Abstract:Research on delay discounting has focused largely on non-drug reinforcers in an isomorphic context in which choice is between alternatives that involve the same type of reinforcer. Less often, delay discounting has been studied with drug reinforcers in a more ecologically valid allomorphic context where choice is between alternatives involving different types of reinforcers. The present experiment is the first to examine discounting of drug and non-drug reinforcers in both isomorphic and allomorphic situations… Show more
“…Bickel et al (2011) found a trend for cocaine addicts to discount delayed money more when the alternative was immediate cocaine than when the alternative was immediate money. Huskinson et al (2015) found that rhesus monkeys discounted delayed food more steeply when the alternative was immediate cocaine than when the alternative was immediate food. These findings are consistent with the steep discounting of delayed food that we observed when the alternative to delayed food was immediate delivery of a 16 µg/kg/inj dose of remifentanil, and they are consistent with similar effects in rhesus monkeys (Maguire et al 2013).…”
Section: Discussionmentioning
confidence: 96%
“…Since the percent choice curve and the area under this curve could be affected by the nondelayed values of the drug and nondrug options, or by the difference between these two values, the shape of the curves obtained in these experiments might not generalize to other amounts of food. More complete information could be obtained by determining indifference points between delayed and nondelayed rewards over a wider range of values (Bickel et al 2011; Huskinson et al 2015; Mazur 1987). However, despite this limitation, the comparisons obtained with the streamlined procedure clearly demonstrate that the nature of the immediate drug option strongly affects the value of the delayed nondrug option.…”
Section: Discussionmentioning
confidence: 99%
“…This maladaptive choice behavior involves delay discounting, the tendency to place less value on rewards that are not received immediately (Bickel et al 2014; Lamb et al 2016). From this perspective, procedures that allow animals to choose between immediate drug injection and delayed delivery of a salient nondrug reward could provide a useful model of addiction (Huskinson et al 2015; Maguire et al 2013; Woolverton and Anderson 2006), with certain advantages over procedures that only involve drug reward or that only provide a choice between immediate drug and immediate nondrug reward.…”
Rationale
Addiction involves maladaptive choice behavior in which immediate drug effects are valued more than delayed nondrug rewards.
Objectives and Methods
To model this behavior and extend our earlier work with the prescription opioid oxycodone, we allowed rats to choose between immediate intravenous delivery of the short-acting opioid remifentanil and delayed delivery of highly palatable food pellets. Treatment drugs were tested on a baseline where remifentanil was preferred over food.
Results
Treatment with a high dose of the opioid antagonist naltrexone decreased but did not reverse the preference for remifentanil. Treatment with the serotonin 5-HT2C agonist lorcaserin decreased remifentanil and food self-administration nonselectively. Across conditions in which the alternative to delayed food was either a moderate dose of oxycodone, a moderate or high dose of remifentanil, a smaller more immediate delivery of food, or timeout with no primary reinforcement, choice was determined by both the length of the delay and the nature of the alternative option. Delayed food was discounted most steeply when the alternative was a high dose of remifentanil, which was preferred over food when food was delayed by 30 s or more. Within-subject comparisons showed no evidence for trait-like impulsivity or sensitivity to delay across these conditions.
Conclusions
Choice was determined more by the current contingencies of reinforcement than by innate individual differences. This finding suggests that people might develop steep delay-discounting functions because of the contingencies in their environment, and it supports the use of contingency management to enhance the relative value of delayed non-drug reinforcers.
“…Bickel et al (2011) found a trend for cocaine addicts to discount delayed money more when the alternative was immediate cocaine than when the alternative was immediate money. Huskinson et al (2015) found that rhesus monkeys discounted delayed food more steeply when the alternative was immediate cocaine than when the alternative was immediate food. These findings are consistent with the steep discounting of delayed food that we observed when the alternative to delayed food was immediate delivery of a 16 µg/kg/inj dose of remifentanil, and they are consistent with similar effects in rhesus monkeys (Maguire et al 2013).…”
Section: Discussionmentioning
confidence: 96%
“…Since the percent choice curve and the area under this curve could be affected by the nondelayed values of the drug and nondrug options, or by the difference between these two values, the shape of the curves obtained in these experiments might not generalize to other amounts of food. More complete information could be obtained by determining indifference points between delayed and nondelayed rewards over a wider range of values (Bickel et al 2011; Huskinson et al 2015; Mazur 1987). However, despite this limitation, the comparisons obtained with the streamlined procedure clearly demonstrate that the nature of the immediate drug option strongly affects the value of the delayed nondrug option.…”
Section: Discussionmentioning
confidence: 99%
“…This maladaptive choice behavior involves delay discounting, the tendency to place less value on rewards that are not received immediately (Bickel et al 2014; Lamb et al 2016). From this perspective, procedures that allow animals to choose between immediate drug injection and delayed delivery of a salient nondrug reward could provide a useful model of addiction (Huskinson et al 2015; Maguire et al 2013; Woolverton and Anderson 2006), with certain advantages over procedures that only involve drug reward or that only provide a choice between immediate drug and immediate nondrug reward.…”
Rationale
Addiction involves maladaptive choice behavior in which immediate drug effects are valued more than delayed nondrug rewards.
Objectives and Methods
To model this behavior and extend our earlier work with the prescription opioid oxycodone, we allowed rats to choose between immediate intravenous delivery of the short-acting opioid remifentanil and delayed delivery of highly palatable food pellets. Treatment drugs were tested on a baseline where remifentanil was preferred over food.
Results
Treatment with a high dose of the opioid antagonist naltrexone decreased but did not reverse the preference for remifentanil. Treatment with the serotonin 5-HT2C agonist lorcaserin decreased remifentanil and food self-administration nonselectively. Across conditions in which the alternative to delayed food was either a moderate dose of oxycodone, a moderate or high dose of remifentanil, a smaller more immediate delivery of food, or timeout with no primary reinforcement, choice was determined by both the length of the delay and the nature of the alternative option. Delayed food was discounted most steeply when the alternative was a high dose of remifentanil, which was preferred over food when food was delayed by 30 s or more. Within-subject comparisons showed no evidence for trait-like impulsivity or sensitivity to delay across these conditions.
Conclusions
Choice was determined more by the current contingencies of reinforcement than by innate individual differences. This finding suggests that people might develop steep delay-discounting functions because of the contingencies in their environment, and it supports the use of contingency management to enhance the relative value of delayed non-drug reinforcers.
“…Moreover, the current findings with remifentanil, taken together with studies using cocaine, support the hypothesis that in nonhuman primates drug reinforcers in general might be discounted less steeply than non-drug reinforcers such as sweetened solutions (see Freeman et al, 2009; 2012). A recent study reported that the rate at which food is discounted depends upon whether food or drug (cocaine) is available as the immediately delivered alternative (Huskinson et al, 2015), demonstrating that the types of commodities that are available, as either the immediate or the delayed option, also impact discounting. It is not known whether monkeys in the current study might discount other opioids (e.g., heroin), drugs with different pharmacological mechanisms (e.g., cocaine), or non-drug reinforcers (e.g., food) at different rates.…”
Section: Discussionmentioning
confidence: 99%
“…Studies to date indicate that delaying delivery of an otherwise preferred reinforcer, whether food (Maguire et al, 2013b; Woolverton and Anderson, 2006; Huskinson et al 2015) or a dose of drug (Maguire et al, 2013a; Woolverton and Anderson, 2006; Woolverton et al, 2007), increases responding for a small and less preferred reinforcer (e.g., small dose of drug). Delaying presentation of preferred commodities increases the effectiveness of small immediately-available commodities.…”
Although increased impulsivity (delay discounting) is an important risk factor for drug abuse, the impact of delay on drug taking has received relatively little attention.
This study examined delay discounting of the mu opioid receptor agonist remifentanil in rhesus monkeys (n=4) responding for intravenous (i.v.) infusions under a concurrent choice procedure. Dose-effect curves for remifentanil were determined by varying the dose available on one lever (0.001-0.32 μg/kg/infusion) while keeping the dose available on the other lever (0.1 μg/kg/infusion) the same. Dose-effect curves were determined when both infusions were delivered immediately and when delivery of the fixed dose was delayed (15-180 s).
When both doses of remifentanil were delivered immediately, monkeys chose the large dose. Delaying delivery of the fixed dose reduced choice of that dose and increased choice of small immediately available doses.
Extending previous studies these results show that the effects of delay on choice between two doses of a mu opioid receptor agonist are consistent with hyperbolic discounting. Delaying delivery of a preferred reinforcer (e.g., large dose of drug) reduces its effectiveness and increases the effectiveness of small immediately available doses. This effect of delay, particularly on drug self-administration, might contribute to drug abuse.
Impulsive choice describes preference for smaller, sooner rewards over larger, later rewards. Excessive delay discounting (i.e., rapid devaluation of delayed rewards) underlies some impulsive choices, and is observed in many maladaptive behaviors (e.g., substance abuse, gambling). Interventions designed to reduce delay discounting may provide therapeutic gains. One such intervention provides rats with extended training with delayed reinforcers. When compared to a group given extended training with immediate reinforcers, delay-exposed rats make significantly fewer impulsive choices. To what extent is this difference due to delay-exposure training shifting preference toward self-control or immediacy-exposure training (the putative control group) shifting preference toward impulsivity? The current study compared the effects of delay- and immediacy-exposure training to a no-training control group and evaluated within-subject changes in impulsive choice across 51 male Wistar rats. Delay-exposed rats made significantly fewer impulsive choices than immediacy-exposed and control rats. Between-group differences in impulsive choice were not observed in the latter two groups. While delay-exposed rats showed large, significant pre- to posttraining reductions in impulsive choice, immediacy-exposed and control rats showed small reductions in impulsive choice. These results suggest that extended training with delayed reinforcers reduces impulsive choice, and that extended training with immediate reinforcers does not increase impulsive choice.
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