone in plasma and on choline acetyltransferase activity and acetylcholine levels in discrete nuclei of rat brain. Neuroendocrinology, 1980, 30, 329–336.

    Article  PubMed  CAS  Google Scholar 

  • Nagle, C. A., & Rosner, J. M. Rat brain norepinephrine release during progesterone-induced LH secretion. Neuroendocrinology, 1980, 30, 33–37.

    Article  PubMed  CAS  Google Scholar 

  • Neckers, L., & Sze, P. Y. Regulation of 5-hydroxytryptamine metabolism in mouse brain by adrenal glucocorticoids. Brain Research, 1976, 93, 123–132.

    Article  Google Scholar 

  • Nemeroff, C. B., & Dunn, A. J. (Eds.). Peptides, hormones and behavior: Molecular and behavioral neuroendocrinology. New York: Spectrum Publications, 1983.

    Google Scholar 

  • Nixon, R. L., Janowsky, D. S., & Davis, J. M. Effects of progesterone, β-estradiol, and testosterone on the uptake and metabolism of 3H-norepinephrine, 3H-dopamine and 3H-serotonin in rat brain synaptosomes. Research Communications in Chemical Pathology and Pharmacology, 1974, 7, 233–236.

    PubMed  CAS  Google Scholar 

  • Nock, B., Blaustein, J. D., & Feder, H. H. Changes in noradrenergic transmission alter the concentration of cytoplasmic progestin receptors in hypothalamus. Society for Neuroscience Abstracts, 1980, 6, 31.

    Google Scholar 

  • Nyakas, C., de Kloet, E. R., & Bohas, B. Hippocampal function and putative corticosterone receptors: Effects of septal lesions. Neuroendocrinology, 1979, 29, 301–312.

    Article  PubMed  CAS  Google Scholar 

  • Orr, E., & Quay, W. The effects of castration on histamine levels and 24-hour rhythm in the male rat hypothalamus. Endocrinology, 1975, 97, 481–484.

    Article  PubMed  CAS  Google Scholar 

  • Packman, P. M., Bragdon, M. J., & Boshans, R. L. Quantitative histochemical studies of the hypothalamus: Control point enzymes during the estrous cycle. Neuroendocrinology, 1977, 23, 76–87.

    Article  PubMed  CAS  Google Scholar 

  • Pandolfo, L., & Macaione, S. Effect of adrenalectomy on activity of GAB A transaminase and glutamic acid decarboxylase from rat brain cortex. Italian Journal of Biochemistry, 1964, 13, 247–252.

    Google Scholar 

  • Paolo, T. D., Labrie, F., Dupont, A., Barden, N., & Langelier, P. Effects of estrogen treatment on normal and sensitized rat striatal dopamine (DA) receptors and DA-sensitive adenylyl cyclase. Society for Neuroscience Abstracts, 1979, 5, 1495.

    Google Scholar 

  • Pardridge, W. M., & Mietus, L. J. Transport of steroid hormones through the rat blood-brain barrier. Primary role of albumin-bound hormone. Journal of Clinical Investigation, 1979, 64, 145–154.

    Article  PubMed  CAS  Google Scholar 

  • Pardridge, W. M., & Mietus, L. J. Effects of progesterone-binding globulin versus a progesterone antiserum on steroid hormone transport through the blood-brain barrier. Endocrinology, 1980, 106, 1137–1141.

    Article  PubMed  CAS  Google Scholar 

  • Parsons, B., MacLusky, N. J., Krey, L., Pfaff, D. W., & McEwen, B. S. The temporal relationship between estrogen-inducible progestin receptors in the female rat brain and the time course of estrogen activation of mating behavior, Endocrinology, 1980, 107, 774–779.

    Article  PubMed  CAS  Google Scholar 

  • Paul, S. M., & Skolnick, P. Catechol oestrogens inhibit oestrogen elicited accumulation of hypothalamic cyclic AMP suggesting role as endogenous anti-oestrogens. Nature, 1977, 266, 559–561.

    Article  PubMed  CAS  Google Scholar 

  • Paul, S. M., Axelrod, J., Saavedra, J. M., & Skolnick, P. Estrogen-induced efflux of endogenous catecholamines from the hypothalamus in vitro. Brain Research, 1979, 178, 499–505.

    Article  PubMed  CAS  Google Scholar 

  • Paul, S. M., Hoffman, A. R., & Axelrod, J. Catechol estrogens: Synthesis and metabolism in brain and other tissues. In L. Martini & W. F. Ganong (Eds.), Frontiers in neuroendocrinology (Vol. 6). New York: Raven Press, 1980.

    Google Scholar 

  • Peck, E. J., Jr., Miller, A. L., & Keiner, K. L. Estrogen receptors and the activation of RNA polymerase by estrogens in the central nervous system. In T. H. Hamilton, J. H. Clark, & W. A. Sandler (Eds.), Ontogeny of receptors and reproductive hormone action. New York: Raven Press, 1979.

    Google Scholar 

  • Perry, B. N., & Lopez, T. A. The binding of 3H-labelled oestradiol- and progesterone-receptor complexes to hypothalamic chromatin of male and female sheep. Biochemical Journal, 1978, 176, 873–883.

    PubMed  CAS  Google Scholar 

  • Pfaff, D. W., & Keiner, M. Atlas of estradiol-concentrating cells in the central nervous system of the female rat. Journal of Comparative Neurology, 1973, 151, 121–158.

    Article  PubMed  CAS  Google Scholar 

  • Pfaff, D. W., & Modianos, D. Neural mechanisms of female reproductive behavior. In N. T. Adler & D. Pfaff (Eds.), Neurobiology of reproduction. Book in preparation, 1983.

    Google Scholar 

  • Portaleone, P., Pagnini, G., Crispino, A., & Genazzani, E. Histamine-sensitive adenylate cyclase in hypothalamus of rat brain: H1 and H2 receptors. Journal of Neurochemistry, 1978, 31, 1371–1374.

    Article  PubMed  CAS  Google Scholar 

  • Portaleone, P., Genazzani, E., Pagnini, G., Crispino, A., & DiCarlo, F. Interaction of estradiol and 2- hydroxy-estradiol with histamine receptors at hypothalamic level. Brain Research, 1980, 187, 216–220.

    Article  PubMed  CAS  Google Scholar 

  • Puca, G. A., Nola, E., Hibner, U., Cicala, G., & Sica, V. Interaction of the estradiol receptor from calf uterus with its nuclear acceptor sites. Journal of Biological Chemistry, 1975, 250, 6452–6459.

    PubMed  CAS  Google Scholar 

  • Rainbow, T. C., Davis, P. G., & McEwen, B. S. Anisomycin inhibits the activation of sexual behavior by estradiol and progesterone. Brain Research, 1980, 194, 548–555.

    Article  PubMed  CAS  Google Scholar 

  • Rastogi, R. B., & Singhal, R. L. Evidence for the role of adrenocortical hormones in the regulation of noradrenaline and dopamine metabolism in certain brain areas. British Journal of Pharmacology, 1978, 62, 131–136. (a)

    PubMed  CAS  Google Scholar 

  • Rastogi, R. B., & Singhal, R. L. Adrenocorticoids control 5-hydroxytryptamine metabolism in rat brain. Journal of Neural Transmission, 1978, 42, 63–71. (b)

    Article  PubMed  CAS  Google Scholar 

  • Raynaud, J. P. R5020, a tag for the progestin receptor. In W. L. McGuire, J. P. Raynaud, & E. E. Baulieu (Eds.), Progesterone receptors in normal and neoplastic tissues. New York: Raven Press, 1977.

    Google Scholar 

  • Reddy, V. V. R. Estriol synthesis in rat brain and pituitary. Brain Research, 1979, 175, 165–168. (a)

    Article  PubMed  CAS  Google Scholar 

  • Reddy, V. V. R. Estrogen metabolism in neural tissues of rabbits: 17’-hydroxysteroid oxidoreductase activity. Steroids, 1979, 34, 207–215. (b)

    Article  PubMed  CAS  Google Scholar 

  • Rees, H. D., & Gray, H. E. Glucocorticoids and mineralocorticoids: actions on brain and behavior. In C. B. Nemeroff & A. J. Dunn (Eds.), Peptides, hormones and behavior: Molecular and behavioral neuroendocrinology. New York: Spectrum Publications, 1983.

    Google Scholar 

  • Rees, H. D., Stumpf, W. E., & Sar, M. Autoradiographic studies with 3H-dexamethasone in the rat brain and pituitary. In W. E. Stumpf & L. D. Grant (Eds.), Anatomical neuroendocrinology. Basel: Karger, 1975.

    Google Scholar 

  • Reiss, N., & Kaye, A. M. Separation of a protein from rat brain resembling the uterine “estrogen- induced protein” in electrophoretic and immunologic properties. Israel Journal of Medicine, 1979, 15, 545.

    Google Scholar 

  • Reiter, R. J. The pineal and its hormones in the control of reproduction in mammals. Endocrine Reviews, 1980, 1, 109–131.

    Article  PubMed  CAS  Google Scholar 

  • Rezek, D. L. Nuclear localization of testosterone, dihydrotestosterone and estradiol- 17’ in basal rat brain. Psychoneuroendocrinology, 1977, 2, 173–178.

    Article  PubMed  CAS  Google Scholar 

  • Rhees, R. W., Grosser, B. I., & Stevens, W. The autoradiographic localization of [3H]dexamethasone in the brain and pituitary of the rat. Brain Research, 1975, 100, 151–156.

    Article  PubMed  CAS  Google Scholar 

  • Ricker, D. K., Sastre, A., Baker, T., Roth, R. H., & Riker, W. F. Regional high-affinity [3H]choline accumulation in cat forebrain: Selective increase in the caudate-putamen after corticosteroid pretreatment. Molecular Pharmacology, 1979, 16, 886–899.

    Google Scholar 

  • Roberts, E., Chase, T. N., & Tower, D. B. GABA in nervous system function. New York: Raven Press, 1976.

    Google Scholar 

  • Rosner, J. M., Denari, J. H., Castro-Vazquez, A., Nagle, C. A., Neuspiller, M. R., Bedes, G. D. D. P., Pedroza, E., Martin, J. L., & Gomez, E. Oestrogen uptake by the central nervous system. Gynecological Investigation, 1972, 3, 30–42.

    Article  CAS  Google Scholar 

  • Roy, E. J., & McEwen, B. S. Oestrogen receptors in cell nuclei of the hypothalamus-preoptic area-amygdala following an injection of oestradiol or the antioestrogen CI-628. Journal of Endocrinology, 1979, 83, 285–293.

    Article  PubMed  CAS  Google Scholar 

  • Roy, E. J., Schmit, E., McEwen, B. S., & Wade, G. N. Anti-estrogens in the central nervous system. In M. K. Agarwal (Ed.), Antihormones. Amsterdam: Elsevier-North Holland Biomedical Press, 1979.

    Google Scholar 

  • Russell, D. H. Ornithine decarboxylase as a biological and pharmacological tool. Pharmacology, 1980, 20, 117–129.

    Article  PubMed  Google Scholar 

  • Saad, S. F. The effect of ovariectomy on the γ-aminobutyric acid content in the cerebral hemispheres of young rats. Journal of Pharmacy and Pharmacology, 1970, 22, 307.

    Article  PubMed  CAS  Google Scholar 

  • Sadasivudu, B., Rao, T. I., & Murphy, C. R. K. Metabolic effects of hydrocortisone in mouse brain. Neurochemical Research, 1977, 2, 521–532.

    Article  CAS  Google Scholar 

  • Saffran, J., & Loeser, B. K. Nuclear binding of guinea pig uterine progesterone receptor in cell- free preparations. Journal of Steroid Biochemistry, 1979, 10, 43–51.

    Article  PubMed  CAS  Google Scholar 

  • Sakaue, Y., & Thompson, E. B. Characterization of two forms of glucocorticoid hormone-receptor complex separated by DEAE-cellulose column chromatography. Biochemical and Biophysical Research Communications, 1977, 77, 533–541.

    Article  PubMed  CAS  Google Scholar 

  • Sando, J. J., Hammond, N. D., Stratford, C. A., & Pratt, W. B. Activation of thymocyte glucocorticoid receptors to the steroid binding form. Journal of Biological Chemistry, 1979, 254,4779–4789.

    PubMed  CAS  Google Scholar 

  • Sando, J. J., LaForest, A. C., & Pratt, W. B. ATP-Dependent activation of L cell glucocorticoid receptors to the steroid binding form. Journal of Biological Chemistry, 1979, 254, 4772–4778.

    PubMed  CAS  Google Scholar 

  • Sar, M., & Stumpf, W. E. Androgen concentration in motor neurons of cranial nerves and spinal cord. Science, 1977, 197, 77–79.

    Article  PubMed  CAS  Google Scholar 

  • Sato, B., Noma, K., Nishizawa, Y., Nakao, K., Matsumoto, K., & Yamamura, Y. Mechanism of activation of steroid receptors: Involvement of low molecular weight inhibitor in activation of androgen, glucocorticoid, and estrogen receptor systems. Endocrinology, 1980, 106, 1142–1148.

    Article  PubMed  CAS  Google Scholar 

  • Scacchi, P., Moguilevsky, J. A., & Szwarcfarb, B. Effect of castration on C1402 production from glucose-U-C14 in the hypothalamus and cerebral cortex. Proceedings of the Society of Experimental Biology and Medicine, 1971, 136, 1068–1071.

    CAS  Google Scholar 

  • Scacchi, P., Moguilevsky, J. A., & Schiaffini, O. Glucose oxidation in the hypothalamus during the sexual cycle in rats: Influence of castration. Neuroendocrinology, 1973, 11, 321–327.

    Article  PubMed  CAS  Google Scholar 

  • Schaeffer, J. M., & Hseuh, A. J. W. 2-Hydroxyestradiol interaction with dopamine receptor binding in rat anterior pituitary. Journal of Biological Chemistry, 1979, 254, 5606–5608.

    PubMed  CAS  Google Scholar 

  • Schaeffer, J. M., Stevens, S. R., & Smith, R. G. 2-Hydroxyestradiol (2-OH-E2) binding to rat anterior pituitary membranes. Endocrine Society Abstracts, 1980, 106, 317.

    Google Scholar 

  • Scheff, S. W., Thorne, D. R., Sasvary, G., Bernardo, L. S., & Cotman, C. W. Chronic glucocorticoid administration alters axonal sprouting in the rat hippocampal formation. Society for Neuroscience Abstracts, 1979, 5, 1555.

    Google Scholar 

  • Schiaffini, O., & Marin, B. Effect of ovariectomy on the oxidative activity of the hypothalamus and of the limbic system of the rat. Neuroendocrinology, 1971, 7, 302–307.

    Article  PubMed  CAS  Google Scholar 

  • Schiaffini, O., & Martini, L. The amygdala and the control of gonadotrophin secretion. Acta Endocrinologica, 1972, 70, 209–219.

    PubMed  CAS  Google Scholar 

  • Schiaffini, O., Moguilevsky, J. A., Libertun, C., & Foglia, V. G. Oxidative and glycolytic metabolism of different hypothalamic areas in diabetic rat. Acta Physiologica Latino Americana, 1968, 18, 257–262.

    PubMed  CAS  Google Scholar 

  • Schiaffini, O., Marin, B., & Foglia, V. G. Metabolic alterations in hypothalamus and limbic structures in female diabetic rats. Experientia, 1970, 26, 610–611.

    Article  PubMed  CAS  Google Scholar 

  • Schwartz, J. -C., Pollard, H., & Quach, T. T. Histamine as a neurotransmitter in mammalian brain: Neurochemical evidence. Journal of Neurochemistry, 1980, 35, 26–33.

    Article  PubMed  CAS  Google Scholar 

  • Seiki, K., Haruki, Y., Imanishi, Y., & Enomoto, T. Further evidence of the presence of progesterone- binding proteins in female rat hypothalamus. Endocrinologia Japonica, 1977, 24, 233–238.

    Article  PubMed  CAS  Google Scholar 

  • Seiki, K., Haruki, Y., Imanishi, Y., & Enomoto, T. Progestin binding in vitro by brain cell nuclei of ovariectomized oestrogen-primed rats. Journal of Endocrinology, 1979, 82, 347–360.

    Article  PubMed  CAS  Google Scholar 

  • Selmanoff, M. K., Brodkin, L. D., Weiner, R. J., & Siiteri, P. Aromatization and 5a-reduction of androgens in discrete hypothalamic and limbic regions of the male and female rat. Endocrinology, 1977, 101, 841–848.

    Article  PubMed  CAS  Google Scholar 

  • Shani, J., Givant, Y., Sulman, F., Eylath, U., & Eckstein, B. Competition of phenothazines with oestradiol receptors in the brain. Neuroendocrinology, 1971, 8, 307–316.

    Article  PubMed  CAS  Google Scholar 

  • Shen, G., Thrower, S., & Lim, L. Uterine oestrogen-receptor binding to oligo(dT)-cellulose: An inhibitor from hypothalamic cytosol. Biochemical Journal, 1979, 182, 241–243.

    PubMed  CAS  Google Scholar 

  • Shen, J. T., & Ganong, W. F. Effect of variations in adrenocortical function on dopamine β-hy-droxylase and norepinephrine in the brain of the rat. Journal of Pharmacology and Experimental Therapeutics, 1976, 199, 639–648.

    PubMed  CAS  Google Scholar 

  • Sheridan, P. J. The nucleus interstitialis striae terminalis and the nucleus amygdaloideus medialis: Prime targets for androgen in the rat forebrain. Endocrinology, 1979, 104, 130–136.

    Article  PubMed  CAS  Google Scholar 

  • Siegel, L. I., & Wade, G. N. Insulin withdrawal impairs sexual receptivity and retention of brain cell nuclear estrogen receptors in diabetic rats. Neuroendocrinology, 1979, 29, 200–206.

    Article  PubMed  CAS  Google Scholar 

  • Simpkins, J. W., Kalra, P. S., & Kalra, S. P. Effects of testosterone on catecholamine turnover and LHRH contents in the basal hypothalamus and preoptic area. Neuroendocrinology, 1980, 30, 94–100.

    Article  PubMed  CAS  Google Scholar 

  • Stevens, W., Reed, D. J., Erickson, S., & Grosser, B. I. The binding of corticosterone to brain proteins: Diurnal variation. Endocrinology, 1973, 93, 1152–1156.

    Article  PubMed  CAS  Google Scholar 

  • Stipek, S., Crkovska, J., Trojan, S., & Prokes, J. The effects of polyamines on RNA synthesis in cell nuclei isolated from the rat brain. Physiologica Bohemoslovaca, 1978, 27, 280–281.

    Google Scholar 

  • Stith, R. D., & Bottoms, G. D. Intracellular binding of [3H]cortisol and its effect on RNA polymerase activity in hypothalamus of the pig. Brain Research, 1972, 41, 423–434.

    Article  PubMed  CAS  Google Scholar 

  • Stith, R. D., Person, R. J., & Dana, R. C. Effects of hippocampal and amygdalar stimulation on the uptake and binding of 3H-hydrocortisone in the hypothalamus of the cat. Journal of Neuroscience Research, 1976, 2, 317–322.

    Article  PubMed  CAS  Google Scholar 

  • Stumpf, W. E., & Grant, L. D. Anatomical neuroendocrinology. Basel: Karger, 1975.

    Google Scholar 

  • Stumpf, W. E., & Sar, M. Anatomical distribution of estrogen, androgen, progestin, corticosteroid and thyroid hormone target sites in the brain of mammals: Phylogeny and ontogeny. American Zoologist, 1978, 18, 435–445.

    CAS  Google Scholar 

  • Stumpf, W. E., & Sar, M. Steroid action in CNS and anterior pituitary: I. Steroid hormone target cells in the extrahypothalamic brain stem and cervical spinal cord: Neuroendocrine significance. Journal of Steroid Biochemistry, 1979, 11, 801–807.

    Article  PubMed  CAS  Google Scholar 

  • Sundberg, D. K., Fawcett, C. P., & McCann, S. M. The involvement of cyclic-3’, 5’AMP in the release of hormones from the anterior pituitary in vitro. Proceedings of the Society of Experimental Biology and Medicine, 1976, 151, 149–154.

    CAS  Google Scholar 

  • Sze, P. Y., Neckers, L., & Towle, A. C. Glucocorticoids as a regulatory factor for brain tryptophan hydroxylase. Journal of Neurochemistry, 1976, 26, 169–173.

    PubMed  CAS  Google Scholar 

  • Tappaz, M. L., Brownstein, M. J., & Kopin, I. J. Glutamate decarboxylase (GAD) and γ-aminobutyric acid (GABA) in discrete nuclei of hypothalamus and substantia nigra. Brain Research, 1977, 125, 109–121.

    Article  PubMed  CAS  Google Scholar 

  • Teyler, T. J., Vardaris, R. M., Lewis, D., & Rawitch, A. B. Gonadal steroids: Effects on excitability of hippocampal pyramidal cells. Science, 1980, 209, 1017–1019.

    Article  PubMed  CAS  Google Scholar 

  • Thrower, S., & Lim, L. Characterization of rat hypothalamic progestin binding by spheroidal hydrox- ylapatite chromatography. Biochemical Journal, 1980, 186, 295–300.

    PubMed  CAS  Google Scholar 

  • Tintner, R., Dunn, A. J., Iuvone, P. M., Shukla, J. B., & Rennert, O. M. Corticotrophin increases cerebral polyamine content. Journal of Neurochemistry, 1979, 33, 1067–1073.

    Article  PubMed  CAS  Google Scholar 

  • Tobias, H., Carr, L., & Vooft, J. Effects of estradiol on catecholamine synthesizing enzymes, luteinizing hormone (LH) and prolactin in the ovariectomized rat. Society for Neuroscience Abstracts, 1979, 5, 1569.

    Google Scholar 

  • Towle, A. C., & Sze, P. Y. Binding of corticosterone to synaptic plasma membrane from rat brain. Society for Neuroscience Abstracts, 1978, 4, 356.

    Google Scholar 

  • Towle, A. C., Sze, P. Y., & Lauder, J. M. Cytosol glucocorticoid receptors in monoaminergic cell groups. Transactions of the American Society of Neurochemistry, 1979, 10, 199.

    Google Scholar 

  • Traish, A. M., Muller, R. E., & Wotiz, H. H. Binding of estrogen receptor to uterine nuclei: Salt-extractable versus salt-resistant receptor estrogen complexes. Journal of Biological Chemistry, 1977, 252, 6823–6830.

    PubMed  CAS  Google Scholar 

  • Tsuboi, S., Kawashima, R., Tomioka, O., Nakata, M., Sakamoto, N., & Fujita, T. Glucocorticoid binding proteins of human brain cytosol. Brain Research, 1979, 179, 181–185.

    Article  PubMed  CAS  Google Scholar 

  • Turner, B. B., & McEwen, B. S. Hippocampal cytosol binding capacity of corticosterone: No depletion with nuclear loading. Brain Research, 1980, 189, 169–182.

    Article  PubMed  CAS  Google Scholar 

  • Turner, B. B., Smith, E. M., & Carroll, B. J. Baboon corticosterone: Substantial brain binding of a ‘minor’ adrenal glucocorticoid. Society for Neuroscience Abstracts, 1979, 5, 462.

    Google Scholar 

  • Ulrich, R., Yuwiler, A., & Geller, E. Effects of hydrocortisone on biogenic amine levels in the hypothalamus. Neuroendocrinology, 1975, 19, 259–268.

    Article  PubMed  CAS  Google Scholar 

  • Vacas, M. I., & Cardinali, D. P. Effect of estradiol on a- and β-adrenoceptor density in medial basal hypothalamus, cerebral cortex and pineal gland of ovariectomized rats. Neuroscience Letters, 1980, 17, 73–77.

    Article  PubMed  CAS  Google Scholar 

  • Veals, J. W., Korduba, C. A., & Symchowicz, S. Effect of dexamethasone on monoamine oxidase inhibition by iproniazid in rat brain. European Journal of Pharmacology, 1977, 41, 291–299.

    Article  PubMed  CAS  Google Scholar 

  • Verdiere, M., Rose, C., & Schwartz, J. C. Turnover of central histamine in a stressful situation. Brain Research, 1977, 129, 107–119.

    Article  PubMed  CAS  Google Scholar 

  • Vermes, I., Telegdy, G., & Lissak, K. Correlation between hypothalamic serotonin content and adrenal function during acute stress. Effect of adrenal corticosteroids on hypothalamic serotonin content. Acta Physiologica Academiae Scientiarum Hungaricae, 1973, 43, 33–42.

    PubMed  CAS  Google Scholar 

  • Vermes, I., Varszegi, M., Toth, E. K., & Telegdy, G. Action of androgenic steroids on brain neurotransmitters in rats. Neuroendocrinology, 1979, 28, 386–393.

    Article  PubMed  CAS  Google Scholar 

  • Vertes, A., Vertes, M., & Kovacs, S. Hypothalamic effect of oestradiol. Acta Physiologica Academiae Scientiarum Hungaricae, 1978, 51, 218–219.

    Google Scholar 

  • Walker, M. D., Negreanu, V., Gozes, I., & Kaye, A. M. Identification of the ‘estrogen-induced protein’ in uterus and brain of untreated immature rats. FEBS Letters, 1979, 98, 187–191.

    Article  PubMed  CAS  Google Scholar 

  • Wallis, C. J. Neuroendocrine influences on gamma-aminobutyric acid metabolism in rodent brain tissue. Unpublished doctoral dissertation, University of Florida, 1976.

    Google Scholar 

  • Wallis, C. J., & Luttge, W. G. Influence of estrogen and progesterone on glutamic acid decarboxylase activity in discrete regions of rat brain. Journal of Neurochemistry, 1980, 34, 609–613.

    Article  PubMed  CAS  Google Scholar 

  • Wallis, C. J., & Printz, M. P. Adrenal regulation of regional brain angiotensinogen content. Endocrinology, 1980, 106, 337–342.

    Article  PubMed  CAS  Google Scholar 

  • Warembourg, M. Radioautographic study of the rat brain after injection of [l,2-3H]corticosterone. Brain Research, 1975, 89, 61–70. (a)

    Article  PubMed  CAS  Google Scholar 

  • Warembourg, M. Radioautographic study of the rat brain and pituitary after injection of 3H-dex- amethasone. Cell and Tissue Research, 1975, 161, 183–191. (b)

    Article  PubMed  CAS  Google Scholar 

  • Warembourg, M. Fixation des steroides au niveau du systeme nerveux central et de l’hypophyse chez differents mammiferes. Annales d’Endocrinologie (Paris), 1977, 38, 41–54.

    PubMed  CAS  Google Scholar 

  • Warembourg, M. Radioautographic study of the rat brain, uterus and vagina after [3H]R-5020. Molecular and Cellular Endocrinology, 1978, 12, 67–79.

    Article  PubMed  CAS  Google Scholar 

  • Watson, G. H., & Muldoon, T. G. Microsomal estrogen receptors in rat uterus and anterior pituitary. Federation Proceedings, 1977, 36, 912.

    Google Scholar 

  • Weichman, B. M., & Notides, A. C. Analysis of estrogen receptor activation by its [3H]estradiol dissociation kinetics. Biochemistry, 1979, 18, 220–225.

    Article  PubMed  CAS  Google Scholar 

  • Weichman, B. M., & Notides, A. C. Estrogen receptor activation and the dissociation kinetics of estradiol, estriol and estrone. Endocrinology, 1980, 106, 434–439.

    Article  PubMed  CAS  Google Scholar 

  • Weidenfeld, J., Siegel, R. A., & Chowers, I. In vitro conversion of pregnenolone to progesterone by discrete brain areas of the male rat. Journal of Steroid Biochemistry, 1980, 13, 961–963.

    Article  PubMed  CAS  Google Scholar 

  • Weissman, B. A., & Johnson, D. F. Possible role of dopamine in diethylstilbestrol-elicited accumulation of cyclic AMP in incubated male rat hypothalamus. Neuroendocrinology, 1976, 21, 1–9.

    Article  PubMed  CAS  Google Scholar 

  • Weissman, B. A., & Skolnick, P. Stimulation of adenosine 3’,5’-monophosphate formation in incubated rat hypothalamus by estrogenic compounds: Relationship to biologic potency and blockade by anti-estrogens. Neuroendocrinology, 1975, 18, 27–34.

    Article  PubMed  CAS  Google Scholar 

  • Weissman, B. A., Daly, J. W., & Skolnick, P. Deithylstilbestrol-elicited accumulation of cyclic AMP in incubated rat hypothalamus. Endocrinology, 1975, 97, 1559–1566.

    Article  PubMed  CAS  Google Scholar 

  • Whalen, R. E., & Olsen, K. L. Chromatin binding of estradiol in the hypothalamus and cortex of male and female rats. Brain Research, 1978, 152, 121–131.

    Article  PubMed  CAS  Google Scholar 

  • Whalen, R. E., Yahr, P., & Luttge, W. G. Hormones, metabolism and sexual behavior. In N. T. Adler & D. Pfaff (Eds.), Neurobiology of reproduction. Book in preparation, 1983.

    Google Scholar 

  • White, J. O., & Lim, L. Unoccupied nuclear oestrogen receptors in the female rat hypothalamus. Increases on oestrogen administration. Biochemical Journal, 1980, 190, 833–837.

    PubMed  CAS  Google Scholar 

  • White, J. O., Thrower, S., & Lim, L. Intracellular relationships of the oestrogen receptor in the rat uterus and hypothalamus during the oestrous cycle. Biochemical Journal, 1978, 172, 37–47.

    PubMed  CAS  Google Scholar 

  • Wilkinson, M., Herdon, H., Pearce, M., & Wilson, C. Radioligand binding studies on hypothalamic noradrenergic receptors during the estrous cycle or after steroid injection in ovariectomized rats. Brain Research, 1979, 168, 652–655.

    Article  PubMed  CAS  Google Scholar 

  • Williams, M. Protein phosphorylation in the mammalian nervous system. Trends in Biochemical Science, 1979, 4, 25–28.

    Article  CAS  Google Scholar 

  • Wilson, E. M., & French, F. S. Effects of proteases and protease inhibitors on the 4.5S and 8S androgen receptor. Journal of Biological Chemistry, 1979, 254, 6310–6319.

    PubMed  CAS  Google Scholar 

  • Wrange, O. A comparison of the glucocorticoid receptor in cytosol from rat liver and hippocampus. Biochimica et Biophysica Acta, 1979, 582, 346–357.

    PubMed  CAS  Google Scholar 

  • Yagi, K., & Sawaki, Y. Recurrent inhibition and facilitation. Demonstration in the tuberinfundibular system and effects of strychnine and picrotoxin. Brain Research, 1975, 84, 155–159.

    Article  PubMed  CAS  Google Scholar 

  • Yamamoto, K. R. Characterization of the 4S and 5S forms of the estradiol receptor protein and their interaction with deoxyribonucleic acid. Journal of Biological Chemistry, 1974, 249, 7068–7075.

    PubMed  CAS  Google Scholar 

  • Zava, D. T., & McGuire, W. L. Estrogen receptor: Unoccupied sites in nuclei of breast tumor cell line. Journal of Biological Chemistry, 1977, 252, 3703–3708.

    PubMed  CAS  Google Scholar 

  • Zigmond, R. E., & McEwen, B. S. Selective retention of oestradiol by cell nuclei in specific brain regions of the ovariectomized rat. Journal of Neurochemistry, 1970, 17, 889–899.

    Article  PubMed  CAS  Google Scholar 

  • Zolovick, A. J., Pearse, R., Boehlke, K. W., & Eleftheriou, B. E. Monoamine oxidase activity in various parts of the rat brain during the estrous cycle. Science, 1966, 154, 649.

    Article  PubMed  CAS  Google Scholar 

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Luttge, W.G. (1983). Molecular Mechanisms of Steroid Hormone Actions in the Brain. In: Svare, B.B. (eds) Hormones and Aggressive Behavior. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-3521-4_11

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