Perinatal exposure to diethylstilbestrol improves olfactory discrimination learning in male and female Swiss-Webster mice

During late prenatal and early postnatal brain development, estrogen induces structural sex differences that correspond to behavioral differences in certain domains such as learning and memory. The typically superior performance of males is attributed to the action of elevated concentrations of estrogen, derived inside neurons from the aromatization of testosterone. In contrast, female performance appears dependent on minimal estrogenic activity. Rat models of the relationship between hormones and cognitive behavior predominate the field, but the advent of genetically modified mice as research tools necessitates development of analogous mouse models. This study examined how early postnatal exposure to the synthetic estrogen diethylstilbestrol (DES) affected the ability of male and female Swiss-Webster mice to learn a two-choice olfactory discrimination and three repeated reversals. Mice treated with subcutaneous injections of DES from postnatal days 1-10 learned reversals more readily than oil-treated controls, a difference that became evident after repeated testing. DES-exposed males and females learned reversals at a comparable rate, suggesting that early postnatal estrogen exposure does not influence this mode of learning through a sexually differentiated mechanism in mice. An analysis of response patterns during qualitatively different phases of reversal learning revealed that DES-induced improvements probably were not due to greater inhibitory control. Instead, DES appeared to enhance associative ability. Early postnatal estrogen exposure may have the potential to preserve certain cognitive skills in adulthood.

[1]  S. Segovia,et al.  Effects of early postnatal gonadal steroids on the successive conditional discrimination reversal learning in the rat , 1986, Physiology & Behavior.

[2]  C. D. Jacobson,et al.  Evidence for the existence of a sexually dimorphic nucleus in the preoptic area of the rat , 1980, The Journal of comparative neurology.

[3]  J. Langlois,et al.  Strain and sex differences on olfactory discrimination learning in C57BL/6J and DBA/2J inbred mice (Mus musculus). , 2000, Journal of comparative psychology.

[4]  C. Viscoli,et al.  Postmenopausal estrogen replacement therapy is associated with adverse breast cancer prognostic indices. , 1999, Journal of women's health & gender-based medicine.

[5]  R. Roof,et al.  Testosterone improves maze performance and induces development of a male hippocampus in females , 1992, Brain Research.

[6]  R. Handa,et al.  Transient elevation of estrogen receptors in the neonatal rat hippocampus. , 1990, Brain research. Developmental brain research.

[7]  Warren H. Meck,et al.  Organizational effects of early gonadal secretions on sexual differentiation in spatial memory. , 1990, Behavioral Neuroscience.

[8]  S Hulley,et al.  Randomized trial of estrogen plus progestin for secondary prevention of coronary heart disease in postmenopausal women. Heart and Estrogen/progestin Replacement Study (HERS) Research Group. , 1998, JAMA.

[9]  M. Mishkin,et al.  Limbic lesions and the problem of stimulus--reinforcement associations. , 1972, Experimental neurology.

[10]  B. Strupp,et al.  Analyses of response patterns clarify lead effects in olfactory reversal and extradimensional shift tasks: assessment of inhibitory control, associative ability, and memory. , 1997, Behavioral neuroscience.

[11]  C. D. Toran-Allerand,et al.  Gonadal Hormones and Brain Development: Implications for the Genesis of Sexual Differentiation a , 1984, Annals of the New York Academy of Sciences.

[12]  Bradley M. Cooke,et al.  Sex difference and laterality in the volume of mouse dentate gyrus granule cell layer , 1999, Brain Research.

[13]  H. Garavan,et al.  Prenatal cocaine exposure impairs selective attention: Evidence from serial reversal and extradimensional shift tasks , 2000 .

[14]  D. Rubinow,et al.  Estrogen protects against beta-amyloid-induced neurotoxicity in rat hippocampal neurons by activation of Akt. , 2001, Neuroreport.

[15]  S. Asthana,et al.  High-dose estradiol improves cognition for women with AD , 2001, Neurology.

[16]  J. Mills,et al.  Sexually dimorphic responses to neonatal basal forebrain lesions in mice: I. Behavior and neurochemistry. , 1998, Journal of neurobiology.

[17]  B. McEwen,et al.  Estrogen-induction of dendritic spines in ventromedial hypothalamus and hippocampus: effects of neonatal aromatase blockade and adult GDX. , 1995, Brain research. Developmental brain research.

[18]  M. Kavaliers,et al.  Sex differences in performance in the Morris water maze and the effects of initial nonstationary hidden platform training. , 1996, Behavioral neuroscience.

[19]  K. Teraoka,et al.  Sex differences in appetitive learning of mice , 1986, Physiology & Behavior.

[20]  K. Marder,et al.  Cognitive function in nondemented older women who took estrogen after menopause , 1998, Neurology.

[21]  W. Greenough,et al.  Sex steroids and the development of the newborn mouse hypothalamus and preoptic area in vitro: III. Effects of estrogen on dendritic differentiation. , 1983, Brain research.

[22]  R. Handa,et al.  Estrogen receptor mRNA alterations in the developing rat hippocampus. , 1995, Brain research. Molecular brain research.

[23]  W. Meck,et al.  The organizational effects of gonadal steroids on sexually dimorphic spatial ability , 1991, Psychoneuroendocrinology.

[24]  H. Eichenbaum,et al.  Hippocampal representation in place learning , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[25]  H Eichenbaum,et al.  Normal olfactory discrimination learning set and facilitation of reversal learning after medial-temporal damage in rats: implications for an account of preserved learning abilities in amnesia , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[26]  S. Tobet,et al.  The preoptic area/anterior hypothalamus of different strains of mice: sex differences and development. , 1999, Brain research. Developmental brain research.

[27]  L. Hermer-Vazquez,et al.  Enduring effects of early lead exposure: evidence for a specific deficit in associative ability. , 2000, Neurotoxicology and teratology.

[28]  S. Asthana,et al.  Cognitive and neuroendocrine response to transdermal estrogen in postmenopausal women with Alzheimer’s disease: results of a placebo-controlled, double-blind, pilot study , 1999, Psychoneuroendocrinology.

[29]  B. Zhivotovsky,et al.  Apoptosis in rat hippocampal dentate gyrus after intraventricular colchicine , 1997, Neuroreport.

[30]  H Eichenbaum,et al.  Selective damage to the hippocampal region blocks long‐term retention of a natural and nonspatial stimulus‐stimulus association , 1995, Hippocampus.

[31]  K. Crofton,et al.  Spatial reversal learning in Aroclor 1254-exposed rats: sex-specific deficits in associative ability and inhibitory control. , 2001, Toxicology and applied pharmacology.

[32]  J. W. Pendleton,et al.  Estrogen receptor-dependent sexual differentiation of dopaminergic neurons in the preoptic region of the mouse. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[33]  Toran-Allerand Cd On the genesis of sexual differentiation of the general nervous system: morphogenetic consequences of steroidal exposure and possible role of alpha-fetoprotein. , 1984 .

[34]  H. Honjo,et al.  Estrogen protects neuronal cells from amyloid β-induced apoptotic cell death , 2001 .

[35]  B. Mcewen,et al.  Estradiol mediates fluctuation in hippocampal synapse density during the estrous cycle in the adult rat [published erratum appears in J Neurosci 1992 Oct;12(10):following table of contents] , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[36]  C. Woolley,et al.  Roles of estradiol and progesterone in regulation of hippocampal dendritic spine density during the estrous cycle in the rat , 1993, The Journal of comparative neurology.

[37]  R. Gerlai Gene-targeting studies of mammalian behavior: is it the mutation or the background genotype? , 1996, Trends in Neurosciences.

[38]  Estrogen use and verbal memory in healthy postmenopausal women. , 1994 .

[39]  K. Döhler The pre- and postnatal influence of hormones and neurotransmitters on sexual differentiation of the mammalian hypothalamus. , 1991, International review of cytology.

[40]  H. Eichenbaum Is the rodent hippocampus just for ‘place’? , 1996, Current Opinion in Neurobiology.

[41]  B. Kudielka,et al.  Two weeks of transdermal estradiol treatment in postmenopausal elderly women and its effect on memory and mood: verbal memory changes are associated with the treatment induced estradiol levels , 1999, Psychoneuroendocrinology.

[42]  J. Mills,et al.  Sex differences in learning and memory in mice: effects of sequence of testing and cholinergic blockade. , 1995 .

[43]  P. Wise,et al.  Estradiol is a protective factor in the adult and aging brain: understanding of mechanisms derived from in vivo and in vitro studies , 2001, Brain Research Reviews.

[44]  Estradiol masculinizes the posteromedial cortical nucleus of the amygdala in the rat , 2000, Brain Research Bulletin.

[45]  R. Wimer,et al.  Three sex dimorphisms in the granule cell layer of the hippocampus in house mice , 1985, Brain Research.

[46]  H. Adlercreutz,et al.  Visual spatial memory is enhanced in female rats (but inhibited in males) by dietary soy phytoestrogens , 2001, BMC Neuroscience.

[47]  J. Cherry,et al.  Sex Difference and Steroid Modulation of Pheromone-Induced Immediate Early Genes in the Two Zones of the Mouse Accessory Olfactory System , 2001, The Journal of Neuroscience.

[48]  D. Sengelaub,et al.  Prenatal Gonadal Steroids Affect Adult Spatial Behavior, CA1 and CA3 Pyramidal Cell Morphology in Rats , 1998, Hormones and Behavior.

[49]  A. Guillamón,et al.  Early postnatal estrogen organizes sex differences in the extinction of a CRF running response , 1993, Brain Research Bulletin.

[50]  D. Purdie Consequences of long-term hormone replacement therapy. , 2000, British medical bulletin.

[51]  Elizabeth Gould,et al.  Regulation of hippocampal neurogenesis in adulthood , 2000, Biological Psychiatry.

[52]  V. Koliatsos,et al.  Estrogens modulate experimentally induced apoptosis of granule cells in the adult hippocampus , 2001, The Journal of comparative neurology.

[53]  Y. Suh,et al.  Estrogen attenuates cell death induced by carboxy‐terminal fragment of amyloid precursor protein in PC12 through a receptor‐dependent pathway , 2001, Journal of neuroscience research.

[54]  Marc D Hauser,et al.  Perseveration, inhibition and the prefrontal cortex: a new look , 1999, Current Opinion in Neurobiology.

[55]  B. McEwen,et al.  Neurotrophic and neuroprotective actions of estrogens and their therapeutic implications. , 2001, Annual review of pharmacology and toxicology.

[56]  M. Morimoto,et al.  Steroid Hormone Effects on Gene Expression, Neuronal Structure, and Differentiation , 1994, Hormones and Behavior.

[57]  G. Keppel,et al.  Design and Analysis: A Researcher's Handbook , 1976 .

[58]  P. Wise,et al.  Estradiol Protects Against Ischemic Brain Injury in Middle-Aged Rats1 , 2000, Biology of reproduction.

[59]  L. Nadel,et al.  The Hippocampus as a Cognitive Map , 1978 .

[60]  W. Beatty,et al.  Hormonal organization of sex differences in play fighting and spatial behavior. , 1984, Progress in brain research.