La maladie de Parkinson en France (serveur d'exploration)

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Subthalamic nucleus high-frequency stimulation modulates neuronal reactivity to cocaine within the reward circuit.

Identifieur interne : 000269 ( PubMed/Checkpoint ); précédent : 000268; suivant : 000270

Subthalamic nucleus high-frequency stimulation modulates neuronal reactivity to cocaine within the reward circuit.

Auteurs : Sabira Hachem-Delaunay [France] ; Marie-Line Fournier [France] ; Candie Cohen [France] ; Nicolas Bonneau [France] ; Martine Cador [France] ; Christelle Baunez [France] ; Catherine Le Moine [France]

Source :

RBID : pubmed:25982833

English descriptors

Abstract

The subthalamic nucleus (STN) is a critical component of a complex network controlling motor, associative and limbic functions. High-frequency stimulation (HFS) of the STN is an effective therapy for motor symptoms in Parkinsonian patients and can also reduce their treatment-induced addictive behaviors. Preclinical studies have shown that STN HFS decreases motivation for cocaine while increasing that for food, highlighting its influence on rewarding and motivational circuits. However, the cellular substrates of these effects remain unknown. Our objectives were to characterize the cellular consequences of STN HFS with a special focus on limbic structures and to elucidate how STN HFS may interfere with acute cocaine effects in these brain areas. Male Long-Evans rats were subjected to STN HFS (130 Hz, 60 μs, 50-150 μA) for 30 min before an acute cocaine injection (15 mg/kg) and sacrificed 10 min following the injection. Neuronal reactivity was analyzed through the expression of two immediate early genes (Arc and c-Fos) to decipher cellular responses to STN HFS and cocaine. STN HFS only activated c-Fos in the globus pallidus and the basolateral amygdala, highlighting a possible role on emotional processes via the amygdala, with a limited effect by itself in other structures. Interestingly, and despite some differential effects on Arc and c-Fos expression, STN HFS diminished the c-Fos response induced by acute cocaine in the striatum. By preventing the cellular effect of cocaine in the striatum, STN HFS might thus decrease the reinforcing properties of the drug, which is in line with the inhibitory effect of STN HFS on the rewarding and reinforcing properties of cocaine.

DOI: 10.1016/j.nbd.2015.05.007
PubMed: 25982833


Affiliations:


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pubmed:25982833

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<div type="abstract" xml:lang="en">The subthalamic nucleus (STN) is a critical component of a complex network controlling motor, associative and limbic functions. High-frequency stimulation (HFS) of the STN is an effective therapy for motor symptoms in Parkinsonian patients and can also reduce their treatment-induced addictive behaviors. Preclinical studies have shown that STN HFS decreases motivation for cocaine while increasing that for food, highlighting its influence on rewarding and motivational circuits. However, the cellular substrates of these effects remain unknown. Our objectives were to characterize the cellular consequences of STN HFS with a special focus on limbic structures and to elucidate how STN HFS may interfere with acute cocaine effects in these brain areas. Male Long-Evans rats were subjected to STN HFS (130 Hz, 60 μs, 50-150 μA) for 30 min before an acute cocaine injection (15 mg/kg) and sacrificed 10 min following the injection. Neuronal reactivity was analyzed through the expression of two immediate early genes (Arc and c-Fos) to decipher cellular responses to STN HFS and cocaine. STN HFS only activated c-Fos in the globus pallidus and the basolateral amygdala, highlighting a possible role on emotional processes via the amygdala, with a limited effect by itself in other structures. Interestingly, and despite some differential effects on Arc and c-Fos expression, STN HFS diminished the c-Fos response induced by acute cocaine in the striatum. By preventing the cellular effect of cocaine in the striatum, STN HFS might thus decrease the reinforcing properties of the drug, which is in line with the inhibitory effect of STN HFS on the rewarding and reinforcing properties of cocaine.</div>
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<QualifierName UI="Q000008" MajorTopicYN="Y">administration & dosage</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D003342" MajorTopicYN="N">Corpus Striatum</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D003598" MajorTopicYN="N">Cytoskeletal Proteins</DescriptorName>
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<DescriptorName UI="D051381" MajorTopicYN="N">Rats</DescriptorName>
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<Keyword MajorTopicYN="N">Addiction</Keyword>
<Keyword MajorTopicYN="N">Arc</Keyword>
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<Keyword MajorTopicYN="N">Deep brain stimulation</Keyword>
<Keyword MajorTopicYN="N">Nucleus accumbens</Keyword>
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<Year>2015</Year>
<Month>05</Month>
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<ArticleId IdType="doi">10.1016/j.nbd.2015.05.007</ArticleId>
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<list>
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<li>France</li>
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<li>Aquitaine</li>
<li>Nouvelle-Aquitaine</li>
<li>Provence-Alpes-Côte d'Azur</li>
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<country name="France">
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<name sortKey="Hachem Delaunay, Sabira" sort="Hachem Delaunay, Sabira" uniqKey="Hachem Delaunay S" first="Sabira" last="Hachem-Delaunay">Sabira Hachem-Delaunay</name>
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<name sortKey="Baunez, Christelle" sort="Baunez, Christelle" uniqKey="Baunez C" first="Christelle" last="Baunez">Christelle Baunez</name>
<name sortKey="Bonneau, Nicolas" sort="Bonneau, Nicolas" uniqKey="Bonneau N" first="Nicolas" last="Bonneau">Nicolas Bonneau</name>
<name sortKey="Cador, Martine" sort="Cador, Martine" uniqKey="Cador M" first="Martine" last="Cador">Martine Cador</name>
<name sortKey="Cohen, Candie" sort="Cohen, Candie" uniqKey="Cohen C" first="Candie" last="Cohen">Candie Cohen</name>
<name sortKey="Fournier, Marie Line" sort="Fournier, Marie Line" uniqKey="Fournier M" first="Marie-Line" last="Fournier">Marie-Line Fournier</name>
<name sortKey="Le Moine, Catherine" sort="Le Moine, Catherine" uniqKey="Le Moine C" first="Catherine" last="Le Moine">Catherine Le Moine</name>
</country>
</tree>
</affiliations>
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