Estrogen and progesterone do not activate Fos in AVPV or LHRH neurons in male rats
In rodents, females but not males, in response to escalating levels of estrogen, express a luteinizing hormone (LH) surge that is prompted by a surge in luteinizing hormone-releasing hormone (LHRH). It cannot take place if estrogen-sensitive afferents located in the anteroventral periventricular nuc...
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description | In rodents, females but not males, in response to escalating levels of estrogen, express a luteinizing hormone (LH) surge that is prompted by a surge in luteinizing hormone-releasing hormone (LHRH). It cannot take place if estrogen-sensitive afferents located in the anteroventral periventricular nucleus (AVPV) are either absent or disabled. Males appear to lack the ability to exhibit an LH surge, but it is unclear what level of the CNS contributes to this dimorphic response. This study was conducted to determine whether estrogen followed by progesterone treatment (E + P) of gonadectomized males evokes Fos activation in LHRH and AVPV neurons as it does in females. The results indicated that, consistent with the males' inability to express an LH surge in response to E + P treatment, LHRH and AVPV neurons in males failed to show increased Fos activation. Examination of neuron nuclear antigen (NeuN, a neuron-specific marker), estrogen receptor (ERα) and progesterone receptor (PR) neurons in AVPV neurons indicated that, while essentially all the neurons of the caudal AVPV in males and females are steroid responsive, the male possessed half the number of steroid responsive neurons within the caudal AVPV (where activation of Fos is maximal in females) compared to the female. Together, these data indicate that the male lacks a substantial population of steroid receptive AVPV neurons and is unable to respond to the presence of E and P and activate either AVPV or LHRH neurons. |
doi_str_mv | 10.1016/j.brainres.2005.06.082 |
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It cannot take place if estrogen-sensitive afferents located in the anteroventral periventricular nucleus (AVPV) are either absent or disabled. Males appear to lack the ability to exhibit an LH surge, but it is unclear what level of the CNS contributes to this dimorphic response. This study was conducted to determine whether estrogen followed by progesterone treatment (E + P) of gonadectomized males evokes Fos activation in LHRH and AVPV neurons as it does in females. The results indicated that, consistent with the males' inability to express an LH surge in response to E + P treatment, LHRH and AVPV neurons in males failed to show increased Fos activation. Examination of neuron nuclear antigen (NeuN, a neuron-specific marker), estrogen receptor (ERα) and progesterone receptor (PR) neurons in AVPV neurons indicated that, while essentially all the neurons of the caudal AVPV in males and females are steroid responsive, the male possessed half the number of steroid responsive neurons within the caudal AVPV (where activation of Fos is maximal in females) compared to the female. Together, these data indicate that the male lacks a substantial population of steroid receptive AVPV neurons and is unable to respond to the presence of E and P and activate either AVPV or LHRH neurons.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/j.brainres.2005.06.082</identifier><identifier>PMID: 16084918</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>London: Elsevier B.V</publisher><subject>Analysis of Variance ; Animals ; Biological and medical sciences ; Cell Count ; Cerebral Ventricles - drug effects ; Estrogen positive feedback ; Estrogen receptor alpha ; Estrogens - pharmacology ; Female ; Fundamental and applied biological sciences. Psychology ; Gene Expression Regulation - drug effects ; General aspects. Hormone interactions. Hormone actions on several organ systems. Adaptive reactions ; GnRH ; Gonadotropin-Releasing Hormone - metabolism ; Hypothalamus ; Immunohistochemistry - methods ; Luteinizing hormone ; Luteinizing Hormone - blood ; Male ; Neurons - drug effects ; Neurons - metabolism ; Oncogene Proteins v-fos - metabolism ; Preoptic area ; Preoptic Area - cytology ; Preoptic Area - drug effects ; Progesterone - pharmacology ; Progesterone receptor ; Radioimmunoassay - methods ; Rats ; Rats, Sprague-Dawley ; Sex Factors ; Sexual dimorphism ; Vertebrates: endocrinology</subject><ispartof>Brain research, 2005-08, Vol.1054 (2), p.116-124</ispartof><rights>2005 Elsevier B.V.</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c427t-deeb625539fc9cd1063c006871312ca1ab6463d1ddcf7cfa7a60b9e0d50227bf3</citedby><cites>FETCH-LOGICAL-c427t-deeb625539fc9cd1063c006871312ca1ab6463d1ddcf7cfa7a60b9e0d50227bf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.brainres.2005.06.082$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17078322$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16084918$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hoffman, G.E.</creatorcontrib><creatorcontrib>Le, W.W.</creatorcontrib><creatorcontrib>Schulterbrandt, T.</creatorcontrib><creatorcontrib>Legan, S.J.</creatorcontrib><title>Estrogen and progesterone do not activate Fos in AVPV or LHRH neurons in male rats</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>In rodents, females but not males, in response to escalating levels of estrogen, express a luteinizing hormone (LH) surge that is prompted by a surge in luteinizing hormone-releasing hormone (LHRH). It cannot take place if estrogen-sensitive afferents located in the anteroventral periventricular nucleus (AVPV) are either absent or disabled. Males appear to lack the ability to exhibit an LH surge, but it is unclear what level of the CNS contributes to this dimorphic response. This study was conducted to determine whether estrogen followed by progesterone treatment (E + P) of gonadectomized males evokes Fos activation in LHRH and AVPV neurons as it does in females. The results indicated that, consistent with the males' inability to express an LH surge in response to E + P treatment, LHRH and AVPV neurons in males failed to show increased Fos activation. Examination of neuron nuclear antigen (NeuN, a neuron-specific marker), estrogen receptor (ERα) and progesterone receptor (PR) neurons in AVPV neurons indicated that, while essentially all the neurons of the caudal AVPV in males and females are steroid responsive, the male possessed half the number of steroid responsive neurons within the caudal AVPV (where activation of Fos is maximal in females) compared to the female. Together, these data indicate that the male lacks a substantial population of steroid receptive AVPV neurons and is unable to respond to the presence of E and P and activate either AVPV or LHRH neurons.</description><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Count</subject><subject>Cerebral Ventricles - drug effects</subject><subject>Estrogen positive feedback</subject><subject>Estrogen receptor alpha</subject><subject>Estrogens - pharmacology</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation - drug effects</subject><subject>General aspects. Hormone interactions. Hormone actions on several organ systems. Adaptive reactions</subject><subject>GnRH</subject><subject>Gonadotropin-Releasing Hormone - metabolism</subject><subject>Hypothalamus</subject><subject>Immunohistochemistry - methods</subject><subject>Luteinizing hormone</subject><subject>Luteinizing Hormone - blood</subject><subject>Male</subject><subject>Neurons - drug effects</subject><subject>Neurons - metabolism</subject><subject>Oncogene Proteins v-fos - metabolism</subject><subject>Preoptic area</subject><subject>Preoptic Area - cytology</subject><subject>Preoptic Area - drug effects</subject><subject>Progesterone - pharmacology</subject><subject>Progesterone receptor</subject><subject>Radioimmunoassay - methods</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Sex Factors</subject><subject>Sexual dimorphism</subject><subject>Vertebrates: endocrinology</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMFq3DAQhkVpabZpXyHo0t7sjCRbkm8NIekGFlpCm6uQpXHR4pVSyRvI21fb3ZJjTqMR38z8fIRcMGgZMHm5bcdsQ8xYWg7QtyBb0PwNWTGteCN5B2_JCgBko4dBnJEPpWxrK8QA78kZk6C7gekVub8pS06_MVIbPX08PMuCOUWkPtGYFmrdEp7sgvQ2FRoivXr48UBTppv1_ZpG3Ff23__OzkizXcpH8m6yc8FPp3pOft3e_LxeN5vv3-6urzaN67haGo84St73Ypjc4DwDKVzNqxUTjDvL7Cg7KTzz3k3KTVZZCeOA4HvgXI2TOCdfjntr6j_7GtvsQnE4zzZi2hcjdd-DVPAqyJTQWrKugvIIupxKyTiZxxx2Nj8bBuag3WzNf-3moN2ANFV7Hbw4XdiPO_QvYyfPFfh8Amxxdp6yjS6UF06B0oIfFn09cljFPQXMpriA0aEPGd1ifAqvZfkLo9qjQA</recordid><startdate>20050830</startdate><enddate>20050830</enddate><creator>Hoffman, G.E.</creator><creator>Le, W.W.</creator><creator>Schulterbrandt, T.</creator><creator>Legan, S.J.</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>20050830</creationdate><title>Estrogen and progesterone do not activate Fos in AVPV or LHRH neurons in male rats</title><author>Hoffman, G.E. ; Le, W.W. ; Schulterbrandt, T. ; Legan, S.J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c427t-deeb625539fc9cd1063c006871312ca1ab6463d1ddcf7cfa7a60b9e0d50227bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Count</topic><topic>Cerebral Ventricles - drug effects</topic><topic>Estrogen positive feedback</topic><topic>Estrogen receptor alpha</topic><topic>Estrogens - pharmacology</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Regulation - drug effects</topic><topic>General aspects. Hormone interactions. Hormone actions on several organ systems. Adaptive reactions</topic><topic>GnRH</topic><topic>Gonadotropin-Releasing Hormone - metabolism</topic><topic>Hypothalamus</topic><topic>Immunohistochemistry - methods</topic><topic>Luteinizing hormone</topic><topic>Luteinizing Hormone - blood</topic><topic>Male</topic><topic>Neurons - drug effects</topic><topic>Neurons - metabolism</topic><topic>Oncogene Proteins v-fos - metabolism</topic><topic>Preoptic area</topic><topic>Preoptic Area - cytology</topic><topic>Preoptic Area - drug effects</topic><topic>Progesterone - pharmacology</topic><topic>Progesterone receptor</topic><topic>Radioimmunoassay - methods</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Sex Factors</topic><topic>Sexual dimorphism</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hoffman, G.E.</creatorcontrib><creatorcontrib>Le, W.W.</creatorcontrib><creatorcontrib>Schulterbrandt, T.</creatorcontrib><creatorcontrib>Legan, S.J.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hoffman, G.E.</au><au>Le, W.W.</au><au>Schulterbrandt, T.</au><au>Legan, S.J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Estrogen and progesterone do not activate Fos in AVPV or LHRH neurons in male rats</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>2005-08-30</date><risdate>2005</risdate><volume>1054</volume><issue>2</issue><spage>116</spage><epage>124</epage><pages>116-124</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>In rodents, females but not males, in response to escalating levels of estrogen, express a luteinizing hormone (LH) surge that is prompted by a surge in luteinizing hormone-releasing hormone (LHRH). It cannot take place if estrogen-sensitive afferents located in the anteroventral periventricular nucleus (AVPV) are either absent or disabled. Males appear to lack the ability to exhibit an LH surge, but it is unclear what level of the CNS contributes to this dimorphic response. This study was conducted to determine whether estrogen followed by progesterone treatment (E + P) of gonadectomized males evokes Fos activation in LHRH and AVPV neurons as it does in females. The results indicated that, consistent with the males' inability to express an LH surge in response to E + P treatment, LHRH and AVPV neurons in males failed to show increased Fos activation. Examination of neuron nuclear antigen (NeuN, a neuron-specific marker), estrogen receptor (ERα) and progesterone receptor (PR) neurons in AVPV neurons indicated that, while essentially all the neurons of the caudal AVPV in males and females are steroid responsive, the male possessed half the number of steroid responsive neurons within the caudal AVPV (where activation of Fos is maximal in females) compared to the female. Together, these data indicate that the male lacks a substantial population of steroid receptive AVPV neurons and is unable to respond to the presence of E and P and activate either AVPV or LHRH neurons.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>16084918</pmid><doi>10.1016/j.brainres.2005.06.082</doi><tpages>9</tpages></addata></record> |
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subjects | Analysis of Variance Animals Biological and medical sciences Cell Count Cerebral Ventricles - drug effects Estrogen positive feedback Estrogen receptor alpha Estrogens - pharmacology Female Fundamental and applied biological sciences. Psychology Gene Expression Regulation - drug effects General aspects. Hormone interactions. Hormone actions on several organ systems. Adaptive reactions GnRH Gonadotropin-Releasing Hormone - metabolism Hypothalamus Immunohistochemistry - methods Luteinizing hormone Luteinizing Hormone - blood Male Neurons - drug effects Neurons - metabolism Oncogene Proteins v-fos - metabolism Preoptic area Preoptic Area - cytology Preoptic Area - drug effects Progesterone - pharmacology Progesterone receptor Radioimmunoassay - methods Rats Rats, Sprague-Dawley Sex Factors Sexual dimorphism Vertebrates: endocrinology |
title | Estrogen and progesterone do not activate Fos in AVPV or LHRH neurons in male rats |
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