Chronic D<sub>2/3sub> agonist ropinirole treatment increases preference for uncertainty in rats regardless of baseline choice patterns
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- 作者：Melanie Tremblay ; Mason M. Silveira ; Sukhbir Kaur ; Jay G. Hosking ; Wendy K. Adams ; Christelle Baunez and Catharine A. Winstanley
- 刊名：European Journal of Neuroscience
- 出版年：2017
- 出版时间：January 2017
- 年：2017
- 卷：45
- 期：1
- 页码：159-166
- 全文大小：765K
- ISSN：1460-9568
文摘
D<sub>2/3sub> receptor agonists are effective treatments for Parkinson's disease (PD), but can precipitate impulse control disorders (ICDs) including gambling disorder (GD). The neurobiological mechanisms underlying this devastating side-effect of dopamine agonist replacement therapy (DRT), and any dependence on the dopamine depletion caused by PD, are unclear. It is also unclear whether previous biases towards risk or uncertainty are a risk factor for developing these ICDs. We investigated whether chronic D<sub>2/3sub> agonist administration (5 mg/kg/day ropinirole for 28 days) altered performance of a rat model of gambling-like behaviour, the rodent betting task (rBT), and examined if baseline behaviour predicted this behavioural change. The rBT captures individual differences in subjective preference for uncertain outcomes: animals choose between guaranteed or probabilistic reinforcement of equal expected value. Chronic ropinirole dramatically increased selection of the uncertain option in two-thirds of animals, regardless of baseline preferences. The effect on choice in the rBT was replicated in a dorsolateral striatal 6-hydroxydopamine (6-OHDA) rat model of early PD. These studies are the first to look at individual differences in response to chronic, rather than pulsatile, dosing of DRT in a rodent model of gambling behaviour. These findings suggest that DRT-induced PG may stem from increases in subjective valuation of uncertainty. Such symptoms likely arise because of changes in dopaminergic striatal signalling caused by DRT rather than from an interaction between pre-morbid behaviours or PD itself.