Psychopharmacological characterisation of the successive negative contrast effect in rats
Author(s)
Phelps, CE
Mitchell, EN
Nutt, DJ
Marston, HM
Robinson, ESJ
Type
Journal Article
Abstract
Rationale
Successive negative contrast (SNC) describes a change in the behaviour of an animal following a downshift in the quantitative or qualitative value of an expected reward. This behavioural response has been hypothesised to be linked to affective state, with negative states associated with larger and/or prolonged shifts in behaviour.
Objective
This study has investigated whether different psychopharmacological treatments have dissociable actions on the SNC effect in rats and related these findings to their actions on different neurotransmitter systems and affective state.
Methods
Animals were trained to perform a nose-poke response to obtain a high-value food reward (four pellets). SNC was quantified during devalue sessions in which the reward was reduced to one pellet. Using a within-subject study design, the effects of acute treatment with anxiolytic, anxiogenic, antidepressant and dopaminergic drugs were investigated during both baseline (four pellets) or devalue sessions (one pellet).
Results
The indirect dopamine agonist, amphetamine, attenuated the SNC effect whilst the D1/D2 antagonist, alpha-flupenthixol, potentiated it. The antidepressant citalopram, anxiolytic buspirone and anxiogenic FG7142 had no specific effects on SNC, although FG7142 induced general impairments at higher doses. The α2-adrenoceptor antagonist, yohimbine, increased premature responding but had no specific effect on SNC. Results for the anxiolytic diazepam were mixed with one group showing an attenuation of the SNC effect whilst the other showed no effect.
Conclusions
These data suggest that the SNC effect is mediated, at least in part, by dopamine signalling. The SNC effect may also be attenuated by benzodiazepine anxiolytics.
Successive negative contrast (SNC) describes a change in the behaviour of an animal following a downshift in the quantitative or qualitative value of an expected reward. This behavioural response has been hypothesised to be linked to affective state, with negative states associated with larger and/or prolonged shifts in behaviour.
Objective
This study has investigated whether different psychopharmacological treatments have dissociable actions on the SNC effect in rats and related these findings to their actions on different neurotransmitter systems and affective state.
Methods
Animals were trained to perform a nose-poke response to obtain a high-value food reward (four pellets). SNC was quantified during devalue sessions in which the reward was reduced to one pellet. Using a within-subject study design, the effects of acute treatment with anxiolytic, anxiogenic, antidepressant and dopaminergic drugs were investigated during both baseline (four pellets) or devalue sessions (one pellet).
Results
The indirect dopamine agonist, amphetamine, attenuated the SNC effect whilst the D1/D2 antagonist, alpha-flupenthixol, potentiated it. The antidepressant citalopram, anxiolytic buspirone and anxiogenic FG7142 had no specific effects on SNC, although FG7142 induced general impairments at higher doses. The α2-adrenoceptor antagonist, yohimbine, increased premature responding but had no specific effect on SNC. Results for the anxiolytic diazepam were mixed with one group showing an attenuation of the SNC effect whilst the other showed no effect.
Conclusions
These data suggest that the SNC effect is mediated, at least in part, by dopamine signalling. The SNC effect may also be attenuated by benzodiazepine anxiolytics.
Date Issued
2015-03-21
Date Acceptance
2015-02-23
Citation
Psychopharmacology, 2015, 232 (15), pp.2697-2709
ISSN
1432-2072
Publisher
Springer Verlag
Start Page
2697
End Page
2709
Journal / Book Title
Psychopharmacology
Volume
232
Issue
15
Copyright Statement
This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
License URL
Subjects
Science & Technology
Life Sciences & Biomedicine
Neurosciences
Pharmacology & Pharmacy
Psychiatry
Neurosciences & Neurology
Anxiety
Antidepressant
Affective state
Behaviour
Monoamine transmitters
ELEVATED-PLUS-MAZE
REACTION-TIME-TASK
ANIMAL-MODELS
OPIOID RECEPTORS
AMPHETAMINE
PERFORMANCE
DEPRESSION
CITALOPRAM
BUSPIRONE
BRAIN
Amphetamine
Animals
Anti-Anxiety Agents
Behavior, Animal
Buspirone
Carbolines
Citalopram
Diazepam
Dopamine Agents
Dopamine Antagonists
Emotions
Flupenthixol
GABA Antagonists
Male
Rats
Reward
Serotonin Receptor Agonists
Serotonin Uptake Inhibitors
11 Medical And Health Sciences
17 Psychology And Cognitive Sciences
Publication Status
Published