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Neurotrophin expression modulated by glucocorticoids and oestrogen in immortalized hippocampal neurons
We have used reverse transcription followed by polymerase chain reaction amplification to investigate changes in expression of nerve growth factor (NGF) mRNA in immortalized hippocampal neurons after treatment with the glucocorticoids dexamethasone and corticosterone, the glucocorticoid antagonist R...
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Published in: | Brain research. Molecular brain research. 1995-07, Vol.31 (1), p.158-164 |
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container_title | Brain research. Molecular brain research. |
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creator | Leach Scully, Jackie Otten, Uwe |
description | We have used reverse transcription followed by polymerase chain reaction amplification to investigate changes in expression of nerve growth factor (NGF) mRNA in immortalized hippocampal neurons after treatment with the glucocorticoids dexamethasone and corticosterone, the glucocorticoid antagonist RU38486, and the gonadal steroids progesterone and 17-beta oestradiol. We found that NGF mRNA levels rise after application of either dexamethasone or corticosterone, and that this rise is prevented by the antagonist. Thus, neurotrophin expression is modulated by the physiological glucocorticoid and is mediated by type II glucocorticoid receptors. Progesterone has no effect, while 17-beta oestradiol suppresses NGF mRNA in a postnatally-derived cell line but does not change levels in an embryonic line. An increase in neurotrophin expression is therefore not a general response to steroid hormone application, and may be a specific defence against the presence of metabolically endangering glucocorticoids. |
doi_str_mv | 10.1016/0169-328X(95)00047-V |
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We found that NGF mRNA levels rise after application of either dexamethasone or corticosterone, and that this rise is prevented by the antagonist. Thus, neurotrophin expression is modulated by the physiological glucocorticoid and is mediated by type II glucocorticoid receptors. Progesterone has no effect, while 17-beta oestradiol suppresses NGF mRNA in a postnatally-derived cell line but does not change levels in an embryonic line. An increase in neurotrophin expression is therefore not a general response to steroid hormone application, and may be a specific defence against the presence of metabolically endangering glucocorticoids.</description><identifier>ISSN: 0169-328X</identifier><identifier>EISSN: 1872-6941</identifier><identifier>DOI: 10.1016/0169-328X(95)00047-V</identifier><identifier>PMID: 7476024</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Animals ; Base Sequence ; Biochemistry and metabolism ; Biological and medical sciences ; Cell Survival - drug effects ; Central nervous system ; Corticosterone - antagonists & inhibitors ; Corticosterone - pharmacology ; Dexamethasone - antagonists & inhibitors ; Dexamethasone - pharmacology ; Estradiol - pharmacology ; Fundamental and applied biological sciences. Psychology ; Glucocorticoid ; Glucocorticoids - antagonists & inhibitors ; Glucocorticoids - pharmacology ; Hippocampus ; Hippocampus - cytology ; Hippocampus - drug effects ; Hippocampus - metabolism ; Mice ; Mifepristone - pharmacology ; Molecular Sequence Data ; Nerve growth factor ; Nerve Growth Factors - genetics ; Neuron ; Neurons - drug effects ; Neurons - metabolism ; Neurotrophin-3 ; Oestrogen ; Progesterone - antagonists & inhibitors ; Progesterone - pharmacology ; RNA, Messenger - biosynthesis ; Tumor Cells, Cultured ; Vertebrates: nervous system and sense organs</subject><ispartof>Brain research. 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Molecular brain research.</title><addtitle>Brain Res Mol Brain Res</addtitle><description>We have used reverse transcription followed by polymerase chain reaction amplification to investigate changes in expression of nerve growth factor (NGF) mRNA in immortalized hippocampal neurons after treatment with the glucocorticoids dexamethasone and corticosterone, the glucocorticoid antagonist RU38486, and the gonadal steroids progesterone and 17-beta oestradiol. We found that NGF mRNA levels rise after application of either dexamethasone or corticosterone, and that this rise is prevented by the antagonist. Thus, neurotrophin expression is modulated by the physiological glucocorticoid and is mediated by type II glucocorticoid receptors. Progesterone has no effect, while 17-beta oestradiol suppresses NGF mRNA in a postnatally-derived cell line but does not change levels in an embryonic line. An increase in neurotrophin expression is therefore not a general response to steroid hormone application, and may be a specific defence against the presence of metabolically endangering glucocorticoids.</description><subject>Animals</subject><subject>Base Sequence</subject><subject>Biochemistry and metabolism</subject><subject>Biological and medical sciences</subject><subject>Cell Survival - drug effects</subject><subject>Central nervous system</subject><subject>Corticosterone - antagonists & inhibitors</subject><subject>Corticosterone - pharmacology</subject><subject>Dexamethasone - antagonists & inhibitors</subject><subject>Dexamethasone - pharmacology</subject><subject>Estradiol - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glucocorticoid</subject><subject>Glucocorticoids - antagonists & inhibitors</subject><subject>Glucocorticoids - pharmacology</subject><subject>Hippocampus</subject><subject>Hippocampus - cytology</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - metabolism</subject><subject>Mice</subject><subject>Mifepristone - pharmacology</subject><subject>Molecular Sequence Data</subject><subject>Nerve growth factor</subject><subject>Nerve Growth Factors - genetics</subject><subject>Neuron</subject><subject>Neurons - drug effects</subject><subject>Neurons - metabolism</subject><subject>Neurotrophin-3</subject><subject>Oestrogen</subject><subject>Progesterone - antagonists & inhibitors</subject><subject>Progesterone - pharmacology</subject><subject>RNA, Messenger - biosynthesis</subject><subject>Tumor Cells, Cultured</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0169-328X</issn><issn>1872-6941</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><recordid>eNqFkc1LHTEUxUOp6NP2P6gwiyLtYmy-Jh-bQpHaCmI3It2FmLnRyEwyJjNF_evN63u8Zbu43MX5ncPlXIQ-EHxKMBFf6uiWUfX7k-4-Y4y5bG_eoBVRkrZCc_IWrXbIATos5aFCRBGyj_YllwJTvkL-Cpac5pym-xAbeJoylBJSbMbUL4OdoW9un5u7YXHJpTwHl0JfGhv7JkGptjuITTWGcayqHcJLNdyHaUrOjpMdmriOj-Ud2vN2KPB-u4_Q9fn367Of7eWvHxdn3y5bx4mcW8osVw4z3FvBuaAKa-e1Fcp3irEOsKcCC6k0Jc5qrkFIRqnW2DtpvWVH6GQTO-X0uNQDzRiKg2GwEdJSjJRCKd3p_4JEqI5zyirIN6DLqZQM3kw5jDY_G4LN-g1m3bFZd2x0Z_6-wdxU2_E2f7kdod-Ztr1X_eNWt8XZwWcbXSg7jAnccdJV7OsGg9rZnwDZFBcgOuhDBjebPoV_3_EKePilyg</recordid><startdate>19950701</startdate><enddate>19950701</enddate><creator>Leach Scully, Jackie</creator><creator>Otten, Uwe</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>19950701</creationdate><title>Neurotrophin expression modulated by glucocorticoids and oestrogen in immortalized hippocampal neurons</title><author>Leach Scully, Jackie ; Otten, Uwe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-23a48c030da64462809cf9a68f58335e0f260678921ca949e67322990fc7afa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Base Sequence</topic><topic>Biochemistry and metabolism</topic><topic>Biological and medical sciences</topic><topic>Cell Survival - drug effects</topic><topic>Central nervous system</topic><topic>Corticosterone - antagonists & inhibitors</topic><topic>Corticosterone - pharmacology</topic><topic>Dexamethasone - antagonists & inhibitors</topic><topic>Dexamethasone - pharmacology</topic><topic>Estradiol - pharmacology</topic><topic>Fundamental and applied biological sciences. 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Molecular brain research.</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Leach Scully, Jackie</au><au>Otten, Uwe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neurotrophin expression modulated by glucocorticoids and oestrogen in immortalized hippocampal neurons</atitle><jtitle>Brain research. Molecular brain research.</jtitle><addtitle>Brain Res Mol Brain Res</addtitle><date>1995-07-01</date><risdate>1995</risdate><volume>31</volume><issue>1</issue><spage>158</spage><epage>164</epage><pages>158-164</pages><issn>0169-328X</issn><eissn>1872-6941</eissn><abstract>We have used reverse transcription followed by polymerase chain reaction amplification to investigate changes in expression of nerve growth factor (NGF) mRNA in immortalized hippocampal neurons after treatment with the glucocorticoids dexamethasone and corticosterone, the glucocorticoid antagonist RU38486, and the gonadal steroids progesterone and 17-beta oestradiol. We found that NGF mRNA levels rise after application of either dexamethasone or corticosterone, and that this rise is prevented by the antagonist. Thus, neurotrophin expression is modulated by the physiological glucocorticoid and is mediated by type II glucocorticoid receptors. Progesterone has no effect, while 17-beta oestradiol suppresses NGF mRNA in a postnatally-derived cell line but does not change levels in an embryonic line. An increase in neurotrophin expression is therefore not a general response to steroid hormone application, and may be a specific defence against the presence of metabolically endangering glucocorticoids.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>7476024</pmid><doi>10.1016/0169-328X(95)00047-V</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Base Sequence Biochemistry and metabolism Biological and medical sciences Cell Survival - drug effects Central nervous system Corticosterone - antagonists & inhibitors Corticosterone - pharmacology Dexamethasone - antagonists & inhibitors Dexamethasone - pharmacology Estradiol - pharmacology Fundamental and applied biological sciences. Psychology Glucocorticoid Glucocorticoids - antagonists & inhibitors Glucocorticoids - pharmacology Hippocampus Hippocampus - cytology Hippocampus - drug effects Hippocampus - metabolism Mice Mifepristone - pharmacology Molecular Sequence Data Nerve growth factor Nerve Growth Factors - genetics Neuron Neurons - drug effects Neurons - metabolism Neurotrophin-3 Oestrogen Progesterone - antagonists & inhibitors Progesterone - pharmacology RNA, Messenger - biosynthesis Tumor Cells, Cultured Vertebrates: nervous system and sense organs |
title | Neurotrophin expression modulated by glucocorticoids and oestrogen in immortalized hippocampal neurons |
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