Neurotransmitter-controlled steroid hormone receptors in the central nervous system

Results are discussed indicating that neurotransmitters affect steroid hormone activity not only by controlling via neuroendocrine events the hypophysial-gonadal and hypophysial-adrenal axes, but also by modulating cell responsiveness to steroids in target cells. Hyper- or hypoactivity of pineal ner...

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Autores principales: Cardinali, D.P., Vacas, M.I., Ritta, M.N., Gejman, P.V.
Formato: JOUR
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_01970186_v5_n2_p185_Cardinali
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spelling todo:paper_01970186_v5_n2_p185_Cardinali2023-10-03T15:09:53Z Neurotransmitter-controlled steroid hormone receptors in the central nervous system Cardinali, D.P. Vacas, M.I. Ritta, M.N. Gejman, P.V. Results are discussed indicating that neurotransmitters affect steroid hormone activity not only by controlling via neuroendocrine events the hypophysial-gonadal and hypophysial-adrenal axes, but also by modulating cell responsiveness to steroids in target cells. Hyper- or hypoactivity of pineal nerves result in enhancement or impairment of estradiol and testosterone effects on pineal metabolism in vivo and in vitro. Pineal cytoplasmic and nuclear estrogen and androgen receptors are modulated by norepinephrine released from nerve endings at the pinealocyte level. Neural activity affects the cycle of depletion-replenishment of pineal estrogen receptors following estradiol administration. Another site of modulation of steroid effects on the pinealocytes is the intracellular metabolism of testosterone and progesterone; nerve activity has a positive effect on testosterone aromatization and a negative effect on testosterone and progesterone 5α-reduction. NE activity on the pineal cells is mediated via β-adrenoceptors and cAMP. In the central nervous system information on the neurotransmitter modulation of steroid hormone action includes the following observations: (a) hypothalamic deafferentation depresses estrogen receptor levels in rat medial basal hypothalamus; (b) changes in noradrenergic transmission affect, via α-adrenoceptors, the estradiol-induced increase of cytosol progestin receptor concentration in guinea pig hypothalamus; (c) cAMP increases testosterone aromatization in cultured neurons from turtle brain; (d) electrical stimulation of dorsal hippocampus augments, and reserpine or 6-hydroxydopamine treatment decrease, corticoid binding in cat hypothalamus. In the adenohypophysis changes in dopaminergic input after median eminence lesions or bromocriptine treatment of rats result in opposite modifications of pituitary estrogen receptor levels. Therefore all these observations support the view that neurotransmitters can modulate the attachment of steroid hormones to their receptors in target cells. © 1983. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_01970186_v5_n2_p185_Cardinali
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
description Results are discussed indicating that neurotransmitters affect steroid hormone activity not only by controlling via neuroendocrine events the hypophysial-gonadal and hypophysial-adrenal axes, but also by modulating cell responsiveness to steroids in target cells. Hyper- or hypoactivity of pineal nerves result in enhancement or impairment of estradiol and testosterone effects on pineal metabolism in vivo and in vitro. Pineal cytoplasmic and nuclear estrogen and androgen receptors are modulated by norepinephrine released from nerve endings at the pinealocyte level. Neural activity affects the cycle of depletion-replenishment of pineal estrogen receptors following estradiol administration. Another site of modulation of steroid effects on the pinealocytes is the intracellular metabolism of testosterone and progesterone; nerve activity has a positive effect on testosterone aromatization and a negative effect on testosterone and progesterone 5α-reduction. NE activity on the pineal cells is mediated via β-adrenoceptors and cAMP. In the central nervous system information on the neurotransmitter modulation of steroid hormone action includes the following observations: (a) hypothalamic deafferentation depresses estrogen receptor levels in rat medial basal hypothalamus; (b) changes in noradrenergic transmission affect, via α-adrenoceptors, the estradiol-induced increase of cytosol progestin receptor concentration in guinea pig hypothalamus; (c) cAMP increases testosterone aromatization in cultured neurons from turtle brain; (d) electrical stimulation of dorsal hippocampus augments, and reserpine or 6-hydroxydopamine treatment decrease, corticoid binding in cat hypothalamus. In the adenohypophysis changes in dopaminergic input after median eminence lesions or bromocriptine treatment of rats result in opposite modifications of pituitary estrogen receptor levels. Therefore all these observations support the view that neurotransmitters can modulate the attachment of steroid hormones to their receptors in target cells. © 1983.
format JOUR
author Cardinali, D.P.
Vacas, M.I.
Ritta, M.N.
Gejman, P.V.
spellingShingle Cardinali, D.P.
Vacas, M.I.
Ritta, M.N.
Gejman, P.V.
Neurotransmitter-controlled steroid hormone receptors in the central nervous system
author_facet Cardinali, D.P.
Vacas, M.I.
Ritta, M.N.
Gejman, P.V.
author_sort Cardinali, D.P.
title Neurotransmitter-controlled steroid hormone receptors in the central nervous system
title_short Neurotransmitter-controlled steroid hormone receptors in the central nervous system
title_full Neurotransmitter-controlled steroid hormone receptors in the central nervous system
title_fullStr Neurotransmitter-controlled steroid hormone receptors in the central nervous system
title_full_unstemmed Neurotransmitter-controlled steroid hormone receptors in the central nervous system
title_sort neurotransmitter-controlled steroid hormone receptors in the central nervous system
url http://hdl.handle.net/20.500.12110/paper_01970186_v5_n2_p185_Cardinali
work_keys_str_mv AT cardinalidp neurotransmittercontrolledsteroidhormonereceptorsinthecentralnervoussystem
AT vacasmi neurotransmittercontrolledsteroidhormonereceptorsinthecentralnervoussystem
AT rittamn neurotransmittercontrolledsteroidhormonereceptorsinthecentralnervoussystem
AT gejmanpv neurotransmittercontrolledsteroidhormonereceptorsinthecentralnervoussystem
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