Related Experiment Video
Updated: May 31, 2026

A Conditioned Place Preference Protocol for Measuring Incubation of Craving in Rats
Published on: November 6, 2018
Relationship between the rewarding and aversive effects of morphine and amphetamine in individual subjects
Andrey Verendeev1, Anthony L Riley
1Psychopharmacology Laboratory, Department of Psychology, American University, Washington, DC 20016, USA. andrey.verendeev@gmail.com
Abstract:
Drugs of abuse have been reported to produce both rewarding and aversive effects, as evidenced by their ability to induce both conditioned place preferences (CPPs) and conditioned taste aversions (CTAs), respectively. Although several attempts have been made to assess the relationship between the rewarding and aversive effects of drugs in independent groups, it is unknown to what extent (if any) preferences and aversions are related in individual animals. The present study assessed this relationship by examining the ability of morphine (5 and 10 mg/kg) and amphetamine (3 and 5 mg/kg) to induce both place preferences and taste aversions in the same animal, using a concurrent CTA/CPP design. There was no consistent relationship between the ability of morphine or amphetamine at either dose to increase time spent on the drug-paired side and the ability to suppress consumption of the drug-paired taste. These results support the position that drugs of abuse have multiple stimulus effects, both rewarding and aversive, that condition place preferences and taste aversions independently.
Related Concept Videos
Drug Abuse and Addiction: Pharmacological Phenomena
Analgesia and Pain Management
Opioid Analgesics: Synthetic and Semisynthetic Opioids
Opioid Receptors: Overview
Opioid Analgesics: Morphine and Other Natural Cogeners
Adrenergic Agonists: Indirect-Acting Agents
One mechanism involves depleting stored catecholamines by displacing them from synaptic vesicles. These agents, known as "displacers," are transported into vesicles at the expense of noradrenaline. Examples include amphetamine and tyramine, which lack a catechol moiety, resulting in prolonged action, improved oral bioavailability, and...

