Literature DB >> 11123512

Oestrogen-induced changes in the synaptology of the monkey (Cercopithecus aethiops) arcuate nucleus during gonadotropin feedback.

A Zsarnovszky1, T L Horvath, L M Garcia-Segura, B Horvath, F Naftolin.   

Abstract

To assess their role in the regulation of gonadotropin secretion in primates, we determined the number of synaptic connections on gondotropin releasing hormone (GnRH)- and non-GnRH neurones of the arcuate nucleus of ovariectomized (OVX) and OVX plus oestradiol benzoate-treated African green monkeys. After 24 h (day 1), 48 h (day 2) and 8 days (day 8), we performed immunostaining for GnRH. Using electron microscopy, synapses on GnRH- and randomly selected non-GnRH neurones were counted and characterized according to the classification of Gray (symmetric/inhibitory or asymmetric/excitatory). Serum concentrations of oestradiol (OVX) needed to 232 pg/ml on day 1, 63 pg/ml on day 2 and 45 pg/ml on day 8. Concentrations of luteinizing hormone (LH) fell after ovariectomy to 9 microg/ml on day 1, surged to 93 microg/ml on day 2 and declined again by day 8. (a) Ten days after ovariectomy, there were no synapses on GnRH neurones, whereas non-GnRH cells received substantial inhibitory innervation and moderate excitatory input. (b) On day 1, GnRH neurones had highest numbers of inhibitory synapses, while inhibitory synapses on non-GnRH neurones decreased, whereas numbers of excitatory synapses remained relatively unchanged compared to OVX monkeys. (c) By day 2, synapses on GnRH neurones decreased, while synapses increased on non-GnRH cells compared to day 1. (d) On day 8, the most pronounced alteration on GnRH cells was an elevated inhibitory input while non-GnRH neurones received the fewest synapses compared to day 2. We conclude that during an oestrogen-induced LH surge, synapses on GnRH- and mixed non-GnRH neurones are differentially regulated. These findings suggest that oestrogen modulation of arcuate nucleus synapses may be important in the regulation of gonadotropin secretion in monkeys.

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Year:  2001        PMID: 11123512     DOI: 10.1046/j.1365-2826.2001.00602.x

Source DB:  PubMed          Journal:  J Neuroendocrinol        ISSN: 0953-8194            Impact factor:   3.627


  5 in total

1.  Rapid signaling of estrogen to WAVE1 and moesin controls neuronal spine formation via the actin cytoskeleton.

Authors:  Angel Matias Sanchez; Marina Ines Flamini; Xiao-Dong Fu; Paolo Mannella; Maria Silvia Giretti; Lorenzo Goglia; Andrea Riccardo Genazzani; Tommaso Simoncini
Journal:  Mol Endocrinol       Date:  2009-05-21

2.  Neuroanatomical organization of gonadotropin-releasing hormone neurons during the oestrus cycle in the ewe.

Authors:  Martine Batailler; Alain Caraty; Benoît Malpaux; Yves Tillet
Journal:  BMC Neurosci       Date:  2004-11-22       Impact factor: 3.288

3.  Ecto-nucleoside triphosphate diphosphohydrolase 3 in the ventral and lateral hypothalamic area of female rats: morphological characterization and functional implications.

Authors:  David S Kiss; Attila Zsarnovszky; Krisztina Horvath; Andrea Gyorffy; Tibor Bartha; Diana Hazai; Peter Sotonyi; Virag Somogyi; Laszlo V Frenyo; Sabrina Diano
Journal:  Reprod Biol Endocrinol       Date:  2009-04-22       Impact factor: 5.211

Review 4.  NTPDases in the neuroendocrine hypothalamus: possible energy regulators of the positive gonadotrophin feedback.

Authors:  Attila Zsarnovszky; Tibor Bartha; Laszlo V Frenyo; Sabrina Diano
Journal:  Reprod Biol Endocrinol       Date:  2009-06-16       Impact factor: 5.211

5.  Preparation of purified perikaryal and synaptosomal mitochondrial fractions from relatively small hypothalamic brain samples.

Authors:  David S Kiss; Istvan Toth; Gergely Jocsak; Agnes Sterczer; Tibor Bartha; Laszlo V Frenyo; Attila Zsarnovszky
Journal:  MethodsX       Date:  2016-05-19
  5 in total

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