<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/CINECAstyle.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-23T19:16:43Z</responseDate><request verb="GetRecord" identifier="oai:iris.unica.it:11584/266368" metadataPrefix="oai_dc">https://iris.unica.it/oai/request</request><GetRecord><record><header><identifier>oai:iris.unica.it:11584/266368</identifier><datestamp>2022-10-20T09:34:34Z</datestamp><setSpec>com_11584_207615</setSpec><setSpec>com_11584_111066</setSpec><setSpec>col_11584_265854</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
<dc:title>Interazioni neurotrasmettitoriali nel meccanismo d’azione della cocaina: ruolo della serotonina e dell’adenosina</dc:title>
<dc:creator>PERRA, VALENTINA</dc:creator>
<dc:subject>5-HT6 receptor</dc:subject>
<dc:subject>autosomministrazione</dc:subject>
<dc:subject>caffeina</dc:subject>
<dc:subject>caffeine</dc:subject>
<dc:subject>cocaina</dc:subject>
<dc:subject>cocaine</dc:subject>
<dc:subject>dopamina</dc:subject>
<dc:subject>dopamine</dc:subject>
<dc:subject>microdialisi</dc:subject>
<dc:subject>recettore 5-HT6</dc:subject>
<dc:subject>self administration</dc:subject>
<dc:subject>Settore BIO/14 - Farmacologia</dc:subject>
<dc:description>The putative 5-HT6 receptor agonist ST1936 has been shown to increase extracellular&#xd;
dopamine (DA) in the n.accumbens (NAc) Shell and in the medial prefrontal cortex (PFCX).&#xd;
These observations suggest that 5-HT6 receptors modulate DA transmission in mesolimbic&#xd;
and mesocortical terminal DA areas. To investigate the behavioral counterpart of this&#xd;
interaction I studied in rats the effect of 5-HT6 receptor blockade on cocaine stimulated&#xd;
overflow of DA in dialysates from the PFCX and from the NAc Shell and on cocaine i.v. selfadministration.&#xd;
Pretreatment with the 5-HT6 antagonist SB271046 reduced cocaine-induced&#xd;
increase of dialysate DA in the NAc Shell but not in the PFCX and impaired i.v. cocaine selfadministration.&#xd;
These suggest that 5-HT6 receptors play a role in cocaine reinforcement via&#xd;
their facilitatore interaction with DA projections to the NAc Shell. This 5-HT/DA interaction&#xd;
might provide the basis for a new pharmacotherapeutic strategy of cocaine addiction.&#xd;
Caffeine is one of the psychoactive substances most widely used as adulterant in illicit drugs,&#xd;
such as cocaine. Animal studies have demonstrated that caffeine is able to potentiate cocaine&#xd;
actions, although the enhancement of the cocaine reinforcing property by caffeine is less&#xd;
reported, and the results depend on the paradigms and experimental protocols used.&#xd;
In the present study I examined the ability of caffeine to enhance the motivational and&#xd;
rewarding properties of cocaine using the intravenous self-administration paradigm in rats.&#xd;
Additionally, the role of caffeine as a primer cue during extinction was evaluated. To this end,&#xd;
we assessed in naïve rats: 1) the ability of the combination of cocaine (0,125&#xd;
mg/kg/infusion) and caffeine (0,0625 mg/kg/infusion) to maintain self-administration in&#xd;
fixed ratio (FR) and progressive ratio (PR) schedules of reinforcement compared with cocaine&#xd;
and caffeine alone; 2) the effect of caffeine in the maintenance of responding in the animals&#xd;
exposed to the combination of the drugs during cocaine extinction.&#xd;
Cocaine and the combination of cocaine and caffeine were self-administered on a FR and PR&#xd;
schedules of reinforcement, and the responding for the combination of the drugs was higher&#xd;
than cocaine alone. Caffeine was not reliably self-administered, but was able to maintain a&#xd;
drug-seeking behavior in rats previously exposed to cocaine plus caffeine.&#xd;
These findings suggest that the presence of caffeine enhances the reinforcing effects of&#xd;
cocaine and the motivational value of the drug. Our results highlight the role of active&#xd;
adulterants commonly used in illicit street drugs.</dc:description>
<dc:date>2015-05-06</dc:date>
<dc:type>info:eu-repo/semantics/doctoralThesis</dc:type>
<dc:identifier>http://hdl.handle.net/11584/266368</dc:identifier>
<dc:language>ita</dc:language>
<dc:relation>numberofpages:65</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:publisher>Università degli Studi di Cagliari</dc:publisher>
<dc:rights>license:Non specificato</dc:rights>
</oai_dc:dc></metadata></record></GetRecord></OAI-PMH>