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Vol. 301, Issue 3, 785-789, June 2002
Departments of Pharmacology and Therapeutics and Psychiatry,
Louisiana State University Health Sciences Center, Shreveport,
Louisiana
The hypothalamo-pituitary-adrenal (HPA) axis is involved in all aspects
of cocaine self-administration. Corticosterone seems to be crucial for
the acquisition of drug use since self-administration does not occur
unless this stress hormone is increased above a critical reward
threshold. Increasing circulating levels of corticosterone also
augments sensitivity to low doses of cocaine, possibly from a
sensitization-associated phenomenon involving dopamine, suggesting that
exposure to stress can increase individual vulnerability to cocaine.
Drugs affecting the synthesis and/or secretion of corticosterone
decrease ongoing, low-dose cocaine self-administration. When higher
doses falling on the descending limb of the cocaine dose-response curve
are self-administered, plasma corticosterone can still reach this
reward threshold even when synthesis is inhibited and drug intake is
not affected. Corticotropin-releasing hormone (CRH) seems to play a
more prominent role in the maintenance of cocaine self-administration
and may even be involved in the incentive motivation for the drug.
Corticosterone and CRH are also critical for the stress- and
cue-induced reinstatement of extinguished cocaine-seeking behavior.
Therefore, cocaine self-administration may represent an attempt to seek
out specific sensations, with the internal state produced being very
similar to that perceived by individuals who engage in risky,
thrill-seeking behavior. During abstinence, exposure to stressors or
cocaine-associated cues can stimulate the HPA axis to remind the
individual about the effects of cocaine, thus producing craving and
promoting relapse. Stress reduction, either alone or in combination
with pharmacotherapies targeting the HPA axis may prove beneficial in
reducing cravings and promoting abstinence in individuals seeking
treatment for cocaine addiction.
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