Progressive ratio and fixed ratio schedules of cocaine-maintained responding in baboons
- PMID: 117480
- DOI: 10.1007/BF00433038
Progressive ratio and fixed ratio schedules of cocaine-maintained responding in baboons
Abstract
Responding maintained under progressive ratio (PR) and fixed ratio (FR 160) schedules of IV saline or cocaine (0.01-4.0 mg/kg) injections was studied in baboons. Each injection was followed by a time-out period which was 3-h with the PR schedule and was either 3 or 12 with the FR schedule. On the PR schedule the ratio requirement was systematically increased each day until reaching the 'breaking point' at which self-injection performance fell below a criterion level (one or zero injections per day). Overall response rates on the PR schedule increased with progressive increases in the ratio until a maximum at which an abrupt reduction in responding occurred. With the 3-h time-out the dose-breaking point function on the PR schedule was similar to the dose-response rate function on the FR schedule. These dose-effect functions were inverted U-shaped curves characterized by a graded ascending limb (0.01-0.32 mg/kg) and a downturn at the highest doses (3.0-4.0 mg/kg). On the FR schedule the downturn in the dose-response rate function was attributable to a cumulative drug effect as revealed by manipulation of time-out duration and analysis of sequential interresponse time distributions and cumulative response records. PR and FR schedules provide similar information about the relative reinforcing efficacy of different cocaine doses.
Similar articles
-
Behavior controlled by scheduled injections of cocaine in squirrel and rhesus monkeys.J Exp Anal Behav. 1976 Jan;25(1):93-104. doi: 10.1901/jeab.1976.25-93. J Exp Anal Behav. 1976. PMID: 814192 Free PMC article.
-
Parametric analysis of cocaine self-administration under a progressive-ratio schedule in rhesus monkeys.Psychopharmacology (Berl). 1996 Jun;125(4):361-70. doi: 10.1007/BF02246019. Psychopharmacology (Berl). 1996. PMID: 8826541
-
Effects of cocaine under concurrent fixed ratio schedules of food and IV drug availability: a novel choice procedure in monkeys.Psychopharmacology (Berl). 2002 Oct;163(3-4):283-91. doi: 10.1007/s00213-002-1180-5. Epub 2002 Jul 30. Psychopharmacology (Berl). 2002. PMID: 12373429
-
A labor-supply analysis of cocaine self-administration under progressive-ratio schedules: antecedents, methodologies, and perspectives.Psychopharmacology (Berl). 2000 Dec;153(1):1-16. doi: 10.1007/s002130000610. Psychopharmacology (Berl). 2000. PMID: 11255919 Review.
-
Progressive ratio schedules in drug self-administration studies in rats: a method to evaluate reinforcing efficacy.J Neurosci Methods. 1996 May;66(1):1-11. doi: 10.1016/0165-0270(95)00153-0. J Neurosci Methods. 1996. PMID: 8794935 Review.
Cited by
-
Addiction as a BAD, a Behavioral Allocation Disorder.Pharmacol Biochem Behav. 2018 Jan;164:62-70. doi: 10.1016/j.pbb.2017.05.002. Epub 2017 May 2. Pharmacol Biochem Behav. 2018. PMID: 28476485 Free PMC article. Review.
-
How to make a rat addicted to cocaine.Prog Neuropsychopharmacol Biol Psychiatry. 2007 Nov 15;31(8):1614-24. doi: 10.1016/j.pnpbp.2007.08.028. Epub 2007 Aug 28. Prog Neuropsychopharmacol Biol Psychiatry. 2007. PMID: 17888555 Free PMC article. Review.
-
Tolerance to the reinforcing effects of cocaine in a progressive ratio paradigm.Psychopharmacology (Berl). 1994 Nov;116(3):326-32. doi: 10.1007/BF02245336. Psychopharmacology (Berl). 1994. PMID: 7892423
-
Contingent reinforcement for carbon monoxide reduction: within-subject effects of pay amount.J Appl Behav Anal. 1984 Winter;17(4):477-83. doi: 10.1901/jaba.1984.17-477. J Appl Behav Anal. 1984. PMID: 6526768 Free PMC article. Clinical Trial.
-
Cocaine and food as reinforcers: effects of reinforcer magnitude and response requirement under second-order fixed-ratio and progressive-ratio schedules.J Exp Anal Behav. 1991 Sep;56(2):261-75. doi: 10.1901/jeab.1991.56-261. J Exp Anal Behav. 1991. PMID: 1955816 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials