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Cross-sensitization between footshock stress and apomorphine on self-injurious behavior and neostriatal catecholamines in a rat model of Lesch–Nyhan syndrome

The effects of footshock sensitization (priming), apomorphine (APO) priming and their combination on behavior and neostriatal and cortical catecholamines were examined in adult rats which had neonatally received bilateral intracerebroventricular injections with 6-hydroxydopamine (6-OHDA; a model of...

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Published in:Brain research 1998-02, Vol.783 (1), p.10-18
Main Authors: Stodgell, Christopher J, Loupe, Pippa S, Schroeder, Stephen R, Tessel, Richard E
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description The effects of footshock sensitization (priming), apomorphine (APO) priming and their combination on behavior and neostriatal and cortical catecholamines were examined in adult rats which had neonatally received bilateral intracerebroventricular injections with 6-hydroxydopamine (6-OHDA; a model of Lesch–Nyhan syndrome (LNS)) or vehicle (unlesioned rats). Lesioned (6-OHDA-treated) rats displayed self-biting (SB; 7/20 rats) and self-injurious behavior (SIB; 1/20 rats) during APO priming, but not during footshock priming. During subsequent acute cumulative APO dosing, 20–30% of lesioned rats primed with APO alone or footshock alone displayed SB and SIB. However, SB and SIB incidence in APO+footshock-primed lesioned rats was nearly tripled. Dopamine (DA) synthesis, metabolism and extracellular concentrations (disposition) in unlesioned rats and in cortices of lesioned animals were unaffected by priming. In lesioned rats primed with APO alone or footshock alone, only neostriatal 3-methoxytyramine (3-MT) was significantly increased. However, neostriatal DA and metabolite concentrations (and norepinephrine (NE)) were all significantly elevated in lesioned rats primed with both APO and footshock. These results confirm that neonatal 6-OHDA-induced neostriatal catecholamine depletion can be antagonized by experiential change, suggest that behavioral and neurochemical cross-sensitization between APO and footshock in such rats is unidirectional and support the view that stress can exacerbate the incidence of SIB in LNS.
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Loupe, Pippa S ; Schroeder, Stephen R ; Tessel, Richard E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c486t-2a35a9fe504beff664d9c470eb1fd6bf7fcfdad1f6531c76178759c81345a52f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>6-Hydroxydopamine</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Apomorphine</topic><topic>Apomorphine - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Catecholamines - metabolism</topic><topic>Disease Models, Animal</topic><topic>Dopamine</topic><topic>Dopamine Agonists - pharmacology</topic><topic>Electroshock</topic><topic>Errors of metabolism</topic><topic>Fixed ratio discrimination training</topic><topic>Injections, Intraventricular</topic><topic>Lesch-Nyhan Syndrome - chemically induced</topic><topic>Lesch-Nyhan Syndrome - metabolism</topic><topic>Lesch-Nyhan Syndrome - psychology</topic><topic>Lesch–Nyhan syndrome</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>Neostriatum - drug effects</topic><topic>Neostriatum - metabolism</topic><topic>Neurotoxins</topic><topic>Oxidopamine</topic><topic>Proteins and glycoproteins</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Self-Injurious Behavior</topic><topic>Stress, Physiological - metabolism</topic><topic>Stress, Physiological - psychology</topic><topic>Striatum</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stodgell, Christopher J</creatorcontrib><creatorcontrib>Loupe, Pippa S</creatorcontrib><creatorcontrib>Schroeder, Stephen R</creatorcontrib><creatorcontrib>Tessel, Richard E</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>Neurosciences Abstracts</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stodgell, Christopher J</au><au>Loupe, Pippa S</au><au>Schroeder, Stephen R</au><au>Tessel, Richard E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cross-sensitization between footshock stress and apomorphine on self-injurious behavior and neostriatal catecholamines in a rat model of Lesch–Nyhan syndrome</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>1998-02-02</date><risdate>1998</risdate><volume>783</volume><issue>1</issue><spage>10</spage><epage>18</epage><pages>10-18</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>The effects of footshock sensitization (priming), apomorphine (APO) priming and their combination on behavior and neostriatal and cortical catecholamines were examined in adult rats which had neonatally received bilateral intracerebroventricular injections with 6-hydroxydopamine (6-OHDA; a model of Lesch–Nyhan syndrome (LNS)) or vehicle (unlesioned rats). Lesioned (6-OHDA-treated) rats displayed self-biting (SB; 7/20 rats) and self-injurious behavior (SIB; 1/20 rats) during APO priming, but not during footshock priming. During subsequent acute cumulative APO dosing, 20–30% of lesioned rats primed with APO alone or footshock alone displayed SB and SIB. However, SB and SIB incidence in APO+footshock-primed lesioned rats was nearly tripled. Dopamine (DA) synthesis, metabolism and extracellular concentrations (disposition) in unlesioned rats and in cortices of lesioned animals were unaffected by priming. In lesioned rats primed with APO alone or footshock alone, only neostriatal 3-methoxytyramine (3-MT) was significantly increased. However, neostriatal DA and metabolite concentrations (and norepinephrine (NE)) were all significantly elevated in lesioned rats primed with both APO and footshock. These results confirm that neonatal 6-OHDA-induced neostriatal catecholamine depletion can be antagonized by experiential change, suggest that behavioral and neurochemical cross-sensitization between APO and footshock in such rats is unidirectional and support the view that stress can exacerbate the incidence of SIB in LNS.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>9479035</pmid><doi>10.1016/S0006-8993(97)01128-1</doi><tpages>9</tpages></addata></record>
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subjects 6-Hydroxydopamine
Animals
Animals, Newborn
Apomorphine
Apomorphine - pharmacology
Biological and medical sciences
Catecholamines - metabolism
Disease Models, Animal
Dopamine
Dopamine Agonists - pharmacology
Electroshock
Errors of metabolism
Fixed ratio discrimination training
Injections, Intraventricular
Lesch-Nyhan Syndrome - chemically induced
Lesch-Nyhan Syndrome - metabolism
Lesch-Nyhan Syndrome - psychology
Lesch–Nyhan syndrome
Male
Medical sciences
Metabolic diseases
Neostriatum - drug effects
Neostriatum - metabolism
Neurotoxins
Oxidopamine
Proteins and glycoproteins
Rats
Rats, Sprague-Dawley
Self-Injurious Behavior
Stress, Physiological - metabolism
Stress, Physiological - psychology
Striatum
title Cross-sensitization between footshock stress and apomorphine on self-injurious behavior and neostriatal catecholamines in a rat model of Lesch–Nyhan syndrome
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