Key result
D1 and D2 dopamine antagonists prevent the rewarding and anxiolytic effects of neurotensin in rats.
Why the study?
Neurotensin in the ventral pallidum has rewarding and anxiolytic effects and interacts with dopamine receptors elsewhere, but this interaction had not been investigated in the ventral pallidum.
p-value: p=<0.05
The activity of D1-like and D2-like dopamine receptors in the ventral pallidum is necessary for the rewarding and anxiolytic effects of neurotensin in rats.
NT-DA receptor interactions in VP warrant further animal work; leaves open any clinical relevance or therapeutic targeting.
BACKGROUND: Neurotensin (NT) acts as a neurotransmitter and neuromodulator in the central nervous system. It was shown previously that NT in the ventral pallidum (VP) has rewarding and anxiolytic effects. NT exerts its effect in interaction with dopamine (DA) receptors in numerous brain areas; however, this has not yet been investigated in the VP. The aim of this study was to examine whether the inhibition of D1-like and D2-like DA receptors of the VP can modify the above mentioned effects of NT. METHODS: Microinjection cannulas were implanted by means of stereotaxic operations into the VP of male Wistar rats. The rewarding effect of NT was examined by means of a conditioned place preference test. Anxiety was investigated with an elevated plus maze test. To investigate the possible interaction, D1-like DA receptor antagonist SCH23390 or D2-like DA receptor antagonist sulpiride were microinjected prior to NT. All of the drugs were also injected independently to analyze their effects alone. RESULTS: In the present experiments, both the rewarding and anxiolytic effects of NT in the VP were prevented by both D1-like and D2-like DA receptor antagonists. Administered on their own, the antagonists did not influence reward and anxiety. CONCLUSION: Our present results show that the activity of the D1-like and D2-like DA receptors of the VP is a necessary requirement for both the rewarding and anxiolytic effects of NT.
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Ollmann et al. (2022) studied Reward and anxiety (animal model) (n=165). D1-like (SCH23390) and D2-like (sulpiride) dopamine receptor antagonists vs. Vehicle or neurotensin alone was evaluated on Conditioned place preference (time spent in treatment quadrant) and elevated plus maze (time spent in open arms) (p=<0.05). Pretreatment with D1-like or D2-like dopamine receptor antagonists prevented both the rewarding and anxiolytic effects of neurotensin in the ventral pallidum of rats.
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