Subsecond dopamine release during compulsive drug taking

R21 DA021793 (NIH/NIDA), PI: Phillips

Phasic dopamine during drug taking. Rapid changes in extracellular dopamine in the nucleus accumbens time locked to a lever-press response for cocaine (black triangle). Dopamine increases just before animals approach the lever (inverted red triangle) and on completion of the press. The light-blue bar represents the cocaine infusion (0.33 mg, 6 s) and the green bar represents the audiovisual stimulus (20 s; truncated). After: Phillips et al, 2003.

The development of drug addiction in humans involves a switch from experimentation and recreational drug use to compulsive drug taking and habit formation. Following this switch, the habit is rarely ‘kicked’, since periods of voluntary abstinence from drug taking are thwarted by intense drug craving that drives relapse. Even after extended periods of abstinence and conscious recognition of the long-term aversive consequences, the probability of relapse is high. This uncontrolled (compulsive) behavior is the hallmark of addiction.

Release of dopamine into the extracellular space has been highly implicated in motivated behavior and is thought to have a central role in drug abuse. However, until recently it was not possible to measure it on a behaviorally-relevant timescale (seconds) in awake animals. With the development of fast-scan cyclic voltammetry, we have now successfully monitored and characterized dopamine release with subsecond resolution during cocaine self-administration in rats that had modest behavioral training, analogous to recreational drug use in humans (see figure).

We now propose to extend this work to address one of the most pertinent questions in the study of addiction: what are the neurochemical correlates of the switch from recreational to compulsive drug use? The proposed work will study subsecond dopamine release in the nucleus accumbens and dorsolateral striatum in an animal model of addiction that incorporates habitual and compulsive drug taking. Insight into the neural substrates that promote these behaviors will be essential in fully understanding the neurobiology of addictions, and isolating therapeutic targets for the prevention and treatment of these devastating disorders.

Supported by
     NIDA