scholarly journals Cue-motivated reward seeking is negatively regulated by expected reward magnitude in Pavlovian-instrumental transfer

2021 ◽  
Author(s):  
Andrew T Marshall ◽  
Sean B. Ostlund

The Pavlovian-instrumental transfer (PIT) paradigm is widely used to assay the motivational influence of reward-paired cues, which is reflected by their ability to stimulate instrumental reward-seeking behavior. Leading models of incentive learning assume that motivational value is assigned to cues based on the total amount of reward they signal (i.e., their state value). Based on recent findings, we lay out the alternative hypothesis that cue-elicited reward predictions may actually suppress the motivation to seek out new rewards through instrumental behavior in order to facilitate efficient retrieval of a reward that is already expected, before it is lost or stolen. According to this view, cue-motivated reward seeking should be inversely related to the magnitude of an expected reward, since there is more to lose by failing to secure a large reward than a small reward. We investigated the influence of expected reward magnitude on PIT expression. Hungry rats were initially trained to lever press for food pellets before undergoing Pavlovian conditioning, in which two distinct auditory cues signaled food pellet delivery at cue offset. Reward magnitude was varied across cues and groups. While all groups had at least one cue that signaled three food pellets, the alternate cue signaled either one (Group 1/3), three (Group 3/3), or nine food pellets (Group 3/9). PIT testing revealed that the motivational influence of reward-predictive cues on lever pressing varied inversely with expected reward magnitude, with the 1-pellet cue augmenting performance and the 3- and 9-pellet cues suppressing performance, particularly near the expected time of reward delivery. This pattern was mirrored by opposing changes in the food-port entry behavior, which varied positively with expected reward magnitude. We discuss how these findings may relate to cognitive control over cue-motivated behavior.

2020 ◽  
Author(s):  
Andrew T. Marshall ◽  
Nigel T. Maidment ◽  
Sean B. Ostlund

AbstractImpulsive behavior during adolescence may stem from a developmental imbalance between motivational and impulse control systems, producing greater urges to pursue reward and weakened capacities to inhibit such actions. Here, we developed a Pavlovian-instrumental transfer (PIT) protocol to assay rats’ ability to suppress cue-motivated reward seeking based on changes in reward expectancy. Traditionally, PIT studies focus on how reward-predictive cues motivate instrumental reward-seeking behavior (lever pressing). However, cues signaling imminent reward delivery also elicit countervailing focal-search responses (food-cup approach). We first examined how reward expectancy (cue-reward probability) influences expression of these competing behaviors. Adult male rats increased rates of lever pressing when presented with cues signaling lower probabilities of reward but focused their activity at the food cup on trials with cues that signaled higher probabilities of reward. We then compared adolescent and adult male rats in their responsivity to cues signaling different reward probabilities. In contrast to adults, adolescent rats did not flexibly adjust their pattern of responding based on the expected likelihood of reward delivery but increased their rate of lever pressing for both weak and strong cues. These findings indicate that impulse control over cue-motivated behavior is fundamentally dysregulated during adolescence, providing a model for studying neurobiological mechanisms of adolescent impulsivity.


eLife ◽  
2018 ◽  
Vol 7 ◽  
Author(s):  
Jocelyn M Richard ◽  
Nakura Stout ◽  
Deanna Acs ◽  
Patricia H Janak

Despite its being historically conceptualized as a motor expression site, emerging evidence suggests the ventral pallidum (VP) plays a more active role in integrating information to generate motivation. Here, we investigated whether rat VP cue responses would encode and contribute similarly to the vigor of reward-seeking behaviors trained under Pavlovian versus instrumental contingencies, when these behavioral responses consist of superficially similar locomotor response patterns but may reflect distinct underlying decision-making processes. We find that cue-elicited activity in many VP neurons predicts the latency of instrumental reward seeking, but not of Pavlovian response latency. Further, disruption of VP signaling increases the latency of instrumental but not Pavlovian reward seeking. This suggests that VP encoding of and contributions to response vigor are specific to the ability of incentive cues to invigorate reward-seeking behaviors upon which reward delivery is contingent.


2012 ◽  
Vol 5 (3) ◽  
pp. 178-189 ◽  
Author(s):  
Oscar Arias-Carrion ◽  
Mohamed Salama

2019 ◽  
Vol 39 (3) ◽  
pp. 435-449 ◽  
Author(s):  
Tania Campos-Ordonez ◽  
David Zarate-Lopez ◽  
Nereida Ibarra-Castaneda ◽  
Jonathan Buritica ◽  
Oscar Gonzalez-Perez

2010 ◽  
Vol 67 (9) ◽  
pp. 864-871 ◽  
Author(s):  
Oz Malkesman ◽  
Maria Luisa Scattoni ◽  
Daniel Paredes ◽  
Tyson Tragon ◽  
Brandon Pearson ◽  
...  

2018 ◽  
Author(s):  
Vikas Navratna ◽  
Dilip K. Tosh ◽  
Kenneth A. Jacobson ◽  
Eric Gouaux

AbstractThe human dopamine transporter(hDAT) plays a major role in dopamine homeostasis and regulation of neurotransmission by clearing dopamine from the extracellular space using secondary active transport. Dopamine is an essential monoamine chemical messenger that regulates reward seeking behavior, motor control, hormonal release, and emotional response in humans. Psychostimulants such as cocaine primarily target the central binding site of hDAT and lock the transporter in an outward-facing conformation, thereby inhibiting dopamine reuptake. The inhibition of dopamine reuptake leads to accumulation of dopamine in the synapse causing heightened signaling. In addition, hDAT is implicated in various neurological disorders and disease-associated neurodegeneration. Despite its significance, the molecular architecture of hDAT and its various conformational states are poorly understood. Instability of hDAT in detergent micelles has been a limiting factor in its successful biochemical, biophysical, and structural characterization. To overcome this hurdle, first we identified ligands that stabilize hDAT in detergent micelles. Then, we screened ∼200 single residue mutants of hDAT using high-throughput scintillation proximity assay, and identified a thermostable variant(I248Y). Here we report a robust strategy to overexpress and successfully purify a thermostable variant of hDAT in an inhibitor and allosteric ligand bound conformation.


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