4.5 Article

Escalation patterns of varying periods of heroin access

Journal

PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR
Volume 98, Issue 4, Pages 570-574

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pbb.2011.03.004

Keywords

Heroin self-administration; Opioid dependence; Drug addiction; Escalation; Naloxone-precipitated withdrawal

Funding

  1. National Institutes of Health, National Institute on Drug Abuse [DA004043]
  2. Pearson Center for Alcoholism and Addiction Research
  3. National Institute on Alcohol Abuse and Alcoholism [T32AA007456]

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The prevalence of opioid abuse and dependence has been on the rise in just the past few years. Animal studies indicate that extended access to heroin produces escalation of intake over time, whereas stable intake is observed under limited-access conditions. Escalation of drug intake has been suggested to model the transition from controlled drug use to compulsive drug seeking and taking. Here, we directly compared the pattern of heroin intake in animals with varying periods of heroin access. Food intake was also monitored over the course of escalation. Rats were allowed to lever press on a fixed-ratio 1 schedule of reinforcement to receive intravenous infusions of heroin for 1, 6, 12, or 23 h per day for 14 sessions. The results showed that heroin intake in the 12 and 23 h groups markedly increased over time, whereas heroin intake in the 1 h group was stable. The 6 h group showed a significant but modest escalation of intake. Total heroin intake was similar in the 12 and 23 h groups, but the rate of heroin self-administration was two-fold higher in the 12 h group compared with the 23 h group. Food intake decreased over sessions only in the 12 h group. The 12 and 23 h groups showed marked physical signs of naloxone-precipitated withdrawal. These findings suggest that 12 h heroin access per day may be the optimal access time for producing escalation of heroin intake. The advantages of this model and the potential relevance for studying drug addiction are discussed. (C) 2011 Elsevier Inc. All rights reserved.

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