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Incubation of Cocaine Craving After Intermittent-Access Self-administration: Sex Differences and Estrous Cycle.

Celine Nicolas, Ph.D.Featured Paper of the Month – June 2019.

We examined whether binge cocaine intake has an impact on drug craving after abstinence and whether it has differential effects between male and female rats. We used an intermittent access cocaine self-administration to mimic binge intake and compare it with a continuous access self-administration. The intermittent access procedure caused stronger cocaine craving following abstinence than the continuous access procedure, and this effect was greater in female than male rats. Importantly, the increased cocaine craving of female rats is dependent on the cycle of female reproductive system. The present study suggests that binge-like self-administration intensifies cocaine craving after abstinence, and that female rats display stronger cocaine craving during the estrus phase than non-estrus phases. An important implication would be to take the menstrual cycle into consideration for addiction treatments in women.

Publication Information

Nicolas, Celine; Russell, Trinity I; Pierce, Anne F; Maldera, Steeve; Holley, Amanda; You, Zhi-Bing; McCarthy, Margaret M; Shaham, Yavin; Ikemoto, Satoshi

Incubation of Cocaine Craving After Intermittent-Access Self-administration: Sex Differences and Estrous Cycle. Journal Article

In: Biol Psychiatry, vol. 85, no. 11, pp. 915–924, 2019, ISSN: 1873-2402 (Electronic); 0006-3223 (Linking).

Abstract | Links

@article{Nicolas:2019aa,
title = {Incubation of Cocaine Craving After Intermittent-Access Self-administration: Sex Differences and Estrous Cycle.},
author = {Celine Nicolas and Trinity I Russell and Anne F Pierce and Steeve Maldera and Amanda Holley and Zhi-Bing You and Margaret M McCarthy and Yavin Shaham and Satoshi Ikemoto},
url = {https://www.ncbi.nlm.nih.gov/pubmed/30846301},
doi = {10.1016/j.biopsych.2019.01.015},
issn = {1873-2402 (Electronic); 0006-3223 (Linking)},
year = {2019},
date = {2019-06-01},
urldate = {2019-06-01},
journal = {Biol Psychiatry},
volume = {85},
number = {11},
pages = {915--924},
address = {Behavioral Neuroscience Branch, Intramural Research Program, National Institute on Drug Abuse, Baltimore, Maryland.},
abstract = {BACKGROUND: Studies using continuous-access drug self-administration showed that cocaine seeking increases during abstinence (incubation of cocaine craving). Recently, studies using intermittent-access self-administration showed increased motivation to self-administer and seek cocaine. We examined whether intermittent cocaine self-administration would potentiate incubation of craving in male and female rats and examined the estrous cycle's role in this incubation. METHODS: In experiment 1, male and female rats self-administered cocaine either continuously (8 hours/day) or intermittently (5 minutes ON, 25 minutes OFF x 16) for 12 days, followed by relapse tests after 2 or 29 days. In experiments 2 and 3, female rats self-administered cocaine intermittently for six, 12, or 18 sessions. In experiment 4, female rats self-administered cocaine continuously followed by relapse tests after 2 or 29 days. In experiments 3 and 4, the estrous cycle was measured using a vaginal smear test. RESULTS: Incubation of cocaine craving was observed in both sexes after either intermittent or continuous drug self-administration. Independent of access condition and abstinence day, cocaine seeking was higher in female rats than in male rats. In both sexes, cocaine seeking on both abstinence days was higher after intermittent drug access than after continuous drug access. In female rats, incubation of craving after either intermittent or continuous drug access was significantly higher during estrus than during non-estrus; for intermittent drug access, this effect was independent of the training duration. CONCLUSIONS: In both sexes, intermittent cocaine access caused time-independent increases in drug seeking during abstinence. In female rats, the time-dependent increase in drug seeking (incubation) is critically dependent on the estrous cycle phase.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}

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BACKGROUND: Studies using continuous-access drug self-administration showed that cocaine seeking increases during abstinence (incubation of cocaine craving). Recently, studies using intermittent-access self-administration showed increased motivation to self-administer and seek cocaine. We examined whether intermittent cocaine self-administration would potentiate incubation of craving in male and female rats and examined the estrous cycle's role in this incubation. METHODS: In experiment 1, male and female rats self-administered cocaine either continuously (8 hours/day) or intermittently (5 minutes ON, 25 minutes OFF x 16) for 12 days, followed by relapse tests after 2 or 29 days. In experiments 2 and 3, female rats self-administered cocaine intermittently for six, 12, or 18 sessions. In experiment 4, female rats self-administered cocaine continuously followed by relapse tests after 2 or 29 days. In experiments 3 and 4, the estrous cycle was measured using a vaginal smear test. RESULTS: Incubation of cocaine craving was observed in both sexes after either intermittent or continuous drug self-administration. Independent of access condition and abstinence day, cocaine seeking was higher in female rats than in male rats. In both sexes, cocaine seeking on both abstinence days was higher after intermittent drug access than after continuous drug access. In female rats, incubation of craving after either intermittent or continuous drug access was significantly higher during estrus than during non-estrus; for intermittent drug access, this effect was independent of the training duration. CONCLUSIONS: In both sexes, intermittent cocaine access caused time-independent increases in drug seeking during abstinence. In female rats, the time-dependent increase in drug seeking (incubation) is critically dependent on the estrous cycle phase.

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  • https://www.ncbi.nlm.nih.gov/pubmed/30846301
  • doi:10.1016/j.biopsych.2019.01.015

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