Regulation of cocaine self-administration in humans: lack of evidence for loading and maintenance phases
- PMID: 20005893
- PMCID: PMC2824073
- DOI: 10.1016/j.pbb.2009.12.005
Regulation of cocaine self-administration in humans: lack of evidence for loading and maintenance phases
Abstract
Background: In rodents, cocaine self-administration under a fixed-ratio schedule and with timeout intervals limited to the duration of the infusions is characterized by an initial burst of drug intake (loading) followed by more stable infusion rates (maintenance). We sought to examine whether similar phases might characterize self-regulated cocaine use in humans.
Methods: 31 Non-treatment seeking, cocaine dependent subjects participated in three (8, 16, and 32 mg/70 kg/infusion), self-regulated, 2-h cocaine self-administration sessions under a fixed-ratio 1, 5-min timeout schedule. Data were assessed for visual (e.g., by graphs of cumulative numbers of infusions) and statistical evidence of change in phase (by step-function analyses of individual infusion rates).
Results: Graphs of cumulative infusions over time suggested a single, linear rate of self-administration over 2h at each cocaine dose. Statistical analyses of infusion data by generalized estimating equation (GEE) models also failed to support a loading/maintenance pattern (suggesting, if anything, the possibility of increasing infusion rates over time).
Conclusions: Our findings fail to support the existence of distinct loading and maintenance phases of self-regulated cocaine administration in humans at behaviorally relevant doses. Several factors may account for these observations including differences between humans and rodents in self-regulated drug intake.
(c) 2010 Elsevier Inc. All rights reserved.
Figures





Similar articles
-
A single-day paradigm of self-regulated human cocaine administration.Pharmacol Biochem Behav. 2012 Nov;103(1):95-101. doi: 10.1016/j.pbb.2012.08.009. Pharmacol Biochem Behav. 2012. PMID: 22922558 Free PMC article.
-
Cocaine self-administration "binges": transition from behavioral and autonomic regulation toward homeostatic dysregulation in rats.Psychopharmacology (Berl). 2000 Feb;148(3):289-98. doi: 10.1007/s002130050053. Psychopharmacology (Berl). 2000. PMID: 10755742
-
A paradigm to investigate the self-regulation of cocaine administration in humans.Psychopharmacology (Berl). 2005 Jul;180(3):436-46. doi: 10.1007/s00213-005-2192-8. Epub 2005 Feb 22. Psychopharmacology (Berl). 2005. PMID: 15726333 Clinical Trial.
-
Acquisition of i.v. amphetamine and cocaine self-administration in rats as a function of dose.Psychopharmacology (Berl). 1997 Feb;129(3):206-14. doi: 10.1007/s002130050182. Psychopharmacology (Berl). 1997. PMID: 9084058
-
Conflation of cocaine seeking and cocaine taking responses in IV self-administration experiments in rats: methodological and interpretational considerations.Neurosci Biobehav Rev. 2013 Nov;37(9 Pt A):2026-36. doi: 10.1016/j.neubiorev.2013.04.017. Epub 2013 May 10. Neurosci Biobehav Rev. 2013. PMID: 23669047 Free PMC article. Review.
Cited by
-
Pharmacotherapeutics directed at deficiencies associated with cocaine dependence: focus on dopamine, norepinephrine and glutamate.Pharmacol Ther. 2012 May;134(2):260-77. doi: 10.1016/j.pharmthera.2012.01.010. Epub 2012 Jan 31. Pharmacol Ther. 2012. PMID: 22327234 Free PMC article. Review.
-
A single-day paradigm of self-regulated human cocaine administration.Pharmacol Biochem Behav. 2012 Nov;103(1):95-101. doi: 10.1016/j.pbb.2012.08.009. Pharmacol Biochem Behav. 2012. PMID: 22922558 Free PMC article.
-
Modeling cocaine relapse in rodents: Behavioral considerations and circuit mechanisms.Prog Neuropsychopharmacol Biol Psychiatry. 2018 Dec 20;87(Pt A):33-47. doi: 10.1016/j.pnpbp.2018.01.002. Epub 2018 Jan 3. Prog Neuropsychopharmacol Biol Psychiatry. 2018. PMID: 29305936 Free PMC article. Review.
-
Effects of Kappa opioid receptor blockade by LY2444296 HCl, a selective short-acting antagonist, during chronic extended access cocaine self-administration and re-exposure in rat.Psychopharmacology (Berl). 2020 Apr;237(4):1147-1160. doi: 10.1007/s00213-019-05444-4. Epub 2020 Jan 8. Psychopharmacology (Berl). 2020. PMID: 31915862
-
Testing the effects of the GLP-1 receptor agonist exenatide on cocaine self-administration and subjective responses in humans with cocaine use disorder.Drug Alcohol Depend. 2021 Apr 1;221:108614. doi: 10.1016/j.drugalcdep.2021.108614. Epub 2021 Feb 15. Drug Alcohol Depend. 2021. PMID: 33621809 Free PMC article. Clinical Trial.
References
-
- Carroll ME, Bickel WK. Behavioral-Environmental Determinants of the reinforcing functions of cocaine. In: Higgins S, Katz JL, editors. Cocaine abuse: basic determinants, cllinical applications, and policy New York Plenum. 1998. pp. 81–105.
-
- de la Garza R, Bergman J, Hartel CR. Food deprivation and cocaine self-administration. Pharmacology, biochemistry, and behavior. 1981;15:141–144. - PubMed
-
- Donny EC, Bigelow GE, Walsh SL. Choosing to take cocaine in the human laboratory: effects of cocaine dose, inter-choice interval, and magnitude of alternative reinforcement. Drug and alcohol dependence. 2003;69:289–301. - PubMed
-
- Ettenberg A, Pettit HO, Bloom FE, Koob GF. Heroin and cocaine intravenous self-administration in rats: mediation by separate neural systems. Psychopharmacology. 1982;78:204–209. - PubMed
-
- Fischman MW. Relationship between self-reported drug effects and their reinforcing effects: studies with stimulant drugs. NIDA research monograph. 1989;92:211–230. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- R01 DA012283/DA/NIDA NIH HHS/United States
- K02 DA000397/DA/NIDA NIH HHS/United States
- R01 DA015857/DA/NIDA NIH HHS/United States
- UL1RR024139/RR/NCRR NIH HHS/United States
- R25 MH071584/MH/NIMH NIH HHS/United States
- DA12283/DA/NIDA NIH HHS/United States
- DA018978/DA/NIDA NIH HHS/United States
- K24 DA017899/DA/NIDA NIH HHS/United States
- DA00397/DA/NIDA NIH HHS/United States
- DA15857/DA/NIDA NIH HHS/United States
- R01 DA011744/DA/NIDA NIH HHS/United States
- UL1 RR024139/RR/NCRR NIH HHS/United States
- T32 MH019961/MH/NIMH NIH HHS/United States
- R03 DA018978/DA/NIDA NIH HHS/United States
LinkOut - more resources
Full Text Sources