Abstract
The dependence of reproductive behavior on sex steroids has been well documented and reviewed for several mammalian species (Beach 1948; Baum 1979; Pfaff 1980). Since behavior in general is a final product of integrative action of the central nervous system, the example of reproductive behavior signifies that sex steroids act on the neural tissue at some level. Also compelling is the evidence of the feedback action of sex steroids and glucocorticoids, which has been shown to be mediated by limbic and hypothalamic structures (Harris 1955; Mangili et al. 1966). Steroid hormones exert their effects on the central nervous system partly through a genomic mechanism which can be blocked by inhibitors of DNA-dependent RNA synthesis or protein synthesis (McEwen et al. 1979). New protein synthesis as a result of the genomic action of steroids has been clearly defined for peripheral target tissues, as, for example, in the action of estrogen in the uterus (O’Malley and Means 1974). Evidence that steroids are incorporated into central neurons includes early demonstration by autoradiography of estrogen, progesterone, and testosterone in the hypothalamus (Pfaff and Keiner 1973; Stumpf and Sar 1976; Sar and Stumpf 1973) and glucocorticoids in the hippocampus (Warembourg 1975). Biochemical studies have shown that these structures contain specific cytosolic and nuclear receptors for estrogen (Zigmond and McEwen 1970), progesterone (Kato and Onouchi 1977), and Cortisol (Chytil and Toft 1972). Estrogenic induction of various enzyme activities and of structural protein synthesis, as measured by incorporation of amino acids, is attributed to this type of receptor mechanism.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Akaishi T, Sakuma Y (1985) Differential routes taken by mesencephalic projections from oestrogensensitive neurones in the rat ventromedial hypothalamus. J Physiol (Lond) (to be published)
Barraclough CA, Cross BA (1963) Unit activity in the hypothalamus of the cyclic female rat. Effect of genital stimuli and progesterone. J Endocrinol 26:339–359
Baum MJ (1979) Differentiation of coital behavior in mammals: a comparative analysis. Neurosci Biobehav Rev 3:265–284
Beach FA (1942) Importance of progesterone to induction of sexual receptivity in spayed female, rats. Proc Soc Exp Biol Med 51:369–371
Beach FA (1948) Hormones and behavior. Hoeber, New York
Bern HA, Gorski RA, Kawashima S (1973) Long-term effects of perinatal hormone administration. Science 181:189–190
Beyer C, Ramirez VD, Whitmoyer DI, Sawyer CH (1967) Effects of hormones on the electrical activity of the brain in the rat and the rabbit. Exp Neurol 18:313–326
Bogdanove EM (1963) Direct gonad-pituitary feedback: An analysis of effects of intracranial estrogenic depots on gonadotropin secretion. Endocrinology 73:696–712
Bolt HM, Kappus H (1976) Interaction by 2-hydroxyestrogens with enzymes of drug metabolism. J Steroid Biochem 7:311–313
Breedlove SM, Arnold AP (1980) Hormone accumulation in a sexually dimorphic motor nucleus of the rat spinal cord. Science 210:564–566
Bueno J, Pfaff DW (1976) Single unit recording in hypothalamus and preoptic area of estrogen-treated and untreated ovariectomized female rats. Brain Res 101:67–78
Catterall WA (1984) The molecular basis of neuronal excitability. Science 223:653–661
Chytil F, Toft D (1972) Corticoid binding component in brain. J Neurochem 19:2877–2880
Conrad LCA, Pfaff DW (1976a) Efferents from medial basal forebrain and hypothalamus in the rat. I. An autoradiographic study of the medial preoptic area. J Comp Neurol 169:185–220
Conrad LCA, Pfaff DW (1976b) Efferents from medial basal forebrain and hypothalamus in the rat. II. An autoradiographic study of the anterior hypothalamus. J Comp Neurol 169:221–262
Costa MRC, Casnellie JE, Catterall WA (1982) Selective phosphorylation of the alpha-subunit of the sodium channel by cAMP-dependent protein kinase. J Biol Chem 257:7918–7921
Davis PG, McEwen BS, Pfaff DW (1979) Localized behavioral effects of tritiated estradiol implants in the ventromedial hypothalamus of female rats. Endocrinology 104:898–903
Dufy B, Partouche C, Dufy-Barbe L, Vincent JD (1976) Effect of oestrogen on the electrical activity of hypothalamic units: correlation with gonadotrophs hormone levels. In: Endroczi E (ed) Cellular and molecular bases of neuroendocrine processes, Akademiai Kiado, Budapest, pp 303–312
Dufy B, Dufy-Barbe L, Vincent JD (1978) Effects of gonadal steroids on the electrical activity of hypothalamic neurons. In: Vincent JD, Kordon C (eds) Biologie cellulare des processes neurosecretoires hypothalamique, CNRS, Bordeaux, pp 207–220
Dyer RG, MacLeod NK, Ellendorff F (1976) Electrophysiological evidence for sexual dimorphism and synaptic convergence in the preoptic and anterior hypothalamic areas of the rat. Proc R Soc Lond B 193:421–440
Feder HH (1981) Perinatal hormones and their role in the development of sexually dimorphic behaviors. In: Adler NT (ed) Neuroendocrinology of reproduction, Plenum, New York, pp 127–157
Feder HH, Whalen RE (1965) Feminine behavior in neonatally castrated and estrogen-treated male rats. Science 147:306–307
Feldman S, Dafny N (1970) Effect of Cortisol on unit activity in the hypothalamus of the rat. Exp Neurol 27:375–387
Fishman J, Norton B (1975) Catechol estrogen formation in the central nervous system of the rat. Endocrinology 96:1054–1059
Gorski RA, Gordon JH, Shryne JE, Southam AM (1978) Evidence for a morphological sex difference in the medial preoptic area of the rat brain. Brain Res 148:333–346
Greengard P (1976) Possible role for cyclic nucleotides and phosphorylated membrane proteins in postsynaptic actions of neurotransmitters. Nature 260:101–108
Greenough WT, Carter CS, Steerman C, DeVoogt TJ (1977) Sex differences in dendritic patterns in hamster preoptic area. Brain Res 126:63–72
Gunaga KD, Kawano A, Menon KM J (1974) In vivo effect of estradiol benzoate on the accumulation of adenosine 3’5’ monophosphate in the rat hypothalamus. Neuroendocrinology 16:273–281
Harlan RE, Shivers BD, Pfaff DW (1983) Midbrain microinfusions of prolactin increase the estrogen-dependent behavior, lordosis. Science 219:1451–1453
Harris GW (1955) Neural control of pituitary gland. Arnold, London
Hart BL (1968) Neonatal castration: influence on neural organization of sexual reflexes in male rats. Science 160:1135–1136
Hart BL (1969) Gonadal hormones and sexual reflexes in the female rat. Horm Behav 1:65–71
Hiemke C, Ghraf R (1982) Effects of short-term exposure to catecholestrogens on catecholamine turnover in the preoptichypothalamic brain of ovariectomized rats. Brain Res 240:295–301
Holzbauer M, Sharman DF, Godden U, Mann SP, Stephens DB (1978) Observations on the function of the dopaminergic nerves innervating the pituitary gland. Neuroscience 3:1251–1262
Kandel E, Schwarz J (1982) Molecular biology of learning: modulation of transmitter release. Science 218:433–443
Kato J, Onouchi T (1977) Specific progesterone receptors in the hypothalamus and anterior hypophysis of the rat. Endocrinology 101:920–928
Kawakami M, Sawyer CH (1959) Neuroendocrine correlates of changes in brain activity thresholds by sex steroids and pituitary hormones. Endocrinology 65:652–668
Kelly MJ, Moss RL, Dudley CA, Fawcett CP (1977a) The specificity of the response of preoptic septal area neurons to estrogen: 17β-estradiol versus 17β-estradiol and the response of extrahypothalamic neurons. Exp Brain Res 30:43–52
Kelly MJ, Moss RL, Dudley CA (1977b) The effects of microelectrophoretically applied estrogen, Cortisol, and acetylcholine on medial preoptic septal unit activity throughout the estrous cycle of the female rat. Exp Brain Res 30:53–64
Kelly MJ, Moss RL, Dudley CA (1978) The effect of ovariectomy on the responsiveness of preoptic-septal neurons to microelectrophoresed estrogen. Neuroendocrinology 25:204–211
Kelly MJ, Kuhnt U, Wuttke W (1980) Hyperpolarization of hypothalamic parvocellular neurons by 17β-estradiol and their identification through intracellular staining with procion yellow. Exp Brain Res 40:440–447
Kelly MJ, Ronnekleiv OK, Eskay RL (1982) Immunocytochemical localization of luteinizing hormone-releasing hormone in neurons in the medial basal hypothalamus of the female rat. Exp Brain Res 48:97–106
Kendrick KM (1982) Inputs to testosterone-sensitive stria terminalis neurones in the rat brain and the effects of castration. J Physiol (Lond) 323:437–447
Kendrick KM, Drewett RF (1979) Testosterone reduces refractory period of stria terminalis neurons in the rat brain. Science 204:877–879
Kendrick KM, Drewett RF (1980) Testosterone-sensitive neurones respond to oestradiol but not to dihydrotestosterone. Nature 286:67–68
Komisaruk BR, McDonald PG, Whitmoyer DI, Sawyer CH (1967) Effects of progesterone and sensory stimulation on EEG and neuronal activity in the rat. Exp Neurol 19:494–507
Kow L-M, Pfaff DW (1975) Induction of lordosis in female rats: two modes of estrogen action and the effect of adrenalectomy. Horm Behav 6:259–276
Kow L-M, Malsbury CW, Pfaff DW (1974) Effects of progesterone on female reproductive behavior in rats: possible modes of action and role in behavioral sex differences. In: Montagna W, Sadler W (eds) Reproductive behavior. Plenum, New York, pp 179–210
Kow L-M, Grill H, Pfaff DW (1978) Elimination of lordosis in decerebrate female rats: observations from acute and chronic preparations. Physiol Behav 20:171–174
Kow L-M, Montgomery MO, Pfaff DW (1979) Triggering of lordosis reflex in female rats with somatosensory stimulation: quantitative determination of stimulus parameters. J Neurophysiol 42:195–202
Krebs EG, Beavo JA (1979) Phosphorylation-dephosphorylation of enzymes. Annu Rev Biochem 48:923–959
Krieger MS, Conrad LCA, Pfaff DW (1979) An autoradiographic study of the efferent connections of the ventromedial nucleus of the hypothalamus. J Comp Neurol 183:785–816
Lincoln DW (1969) Effects of progesterone on the electrical activity of the forebrain. J Endocrinol 45:585–596
MacLeod NK, Mayer ML (1980) Electrophysiological analysis of pathways connecting the medial preoptic area with the mesencephalic central grey matter in rats. J Physiol (Lond) 298:53–70
McEwen BS, Davis PG, Parsons B, Pfaff DW (1979) The brain as a target for steroid hormone action. Annu Rev Neurosci 2:65–112
MacLusky NJ, Chaptal C, Lieberberg I, McEwen BS (1976) Properties and subcellular interrelationships of presumptive estrogen receptor macromolecules in the brains of neonatal and prepubertal female rats. Brain Res 114:158–165
MacLusky NJ, McEwen BS (1978) Oestrogen modulates progestin receptor concentrations in some rat brain regions but not in the others. Nature 274:276–277
McGlone J (1980) Sex differences in human brain asymmetry: a critical survey. Behav Brain Sci 3:215–263
Malsbury CW, Daood JT (1978) Sexual receptivity: critical importance of supraoptic connections of the ventromedial hypothalamus. Brain Res 159:451–457
Malsbury CW, Pfaff DW, Malsbury AM (1980) Suppression of sexual receptivity in the female hamster: neuroanatomical projections from preoptic and anterior hypothalamic electrode sites. Brain Res 181:267–284
Mangili G, Motta M, Martini L (1966) Control of adrenocorticotropic hormone secretion. In: Martini L, Ganong WF (eds) Neuroendocrinology, vol 1. Academic, New York, pp 297–370
Manogue K, Kow L-M, Pfaff DW (1980) Transections affecting reproductive behavior of female rats: the role of hypothalamic output to the midbrain. Horm Behav 14:277–302
Matsumoto A, Arai Y (1980) Sexual dimorphism in wiring pattern in the hypothalamic arcuate nucleus and its modification by neonatal hormonal environment. Brain Res 190:238–242
Matsumoto A, Arai Y (1983) Sex difference in volume of the ventromedial nucleus of the hypothalamus in the rat. Endocrinol Jpn 30:277–280
Meyerson BJ (1964) Central nervous monoamines and hormone-induced estrous behaviour in the spayed rat. Acta Physiol Scand [Suppl] 63:241
Morin LP (1977) Progesterone: inhibition of rodent sexual behavior. Physiol Behav 18:701–715
Morris R, Salt TE, Sofroniew M, Hill RG (1980) Actions of mieroiontophoretically applied oxytocin, and immunohistochemical localization of oxytocin, vasopressin and neurophysin in the rat caudal medulla. Neurosci Lett 18:163–168
Moss RL, McCann SM (1973) Induction of mating behavior in rats by luteinizing hormone-releasing factor. Science 181:177–179
Negoro H, Akaishi T (1981) Effect of anterior or posterior deafferentation of the hypothalamus on unit activity in the paraventricular nucleus of ovariectomized female rats with or without estrogen treatment. Endocrinol Jpn 28:37–43
Nishizuka M, Arai Y (1981) Sexual dimorphism in synaptic organization in the amygdala and its dependence on neonatal hormone environment. Brain Res 212:31–38
Nottebohm F, Arnold AP (1976) Sexual dimorphism in vocal control areas of the songbird brain. Science 194:211–213
O’Malley BW, Means AR (1974) Female steroid hormones and target cell nuclei. Science 183:610–620
Paden CM, McEwen BS, Fishman J (1983) Binding of catechol estrogens to cell membranes. In: Merriam GR, Lipsett MB (ed) Catechol estrogens, Raven, New York, pp 189–201
Paul SM, Axelrod J, Saavedra JM, Skolnick P (1979) Estrogen-induced efflux of endogenous catecholamines from the hypothalamus in vitro. Brain Res 178:499–505
Pfaff DW (1973) Luteinizing hormone releasing factor (LRF) potentiates lordosis behavior in hypophysectomized ovariectomized female rats. Science 182:1148–1149
Pfaff DW (1980) Estrogens and brain function. Springer, Berlin Heidelberg New York
Pfaff DW, Keiner M (1973) Atlas of estradiol-concentrating cells in the central nervous system of the female rat. J Comp Neurol 151:121–158
Pfaff DW, Sakuma Y (1979a) Facilitation of the lordosis reflex of female rats from the ventromedial nucleus of the hypothalamus. J Physiol (Lond) 288:189–202
Pfaff DW, Sakuma Y (1979b) Deficit in the lordosis reflex of female rats caused by lesions in the ventromedial nucleus of the hypothalamus. J Physiol (Lond) 288:203–210
Pfaff DW, Silva MTA, Weiss JM (1971) Telemetered recording of hormone effects on hippocampal neurons. Science 172:394–395
Phoenix CH, Goy RW, Gerall AA, Young WC (1959) Organizational action of prenatally administered testosterone propionate on the tissues mediating mating behavior in the female guinea pig. Endocrinology 65:369–382
Pietras J, Szego CM (1977) Specific binding sites for oestrogen at the outer surfaces of isolated endometrial cells. Nature 265:69–72
Poulain DA, Wakerley JB (1982) Electrophysiology of hypothalamic magnocellular neurons secreting oxytocin and vasopressin. Neuroscience 7:773–808
Powers B, Valenstein ES (1972) Sexual receptivity: facilitation by medial preoptic lesions in female rats. Science 175:1003–1005
Raisman G, Field PM (1971) Sexual dimorphism in the preoptic area of the rat. Science 173:731–733
Raisman G, Field PM (1973) Sexual dimorphism in the neuropil of the preoptic area of the rat and its dependence on neonatal androgen. Brain Res 54:1–29
Ramirez V, Komisaruk BR, Whitmoyer DI, Sawyer CH (1969) Effects of hormones and vaginal stimulation on the EEG and hypothalamic units in rats. Am J Physiol 212:1376–1384
Rhodes CH, Morrell JI, Pfaff DW (1982) Estrogen-concentrating neurophysin-containing hypothalamic magnocellular neurons in the vasopressin-deficient (Brattleboro) rat: a study combining steroid autoradiography and immunocytochemistry. J Neurosci 2:1718–1724
Ross J, Claybaugh C, Clemens LG, Gorski RA (1971) Short latency induction of estrous behavior with intracerebral gonadal hormones in ovariectomized rats. Endocrinology 89:32–38
Sakuma Y (1984) Influences of neonatal gonadectomy or androgen exposure on the sexual differentiation of the rat ventromedial hypothalamus. J Physiol (Lond) 349:273–286
Sakuma Y, Pfaff DW (1979a) Facilitation of female reproductive behavior from mesencephalic central gray in the rat. Am J Physiol 237:R278-R284
Sakuma Y, Pfaff DW (1979b) Mesencephalic mechanisms for integration of female reproductive behavior in the rat. Am J Physiol 237:R285-R290
Sakuma Y, Pfaff DW (1980a) LH-RH in the mesencephalic central grey can potentiate lordosis reflex of female rats. Nature 283:566–567
Sakuma Y, Pfaff DW (1980b) Cells of origin of medullary projections in the central gray of the rat mesencephalon. J Neurophysiol 44:1002–1011
Sakuma Y, Pfaff DW (1980c) Excitability of female rat central gray cells with medullary projection: changes produced by hypothalamic stimulation and estrogen treatment. J Neurophysiol 44:1012–1023
Sakuma Y, Pfaff DW (1980d) Convergent effects of lordosis-relevant somatosensory and hypothalamic influences on central grey cells in the rat mesencephalon. Exp Neurol 70:269–281
Sakuma Y, Pfaff DW (1981) Electrophysiologic determination of projections from ventromedial hypothalamus to midbrain central gray: differences between female and male rats. Brain Res 225:184–188
Sakuma Y, Pfaff DW (1982) Properties of ventromedial hypothalamic neurons with axons to midbrain central gray. Exp Brain Res 46:292–300
Sakuma Y, Pfaff DW (1983) Modulation of the lordosis reflex of female rats by LHRH, its antiserum and analogs in the mesencephalic central gray. Neuroendocrinology 36:218–224
Sakuma Y, Tada K (1984) Evidence that two sizes of ventromedial hypothalamic neurones project to the mesencephalic central grey matter in rats. J Physiol (Lond) 49:287–297
Sakuma Y, Akaishi T, Ohtake M (1984) Effects of estrogen on the neurosecretory cells in the rat paraventricular nucleus: differential responses in the neurons with tonic or phasic activity. Neurosci Lett [Suppl] 17:S 96
Saper CB, Swanson LW, Cowan WM (1976) The efferent connections of the ventromedial nucleus of the hypothalamus of the rat. J Comp Neurol 169:409–442
Sar M, Stumpf WE (1973) Autoradiographic localization of radioactivity in the rat brain after injection of l,2-3H-testosterone using dry mount autoradiography. Endocrinology 92:251–256
Sheridan PJ (1979) Estrogen binding in the neonatal cortex. Brain Res 178:201–206
Shivers BD, Harlan RE, Morrell JI, Pfaff DW (1983) Immunocytochemical localization of luteinizing hormone-releasing hormone in male and female rat brains. Neuroendocrinology 36:1–12
Siggins GR, Hoffer BJ, Bloom FE (1971) Studies on norepinephrine-containing afferents to Purkinje cells of rat cerebellum. III. Evidence for mediation of norepinephrine effects by cyclic 3’,5’-adenosine monophosphate. Brain Res 25:535–539
Sirinathsinghji DJS, Whittington PE, Audsley A, Fraser HM (1983a) β-Endorphin regulates lordosis in female rats by modulating LH-RH release. Nature 301:62–64
Sirinathsinghji DJS, Rees LH, Rivier J, Vale W (1983b) Cortieotropin-releasing factor is a potent inhibitor of sexual receptivity in the female rat. Nature 305:232–235
Steiner FA (1971) Neurotransmitter und Neuromodulatoren. Thieme, Stuttgart
Stumpf WE, Sar M (1976) Steroid hormone target sites in the brain: the differential distribution of estrogen, progestin, androgen and glucocorticoid. J Steroid Biochem 7:1163–1170
Suzuki Y, Ishii H, Furuya Y, Arai Y (1982) Developmental changes of the hypogastric ganglion associated with the differentiation of the reproductive tract in the mouse. Neurosci Lett 32:271–276
Terasawa E, Sawyer CH (1970) Diurnal variation in the effects of progesterone on multiple unit activity in the rat hypothalamus. Exp Neurol 27:359–374
Teyler TJ, Vardaris RM, Lewis D, Rawitch AB (1980) Gonadal steroid effects on excitability of hippocampal pyramidal cells. Science 209:1017–1019
Toran-Allerand DC (1976) Sex steroids and the development of the newborn mouse hypothalamus and preoptic area in vitro: implications for sexual differentiation. Brain Res 106:407–412
Tweedle CD (1983) Ultrastructural manifestations of increased hormone release in the neurohypophysis. In: Cross BA, Leng G (eds) The neurohypophysis: structure, function and control. Elsevier, Amsterdam, pp 259–272 (Progress of brain research, vol 60)
Warembourg M (1975) Radioautographic study of the rat brain after injection of 1,2-3Hcorticosterone. Brain Res 89:61–70
Weissman BA, Johnson DF (1976) Possible role of dopamine in diethylstilbesterol-elicited accumulation of cyclic AMP in incubated male rat hypothalamus. Neuroendocrinology 21:1–9
Weissman BA, Daly JW, Skolnik P (1975) Diethylstilbesterol-elicited accumulation of cyclic-AMP in incubated rat hypothalamus. Endocrinology 97:1559–1566
Welshons WV, Lieberman ME, Gorski J (1984) Nuclear localization of unoccupied oestrogen receptors. Nature 307:747–749
Whitehead SA, Ruf KB (1974) Response of antidromically identified preoptic neurons in the rat to neurotransmitters and to estrogen. Brain Res 79:185–198
Wooley DE, Timiras PS (1962) The gonad-brain relationship: effects of female sex hormones on electroshock convulsions in the rat. Endocrinology 70:196–209
Yagi K (1973) Changes in firing rates of single preoptic and hypothalamic units following an intravenous administration of estrogen in the castrated female rat. Brain Res 53:343–352
Yagi K, Azuma T, Matsuda K (1966) Neurosecretory cell: capable of conducting impulse in rats. Science 154:778–779
Yamada Y (1979) Effects of testosterone on unit activity in rat hypothalamus and septum. Brain Res 172:165–168
Yamada Y, Nishida E (1978) Effects of estrogen and adrenal androgen on unit activity of the rat brain. Brain Res 142:187–190
Yamaguchi K-I, Akaishi T, Negoro H (1979) Effect of estrogen treatment on plasma oxytocin and vasopressin in ovariectomized rats. Endocrinol Jpn 26:197–205
Yamanouchi K, Arai Y (1978) Lordosis behaviour in male rats: effects of deafferentation in the preoptic area and hypothalamus. J Endocrinol 76:381–382
Yamanouchi K, Arai Y (1983) Forebrain and lower brainstem participation in facilitatory and inhibitory regulation of the display of lordosis in female rats. Physiol Behav 30:155–159
Zigmond RE, McEwen BS (1970) Selective retention of oestradiol by cell nuclei in specific brain regions of the ovariectomized rat. J Neurochem 17:889–899
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1985 Spriger-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Sakuma, Y. (1985). Effects of Estrogen and Progesterone as Revealed by Neurophysiological Methods. In: Ganten, D., Pfaff, D. (eds) Actions of Progesterone on the Brain. Current Topics in Neuroendocrinology, vol 5. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-69728-9_3
Download citation
DOI: https://doi.org/10.1007/978-3-642-69728-9_3
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-69730-2
Online ISBN: 978-3-642-69728-9
eBook Packages: Springer Book Archive