The biosynthesis and secretion of somatostatin (SRIH) within the hypothalamic periventricular-median eminence (PeN-ME) pathway follows a sexually differentiated developmental pattern beginning in the early neonatal period. It is generally accepted that testosterone plays a role in these processes, but the mechanisms underlying the age and sex differences are poorly understood. The present study sought to investigate the hypothesis that γ-aminobutyric acid (GABA) may play a role in determining sex differences in SRIH neuronal activity. Using an in vitro hypothalamic preparation where more than 97% of the immunoreactive SRIH is contained within the PeN-ME pathway, peptide release in response to the GABAA receptor antagonist, bicuculline, was followed through development. In the male a stimulatory response, indicative of an inhibitory GABAergic tone on SRIH secretion, was observed as early as postnatal day (P) 5. This persisted throughout juvenile development (P10, P17) and was present also in the adult male (P75), but in the peripubertal period the response to bicuculline was first lost (P25) and then reversed to an inhibition (P40), suggesting a transient switch to an apparent stimulatory GABAergic tone on SRIH release. By contrast, in the female, no bicuculline responsiveness was seen until P25 when it caused a decrease in SRIH release which persisted into adulthood. Using in situ hybridization studies we found no evidence to support the view that these age- and sex-dependent differences were due to changes in the expression of GABAA receptor α-subunits (α1 and α2) which are colocalised in the PeN SRIH neurons. Following adult gonadectomy, the bicuculline response was abolished in the male, whereas, in the female it was reversed and identical in magnitude to the response in the intact male. These results demonstrate marked sex differences in GABAA-receptor-mediated influences on SRIH release which develop soon after birth and, in the adult, depend on gonadal factors. In the male these factors activate a primarily inhibitory influence, whereas in the female they facilitate an apparently stimulatory tone of GABA on SRIH secretion via the GABAA receptor. Our findings thus support the view that GABAergic transmission may play a key role in generating sex differences in the mode of SRIH secretion from the hypothalamus which has been shown to be a major factor in determining the sexually dimorphic patterns of growth hormone secretion.

1.
Chowen-Breed JA, Steiner RA, Clifton DK: Sexual dimorphism and testosterone-dependent regulation of somatostatin gene expression in the periventricular nucleus of the rat brain. Endocrinology 1989;125:357–362.
2.
Murray HE, Simonian SX, Herbison AE, Gillies GE: Correlation of hypothalamic somatostatin mRNA and peptide content with secretion: Sexual dimorphism and differential regulation by gonadal factors. J Neuroendocrinol 1999;11:27–33.
3.
Murray HE, Simonian SX, Herbison AE, Gillies GE: Ontogeny and sexual differentiation of somatostatin biosynthesis and secretion in the hypothalamic periventricular-median eminence pathway. J Neuroendocrinol 1999;11:35–42.
4.
Argente J, Chowen-Breed JA, Steiner RA, Clifton DK: Somatostatin messenger RNA in hypothalamic neurones is increased by testosterone through activation of androgen receptors and not by aromatization to estradiol. Neuroendocrinology 1990;52:342–349.
5.
Chowen JA, Argente J, Gonzalezparra S, Garciasegura LM: Differential effects of the neonatal and adult sex steroid environments on the organization and activation of hypothalamic growth hormone-releasing hormone and somatostatin neurons. Endocrinology 1993;133:2792–2802.
6.
Simonian SX, Murray HE, Gillies GE, Herbison AE: Estrogen dependent ontogeny of sex differences in somatostatin neurons of the hypothalamic periventricular nucleus. Endocrinology 1998;139:1420–1428.
7.
Herbison AE: Sexually dimorphic expression of androgen receptor immunoreactivity by somatostatin neurones in the rat hypothalamic periventricular nucleus and the bed nucleus of the stria terminalis. J Neuroendocrinol 1995;7:543–553.
8.
Painson JC, Thorner MO, Krieg RJ, Tannenbaum GS: Short term adult exposure to estradiol feminizes the male pattern of spontaneous and growth hormone-releasing factor-stimulated growth hormone secretion in the rat. Endocrinology 1992;130:511–519.
9.
Herbison AE, Theodosis DT: Absence of estrogen receptor immunoreactivity in somatostatin (SRIF) neurons of the periventricular nucleus but sexually dimorphic colocalization of estrogen receptor and SRIF immunoreactivities in neurons of the bed nucleus of the stria terminalis. Endocrinology 1993;132:1707–1714.
10.
Simonian SX, Herbison AE: Differential expression of estrogen receptor α and β immunoreactivity by oxytocin neurons of rat paraventricular nucleus. J Neuroendocrinol 1997;9:803–806.
11.
Ishikawa K, Taniguchi Y, Kurosumi K: Immunohistochemical identification of somatostatin-containing neurons projecting to the median eminence of the rat. Endocrinology 1987;121:94–97.
12.
Willoughby JO, Beroukas D, Blessing WW: Ultrastructural evidence for gamma-aminobutyric acid-immunoreactive synapses on somatostatin-immunoreactive perikarya in the periventricular anterior hypothalamus. Neuroendocrinology 1987;46:268–272.
13.
Rage F, Jalaguier S, Rougeot C, TapiaArancibia L: GABA inhibition of somatostatin gene-expression in cultured hypothalamic neurons. Neuroreport 1993;4:320–322.
14.
Rage F, Rougeot C, TapiaArancibia L: GABAA and NMDA receptor activation controls somatostatin messenger RNA expression in primary cultures of hypothalamic neurons. Neuroendocrinology 1994;60:470–476.
15.
Gillies GE, Davidson K: GABA-ergic influences on somatostatin secretion from hypothalamic neurones cultured in defined medium. Neuroendocrinology 1992;55:248–256.
16.
Rage F, Benyassi A, Arancibia S, Tapia Arancibia L: Gamma-aminobutyric acid-glutamate interactions in control of SRIH release from hypothalamic neurons in primary culture: In vivo corroboration. Endocrinology 1992;130:1056–1062.
17.
Arancibia S, Estupina C, Pesco J, Belmar J, TapiaArancibia L: Responsiveness to depolarization of hypothalamic neurons secreting somatostatin under stress and estrous cycle conditions: Involvement of GABAergic and steroidal interactions. J Neurosci Res 1997;50:575–584.
18.
Herbison AE, Augood SJ: Expression of GABAA receptor alpha(2) subunit messenger-RNA by periventricular somatostatin neurons in the rat hypothalamus. Neurosci Lett 1994;173:9–13.
19.
Pericic D, Maneu H, Lakic N: Sex differences in the response of rats to drugs affecting GABA-ergic transmission. Life Sci 1985;36:541–547.
20.
Perez J, Zucchi I, Maggi A: Sexual dimorphism in the response of the GABA-ergic system to estrogen administration. J Neurochem 1986;47:1798–1803.
21.
Carbone S, Szwarcfarb B, Moguilevsky JA: Differences in the effect of ovarian hormones on hypothalamic GABA-ergic activity and on LH-release during sexual-maturation in female rats. Neuroendocr Lett 1992;14:103–111.
22.
Herbison AE: Estrogen regulation of GABA transmission in rat preoptic area. Brain Res Bull 1997;44:321–326.
23.
Herbison AE, Augood SJ, McGowan E: Expression of glutamic acid decarboxylase messenger RNA in rat medial preoptic area neurons during the oestrous cycle and after ovariectomy. Mol Brain Res 1992;14:310–316.
24.
Duvilanzki BH, Munoz-Maines V, Debeljuk L: GABA-related enzymes in the hypothalamus of rats treated with estradiol. Eur J Pharmacol 1983;89:259–264.
25.
Herbison AE, Fenelon VS: Estrogen regulation of GABAA receptor subunit messenger-RNA expression in preoptic area and bed nucleus of the stria terminalis of female rat brain. J Neurosci 1995;15:2328–2337.
26.
Jussofie A: Steroid modulation of central nervous GABAA receptor binding in three female rat brain areas during postnatal development. Dev Neurosci 1995;17:335–342.
27.
Morisette M, DiPaolo T: Sex and estrous cycle variations of rat striatal dopamine uptake sites. Neuroendocrinology 1993;58:16–22.
28.
McAbee MD, DonCarlos LL: Ontogeny of region-specific sex differences in androgen receptor messenger ribonucleic acid expression in the rat forebrain. Endocrinology 1998;139:1738–1745.
29.
Fenelon VS, Herbison AE: In-vivo regulation of specific GABAA receptor subunit messenger-RNAs by increased GABA concentrations in rat brain. Neuroscience 1996;7:661–670.
30.
Swanson L: Brain Maps: Structure of the Rat Brain. Amsterdam; Elsevier, 1992.
31.
Laurie DJ, Wisden W, Seeberg PH: The distribution of thirteen GABAA receptor subunit mRNAs in the rat brain. III. Embryonic and postnatal development. J Neurosci 1992;12:4151–4172.
32.
Bourguignon JP, Gerard A, Purnelle G, Czajkowski V, Yamanaka C, Lemaitre M, Rigo JM, Moonen G, Franchimont P: Duality of glutamatergic and GABA-ergic control of pulsatile GnRH secretion by rat hypothalamic explants. 2. Reduced NR2C- and GABAA receptor-mediated inhibition at initiation of sexual maturation. J Neuroendocrinol 1997;9:193–199.
33.
Szwarcfarb B, Carbone S, Stein ML, Medina J, Moguilevsky JA: Sexual differences in the effect of the GABA-ergic system on LH secretion and in the hypothalamic ontogeny of GABAA receptors in prepubertal rats. Brain Res 1994;646:351–355.
34.
McKernan RM, Fox P, Gillard NP, Whiting P: Differential expression of GABAA receptor alpha subunits in rat brain development. FEBS Lett 1991;286:44–46.
35.
Fritschy JM, Paysan J, Enna A, Mohler H: Switch in the expression of rat GABAA-receptor subtypes during postnatal development: An immunohistochemical study. J Neurosci 1994;14:5302–5324.
36.
Grattan DR, Rocca MS, Sagrillo CA, McCarthy MM, Selmanoff M: Antiandrogen microimplants into the rostral medial preoptic area decrease gamma-aminobutyric acidergic neuronal-activity and increase luteinizing-hormone secretion in the intact male rat. Endocrinology 1996;137:4167–4173.
37.
Lasaga M, Seilicovich A, Delcarmendiaz M, Pisera D, Debeljuk L, Duvilanski B: Effect of sex steroids on hypothalamic GABA. Neuroendocri Lett 1994;16:111–119.
38.
MacLusky NJ, Naftolin F: Sexual differentiation of the central nervous system. Science 1981;211:1294–1311.
39.
McCarthy MM, Davis AM, Mong JA: Excitatory neurotransmission and sexual differentiation of the brain. Brain Res Bull 1997;44:487–495.
40.
Davis AM, Ward SC, Selmanoff M, Herbison AE, McCarthy MM: Developmental sex differences in amino acid neurotransmitter levels in hypothalamic and limbic areas of rat brain. Neuroscience, in press.
41.
Kalia K, Lamsa K, Smirnov S, Taira T, Voipio J: Long-lasting GABA-mediated depolarization evoked by high-frequency stimulation in pyramidal neurons of rat hippocampal slice is attributable to a network-driven, bicarbonate-dependent K transient. J Neurosci 1997;17:7662–7672.
42.
Wagner S, Castel M, Gainer H, Yarom H: GABA in the mammalian suprachiasmatic nucleus and its role in diurnal rhythmicity. Nature 1998;387:598–603.
43.
Plotsky P, Vale W: Patterns of growth hormone releasing factor and somatostatin secretion into the hypophysial portal circulation of the rat. Science 1985;230:461–463.
44.
Arancibia S, Lyonnet D, Roussel JP, Ixart G, Astier H: The inhibitory effect of picrotoxin on basal and cold-induced thyrotropin secretion involves somatostatin mediation. Neurosci Lett 1995;185:139–143.
45.
Clarke RG, Robinson ICAF: Growth hormone responses to multiple injections of a fragment of human growth hormone-releasing factor in the conscious male and female rat. J Endocrinol 1985;106:281–289.
46.
Gabriel S, Millard W, Koenig J, Badger T, Russell W, Maiter D, Martin J: Sexual and developmental differences in peptides regulating growth hormone secretion in the rat. Neuroendocrinology 1989;50:299–307.
47.
Jansson JO, Eden S, Isaksson O: Sexual dimorphism in the control of growth hormone secretion. Endocr Rev 1985;6:128–150.
48.
Tannenbaum GS, Ling N: The interrelationship of growth hormone (GH)-releasing factor and somatostatin in generation of the ultradian rhythm of GH secretion. Endocrinology 1984;115:1952–1957.
49.
Painson JC, Tannenbaum G: Sexual dimorphism of somatostatin and growth hormone-releasing factor signalling in the control of pulsatile growth hormone secretion in the rat. Endocrinology 1991;128:2858–2866.
50.
Eden S: Age- and sex-related differences in episodic growth hormone secretion in the rat. Endocrinology 1979;105:555–560.
51.
Ojeda SR, Jameson HE: Developmental patterns of plasma and pituitary growth hormone (GH) in the female rat. Endocrinology 1977;100:881–889.
Copyright / Drug Dosage / Disclaimer
Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.
You do not currently have access to this content.