2009
DOI: 10.1007/s00213-009-1707-0
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Evidence of long-term expression of behavioral sensitization to both cocaine and ethanol in dopamine transporter knockout mice

Abstract: These findings, showing that DAT deletion facilitates sensitization, suggest a cross-sensitization-like effect between genetic- and pharmacological-induced hyperdopaminergia.

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Cited by 27 publications
(12 citation statements)
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“…Interestingly, DAT-KO mice were still able to express conditioned place preference (CPP) to cocaine (Sora et al 1998), long term behavioral sensitization (Morice et al 2010) and the ability to self-administer the drug, although less than control (Rocha et al 1998). While DAT-KO still showed rewarding properties to amphetamine (Budygin et al, 2004), this psychostimulant was also able to significantly reduce the locomotor activity of the DAT-KO mice when given in a novel environment.…”
Section: Genetic Manipulations Of the Dat And Responses To Drugs Of Amentioning
confidence: 99%
“…Interestingly, DAT-KO mice were still able to express conditioned place preference (CPP) to cocaine (Sora et al 1998), long term behavioral sensitization (Morice et al 2010) and the ability to self-administer the drug, although less than control (Rocha et al 1998). While DAT-KO still showed rewarding properties to amphetamine (Budygin et al, 2004), this psychostimulant was also able to significantly reduce the locomotor activity of the DAT-KO mice when given in a novel environment.…”
Section: Genetic Manipulations Of the Dat And Responses To Drugs Of Amentioning
confidence: 99%
“…In DAT-KO mice cocaine still possesses rewarding properties that can be seen in a conditional place preference test (Sora et al, 1998). Also, DAT-KO mice are able to develop long-term expression of sensitization to cocaine (Morice et al, 2009). Importantly, when self-administration of cocaine was tested, DAT-KO mice showed the ability to perform the task (Rocha et al, 1998), albeit much reduced, whereas performance to food reinforcement remained normal (Thomsen et al, 2009a).…”
Section: Dat Knockout (Dat-ko) Micementioning
confidence: 99%
“…Despite the increased DA levels, mice genetically modified to be hyperdopaminergic do not learn faster than normal mice. They do, however, demonstrate increased motivation for food (Cagniard et al, 2006a; Cagniard et al, 2006b), morphine (Spielewoy et al, 2000a), endocannabinoid (Tzavara et al, 2006), and cocaine (Morice et al, 2009). In addition, persistent hyperdopaminergia could also change many other functions, including various behavioral disturbances (Spielewoy et al, 2000b) such as disrupted responses in social interaction (Rodriguiz et al, 2004), enhanced resistance to extinction (Hironaka et al, 2004), reduced behavioral lateralization (Morice et al, 2005), and reduced cognitive flexibility (Morice et al, 2007); marked changes in functional interaction between DA and glutamate (Gainetdinov et al, 2001a); motor dysfunction and selective degeneration of striatal GABAergic neurons (Cyr et al, 2003); and decreased hippocampal theta oscillations (Dzirasa et al, 2009b) and disrupted neural phase signaling (Dzirasa et al, 2009a).…”
Section: Dysfunction Of Dopaminergic Transmission — Hypodopaminergmentioning
confidence: 99%