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      <dc:title>Persistent drug-associated memories coexist with hippocampal-dependent cognitive decline and altered adult hippocampal neurogenesis in mice withdrawn from cocaine.</dc:title>
      <dc:creator>Mañas-Padilla, María del Carmen</dc:creator>
      <dc:creator>Gil-Rodríguez, Sara</dc:creator>
      <dc:creator>Sampedro-Piquero, Patricia</dc:creator>
      <dc:creator>Ávila-Gámiz, Fabiola</dc:creator>
      <dc:creator>Rodriguez-de-Fonseca, Fernando</dc:creator>
      <dc:creator>Santín-Núñez, Luis Javier</dc:creator>
      <dc:creator>Castilla-Ortega, María Estela</dc:creator>
      <dc:subject>Toxicomanía - Complicaciones y secuelas</dc:subject>
      <dc:subject>Cocaina</dc:subject>
      <dc:subject>Hipocampo (Cerebro)</dc:subject>
      <dc:subject>Experimentación animal</dc:subject>
      <dc:description>Aims: Using a new animal model (‘chronic’ cocaine-induced conditioned place preference –CPP- paradigm), this work studied whether the long-term maintenance of cocaine-associated memories was concomitant to cognitive impairment and adult hippocampal neurogenesis (AHN) alterations. Methods: Male c57BL/6J mice were submitted to a CPP task treated either with cocaine (20 mg/kg/day) or saline for 14 days (n=10 per group). Bromodeoxyuridine (BrdU) was administered to label the new hippocampal neurons generated one week after the last cocaine dose. After 28 drug-free days, mice were assessed for the CPP memory and on a battery of emotional and cognitive behavioral tests. After completion of behavior, brains were collected for AHN analysis. Results: In mice treated with cocaine, preference for the cocaine-paired compartment (CPP memory) persisted over time. In addition, the cocaine-withdrawn mice overall displayed normal emotional behavior but they showed hippocampal-dependent cognitive impairment for novelty recognition (object and place) and spatial (reference and working) memory. The number of BrdU+ cells was unaffected, suggesting that cocaine withdrawal did not impair basal AHN. However, the cocaine-withdrawn mice excessively increased the number immature hippocampal neurons (doublecortin+) after behavioral training, in direct correlation with their cognitive performance, probably as a result of effortful learning. Conclusions: The CPP memory induced by cocaine remains unaltered after a prolonged period of abstinence, accompanied by defective acquisition of new learnings. Since the doublecortin+ neurons correlated with better cognitive performance in the cocaine-withdrawn mice, strategies that increase AHN could alleviate neurocognitive deficits induced by cocaine.</dc:description>
      <dc:date>2019-10-01T11:08:14Z</dc:date>
      <dc:date>2019-10-01T11:08:14Z</dc:date>
      <dc:date>2019</dc:date>
      <dc:date>2019-10-01</dc:date>
      <dc:type>conference output</dc:type>
      <dc:identifier>https://hdl.handle.net/10630/18503</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:relation>48th Annual General Meeting of European Brain and Behaviour Society (EBBS)</dc:relation>
      <dc:relation>Praga</dc:relation>
      <dc:relation>21 a 24 de septiembre, 2019</dc:relation>
      <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
      <dc:rights>open access</dc:rights>
      <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dc:rights>
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