Role of dopamine D2 receptors in plasticity of stress-induced addictive behaviours
Dopaminergic systems are implicated in stress-related behaviour. Here we investigate behavioural responses to chronic stress in dopamine D2 receptor knockout mice and find that anxiety-like behaviours are increased compared with wild-type mice. Repeated stress exposure suppresses cocaine-induced beh...
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Veröffentlicht in: | Nature communications 2013, Vol.4 (1), p.1579-1579, Article 1579 |
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Sprache: | eng |
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Zusammenfassung: | Dopaminergic systems are implicated in stress-related behaviour. Here we investigate behavioural responses to chronic stress in dopamine D2 receptor knockout mice and find that anxiety-like behaviours are increased compared with wild-type mice. Repeated stress exposure suppresses cocaine-induced behavioural sensitization, cocaine-seeking and relapse behaviours in dopamine D2 receptor knockout mice. Cocaine challenge after drug withdrawal in cocaine-experienced wild-type or dopamine D2 receptor knockout mice is associated with inhibition of long-term depression in the nucleus accumbens, and chronic stress during withdrawal prevents inhibition after cocaine challenge in cocaine-experienced dopamine D2 receptor knockout mice, but not in wild-type mice. Lentiviral-induced knockdown of dopamine D2 receptors in the nucleus accumbens of wild-type mice does not affect basal locomotor activity, but confers stress-induced inhibition of the expression of cocaine-induced behavioural sensitization. Stressed mice depleted of dopamine D2 receptors do not manifest long-term depression inhibition. Our results suggest that dopamine D2 receptors have roles in regulating synaptic modification triggered by stress and drug addiction.
Synaptic plasticity in the nucleus accumbens is implicated in stress and addiction. Sim
et al
. study mice deficient in dopamine D2 receptors, and find an increase in anxiety behaviour and reduced addictive behaviour in response to stress, both of which are associated with changes in nucleus accumbens activity. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/ncomms2598 |