4.4 Article

MDPV self-administration in female rats: influence of reinforcement history

期刊

PSYCHOPHARMACOLOGY
卷 238, 期 3, 页码 735-744

出版社

SPRINGER
DOI: 10.1007/s00213-020-05726-2

关键词

Cocaine; MDPV; Synthetic cathinone; Self-administration; Females; Individual differences; Rat; Reinforcement history; Sex differences

资金

  1. National Institutes of Health
  2. National Institute on Drug Abuse [R01DA039146, R36DA050955]
  3. National Institutes of Health Predoctoral Training Program in the Neurosciences [T32NS082145]
  4. Intramural Research Programs of the National Institute on Drug Abuse
  5. National Institute of Alcohol Abuse and Alcoholism

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A subset of female rats showed high levels of MDPV self-administration, which was influenced by their reinforcement history with cocaine or food. Individual differences in MDPV intake were observed under different reinforcement schedules, indicating the potential impact of individual variability on drug-taking behavior.
Rationale A subset of male rats that self-administer 3,4-methylenedioxypyrovalerone (MDPV) have unusually high levels of drug intake; however, factor(s) that influence this behavior (e.g., reinforcement history and sex) are unknown. Objectives Characterize the reinforcing potency and effectiveness of MDPV in female rats to determine whether (1) a subset of females also develop high levels of MDPV self-administration (i.e., a high-responder phenotype) and (2) the degree to which the high-responder phenotype is influenced by various reinforcement histories (i.e., responding for cocaine or food). Methods Female Sprague Dawley rats initially responded for MDPV (0.032 mg/kg/infusion), cocaine (0.32 mg/kg/infusion), or food (45-mg grain pellet) under fixed ratio (FR) 1 and FR5 schedules of reinforcement. After 20 sessions, the cocaine- and food-history rats responded for MDPV for 20 additional sessions. Dose-response curves for MDPV were generated under FR5 and progressive ratio (PR) schedules of reinforcement. Results A subset of rats responding for MDPV developed high levels of MDPV intake. A history of responding for cocaine, but not food, inhibited the development of high levels of MDPV intake. Large individual differences were observed in the level of self-administration when MDPV was available under an FR5, but not PR, schedule of reinforcement. Conclusions MDPV functions as a powerful reinforcer in female rats, as has been previously reported in male rats. The substantial variability in MDPV self-administration between subjects may be related to individual differences in human drug-taking behavior.

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