Role of steroid hormones and morphine treatment in the modulation of opioid receptor gene expression in brain structures in the female rat

This study determined the effects of acute treatment with morphine on the expression of the Oprm1, Oprk1, and Oprd1 genes (which encode μ, κ, and δ receptors, respectively) in the striatum, hypothalamus, and periaqueductal gray (PAG) in ovariectomized female rats treated with estrogen. Ovariectomize...

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Main Authors: Cruz, Wesley Soares, Pereira, Lucas Assis, Cezar, Luana Carvalho, Camarini, Rosana, Felicio, Luciano Freitas, Bernardi, Maria Martha, Teodorov, Elizabeth
Format: Online
Language:English
Published: Springer International Publishing 2015
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4503706/
id pubmed-4503706
recordtype oai_dc
spelling pubmed-45037062015-07-17 Role of steroid hormones and morphine treatment in the modulation of opioid receptor gene expression in brain structures in the female rat Cruz, Wesley Soares Pereira, Lucas Assis Cezar, Luana Carvalho Camarini, Rosana Felicio, Luciano Freitas Bernardi, Maria Martha Teodorov, Elizabeth Research This study determined the effects of acute treatment with morphine on the expression of the Oprm1, Oprk1, and Oprd1 genes (which encode μ, κ, and δ receptors, respectively) in the striatum, hypothalamus, and periaqueductal gray (PAG) in ovariectomized female rats treated with estrogen. Ovariectomized female rats were divided into five equal groups. Two groups received estrogen (50 µg/kg, 54 h before testing) and saline (ES group) or 3.5 mg/kg morphine (EM group) 2 h before euthanasia. The SS group received saline solution 54 and 2 h before the experiments. The SM group received saline 54 h and 3.5 mg/kg morphine 2 h before the experiments. The W group remained undisturbed. The genes expression were evaluated. Oprm1 and Oprk1 expression were activated, respectively, in the hypothalamus and PAG and in the striatum and PAG by morphine only in estrogen-treated animals. Oprd1 expression in the hypothalamus and PAG was activated by morphine in both estrogen-treated and -nontreated animals. The Oprm1 and Oprk1 gene response to morphine might depend on estrogen, whereas the Oprd1 gene response to morphine might not depend on estrogen, supporting the hypothesis of a functional role for ovarian hormones in opioid receptor-mediated functional adaptations in the female brain. Springer International Publishing 2015-07-16 /pmc/articles/PMC4503706/ /pubmed/26191482 http://dx.doi.org/10.1186/s40064-015-1021-8 Text en © Cruz et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Cruz, Wesley Soares
Pereira, Lucas Assis
Cezar, Luana Carvalho
Camarini, Rosana
Felicio, Luciano Freitas
Bernardi, Maria Martha
Teodorov, Elizabeth
spellingShingle Cruz, Wesley Soares
Pereira, Lucas Assis
Cezar, Luana Carvalho
Camarini, Rosana
Felicio, Luciano Freitas
Bernardi, Maria Martha
Teodorov, Elizabeth
Role of steroid hormones and morphine treatment in the modulation of opioid receptor gene expression in brain structures in the female rat
author_facet Cruz, Wesley Soares
Pereira, Lucas Assis
Cezar, Luana Carvalho
Camarini, Rosana
Felicio, Luciano Freitas
Bernardi, Maria Martha
Teodorov, Elizabeth
author_sort Cruz, Wesley Soares
title Role of steroid hormones and morphine treatment in the modulation of opioid receptor gene expression in brain structures in the female rat
title_short Role of steroid hormones and morphine treatment in the modulation of opioid receptor gene expression in brain structures in the female rat
title_full Role of steroid hormones and morphine treatment in the modulation of opioid receptor gene expression in brain structures in the female rat
title_fullStr Role of steroid hormones and morphine treatment in the modulation of opioid receptor gene expression in brain structures in the female rat
title_full_unstemmed Role of steroid hormones and morphine treatment in the modulation of opioid receptor gene expression in brain structures in the female rat
title_sort role of steroid hormones and morphine treatment in the modulation of opioid receptor gene expression in brain structures in the female rat
description This study determined the effects of acute treatment with morphine on the expression of the Oprm1, Oprk1, and Oprd1 genes (which encode μ, κ, and δ receptors, respectively) in the striatum, hypothalamus, and periaqueductal gray (PAG) in ovariectomized female rats treated with estrogen. Ovariectomized female rats were divided into five equal groups. Two groups received estrogen (50 µg/kg, 54 h before testing) and saline (ES group) or 3.5 mg/kg morphine (EM group) 2 h before euthanasia. The SS group received saline solution 54 and 2 h before the experiments. The SM group received saline 54 h and 3.5 mg/kg morphine 2 h before the experiments. The W group remained undisturbed. The genes expression were evaluated. Oprm1 and Oprk1 expression were activated, respectively, in the hypothalamus and PAG and in the striatum and PAG by morphine only in estrogen-treated animals. Oprd1 expression in the hypothalamus and PAG was activated by morphine in both estrogen-treated and -nontreated animals. The Oprm1 and Oprk1 gene response to morphine might depend on estrogen, whereas the Oprd1 gene response to morphine might not depend on estrogen, supporting the hypothesis of a functional role for ovarian hormones in opioid receptor-mediated functional adaptations in the female brain.
publisher Springer International Publishing
publishDate 2015
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4503706/
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