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Sexually dimorphic dopaminergic dysfunction in a transgenic mouse model of Huntington's disease.

Identifieur interne : 003254 ( PubMed/Corpus ); précédent : 003253; suivant : 003255

Sexually dimorphic dopaminergic dysfunction in a transgenic mouse model of Huntington's disease.

Auteurs : Thibault Renoir ; Andrew Argyropoulos ; Caroline Chevarin ; Laurence Lanfumey ; Anthony J. Hannan

Source :

RBID : pubmed:25316307

English descriptors

Abstract

Using the R6/1 transgenic mouse model of Huntington's disease (HD), we have recently shown that acute administration with the dopamine-norepinephrine reuptake inhibitor bupropion was able to rescue depressive-like behaviours in female HD mice at 12weeks of age.

DOI: 10.1016/j.pbb.2014.10.004
PubMed: 25316307

Links to Exploration step

pubmed:25316307

Le document en format XML

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<nlm:affiliation>Florey Institute of Neuroscience and Mental Health, Melbourne Brain Centre, University of Melbourne, Parkville, Australia. Electronic address: thibault.renoir@unimelb.edu.au.</nlm:affiliation>
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<name sortKey="Argyropoulos, Andrew" sort="Argyropoulos, Andrew" uniqKey="Argyropoulos A" first="Andrew" last="Argyropoulos">Andrew Argyropoulos</name>
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<name sortKey="Chevarin, Caroline" sort="Chevarin, Caroline" uniqKey="Chevarin C" first="Caroline" last="Chevarin">Caroline Chevarin</name>
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<name sortKey="Lanfumey, Laurence" sort="Lanfumey, Laurence" uniqKey="Lanfumey L" first="Laurence" last="Lanfumey">Laurence Lanfumey</name>
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<name sortKey="Hannan, Anthony J" sort="Hannan, Anthony J" uniqKey="Hannan A" first="Anthony J" last="Hannan">Anthony J. Hannan</name>
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<term>Animals</term>
<term>Disease Models, Animal</term>
<term>Dopamine (metabolism)</term>
<term>Dopamine Uptake Inhibitors (pharmacology)</term>
<term>Dopamine Uptake Inhibitors (therapeutic use)</term>
<term>Female</term>
<term>Huntington Disease (drug therapy)</term>
<term>Huntington Disease (genetics)</term>
<term>Huntington Disease (metabolism)</term>
<term>Male</term>
<term>Mice</term>
<term>Mice, Inbred C57BL</term>
<term>Mice, Inbred CBA</term>
<term>Mice, Transgenic</term>
<term>Receptors, Dopamine D1 (antagonists & inhibitors)</term>
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<term>Huntington Disease</term>
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<term>Huntington Disease</term>
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<term>Animals</term>
<term>Disease Models, Animal</term>
<term>Female</term>
<term>Male</term>
<term>Mice</term>
<term>Mice, Inbred C57BL</term>
<term>Mice, Inbred CBA</term>
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<div type="abstract" xml:lang="en">Using the R6/1 transgenic mouse model of Huntington's disease (HD), we have recently shown that acute administration with the dopamine-norepinephrine reuptake inhibitor bupropion was able to rescue depressive-like behaviours in female HD mice at 12weeks of age.</div>
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<Day>28</Day>
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<Title>Pharmacology, biochemistry, and behavior</Title>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Using the R6/1 transgenic mouse model of Huntington's disease (HD), we have recently shown that acute administration with the dopamine-norepinephrine reuptake inhibitor bupropion was able to rescue depressive-like behaviours in female HD mice at 12weeks of age.</AbstractText>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">In this present study, we aimed to further investigate the dopamine system as well as specifically measure dopamine transporter (DAT) and D1 receptor function in female versus male R6/1 HD mice at a very early stage of the disease.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">We assessed the effects of acute administration of bupropion and the dopamine D1 receptor agonist SKF-8129 on spontaneous locomotor activity in 8-week-old HD and wild-type (WT) mice. We also measured dopamine levels in striatum via high performance liquid chromatography (HPLC).</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">We found that female (but not male) HD mice were hyposensitive to bupropion when compared to WT littermates. However, both female and male HD mice were less sensitive to SKF-81297 locomotor effects. We also found that striatal dopamine levels and dopamine turnover were reduced in HD animals, regardless of sex.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Our present findings suggest that whereas only female HD mice exhibit an impaired response to bupropion, dopamine D1 receptor function is altered in both female and male HD animals. These data are the first in vivo evidence of impaired dopamine D1 receptor-dependent function in pre-motor symptomatic HD mice suggesting that this is a candidate target for early therapeutic interventions.</AbstractText>
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