Matches in SemOpenAlex for { <https://semopenalex.org/work/W2004451864> ?p ?o ?g. }
- W2004451864 endingPage "636" @default.
- W2004451864 startingPage "628" @default.
- W2004451864 abstract "Extinction of drug-seeking is an integral part of addiction treatment, and can profoundly reverse or ameliorate the harmful consequences of drug use. These consequences may be the most deleterious during adolescence. The studies presented here build from recent evidence that adolescent rats are more resistant to extinction training than adults, and therefore may require unique treatment strategies. We used unbiased place-conditioning in male rats to show that passive, un-explicit extinction pairings resulted in delayed extinction in 40-day-old adolescents relative to 80-day-old adults. However, explicit-pairing of a previously cocaine-associated context with the absence of drug produces extinction in adolescents as rapidly as in adults. These data suggest that successful extinction of drug-paired associations in adolescents may be facilitated by stronger acquisition of a new (extinction) memory. Drug-paired associations are largely controlled by the prelimbic prefrontal cortex (plPFC) and its influence on the nucleus accumbens (NAc). This pathway mediates the motivational salience attributed to incoming stimuli through the D1 dopamine receptor. D1 receptors on plPFC outputs to the accumbens are transiently overproduced during adolescence. Since D1 receptors are selectively responsive to potent stimuli, we hypothesized that the adolescent plPFC hinders competition between potent drug-paired associations and the subtler, drug-free information necessary for extinction. To harness this unique profile of the adolescent plPFC, we aimed to increase the salience of unrewarded extinction memories by activating plPFC D1 receptors during extinction training. In a second study, extinction of drug-cue associations was facilitated in adolescents by elevating dopamine and norepinephrine in the PFC during extinction training with atomoxetine. In a third study, direct microinjection of the D1 receptor agonist SKF38393 mimicked this effect, also facilitating extinction in adolescent subjects. Furthermore, pharmacological intervention attenuated subsequent drug-primed reinstatement of cocaine-conditioned preferences. We establish a potential direction for distinct strategies to treat this vulnerable population." @default.
- W2004451864 created "2016-06-24" @default.
- W2004451864 creator A5012854700 @default.
- W2004451864 creator A5028983848 @default.
- W2004451864 creator A5074317112 @default.
- W2004451864 date "2010-08-01" @default.
- W2004451864 modified "2023-10-14" @default.
- W2004451864 title "Enhancing the salience of dullness: behavioral and pharmacological strategies to facilitate extinction of drug-cue associations in adolescent rats" @default.
- W2004451864 cites W1544565990 @default.
- W2004451864 cites W1605427252 @default.
- W2004451864 cites W1946000001 @default.
- W2004451864 cites W1964528322 @default.
- W2004451864 cites W1967292256 @default.
- W2004451864 cites W1972075913 @default.
- W2004451864 cites W1973371295 @default.
- W2004451864 cites W1977798186 @default.
- W2004451864 cites W1985645068 @default.
- W2004451864 cites W1988068086 @default.
- W2004451864 cites W1996885013 @default.
- W2004451864 cites W2001074622 @default.
- W2004451864 cites W2003039924 @default.
- W2004451864 cites W2005856089 @default.
- W2004451864 cites W2007760226 @default.
- W2004451864 cites W2012804248 @default.
- W2004451864 cites W2013924762 @default.
- W2004451864 cites W2014262050 @default.
- W2004451864 cites W2015905229 @default.
- W2004451864 cites W2018650416 @default.
- W2004451864 cites W2020406157 @default.
- W2004451864 cites W2027143836 @default.
- W2004451864 cites W2029383300 @default.
- W2004451864 cites W2035771644 @default.
- W2004451864 cites W2037663859 @default.
- W2004451864 cites W2043575141 @default.
- W2004451864 cites W2047747458 @default.
- W2004451864 cites W2049120251 @default.
- W2004451864 cites W2054400557 @default.
- W2004451864 cites W2055409618 @default.
- W2004451864 cites W2057760214 @default.
- W2004451864 cites W2062574700 @default.
- W2004451864 cites W2068735847 @default.
- W2004451864 cites W2074754417 @default.
- W2004451864 cites W2088753284 @default.
- W2004451864 cites W2089816026 @default.
- W2004451864 cites W2090500826 @default.
- W2004451864 cites W2100804779 @default.
- W2004451864 cites W2103791867 @default.
- W2004451864 cites W2105758413 @default.
- W2004451864 cites W2113375740 @default.
- W2004451864 cites W2124405898 @default.
- W2004451864 cites W2124464181 @default.
- W2004451864 cites W2128946570 @default.
- W2004451864 cites W2130838343 @default.
- W2004451864 cites W2141376829 @default.
- W2004451864 cites W2141405812 @default.
- W2004451864 cites W2143384095 @default.
- W2004451864 cites W2148399921 @default.
- W2004451864 cites W2156900283 @default.
- W2004451864 cites W2165725596 @default.
- W2004451864 cites W2175523146 @default.
- W2004451864 cites W4234620288 @default.
- W2004451864 cites W4322703236 @default.
- W2004451864 doi "https://doi.org/10.1016/j.neuroscience.2010.05.063" @default.
- W2004451864 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2907356" @default.
- W2004451864 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/20639130" @default.
- W2004451864 hasPublicationYear "2010" @default.
- W2004451864 type Work @default.
- W2004451864 sameAs 2004451864 @default.
- W2004451864 citedByCount "37" @default.
- W2004451864 countsByYear W20044518642012 @default.
- W2004451864 countsByYear W20044518642013 @default.
- W2004451864 countsByYear W20044518642014 @default.
- W2004451864 countsByYear W20044518642015 @default.
- W2004451864 countsByYear W20044518642016 @default.
- W2004451864 countsByYear W20044518642017 @default.
- W2004451864 countsByYear W20044518642018 @default.
- W2004451864 countsByYear W20044518642020 @default.
- W2004451864 countsByYear W20044518642021 @default.
- W2004451864 countsByYear W20044518642022 @default.
- W2004451864 crossrefType "journal-article" @default.
- W2004451864 hasAuthorship W2004451864A5012854700 @default.
- W2004451864 hasAuthorship W2004451864A5028983848 @default.
- W2004451864 hasAuthorship W2004451864A5074317112 @default.
- W2004451864 hasBestOaLocation W20044518642 @default.
- W2004451864 hasConcept C101991246 @default.
- W2004451864 hasConcept C108154423 @default.
- W2004451864 hasConcept C138496976 @default.
- W2004451864 hasConcept C151730666 @default.
- W2004451864 hasConcept C15744967 @default.
- W2004451864 hasConcept C169760540 @default.
- W2004451864 hasConcept C169900460 @default.
- W2004451864 hasConcept C2776552330 @default.
- W2004451864 hasConcept C2779343474 @default.
- W2004451864 hasConcept C2779934784 @default.
- W2004451864 hasConcept C2781195155 @default.
- W2004451864 hasConcept C48856860 @default.
- W2004451864 hasConcept C513476851 @default.
- W2004451864 hasConcept C86803240 @default.