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Reduced Efficacy of 8-OH-DPAT's Inhibition of Lordosis Behavior by Prior Estrogen Treatment
The effects of bilateral VMN infusion with the 5-HT1A receptor agonist, (±)-8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT; 200, 1000, or 2000 ng), on lordosis behavior were examined in hormonally primed ovariectomized rats. When rats were given a single injection with 25 μg estradiol benzoate fo...
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Published in: | Hormones and behavior 1999-06, Vol.35 (3), p.215-223 |
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description | The effects of bilateral VMN infusion with the 5-HT1A receptor agonist, (±)-8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT; 200, 1000, or 2000 ng), on lordosis behavior were examined in hormonally primed ovariectomized rats. When rats were given a single injection with 25 μg estradiol benzoate followed 48 h later with 500 μg progesterone, inhibition of lordosis behavior was evident at all doses of 8-OH-DPAT. However, when rats were treated with 25 μg estradiol benzoate followed 7 days later with a second injection of 25 μg estradiol benzoate and then progesterone, none of the doses of 8-OH-DPAT effectively inhibited lordosis behavior. In some rats, cannulae were located near the most rostral portion of the VMN. In these rats, there was no effect of the second estrogen treatment on the response to 8-OH-DPAT. Therefore, a second experiment was performed to specifically evaluate the effects of two estradiol benzoate treatments on the response to bilateral 8-OH-DPAT infusion in the rostral VMN. In contrast to the reduced effectiveness of the 8-OH-DPAT infusion in the mid to caudal VMN in rats given two injections with estradiol benzoate, 2000 ng 8-OH-DPAT continued to effectively inhibit lordosis behavior following the 5-HT1A receptor agonist's infusion into the more rostral areas. These findings are discussed in relation to earlier studies in which the potency, but not the efficacy, of 8-OH-DPAT was reduced following systemic treatment with the 5-HT1A receptor agonist. |
doi_str_mv | 10.1006/hbeh.1999.1515 |
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When rats were given a single injection with 25 μg estradiol benzoate followed 48 h later with 500 μg progesterone, inhibition of lordosis behavior was evident at all doses of 8-OH-DPAT. However, when rats were treated with 25 μg estradiol benzoate followed 7 days later with a second injection of 25 μg estradiol benzoate and then progesterone, none of the doses of 8-OH-DPAT effectively inhibited lordosis behavior. In some rats, cannulae were located near the most rostral portion of the VMN. In these rats, there was no effect of the second estrogen treatment on the response to 8-OH-DPAT. Therefore, a second experiment was performed to specifically evaluate the effects of two estradiol benzoate treatments on the response to bilateral 8-OH-DPAT infusion in the rostral VMN. In contrast to the reduced effectiveness of the 8-OH-DPAT infusion in the mid to caudal VMN in rats given two injections with estradiol benzoate, 2000 ng 8-OH-DPAT continued to effectively inhibit lordosis behavior following the 5-HT1A receptor agonist's infusion into the more rostral areas. 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When rats were given a single injection with 25 μg estradiol benzoate followed 48 h later with 500 μg progesterone, inhibition of lordosis behavior was evident at all doses of 8-OH-DPAT. However, when rats were treated with 25 μg estradiol benzoate followed 7 days later with a second injection of 25 μg estradiol benzoate and then progesterone, none of the doses of 8-OH-DPAT effectively inhibited lordosis behavior. In some rats, cannulae were located near the most rostral portion of the VMN. In these rats, there was no effect of the second estrogen treatment on the response to 8-OH-DPAT. Therefore, a second experiment was performed to specifically evaluate the effects of two estradiol benzoate treatments on the response to bilateral 8-OH-DPAT infusion in the rostral VMN. In contrast to the reduced effectiveness of the 8-OH-DPAT infusion in the mid to caudal VMN in rats given two injections with estradiol benzoate, 2000 ng 8-OH-DPAT continued to effectively inhibit lordosis behavior following the 5-HT1A receptor agonist's infusion into the more rostral areas. These findings are discussed in relation to earlier studies in which the potency, but not the efficacy, of 8-OH-DPAT was reduced following systemic treatment with the 5-HT1A receptor agonist.</description><subject>5-HT1A receptors</subject><subject>8-Hydroxy-2-(di-n-propylamino)tetralin - pharmacology</subject><subject>Animals</subject><subject>Behavioral psychophysiology</subject><subject>Biological and medical sciences</subject><subject>Brain Chemistry - drug effects</subject><subject>Brain Chemistry - physiology</subject><subject>Estradiol - analogs & derivatives</subject><subject>Estradiol - pharmacology</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>hormones</subject><subject>Hormones and behavior</subject><subject>Injections, Intraventricular</subject><subject>Ovariectomy</subject><subject>Posture - physiology</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychology. Psychophysiology</subject><subject>Rats</subject><subject>Rats, Inbred F344</subject><subject>Receptors, Serotonin - physiology</subject><subject>Receptors, Serotonin, 5-HT1</subject><subject>serotonin</subject><subject>Serotonin Receptor Agonists - pharmacology</subject><subject>sexual behavior</subject><subject>Sexual Behavior, Animal - drug effects</subject><subject>Space life sciences</subject><issn>0018-506X</issn><issn>1095-6867</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkc1LIzEUwIO4aHW9epQ5yHqamsxMMsnR7dYPKCjSBcFDyMeLjbQTTaZC__vN0IJeZE8v4f3y3svvIXRK8JhgzC4XGhZjIoQYE0roHhoRLGjJOGv30QhjwkuK2dMhOkrpNV8JbZoDdEhw3dZ13YzQ8yPYtQFbTJ3zRplNEVzBy_vb8s_D1fwiFXfdwmvf-9ANmVmINiSfit-wUB8-xEJvioc4HKapj-EFumIeQfUr6Pqf6IdTywQnu3iM_l5P55PbcnZ_cze5mpWmwbgvq1oJRVputBCaNqStVFXrVjmoKLeUC-tYZWkLGKDVTDtTG2gotdSpitKqPka_tnXfYnhfQ-rlyicDy6XqIKyTZILnv3LyXzC35g2veAbHW9DEkFIEJ9-iX6m4kQTLwbscvMvBuxy85wdnu8prvQL7Bd-KzsD5DlDJqKWLqjM-fXK5L2YsY3yLQfb14SHKZDx0eUE-gumlDf67Ef4BskGdOA</recordid><startdate>19990601</startdate><enddate>19990601</enddate><creator>Trevino, Angelita</creator><creator>Wolf, Amy</creator><creator>Jackson, Astra</creator><creator>Price, Tiffany</creator><creator>Uphouse, Lynda</creator><general>Elsevier Inc</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>7QG</scope><scope>7X8</scope></search><sort><creationdate>19990601</creationdate><title>Reduced Efficacy of 8-OH-DPAT's Inhibition of Lordosis Behavior by Prior Estrogen Treatment</title><author>Trevino, Angelita ; Wolf, Amy ; Jackson, Astra ; Price, Tiffany ; Uphouse, Lynda</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-23a9a178cb99b54172a23b7afe258d589df62d57e0ee7b6bfc3ce455d5fa25523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>5-HT1A receptors</topic><topic>8-Hydroxy-2-(di-n-propylamino)tetralin - pharmacology</topic><topic>Animals</topic><topic>Behavioral psychophysiology</topic><topic>Biological and medical sciences</topic><topic>Brain Chemistry - drug effects</topic><topic>Brain Chemistry - physiology</topic><topic>Estradiol - analogs & derivatives</topic><topic>Estradiol - pharmacology</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>hormones</topic><topic>Hormones and behavior</topic><topic>Injections, Intraventricular</topic><topic>Ovariectomy</topic><topic>Posture - physiology</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychology. Psychophysiology</topic><topic>Rats</topic><topic>Rats, Inbred F344</topic><topic>Receptors, Serotonin - physiology</topic><topic>Receptors, Serotonin, 5-HT1</topic><topic>serotonin</topic><topic>Serotonin Receptor Agonists - pharmacology</topic><topic>sexual behavior</topic><topic>Sexual Behavior, Animal - drug effects</topic><topic>Space life sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Trevino, Angelita</creatorcontrib><creatorcontrib>Wolf, Amy</creatorcontrib><creatorcontrib>Jackson, Astra</creatorcontrib><creatorcontrib>Price, Tiffany</creatorcontrib><creatorcontrib>Uphouse, Lynda</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>Animal Behavior Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Hormones and behavior</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Trevino, Angelita</au><au>Wolf, Amy</au><au>Jackson, Astra</au><au>Price, Tiffany</au><au>Uphouse, Lynda</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reduced Efficacy of 8-OH-DPAT's Inhibition of Lordosis Behavior by Prior Estrogen Treatment</atitle><jtitle>Hormones and behavior</jtitle><addtitle>Horm Behav</addtitle><date>1999-06-01</date><risdate>1999</risdate><volume>35</volume><issue>3</issue><spage>215</spage><epage>223</epage><pages>215-223</pages><issn>0018-506X</issn><eissn>1095-6867</eissn><coden>HOBEAO</coden><abstract>The effects of bilateral VMN infusion with the 5-HT1A receptor agonist, (±)-8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT; 200, 1000, or 2000 ng), on lordosis behavior were examined in hormonally primed ovariectomized rats. When rats were given a single injection with 25 μg estradiol benzoate followed 48 h later with 500 μg progesterone, inhibition of lordosis behavior was evident at all doses of 8-OH-DPAT. However, when rats were treated with 25 μg estradiol benzoate followed 7 days later with a second injection of 25 μg estradiol benzoate and then progesterone, none of the doses of 8-OH-DPAT effectively inhibited lordosis behavior. In some rats, cannulae were located near the most rostral portion of the VMN. In these rats, there was no effect of the second estrogen treatment on the response to 8-OH-DPAT. Therefore, a second experiment was performed to specifically evaluate the effects of two estradiol benzoate treatments on the response to bilateral 8-OH-DPAT infusion in the rostral VMN. In contrast to the reduced effectiveness of the 8-OH-DPAT infusion in the mid to caudal VMN in rats given two injections with estradiol benzoate, 2000 ng 8-OH-DPAT continued to effectively inhibit lordosis behavior following the 5-HT1A receptor agonist's infusion into the more rostral areas. These findings are discussed in relation to earlier studies in which the potency, but not the efficacy, of 8-OH-DPAT was reduced following systemic treatment with the 5-HT1A receptor agonist.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>10373334</pmid><doi>10.1006/hbeh.1999.1515</doi><tpages>9</tpages></addata></record> |
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subjects | 5-HT1A receptors 8-Hydroxy-2-(di-n-propylamino)tetralin - pharmacology Animals Behavioral psychophysiology Biological and medical sciences Brain Chemistry - drug effects Brain Chemistry - physiology Estradiol - analogs & derivatives Estradiol - pharmacology Female Fundamental and applied biological sciences. Psychology hormones Hormones and behavior Injections, Intraventricular Ovariectomy Posture - physiology Psychology. Psychoanalysis. Psychiatry Psychology. Psychophysiology Rats Rats, Inbred F344 Receptors, Serotonin - physiology Receptors, Serotonin, 5-HT1 serotonin Serotonin Receptor Agonists - pharmacology sexual behavior Sexual Behavior, Animal - drug effects Space life sciences |
title | Reduced Efficacy of 8-OH-DPAT's Inhibition of Lordosis Behavior by Prior Estrogen Treatment |
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