Sexual differentiation of the adolescent rodent brain: Hormonal influences and developmental mechanisms

This article is part of a Special Issue "Puberty and Adolescence". Sexual differentiation is the process by which the nervous system becomes structurally and functionally dissimilar in females and males. In mammals, this process has been thought to occur during prenatal and early postnatal development, when a transient increase in testosterone secretion masculinizes and defeminizes the developing male nervous system. Decades of research have led to the views that structural sexual dimorphisms created during perinatal development are passively maintained throughout life, and that ovarian hormones do not play an active role in feminization of the nervous system. Furthermore, perinatal testosterone was thought to determine sex differences in neuron number by regulating cell death and cell survival, and not by regulating cell proliferation. As investigations of neural development during adolescence became more prominent in the late 20th century and revealed the extent of brain remodeling during this time, each of these tenets has been challenged and modified. Here we review evidence from the animal literature that 1) the brain is further sexually differentiated during puberty and adolescence; 2) ovarian hormones play an active role in the feminization of the brain during puberty; and 3) hormonally modulated, sex-specific addition of new neurons and glial cells, as well as loss of neurons, contribute to sexual differentiation of hypothalamic, limbic, and cortical regions during adolescence. This architectural remodeling during the adolescent phase of sexual differentiation of the brain may underlie the known sex differences in vulnerability to addiction and psychiatric disorders that emerge during this developmental period.

[1]  F. Davis,et al.  Differentiation of the sexually dimorphic nucleus in the preoptic area of the rat brain is determined by the perinatal hormone environment , 1982, Neuroscience Letters.

[2]  S. Segovia,et al.  The development of sex differences in the locus coeruleus of the rat , 2001, Brain Research Bulletin.

[3]  S. Segovia,et al.  Effects of sex steroids on the development of the locus coeruleus in the rat. , 1988, Brain research.

[4]  Cynthia L. Jordan,et al.  Sexual dimorphism in neuronal number of the posterodorsal medial amygdala is independent of circulating androgens and regional volume in adult rats , 2008, The Journal of comparative neurology.

[5]  L. Doncarlos,et al.  Pubertal hormones modulate the addition of new cells to sexually dimorphic brain regions , 2008, Nature Neuroscience.

[6]  S. Breedlove,et al.  Sexual Differentiation of the Brain , 2009 .

[7]  S. Pellis,et al.  Play fighting in androgen-insensitive tfm rats: evidence that androgen receptors are necessary for the development of adult playful attack and defense. , 2006, Developmental psychobiology.

[8]  A. Arnold,et al.  Minireview: Sex chromosomes and brain sexual differentiation. , 2004, Endocrinology.

[9]  T. Insel,et al.  The ontogeny of excitatory amino acid receptors in rat forebrain—I.N-methyl-d-aspartate and quisqualate receptors , 1990, Neuroscience.

[10]  Ivo D. Dinov,et al.  Sex Matters during Adolescence: Testosterone-Related Cortical Thickness Maturation Differs between Boys and Girls , 2012, PloS one.

[11]  Y. Kondo,et al.  Role of septum and preoptic area in regulating masculine and feminine sexual behavior in male rats , 1990, Hormones and Behavior.

[12]  C. Barraclough,et al.  Suppression of spontaneous LH surges in estrogen-treated ovariectomized rats by microimplants of antiestrogens into the preoptic brain , 1989, Brain Research.

[13]  L. Doncarlos,et al.  Astrocytes in the rat medial amygdala are responsive to adult androgens , 2012, The Journal of comparative neurology.

[14]  C. Sisk,et al.  Pubertal hormones, the adolescent brain, and the maturation of social behaviors: Lessons from the Syrian hamster , 2006, Molecular and Cellular Endocrinology.

[15]  B. Hankin Development of Sex Differences in Depressive and Co-Occurring Anxious Symptoms During Adolescence: Descriptive Trajectories and Potential Explanations in a Multiwave Prospective Study , 2009, Journal of clinical child and adolescent psychology : the official journal for the Society of Clinical Child and Adolescent Psychology, American Psychological Association, Division 53.

[16]  W. C. Young,et al.  Organizing action of prenatally administered testosterone propionate on the tissues mediating mating behavior in the female guinea pig. , 1959, Endocrinology.

[17]  H. Cameron,et al.  New Interneurons in the Adult Neocortex: Small, Sparse, but Significant? , 2008, Biological Psychiatry.

[18]  P. Rakić,et al.  Changes of synaptic density in the primary visual cortex of the macaque monkey from fetal to adult stage , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[19]  C. Woolley,et al.  Effects of prepubertal gonadectomy on a male‐typical behavior and excitatory synaptic transmission in the amygdala , 2009, Developmental neurobiology.

[20]  C. Woolley,et al.  Morphological sex differences and laterality in the prepubertal medial amygdala , 2007, The Journal of comparative neurology.

[21]  F. Benes,et al.  Amygdalo‐cortical sprouting continues into early adulthood: Implications for the development of normal and abnormal function during adolescence , 2002, The Journal of comparative neurology.

[22]  P. Huttenlocher Synaptic density in human frontal cortex - developmental changes and effects of aging. , 1979, Brain research.

[23]  W. Le,et al.  Estrogen and progesterone do not activate Fos in AVPV or LHRH neurons in male rats , 2005, Brain Research.

[24]  C. Sisk,et al.  Testosterone programs adult social behavior before and during, but not after, adolescence. , 2009, Endocrinology.

[25]  Y. Arai,et al.  Neuronal death in the developing sexually dimorphic periventricular nucleus of the preoptic area in the female rat: Effect of neonatal androgen treatment , 1989, Neuroscience Letters.

[26]  Y. Arai,et al.  Androgen Enhances Neuronal Degeneration in the Developing Preoptic Area: Apoptosis in the Anteroventral Periventricular Nucleus (AVPvN-POA) , 1994, Hormones and Behavior.

[27]  B. Berdel,et al.  Acetylcholinesterase activity as a marker of maturation of the basolateral complex of the amygdaloid body in the rat , 1996, International Journal of Developmental Neuroscience.

[28]  J. Townsend,et al.  Normal brain development and aging: quantitative analysis at in vivo MR imaging in healthy volunteers. , 2000, Radiology.

[29]  S. Breedlove,et al.  Sex differences and laterality in astrocyte number and complexity in the adult rat medial amygdala , 2008, The Journal of comparative neurology.

[30]  J. Juraska,et al.  Neuron and glia numbers in the basolateral nucleus of the amygdala from preweaning through old age in male and female rats: A stereological study , 2009, The Journal of comparative neurology.

[31]  H. Uylings,et al.  Postnatal volumetric development of the prefrontal cortex in the rat , 1985, The Journal of comparative neurology.

[32]  Y. Arai,et al.  Estrogen and apoptosis in the developing sexually dimorphic preoptic area in female rats , 1996, Neuroscience Research.

[33]  F. Davis,et al.  Pre- and postnatal influence of testosterone propionate and diethylstilbestrol on differentiation of the sexually dimorphic nucleus of the preoptic area in male and female rats , 1984, Brain Research.

[34]  S. Andersen Trajectories of brain development: point of vulnerability or window of opportunity? , 2003, Neuroscience & Biobehavioral Reviews.

[35]  Lennart Heimer,et al.  The basolateral amygdaloid complex as a cortical-like structure , 1988, Brain Research.

[36]  A. Toga,et al.  Localizing Age-Related Changes in Brain Structure between Childhood and Adolescence Using Statistical Parametric Mapping , 1999, NeuroImage.

[37]  H. Moore,et al.  Prefrontal cortical inputs to the basal amygdala undergo pruning during late adolescence in the rat , 2010, The Journal of comparative neurology.

[38]  S. Swithers,et al.  Influence of ovarian hormones on development of ingestive responding to alterations in fatty acid oxidation in female rats , 2008, Hormones and Behavior.

[39]  J. Juraska,et al.  Sex differences in the gross size of the rat neocortex , 1992, The Journal of comparative neurology.

[40]  R. Mills,et al.  Prepubertal testosterone treatment of neonatally gonadectomized male rats: Defeminization and masculinization of behavioral and endocrine function in adulthood , 1995, Neuroscience & Biobehavioral Reviews.

[41]  J. Juraska,et al.  Increases in size and myelination of the rat corpus callosum during adulthood are maintained into old age , 2007, Brain Research.

[42]  P S Goldman-Rakic,et al.  Synaptogenesis in the prefrontal cortex of rhesus monkeys. , 1994, Cerebral cortex.

[43]  J. Juraska,et al.  Neonatal cryoanesthesia affects the morphology of the visual cortex in the adult rat. , 1998, Brain research. Developmental brain research.

[44]  J. Juraska,et al.  A re-examination of sex differences in axon density and number in the splenium of the rat corpus callosum , 1996, Brain Research.

[45]  J. H. Kim,et al.  Myelination in the splenium of the corpus callosum in adult male and female rats. , 2000, Brain research. Developmental brain research.

[46]  J. Juraska,et al.  Sex differences in neuron number in the binocular area of the rat visual cortex , 1992, The Journal of comparative neurology.

[47]  Alan C. Evans,et al.  Brain development during childhood and adolescence: a longitudinal MRI study , 1999, Nature Neuroscience.

[48]  R. Gorski,et al.  Structural sexual dimorphisms in the anteroventral periventricular nucleus of the rat hypothalamus are sensitive to gonadal steroids perinatally, but develop peripubertally. , 1996, Neuroendocrinology.

[49]  J. Juraska,et al.  Ovarian hormones after postnatal day 20 reduce neuron number in the rat primary visual cortex. , 2002, Journal of neurobiology.

[50]  William D S Killgore,et al.  Sex-specific developmental changes in amygdala responses to affective faces , 2001, Neuroreport.

[51]  C. D. Jacobson,et al.  Formation of the sexually dimorphic nucleus of the preoptic area: neuronal growth, migration and changes in cell number. , 1985, Brain research.

[52]  C. Kellogg,et al.  Gonadal hormones during puberty organize environment-related social interaction in the male rat , 1990, Hormones and Behavior.

[53]  C. Woolley,et al.  Sexually Dimorphic Synaptic Organization of the Medial Amygdala , 2005, The Journal of Neuroscience.

[54]  J. Juraska,et al.  Pubertal ovarian hormone exposure reduces the number of myelinated axons in the splenium of the rat corpus callosum , 2008, Experimental Neurology.

[55]  J. Juraska,et al.  Sex differences in the development of axon number in the splenium of the rat corpus callosum from postnatal day 15 through 60. , 1997, Brain research. Developmental brain research.

[56]  N. Forger Cell Death and Sexual Differentiation of the Nervous System , 2006 .

[57]  S. Tobet,et al.  Estrogenic control of preoptic area development in a carnivore, the ferret , 1996, Cellular and Molecular Neurobiology.

[58]  S. Breedlove,et al.  Androgen receptors mediate masculinization of astrocytes in the rat posterodorsal medial amygdala during puberty , 2013, The Journal of comparative neurology.

[59]  R. Gorski,et al.  The role of apoptosis in sexual differentiation of the rat sexually dimorphic nucleus of the preoptic area , 1996, Brain Research.

[60]  S. Wiegand,et al.  Discrete lesions reveal functional heterogeneity of suprachiasmatic structures in regulation of gonadotropin secretion in the female rat. , 1982, Neuroendocrinology.

[61]  P. Huttenlocher,et al.  Regional differences in synaptogenesis in human cerebral cortex , 1997, The Journal of comparative neurology.

[62]  J. Juraska,et al.  Sex differences in the number of synaptic junctions in the binocular area of the rat visual cortex , 1995, The Journal of comparative neurology.

[63]  C. Sisk,et al.  Puberty and the maturation of the male brain and sexual behavior: recasting a behavioral potential , 2002, Neuroscience & Biobehavioral Reviews.

[64]  Julie A. Markham,et al.  Neuron number decreases in the rat ventral, but not dorsal, medial prefrontal cortex between adolescence and adulthood , 2007, Neuroscience.

[65]  A. McDonald Cortical pathways to the mammalian amygdala , 1998, Progress in Neurobiology.

[66]  J. Rapoport,et al.  Quantitative MRI of the temporal lobe, amygdala, and hippocampus in normal human development: Ages 4–18 years , 1995, The Journal of comparative neurology.

[67]  A. Ruiz-Marcos,et al.  Developmental sex differences and effect of ovariectomy on the number of cortical pyramidal cell dendritic spines , 1990, Brain Research.

[68]  H. Uylings,et al.  Cytoarchitectonic development of the prefrontal cortex in the rat , 1985, The Journal of comparative neurology.

[69]  G. Bartzokis,et al.  Age-related changes in frontal and temporal lobe volumes in men: a magnetic resonance imaging study. , 2001, Archives of general psychiatry.

[70]  J. S. Lund,et al.  Synchronous development of pyramidal neuron dendritic spines and parvalbumin-immunoreactive chandelier neuron axon terminals in layer III of monkey prefrontal cortex , 1995, Neuroscience.