Literature DB >> 8006224

Effects of estrogen on the number of neurons expressing beta-endorphin in the medial basal hypothalamus of the female guinea pig.

J E Thornton1, M D Loose, M J Kelly, O K Rönnekleiv.   

Abstract

The distribution pattern of immunoreactive beta-endorphin neurons was studied in female guinea pigs that were ovariectomized, and one week later were injected with 25 micrograms estradiol benzoate or oil. The animals (5 from each group) were perfused after 24 hours with 4% paraformaldehyde. The locations of beta-endorphin cells and fibers were determined using avidin-biotin immunohistochemistry on free-floating vibratome sections. beta-endorphin-immunoreactive fibers were distributed widely throughout specific regions of the rostral forebrain, similar to what has been described in other species. beta-endorphin cell bodies were found in the arcuate nucleus and in adjacent ventrolateral areas throughout the rostrocaudal extent of the basal hypothalamus. Cells immunoreactive to beta-endorphin were also present in the caudal part of the ventromedial nucleus of the hypothalamus. The number of beta-endorphin neurons was quantified in anatomically matched sections through the rostral, medial and caudal basal hypothalamus of estradiol benzoate- and oil-treated guinea pigs. Analysis of variance revealed that the number of immunoreactive beta-endorphin cells was significantly increased in all regions of the basal hypothalamus of estrogen-treated guinea pigs as compared to vehicle-treated animals (P < 0.01). These data indicate that in the guinea pig, the number of neurons expressing beta-endorphin is increased in the arcuate nucleus 24 hours after estrogen treatment.

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Year:  1994        PMID: 8006224     DOI: 10.1002/cne.903410107

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  31 in total

1.  Estrogen modulation of two subpopulations of β-endorphin neurons in ovariectomized guinea pigs distinguished by peripherally injected fluorogold.

Authors:  M D Loose; J C Niu; T T Nguyen; J E Thornton
Journal:  Endocrine       Date:  1995-11       Impact factor: 3.633

2.  Pronociceptive and antinociceptive effects of estradiol through endogenous opioid neurotransmission in women.

Authors:  Yolanda R Smith; Christian S Stohler; Thomas E Nichols; Joshua A Bueller; Robert A Koeppe; Jon-Kar Zubieta
Journal:  J Neurosci       Date:  2006-05-24       Impact factor: 6.167

Review 3.  Diverse actions of estradiol on anorexigenic and orexigenic hypothalamic arcuate neurons.

Authors:  Todd L Stincic; Oline K Rønnekleiv; Martin J Kelly
Journal:  Horm Behav       Date:  2018-04-21       Impact factor: 3.587

Review 4.  Estradiol and the control of feeding behavior.

Authors:  H M Rivera; T L Stincic
Journal:  Steroids       Date:  2017-11-24       Impact factor: 2.668

Review 5.  Minireview: neural signaling of estradiol in the hypothalamus.

Authors:  Martin J Kelly; Oline K Rønnekleiv
Journal:  Mol Endocrinol       Date:  2015-03-09

6.  Gonadal steroids differentially modulate the actions of orphanin FQ/nociceptin at a physiologically relevant circuit controlling female sexual receptivity.

Authors:  A Borgquist; V M Rivas; M Kachani; K Sinchak; E J Wagner
Journal:  J Neuroendocrinol       Date:  2014-05       Impact factor: 3.627

Review 7.  Oestrogen modulates hypothalamic control of energy homeostasis through multiple mechanisms.

Authors:  T A Roepke
Journal:  J Neuroendocrinol       Date:  2008-12-06       Impact factor: 3.627

Review 8.  A selective membrane estrogen receptor agonist maintains autonomic functions in hypoestrogenic states.

Authors:  Martin J Kelly; Oline K Rønnekleiv
Journal:  Brain Res       Date:  2013-03-25       Impact factor: 3.252

Review 9.  Cross-talk between membrane-initiated and nuclear-initiated oestrogen signalling in the hypothalamus.

Authors:  T A Roepke; J Qiu; M A Bosch; O K Rønnekleiv; M J Kelly
Journal:  J Neuroendocrinol       Date:  2009-03       Impact factor: 3.627

Review 10.  Membrane-initiated estrogen signaling via Gq-coupled GPCR in the central nervous system.

Authors:  Gwyndolin Vail; Troy A Roepke
Journal:  Steroids       Date:  2018-01-31       Impact factor: 2.668

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