ADC 655 Module 1 The Brain's Reward System Example

Reviewed by Frances Ledbetter, MA Aspen University Updated October 2026

This ADC 655 Module 1 sample paper begins Aspen University's course on the neurobiology of addiction with the brain's reward system, explained through a composite counselor preparing a psychoeducation group at an invented residential program in Colorado Springs. Olds and Milner found in 1954 that rats would press a lever repeatedly to stimulate certain brain areas, the first evidence of dedicated reward circuitry. Schultz, Dayan and Montague showed that dopamine cells fire according to how much better or worse a reward turns out than predicted, a prediction error that drives learning. Berridge and Robinson argued that dopamine creates wanting rather than liking, which helps explain why people in addiction crave drugs they no longer enjoy.

CourseADC 655 Neurobiology of Addiction
ModuleModule 1
Paper typeNeuroscience foundations paper
LengthAbout 1,021 words, 6 pages
FormatAPA 7 student paper
SchoolAspen University
ProgramPsychology and Addiction Studies
UpdatedOctober 2026

Free sample paper for ADC 655 Module 1

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Wanting, Liking and Learning: How the Brain's Reward System Was Discovered

Student Name

Psychology and Addiction Studies Program, Aspen University

ADC 655: Neurobiology of Addiction

Instructor Name

Month Day, Year

What this page is doingThe title names the three functions research has separated within the reward system. APA 7 student title page.
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Wanting, Liking and Learning: How the Brain's Reward System Was Discovered

Nadia, a counselor at a residential addiction treatment program in Colorado Springs, leads a weekly psychoeducation group. Both she and her program were made up for teaching. Last week a client, Marcus, asked a question she could not fully answer: "Why do I still crave meth when it doesn't even feel good anymore?" This paper reviews the science of the brain's reward system that she will draw on in her next session.

The Discovery of Reward Circuitry

Olds and Milner (1954) implanted electrodes in the brains of rats and allowed the animals to press a lever that delivered mild electrical stimulation. When electrodes were placed in certain areas, including regions along a pathway later associated with dopamine, rats pressed the lever repeatedly, sometimes thousands of times an hour, in preference to other activities. The finding showed that the brain contains circuitry whose activation is strongly reinforcing. It was quickly interpreted as the discovery of pleasure centers, a label later research would complicate.

Dopamine and Prediction Error

Schultz et al. (1997) recorded the activity of dopamine neurons in monkeys learning to associate a cue with a reward. Before learning, the neurons fired when an unexpected reward arrived. After learning, they fired when the cue appeared and no longer fired at the reward itself, which was now expected. If an expected reward failed to arrive, their activity dropped below baseline. The authors showed that this pattern matched a computational learning signal known as a prediction error: the difference between the reward expected and the reward received. Dopamine, in this view, teaches the brain which cues predict rewards and updates those predictions when outcomes differ from expectations.

Wanting Versus Liking

Berridge and Robinson (1998) reviewed evidence on what dopamine does in reward. They argued that dopamine is not necessary for liking, the pleasure of a reward: animals with dopamine depleted still showed facial reactions of pleasure to sweet tastes. Nor, they argued, is it primarily a teaching signal. Instead, they proposed that dopamine mediates incentive salience, or wanting: the attribution of motivational value to rewards and the cues that predict them, which makes them attractive and attention-grabbing. Wanting and liking usually go together, but they can separate.

DiscoveryStudyWhat it changed
Reward circuitry existsOlds and Milner, 1954Brain stimulation can be powerfully reinforcing
Dopamine signals prediction errorSchultz, Dayan and Montague, 1997Dopamine teaches which cues predict reward
Dopamine drives wanting, not likingBerridge and Robinson, 1998Craving and pleasure can come apart
Drugs act on this systemLater researchAddictive drugs hijack circuits built for natural rewards
What this page is doingBerridge and Robinson's distinction answers Marcus's question directly: wanting can grow even as liking fades.
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Connecting to Addiction

Natural rewards, such as food, water and social contact, activate this system, which evolved to motivate behaviors that help survival. Addictive drugs activate it too, often more strongly and more directly. Repeated drug use, the later modules will show, can sensitize the wanting system to drug cues while tolerance reduces the pleasure the drug provides. The result is a person who wants a drug intensely while enjoying it less, exactly the experience Marcus described.

From Animals to People

Most of this research was done in animals, and the step to people requires care. Brain imaging in humans, discussed in later modules, has found dopamine release in response to drugs and drug cues, consistent with the animal work. But human experience involves memory, meaning, relationships and choice in ways no animal model captures. The reward system is part of the explanation for addiction, not the whole of it.

Natural Rewards and Recovery

The same system that drugs overstimulate also responds to food, exercise, music, accomplishment and connection with other people. In early recovery these natural rewards may feel flat, since the system has adapted to stronger stimulation. Over time, many people find that ordinary pleasures return. This is one reason treatment encourages building routines around activities and relationships that provide natural reward.

Why the Prediction Error Matters for Addiction

Schultz and colleagues' finding helps explain the power of drug cues. Through repeated use, cues such as a lighter, a street corner or a payday come to predict the drug, and dopamine neurons begin to fire at the cue itself. The cue then carries the motivational charge. For someone in recovery, encountering such a cue can produce a surge of wanting even when no drug is present.

Explaining It to the Group

Nadia planned to explain the science in three steps. First, the brain has a system whose job is to say "this matters, go get it," which keeps us eating, drinking and connecting with others. Second, that system is separate from the one that makes things feel good; the two usually agree but not always. Third, repeated meth use turned up the "go get it" signal for meth and its cues while the good feeling wore down, so the craving can be loud even when the high is disappointing. She would add that the system can recalibrate with time away from the drug and with other rewards, a point later sessions will develop.

What Changes With Recovery

Research suggests that some of the changes in reward signaling seen in addiction partly reverse with sustained abstinence, though the pace varies and cue-triggered wanting can persist. For clients, this means two things at once: craving may stay strong for a while after the pleasure has gone, and the balance can shift with time, new routines and other rewards.

Cautions in Translating the Science

Animal studies show mechanisms that are not always simple in people, and brain systems interact in complex ways. Nadia would avoid suggesting that clients are controlled by their dopamine, which could undermine their sense of agency. The aim is understanding, not fatalism: knowing why craving persists can make it less frightening and easier to plan for.

Conclusion

Olds and Milner revealed that the brain contains reward circuitry, Schultz, Dayan and Montague showed dopamine signaling prediction errors and Berridge and Robinson distinguished wanting from liking. Together these findings explain why people in addiction can crave a drug they no longer enjoy, and they give Nadia a clear, accurate answer for Marcus.

References

Berridge, K. C., & Robinson, T. E. (1998). What is the role of dopamine in reward: Hedonic impact, reward learning, or incentive salience? Brain Research Reviews, 28(3), 309-369. https://doi.org/10.1016/S0165-0173(98)00019-8

Olds, J., & Milner, P. (1954). Positive reinforcement produced by electrical stimulation of septal area and other regions of rat brain. Journal of Comparative and Physiological Psychology, 47(6), 419-427. https://doi.org/10.1037/h0058775

Schultz, W., Dayan, P., & Montague, P. R. (1997). A neural substrate of prediction and reward. Science, 275(5306), 1593-1599. https://doi.org/10.1126/science.275.5306.1593

Reading the ADC 655 Module 1 assignment instructions

The first module of ADC 655 usually asks for a paper on the brain's reward system. Your Aspen course's Module 1 instructions govern the details; the counselor and clients are invented. Trace the major discoveries about reward circuitry, in order, and say what each one changed. Explain dopamine's role accurately, avoiding the oversimplification that dopamine is the pleasure chemical. Distinguish learning, wanting and liking, with evidence for each distinction. Connect the science to addiction, especially to craving that outlasts pleasure. If your prompt involves clients, explain the science in plain terms. List every source in APA 7 form, and include the years of the studies to show how understanding developed. Note where animal findings may not translate directly to people, and say what the science does and does not imply about responsibility and choice.

How the ADC 655 Module 1 example is put together

Nadia, a composite counselor at a Colorado Springs residential program, prepares a group session after a client asks why he still craves meth "even though it doesn't feel good anymore." Olds and Milner's Journal of Comparative and Physiological Psychology study shows rats working for brain stimulation. Schultz, Dayan and Montague's Science article shows dopamine neurons signaling prediction error. Berridge and Robinson's Brain Research Reviews article separates wanting from liking. A four-row table shows how each discovery changed understanding. The group explanation uses a simple image: the brain's alarm for "this matters, go get it" stays loud even after the reward fades. A short section on cautions keeps the explanation from sounding fatalistic.

Reading the ADC 655 Module 1 grading rubric

Neuroscience foundations papers earn credit for accurate history, correct explanation of mechanisms and translation that does not distort. This example traces discoveries in order and explains what each added. It corrects the common myth that dopamine equals pleasure, using Berridge and Robinson's evidence from animals whose dopamine was depleted. The prediction error idea is explained clearly, including what happens when an expected reward fails to arrive. The client explanation simplifies without misleading, answering the client's actual question about craving without enjoyment. The cautions about agency and the limits of animal research show judgment about how neuroscience should be used with clients.

ADC 655 Module 1 help from the desk

Neuroscience papers often call dopamine the pleasure chemical, a shorthand that misleads clients about why they crave. Explain its roles in learning and motivation instead. Trace how understanding developed through specific studies. Distinguish liking, wanting and learning. Avoid overstating what animal studies show about people, and note where human imaging has confirmed the findings. Translate carefully for clients; simple images help, but check that they do not mislead. Answer the question clients actually ask, which is often why they want something they no longer enjoy. Avoid images that suggest the brain is permanently broken; emphasize that it can recalibrate.

Write yours, or have the desk draft it

This paper is an original model document written by our desk, not a submitted student paper and not an official Aspen University document. Read it for the moves, then write your own to the instructions in your classroom. If you want one built to your exact prompt and rubric, the first custom sample is free and arrives in 24 to 48 hours.

More ADC 655 and Psychology and Addiction Studies sample papers

ADC 655 Module 1 questions, answered

What does ADC 655 Module 1 usually ask for?

Aspen's ADC 655 opens with the brain's reward system, so a paper on reward circuitry, dopamine and how they relate to addiction is typical. Look at your Module 1 prompt.

Is dopamine the pleasure chemical?

Not exactly. Research by Berridge and Robinson suggests dopamine drives wanting, or motivation, more than liking, the pleasure itself.

What is a reward prediction error?

The difference between expected and actual reward; Schultz, Dayan and Montague showed dopamine neurons signal this difference, which drives learning.

Where can I find a free ADC 655 Module 1 sample paper?

This page has the full paper: the discovery of reward circuitry, prediction error, wanting versus liking and a plain-language explanation for clients.

What did Olds and Milner discover?

That rats would repeatedly press a lever to receive electrical stimulation in certain brain areas, revealing circuitry dedicated to reward.