Postnatal Handling Increases the Expression of cAMP-Inducible Transcription Factors in the Rat Hippocampus: The Effects of Thyroid Hormones and Serotonin

Postnatal handling increases glucocorticoid receptor expression in the rat hippocampus, thus altering the regulation of hypothalamic synthesis of corticotropin-releasing hormone and the hypothalamic–pituitary–adrenal response to stress. The effect on glucocorticoid receptor gene expression represents one mechanism by which the early environment can exert a long-term effect on neural development. The handling effect on hippocampal glucocorticoid receptor expression is dependent on peripheral thyroid hormone release and the activation of ascending serotonergic pathways. In primary hippocampal cell cultures, serotonin (5-HT) increases glucocorticoid receptor expression, and this effect appears to be mediated by increased cAMP levels. In the current studies we examined the in vivoeffects of handling on hippocampal cAMP–protein kinase A (PKA) activity. In 7-d-old rat pups, we found that (1) postnatal handling increased adenylyl cyclase activity and hippocampal cAMP levels, (2) the effect of handling on cAMP levels was completely blocked by treatment with either propylthiouracil (PTU), a thyroid hormone synthesis inhibitor, or the 5-HT receptor antagonist, ketanserin, and (3) handling also increased hippocampal PKA activity. We then examined the effects of handling on cAMP-inducible transcription factors. Handling rapidly increased levels of the mRNAs for nerve growth factor-inducible factor A (NGFI-A) (zif268,krox24) and activator protein-2 (AP-2) as well as for NGFI-A and AP-2 immunoreactivity throughout the hippocampus. Finally, we found that the effects of handling on NGFI-A and AP-2 expression were significantly reduced by concurrent treatment with either PTU or ketanserin, effects that paralleled those on cAMP formation. NGFI-A and AP-2 have been implicated in the regulation of glucocorticoid receptor expression during development. Thus, these findings suggest that postnatal handling might alter glucocorticoid receptor gene expression via cAMP–PKA pathways involving the activation of NGFI-A and AP-2.

[1]  M. Meaney,et al.  Nongenomic transmission across generations of maternal behavior and stress responses in the rat. , 1999, Science.

[2]  M. Campillos,et al.  Transcription factor AP‐2 activity is modulated by protein kinase A‐mediated phosphorylation , 1999, FEBS letters.

[3]  G. Levi,et al.  Thyroid hormone effects on Krox-24 transcription in the post-natal mouse brain are developmentally regulated but are not correlated with mitosis , 1999, Oncogene.

[4]  K. Seamon,et al.  Binding of [ 3 H ] forskolin to rat brain membranes , 1999 .

[5]  S. Her,et al.  Phenylethanolamine N-methyltransferase gene expression: synergistic activation by Egr-1, AP-2 and the glucocorticoid receptor. , 1998, Brain research. Molecular brain research.

[6]  U. Kang,et al.  Electroconvulsive shock does not induce c-fos and junB, but TIS1 and TIS8/zif-268, in neonatal rat hippocampus. , 1998, Brain research. Developmental brain research.

[7]  M. Joëls,et al.  Brain corticosteroid receptor balance in health and disease. , 1998, Endocrine reviews.

[8]  Shakti Sharma,et al.  Maternal care, hippocampal glucocorticoid receptors, and hypothalamic-pituitary-adrenal responses to stress. , 1997, Science.

[9]  C. Vargas,et al.  Expression of 5-HT7 receptor mRNA in rat brain during postnatal development , 1997, Neuroscience Letters.

[10]  J. Herman,et al.  Neurocircuitry of stress: central control of the hypothalamo–pituitary–adrenocortical axis , 1997, Trends in Neurosciences.

[11]  J. Zwiller,et al.  5‐Hydroxytryptamine Induces TIS8/egr‐1 and c‐fos Expression in PC12 Cells. Involvement of Tyrosine Protein Phosphorylation , 1997, The European journal of neuroscience.

[12]  Eric R. Kandel,et al.  Cell Adhesion Molecules, CREB, and the Formation of New Synaptic Connections , 1996, Neuron.

[13]  M. Meaney,et al.  The Role of Early Environmental Events in Regulating Neuroendocrine Development: Moms, Pups, Stress, and Glucocorticoid Receptors , 1996, Annals of the New York Academy of Sciences.

[14]  Shakti Sharma,et al.  Early environmental regulation of forebrain glucocorticoid receptor gene expression: implications for adrenocortical responses to stress. , 1996, Developmental neuroscience.

[15]  I. Weiler,et al.  Correspondence between sites of NGFI-A induction and sites of morphological plasticity following exposure to environmental complexity. , 1995, Brain research. Molecular brain research.

[16]  J. Seckl,et al.  Induction of transcription factor AP2 mRNA expression in rat primary afferent neurons during acute inflammation , 1995, Neuroscience Letters.

[17]  S. Detera-Wadleigh,et al.  Characterization of the human glucocorticoid receptor promoter. , 1995, Biochemistry.

[18]  M. Vallejo Transcriptional Control of Gene Expression by cAMP‐Response Element Binding Proteins , 1994, Journal of neuroendocrinology.

[19]  M. Meaney,et al.  Environmental Regulation of the Development of Glucocorticoid Receptor Systems in the Rat Forebrain. The Role of Serotonin , 1994, Annals of the New York Academy of Sciences.

[20]  Michael E. Greenberg,et al.  CREB: A mediator of long-term memory from mollusks to mammals , 1994, Cell.

[21]  P. Mitchell,et al.  Cell type-specific regulation of expression of transcription factor AP-2 in neuroectodermal cells. , 1994, Developmental biology.

[22]  M. Meaney,et al.  Postnatal handling alters glucocorticoid, but not mineralocorticoid messenger RNA expression in the hippocampus of adult rats. , 1994, Brain research. Molecular brain research.

[23]  B. Mellström,et al.  Differential effect of thyroid hormone on NGFI-A gene expression in developing rat brain. , 1994, Endocrinology.

[24]  A. Tsou,et al.  Cloning and Expression of a 5‐Hydroxytryptamine7 Receptor Positively Coupled to Adenylyl Cyclase , 1994, Journal of neurochemistry.

[25]  M. Meaney,et al.  Neonatal handling alters serotonin (5-HT) turnover and 5-HT2 receptor binding in selected brain regions: relationship to the handling effect on glucocorticoid receptor expression. , 1994, Brain research. Developmental brain research.

[26]  M. McMillian,et al.  Ontogeny of Kainate‐Induced Gene Expression in Rat Hippocampus , 1994, Journal of neurochemistry.

[27]  J. Seckl,et al.  Environmental influences on the central nervous system and their implications for the aging rat , 1993, Behavioural Brain Research.

[28]  M. Erlander,et al.  A novel adenylyl cyclase-activating serotonin receptor (5-HT7) implicated in the regulation of mammalian circadian rhythms , 1993, Neuron.

[29]  D. Sibley,et al.  Molecular cloning and expression of a 5-hydroxytryptamine7 serotonin receptor subtype. , 1993, The Journal of biological chemistry.

[30]  J. Plassat,et al.  Molecular cloning of a mammalian serotonin receptor that activates adenylate cyclase. , 1993, Molecular pharmacology.

[31]  M. Meaney,et al.  Early, postnatal experience alters hypothalamic corticotropin-releasing factor (CRF) mRNA, median eminence CRF content and stress-induced release in adult rats. , 1993, Brain research. Molecular brain research.

[32]  Shakti Sharma,et al.  Increased plasma ACTH responses to stress in nonhandled compared with handled rats require basal levels of corticosterone and are associated with increased levels of ACTH secretagogues in the median eminence , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[33]  M. Meaney,et al.  Serotonergic regulation of type II corticosteroid receptor binding in hippocampal cell cultures: Evidence for the importance of serotonin-induced changes in cAMP levels , 1992, Neuroscience.

[34]  Shakti Sharma,et al.  Basal ACTH, corticosterone and corticosterone-binding globulin levels over the diurnal cycle, and age-related changes in hippocampal type I and type II corticosteroid receptor binding capacity in young and aged, handled and nonhandled rats. , 1992, Neuroendocrinology.

[35]  A. Pérez-Castillo,et al.  Thyroid hormone up-regulates NGFI-A gene expression in rat brain during development. , 1992, The Journal of biological chemistry.

[36]  R. Sapolsky,et al.  The role of the hippocampus in feedback regulation of the hypothalamic-pituitary-adrenocortical axis. , 1991, Endocrine reviews.

[37]  R. Sapolsky,et al.  Postnatal handling attenuates certain neuroendocrine, anatomical, and cognitive dysfunctions associated with aging in female rats , 1991, Neurobiology of Aging.

[38]  P. Plotsky,et al.  Pathways to the Secretion of Adrenocorticotropin: A View from the Portal * , 1991, Journal of neuroendocrinology.

[39]  T. Curran,et al.  Proto-oncogene transcription factors and epilepsy. , 1991, Trends in pharmacological sciences.

[40]  R. Tjian,et al.  Transcription factor AP-2 is expressed in neural crest cell lineages during mouse embryogenesis. , 1991, Genes & development.

[41]  M. Meaney,et al.  The role of serotonin in the development and environmental regulation of type II corticosteroid receptor binding in rat hippocampus. , 1990, Brain research. Developmental brain research.

[42]  J. Habener Cyclic AMP response element binding proteins: a cornucopia of transcription factors. , 1990, Molecular endocrinology.

[43]  M. Meaney,et al.  Serotonin regulates type II corticosteroid receptor binding in hippocampal cell cultures , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[44]  D H Aitken,et al.  Neonatal handling alters adrenocortical negative feedback sensitivity and hippocampal type II glucocorticoid receptor binding in the rat. , 1989, Neuroendocrinology.

[45]  D. Brindley,et al.  Possible connections between stress, diabetes, obesity, hypertension and altered lipoprotein metabolism that may result in atherosclerosis. , 1989, Clinical science.

[46]  D. Pfaff,et al.  Graphical and statistical approaches to data analysis for in situ hybridization. , 1989, Methods in enzymology.

[47]  Shakti Sharma,et al.  Postnatal development and environmental regulation of hippocampal glucocorticoid and mineralocorticoid receptors. , 1988, Brain research.

[48]  M. Karin,et al.  Transcription factor AP-2 mediates induction by two different signal-transduction pathways: Protein kinase C and cAMP , 1987, Cell.

[49]  R. Sapolsky,et al.  Thyroid hormones influence the development of hippocampal glucocorticoid receptors in the rat: a mechanism for the effects of postnatal handling on the development of the adrenocortical stress response. , 1987, Neuroendocrinology.

[50]  S. Snyder,et al.  Mapping second messenger systems in the brain: differential localizations of adenylate cyclase and protein kinase C. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[51]  T. Dawson,et al.  Quantitative autoradiography of [3H]forskolin binding sites in the rat brain , 1985, Brain Research.

[52]  M. Meaney,et al.  The effects of early postnatal handling on hippocampal glucocorticoid receptor concentrations: temporal parameters. , 1985, Brain research.

[53]  J. Daly,et al.  Binding of [3H]forskolin to rat brain membranes. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[54]  H. Towbin,et al.  Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[55]  M. M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.

[56]  B. Brown,et al.  A simple and sensitive saturation assay method for the measurement of adenosine 3':5'-cyclic monophosphate. , 1971, The Biochemical journal.