Human choices are shaped by awareness of past experiences and anticipation of future possibilities. Faced with choices in the here and now, we draw on memories to imagine the different paths before us depending on which way we choose. These memories drive us forward one way or another, as we seek to avoid prior mistakes or relive past experiences. Such memory-based decision-making is familiar from our own lives and a core topic in the cognitive neuroscience of memory. It is also a prevalent theme within clinical contexts and addiction folklore, as demonstrated by the trope of “chasing the first high”:

“The first time I took a drink it was like the black and white world became Technicolor… The first time I smoked a cigarette, I can act it out for you, but then you can't record that. It felt like this. (Demonstrates – sighs.) […]. It relaxed my mind, my body, my breathing, everything. And that is what I was continuing to search for every time I smoked a cigarette after that” [1].

Yet despite empirical data showing that hippocampus and adjacent structures, which in humans are tightly linked to episodic memory, are critical to addiction-related behaviors [2,3,4], and recent work highlighting the role of drugs in memory encoding [5, 6], the role of memory retrieval remains less well-understood, and potentially crucial [7,8,9,10].

In the field of decision making, there is emerging consensus that processes occurring during memory retrieval play a distinct role in biasing choice [11,12,13]. Our aim in this article is to situate memory retrieval within the theory of addiction mechanisms. Drawing on recent work that identifies a key role for episodic memory in decisions for reward [14,15,16,17,18,19,20], we propose a framework in which drug choices are biased by selective sampling of individual memories during two key phases of addiction: (i) downward spiral into persistent use and (ii) relapse. Existing mechanistic accounts that posit addiction as a disorder of value learning [21,22,23,24] or as uniquely determined by incentive sensitization and cue-induced craving [25,26,27] or habit-like compulsion [28,29,30] have difficulty explaining both phases. Memory sampling offers a framework for value-based choice which incorporates features of these mechanisms, allowing flexibility in choice while explaining the outsized influence of particular past experiences (Box 1). In essence, the core idea is that episodic memories of highly rewarding past experiences [31,32,33] can be elicited by associated cues and contexts and come to bias present choices, as opposed to these choices either being determined by a static summary of past outcomes or driven by inflexible compulsion; importantly, these memories and processes can be conscious or unconscious (Box 2). Memory sampling as a mechanism is therefore distinct from, but complementary to, incentive sensitization and craving [25,26,27] in functioning as a causal intermediary between drug-associated cues and contexts on the one hand, and drug choices and behavior on the other.

The puzzle of addiction

All addiction originates in non-addictive psychoactive drug consumption. In humans, this consumption is goal-directed: a means to achieve represented outcomes, such as their anticipated effects on mental states [8, 34]. These effects may be intrinsically valuable, e.g., hedonia, or relief from boredom, pain, stress and psychological suffering; or they may facilitate valued behaviors, e.g., sociability, sex, and task performance. Regardless of the goal of consumption, the majority of users do not transition to addiction [35,36,37], maintaining patterns of consumption that exploit drug benefits while incurring minimal costs.

The transition from non-addictive use to addiction occurs when this balance tips and drug costs come to outweigh drug benefits [38]. However, this immediately complicates demarcating non-addicted and addicted use. Costs and benefits must be weighed relative to values, which vary between individuals, including people with SUDs and observers; moreover, contingent, environmental factors, e.g., status and wealth, can protect against costs [38, 39]. This individuality and complexity is reflected in the DSM-5 [40] diagnostic criteria for SUD that is both polythetic and graded from mild to severe. These criteria include: (i) cravings and failures to limit use as intended, as (ii) drugs come to occupy increasing time and attentional focus, despite (iii) incurring severe risks and negative consequences, including e.g., drug-related mental and physical health problems, and loss of important relationships, social standing, employment, or housing. In countries that criminalize drug possession and stigmatize drug users, there is also risk of criminal sanction and social ostracization.

Continued consumption at the expense of other goods and despite costs is central to the construct of addiction and defines what is so puzzling about it as a form of behavior. Even though drug choices are initially goal-directed, they come to appear to have features not in keeping with purposive behavior, in so far as they contradict first-person reports of desired abstinence and incur costs that, at least from an observer’s vantage point, ought to tip the balance and disincentivize use. Put crudely, the puzzle of addiction is to understand why individuals keep using when drugs no longer appear worth it [38].

This general puzzle of addiction is particularly striking in relation to two key phases of the addiction process:

(i) Spiraling into addiction. Initial stages of consumption prior to addiction typically involve highly rewarding drug experiences. By contrast, the spiral into addiction is characterized not only by increasing negative consequences but by diminishing drug returns: as tolerance increases, hedonia is often claimed to decrease [25, 27]. This behavior is frustrating for standard RL accounts of value-based choice (RL; Box 1), which base decisions on a “running average” of experienced reward (and punishment) outcomes. Taken alone, these models predict that drug choice would eventually cease of its own accord. This gap can be accounted for by introducing disordered learning signals that result in persistent drug preference [21]; however, this leaves abstinence to be explained via “unlearning”, which compromises the model’s capacity to explain relapse [41]. Further, while this model succeeds in predicting drug choice behavior that is sensitive to the rational tradeoff against other rewards [42], it fails to capture the rich repertoire of flexible, goal-directed drug-seeking behaviors evident in human drug choice [24, 43].

(ii) Relapse. Quit attempts often occur when individuals hit “rock bottom” [44] and cannot avoid facing the most severe negative consequences of consumption [45,46,47]. Although medical management can ease the effects of withdrawal, it typically remains physically and psychologically painful to endure. Post-withdrawal, ex-users must maintain resolve and fashion a drug-free life. Successful quit attempts therefore not only indicate awareness of negative consequences and motivation to abstain; they also involve sunk costs. Why, if an ex-user is aware of drug costs and has lived through the pain of withdrawal and its aftermath, would they suddenly and spontaneously choose to use again? This puzzle is similarly frustrating for standard learning accounts of value-guided decisions, as they predict that recent experience should be the primary determining factor in choice; instead, people with SUD appear suddenly to reinstate past preferences without any apparent learning in the intervening period, consistent with the view that extinction is itself a process of new learning, rather than overwriting previous associations [48,49,50].

RL accounts can be extended to incorporate atypically persistent preferences, for instance by adding a term to the standard value update calculation (Box 1) that reflects a dopamine “surge” at the time of consumption [21]. Because dopamine is thought to signal the difference between reward expected and reward received, based on which expectation of future reward is updated, additional dopamine distorts the signal, causing expectations to remain high even as outcomes diminish. However, these approaches suffer from three related problems. First, a focus on dopamine leaves the model underspecified in its account of non-dopaminergic drugs. Many non-dopaminergic drugs are known to indirectly cause dopamine release [51], but this predicts a quantitative asymmetry in addictive potential, yet to be substantiated by empirical findings [52]. More importantly, this focus also fails to address the second puzzle of relapse after abstinence. This second puzzle is often explained as a form of context-dependent preference [22,23,24]. But this raises two additional problems for RL accounts that must in turn be answered, namely: where these context-dependent preferences are stored, and how they come to be reinstated after long periods of dormancy.

Redish et al. [22, 23] identified these challenges and proposed a “situation recognition” component, realized by interactions between hippocampus and PFC, that reinstates past preferences on the basis of similarity to current context. Our proposal is consistent with this idea and connects it with known mechanisms of memory-guided decision-making. Specifically, we link this “situation recognition” component to the episodic memory system, and place particular emphasis on the dynamics of situation recognition that are entailed by context-guided memory sampling. We further predict that this system is instrumental not only in relapse, but in persistent use as well. Notably, our proposed mechanism does not exclude the possibility of atypical dopamine response. Indeed, dopamine release is associated with enhanced memory encoding [53, 54], which may explain why some early drug memories are often vivid and persistent. However, in our framework, atypical dopamine is not required to explain behaviors of interest, consistent with the failure to find outsized addiction potential for directly-dopaminergic drugs.

Cue-induced craving

Research into cue-induced craving contributes to the explanation of both puzzles of (i) downward spiral and (ii) relapse. In animal models, drug-associated cues, similarly to drug priming, reinstate drug-seeking behavior after extinction and forced abstinence [55,56,57]. Although an association between craving and consumption in human addiction studies is contested and remains far from well established [58, 59], there is nonetheless evidence that in human laboratory settings, stress and drug-associated cues predict first-person reports of craving, which is associated with subsequent relapse in cocaine ex-users [60]; and that, outside of the laboratory, craving is associated with consumption in smokers [61] and cocaine users [62]. Cue-induced craving not only characterizes periods of active use but endures for months, possibly years, post-cessation [25,26,27]. Crucially, craving requires effort to resist, which entails both costs (that can be rationally traded off against benefits [63]) and the likelihood of failure due to simple mechanistic fallibility [64]. Together, these predict that there will be occasions when consumption results from stress or encounters with drug-associated cues. This is part of the explanation of both puzzles.

Nonetheless, cue-induced craving alone cannot provide a complete explanation of the puzzles, for the simple reason that it does not necessitate drug-taking: craving may be associated with consumption, but it does not compel it. This is demonstrated by converging lines of evidence from animal models and human addiction studies establishing that the majority of animals and humans alike respond to context-specific contingencies and choose non-drug alternatives across multiple choice settings, cues and craving notwithstanding [38, 65, 66].

Research in laboratory animals has demonstrated that although rodents will escalate drug self-administration in deprived settings where no alternative rewards are available, the vast majority will choose food or social rewards over drugs in forced-choice studies [65, 66]. Recent research suggests that social reward in particular is a potent alternative for rodents, with 100% choosing it over drug reward in the presence of drug-associated cues and irrespective of sex, drug class, dose, training conditions, abstinence duration, social housing, or “addiction score” based on a DSM-style model; only delay or punishment of social reward choices affects choice [67].

Human studies demonstrate similar flexibility in drug choice and behavior. Although drug choices in SUD have features that resemble habitual behavior [28], there is nonetheless limited evidence in support of a habit theory of addiction [68]: in the majority of cases, consumption appears to remain goal-directed [69]. In forced-choice studies offering the immediate opportunity to use crack cocaine or receive money reward, individuals with SUD frequently choose money over drug reward [42]. In addition, contingency management treatment is highly effective [70] and offers positive reward contingent on drug-free urine samples in the form of money, prizes, and most recently and successfully, employment [71]; rates of use are cost-sensitive [72]; and correctional services and courts can succeed in establishing abstinence by imposing costs for failure [73]. Lastly, epidemiological data suggests that the majority of people with SUD (including those with physical dependence) recover without clinical intervention by their late 20 s or early 30s [35].

These lines of evidence converge to establish that on the whole, individuals with SUD choose non-drug alternatives in the presence of drug options across multiple choice settings. Together, they underscore that drug consumption, even in addiction, typically remains purposive [74] and involves choice, as opposed to being compelled by craving alone. Hence, although craving is part of the solution to the puzzles of downward spiral and relapse, it cannot be the whole of it. Given the evidence demonstrating flexibility in behavior and responsiveness to incentives, why do individuals choose to use drugs in both stages of the addiction process, despite the evident costs?

The answer in part lies in a multi-factorial approach to how choice can be biased in addiction. Individuals with SUD display a range of decision-making anomalies, including reflective impulsivity, risk and ambiguity tolerance [75], impatience in delay discounting [76, 77], reduced insight and self-awareness [78], and denial of the severe consequences of use [79]. These may influence subjective expected utility of drug and non-drug choices, such that immediate, certain drug reward is strongly preferred to the delayed, uncertain rewards of abstinence, while drug risks are minimized and drug harms fail to be processed at all. We propose that memory sampling is a further previously unexplored factor that interacts with—and potentially provides a cohesive mechanistic framework giving rise to [80]—many of these decision-making anomalies. The selective sampling of individual episodic memories of rewarding past drug use to anticipate future possibilities can bias present choices towards drugs; and, like incentive salience and craving, is affected by cues and context. This mechanism can lead to individuals “chasing the first high” when exposed to drug-associated cues and context: imagining future possibilities of use that are ripe with rewards of the sorts previously experienced and elaborated—even when recent outcomes should encourage a more sober outlook.

The memory sampling framework

The standard account of value-based choice assumes that choices are based on values learned incrementally, over repeated experience. Therefore, it cannot account for addictive choices, where preferences persist despite repeated counterevidence, or change suddenly after long periods of stability.

Memory sampling offers an alternative account, in which values are estimated at the time of choice, guided by selected memories of similar past experience [13,14,15,16,17,18, 20]. This model treats outcomes of previous choices as “samples” of what may result from the current decision. When these memories are reinstated, they serve as evidence for the favorability of one option or another. Therefore, choices depend on which memories come to mind at the time of decision. In this way, memory sampling can explain puzzling choices as a consequence of known cognitive and neurobiological mechanisms of memory retrieval.

There are two critical relevant differences between memory sampling and incremental RL:

Choice variability

In the standard incremental-learning model there is a degree of “noise”—choices sometimes go against what would be predicted based on learned values alone. But it has difficulty capturing choices that consistently deviate from recent learning, e.g., appearing to “underweight” (ignore) or “overweight” (fixate) on recent experiences [13, 17, 80, 81]. Memory sampling attributes these variations to situational and environmental factors which naturally persist between decisions, predicting consistent deviations from RL of the sort observed in addiction (see Box 1 for a further contrast of choice variability in both models).

Learning history

In the standard incremental-learning model, values are learned as a running average, a single summary representation of past rewards. In essence, previous experiences are lost, reflected only in the learned value. Once a behavior is abandoned, the model predicts that a return ought to be preceded by re-learning the values that guided it. This is inconsistent with recent work demonstrating that incidental reminders of individual past decision outcomes and contexts meaningfully affect choice [17, 18, 82,83,84]. Memory sampling explains these effects because the full history of individual past outcomes and contexts is available for sampling.

Memories of past experiences can be brought to mind by incidental reminders, such as external stimulus (or internal stimulus [85, 86] e.g., stress [6]). At a neural level, partial reactivation of activity patterns formed during the initial experience can lead to reactivation of all of the pattern. This function, pattern completion [87], has particular relevance for memory-guided decisions, because it predicts that memories of past rewards can be reinstated on the basis of stimuli only fleetingly associated with a given valuable outcome. Crucially, this means that decisions are guided by memoranda recalled at the time of choice (Box 1).

The extended set of associations and activity patterns that follow memory retrieval are referred to as context memory [88, 89]. Computational and neurobiological models of context memory emphasize the influence that context has not just on how memories are organized, but on how they are retrieved [90]: memories which share context tend to be retrieved together. For instance: When trying to decide where to eat, we may recall a night at a particular restaurant; context theories suggest that the next recollection will likely be another restaurant nearby in space, or an evening nearby in time. A recent study demonstrated that which context is retrieved can have sizable and specific impact on decisions for reward, separate from that of the initial retrieved memory [18]. Therefore, factors that influence the process or content of context retrieval—such as acute stress [91, 92]—should also influence choice. A more direct analogy to drug relapse can be seen in another study showing that acute stress prior to the presentation of a conditioned fear cue can preferentially diminish recall of the extinction context—though not the cue itself, nor the associated fear response [93].

Importantly, this context-guided “clustering” in memory retrieval is additive: speed and consistency is enhanced when retrieved context is consistent with other internally-guided factors, such as goals, intentions, and mood [85, 86, 94]. This is critical because the dynamics of memory retrieval are instrumental in adjudicating its influence on behavior [13, 95,96,97]: a memory that comes to mind more quickly has a better chance of influencing choice, and of overcoming competing values based on representations other than individual episodic memories [13].

Lastly, memory’s role in decision-making is not simply to bind us to the past. Extensive research demonstrates a role for memory retrieval in imagining novel future scenarios [98, 99], in particular the possible outcomes of decisions about the future being made in the current moment [100,101,102,103]. Suggestively, these imagined future scenarios may have an optimistic bias [104].

Solving the puzzles

Memory sampling addresses both puzzles of (i) downward spiral and (ii) relapse where previous models fail by introducing flexibility to capture both persistent and also reawakened preferences.

Spiraling into addiction:

“Crystallized Molly you can snort it and shoot it. My personal choice was to inject it. I have injected crystal meth and everything but literally the first time with Molly was so intense. Everyone says the first time with anything is intense but for me I overdosed twice in the same week. That was because I was chasing that first high. It was so intense and I just wanted to feel it again. It was just way overwhelming. You just want to chase that first high and that’s why people just keep doing it especially where I’m from.” (from an interview published on the forum Inspirations Youth).


“I was several years sober. Walking past a museum cafe at lunch, I saw white table cloths, nice silverware, attractively dressed people, perfectly framed by goblets of red wine. I was gripped by the sight of a handsome couple, and overcome by the powerful thought that I could and should be doing that—sipping red wine like a gentleman with a beautiful woman in an elegant restaurant. All the possibilities were alive—romance, love, joyful, generous conversation—and required, almost as a necessity, the red wine. The experience repeats when I observe that sort of scene. No craving. But my entire being is sucked into that experience… I don’t believe I ever kissed a girl — let alone fell in love, etc—without spirits being involved until I was over 45. My whole upbringing and history taught me that alcohol made love possible.” (anonymous individual in recovery, personal communication)

These reports describe the subjective experience of memory in both phases of addiction. With respect to the downward spiral, the person wants to re-experience the intensity of the first high. With respect to relapse, they report being swayed not simply by craving for alcohol itself, but by the allure of associated goods, e.g., love, sex, and intimacy. Memory sampling allows us to model the effect of this subjective experience, offering new understanding of both puzzles.

We propose that memory for drug choices develops over four distinct stages (Fig. 1a–d). We illustrate this development via the progressive cognitive implications of an initial drug-associated cue. This cue can be an external stimulus previously experienced during consumption (e.g., a physical object or location, or a social setting); or an internal stimulus that previously led to spontaneous drug-seeking (e.g., a mood or an emotion). Importantly, drug-associated cues can be multitudinous as well as highly contingent: incidental, ephemeral associations can reinstate entire patterns of experience, even after long periods of dormancy.

Fig. 1: The four stages of memory-guided drug choice.
figure 1

a During early use, various memoranda (“cues”—such as people, places, things, or even internal signals) are bound to the memory of positive drug experiences and also to drug-related “fantasies”—episodes which did not occur, but which are imagined on the basis of the material provided by drug experiences and associated rewards. b Over persistent use, these associations between cues, experience memories, and fantasies are strengthened, leading to rapid, involuntary reinstatement of the latter when presented with the former. These signals carry positive reward, thereby encouraging consumption and explaining persistent use despite lessening actual rewards and/or increasing negative consequences. c During treatment or other forms of abstinence, drug memories and fantasies persist and can be recalled, but now have competition in their effect on action selection, in the form of “drug-inconsistent” mental context: memories and imagined scenarios of alternative goods, e.g., of relationships, employment, health. Persistent abstinence suggests these memories have become bound to widely available cues, or are otherwise easily recalled. d However, the original, drug-consistent, memories are still available to recall. If a momentary influence—such as a shift in the environment, or an acute stressor—disrupts recall of drug-inconsistent associations, their effect on behavior can reduce, allowing drug-related memories to prevail.

The first stage occurs during early and highly rewarding experiences, when drugs become associated with the cue in question (Fig. 1a). In this stage, memory is critical not only to the formation of the association between cue and intrinsic drug reward, but equally to the formation of the association between drug and other rewards present during these early experiences. These associated rewards can be contingent upon or coincidental with consumption, and may include e.g., increased confidence, sociability, promiscuity, or feelings of safety. We call these drug-associated rewards the drug “fantasy” as they are components of both the memory of previous drug experiences and the episodic simulation of future drug experiences. As drug choice and consumption persist over time, these associations are elaborated and strengthened, leading to the near-simultaneous retrieval of memory and fantasy.

The second stage occurs when drug choice and consumption become less rewarding (Fig. 1b). Though use may no longer be reinforced by high reward, the early memories and associated fantasies nonetheless persist and are triggered by the same drug-associated cues. These associations between cues, early memories, and drug fantasies evoke reward signals that affect decisions similarly to externally-provided reward [13, 105]. In this way, memory sampling explains the first puzzle of drug choice: the downward spiral into addiction. Individuals with SUD may persist in using drugs despite decreasing drug returns because they are basing their choice on episodic memories of early highly rewarding drug experience and associated drug fantasies.

Importantly, memory and fantasy can also play a role in abstinence (Fig. 1c). A core aim of various therapies for SUD is to instill a vivid sense of the value of a drug-free life: the clear recognition of goods and rewards that are contingent upon abstinence, such as improved personal relationships, employment opportunities, health, and other drug-inconsistent personally meaningful pursuits. This is a feature of twelve-step fellowships [106, 107], group therapy [108], as well as harm reduction approaches [109]; in addition, experience of life meaning has been shown to predict better treatment outcomes for alcohol dependence [110]; and, intriguingly, a recent study suggests that meaning interventions reduce alcohol-cue interference in Stroop tasks [111]. When faced with a drug-associated cue, people with SUD must learn to recall and act to secure this alternative rewarding future, by choosing against present consumption. Over time, drug cues may as a result become associated not only with drug memories and drug fantasies, but with the rewards of a drug-free life (“drug-inconsistent associations” in Fig. 1c, d), as abstinence persists and a series of choices are made against consumption, and in favor of this alternative.

However, drug memories and fantasies do not disappear simply because a competing association between drug cue and a drug-free life is well established. Memory sampling therefore offers a model for explaining the puzzle of relapse: relapse occurs precisely when drug memories and drug fantasies– as opposed to non-drug associations– are retrieved when cued thereby once again exerting an influence on present decisions (Fig. 1d). A crucial issue to preventing relapse is therefore to understand the factors that disrupt the retrieval of cue-associated non-drug alternatives and to design interventions accordingly.

Of the many factors that influence memory retrieval, acute stress may be particularly important in explaining drug choices post abstinence. Acute stress (i) triggers relapse (a process correlated with atypicality in the hippocampal response to drug-associated cues [3]); (ii) shifts reward decisions from goal-directed to seemingly habit-like [112, 113]; and (iii) preferentially lessens retrieval of contextually-linked memories [91,92,93] e.g., the drug-inconsistent associations illustrated above. The precise mechanisms by which stress exposure yields each of the above effects remains an open question. But a tantalizing possibility is that the effects of stress on choice are mediated by the effects of stress on memory retrieval. When context memories are not recalled, decisions may be swayed by the first memory that comes to mind [18]. Suggestively, recent work has shown that memory recall prioritizes events with highly salient, surprising rewards [114,115,116]–which may describe early, positive drug experiences; and that stress may cue retrieval of past stressful occasions—which, in SUD populations, may include or cause drug use [6, 85]. Together, these findings support two routes by which acute stress may influence memory retrieval and yield relapse: (a) diminishing retrieval of drug-inconsistent context memories, leaving initial drug-related memories to guide behavior; and (b) promoting retrieval of drug-consistent context memories and hence drug memories themselves.

Translational implications

There are two routes by which research into the mechanisms of addiction can inform treatment. It can illuminate why existing psychological and pharmacological interventions are successful; or it can suggest new interventions. Recognizing the potential role of memory sampling in explaining drug choices promises both.

Complementing various therapies (see above), qualitative sociological research has long suggested that overcoming SUD is facilitated by the capacity to vividly and realistically imagine an alternative drug-free life of personal value [46, 117,118,119]. In addition, recent experimental studies converge on an emerging theoretical framework that posits memory-guided simulation as a core component of intertemporal choices in all domains [100, 101, 120, 121]. A set of targeted studies [102, 103] probing the effect of episodic future thinking about drug-inconsistent future goods on rates of delay discounting in smokers is concordant with this outlook; as is recent work on orbitofrontal deficits and targeted neural activation in animal models of addiction [122]. These findings suggest that individuals with SUD can be motivated to abstain not simply because they recognize that drugs have negative consequences, but because they recognize that abstinence has positive consequences, in so far as it brings personally meaningful drug-inconsistent rewards into reach [7].

Much existing treatment uses psychological and pharmacological interventions to block the association between drugs and positive reward, e.g., naltrexone and opiate-replacement therapy aim to do so directly by acting on opioid receptors, while cognitive-behavioral therapy and techniques such as motivational interviewing aim to refocus attention away from drug reward onto the negative consequences of use. But once established via real-world experience, memories are difficult, if not impossible, to extinguish [41, 93, 123,124,125,126]. Evidence for the idea that extinction is mediated by creation of new memories, rather than unlearning of previous associations, is found in recent observations that extinction and fear memories are supported by parallel engrams [127, 128]. The memory sampling framework presented here is consistent with these findings from neurobiology, and also supports the clinical and sociological insight that it can be effective to focus treatment on the development of the capacity to imagine an alternative drug-free life when confronted with drug cues: to harness what has been called “meaning in life” [111] or “a stake in conventional life” [118] to recovery. Rather than try to break the association between drug cues and drug reward, treatment should aim to strengthen existing and/or create new associations between drug cues and drug-inconsistent rewards (Fig. 1c), which can compete with and over time potentially dominate drug reward in memory retrieval.


We propose a framework for explaining drug choices in addiction as guided by memories of individual past experiences of drug use. The memory sampling model predicts that such choices can exhibit persistence beyond that captured by incremental learning models, consistent with known drug choice behavior in the downward spiral into addiction and relapse alike.

This framework offers a new perspective on existing, but undertheorized, treatment strategies, as well as suggesting new approaches that center on the life narrative of the person who is suffering. Ultimately, this may facilitate targeting of individual contextual influences, by providing a mechanism for their effect on choice.

The idea that memories can guide choices toward undesirable outcomes might seem cause for despair: if memory can never fully be extinguished, what hope is there for fully overcoming its effects? But the model presented here offers an opportunity for rethinking conceptual frameworks that sometimes threaten to equate people who struggle with addiction with automatons. Specifically, by linking drug choices to the retrieval of memories in the moment, it suggests that the effect of the past on the present is always dynamic—and so potentially subject to interventions leading towards a more desirable future.