Home LiteratureArticle Details
PMID: 6440188 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Enhanced behavioural control by conditioned reinforcers following microinjections of d-amphetamine into the nucleus accumbens.

Psychopharmacology ·Vol. 84 ·No. 3 ·1984-00-00 ·Pages 405-12

Taylor JR, Robbins TW

Abstract

Stimulant drugs have been shown to enhance the control over behaviour exerted by stimuli previously correlated with primary reinforcers, termed conditioned reinforcers (CR). Experiment 1 examined the possible neuroanatomical specificity of the enhancement of conditioned reinforcement following intracerebral injections of d-amphetamine. Thirsty rats were trained to associate a light with water. In the test phase, water was no longer presented but the light (CR) was intermittently produced by responding on one of two novel levers. Rats with bilateral guide cannulae aimed at the nucleus accumbens, posterior caudate nucleus, or medio-dorsal nucleus of the thalamus received four counterbalanced microinfusions of d-amphetamine (10, 20, 30 micrograms/2 microliters) or vehicle (control) over 4 test days. There was a dose-dependent selective increase in responding on the lever that produced the light (CR) with intra-accumbens d-amphetamine infusions. Quantitatively similar, but much more variable effects were found with intra-caudate infusions and no effects following intra-thalamic d-amphetamine. Experiment 2 provided evidence that the enhanced control over responding by a CR with intra-accumbens d-amphetamine is behaviourally specific. Three groups of rats received a compound tone--plus--light stimulus that was positively, negatively or randomly correlated with water during training. Intra-accumbens d-amphetamine produced selective increases in responding only if the contingent stimulus had been positively correlated. The results suggest that the nucleus accumbens may play an important role in d-amphetamine's enhanced control over behaviour exerted by conditioned reinforcers.

MeSH Terms
Animals Behavior, Animal/drug effects Brain/anatomy & histology Caudate Nucleus Conditioning, Operant/drug effects Dextroamphetamine/pharmacology Male Microinjections Nucleus Accumbens/drug effects,physiology Rats Rats, Inbred Strains Septal Nuclei/physiology Thalamus
Chemicals
Dextroamphetamine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Taylor J R
Robbins T W
References (19)
19 references, click to expand
  1. The acquisition of responding with conditioned reinforcement: effects of pipradrol, methylphenidate, d-amphetamine, and nomifensine.
    Psychopharmacology (Berl). 1978 Jun 15;58(1):79-87 PMID: 27837
  2. Temporal properties of the rewarding and aversive effects of amphetamine in rats.
    Pharmacol Biochem Behav. 1980 Oct;13(4):597-9 PMID: 7433491
  3. Enhancement of drug-seeking behavior by environmental stimuli associated with cocaine or morphine injections.
    Neuropharmacology. 1979 Dec;18(12):1015-7 PMID: 119167
  4. Drug reinforcement studied by the use of place conditioning in rat.
    Brain Res. 1982 Jul 8;243(1):91-105 PMID: 6288174
  5. The effects of pipradrol on the acquisitionof responding with conditioned reinforcement: a role for sensory preconditioning.
    Psychopharmacology (Berl). 1980;69(3):235-42 PMID: 6106257
  6. The acquisition of responding with conditioned reinforcement: effects of cocaine, (+)-amphetamine and pipradrol.
    Br J Pharmacol. 1981 Sep;74(1):149-54 PMID: 6115694
  7. On the role of ascending catecholaminergic systems in intravenous self-administration of cocaine.
    Pharmacol Biochem Behav. 1977 Jun;6(6):615-20 PMID: 122445
  8. Effects of chemical stimulation of the mesolimbic dopamine system upon locomotor activity.
    Eur J Pharmacol. 1976 Jan;35(1):45-58 PMID: 3421
  9. Contrasting interactions of pipradrol, d-amphetamine, cocaine, cocaine analogues, apomorphine and other drugs with conditioned reinforcement.
    Psychopharmacology (Berl). 1983;80(2):113-9 PMID: 6136060
  10. Destruction of dopaminergic nerve terminals in nucleus accumbens: effect on d-amphetamine self-administration.
    Pharmacol Biochem Behav. 1979 Nov;11(5):553-6 PMID: 531077
  11. Effects of d-amphetamine and apomorphine upon operant behavior and schedule-induced licking in rats with 6-hydroxydopamine-induced lesions of the nucleus accumbens.
    J Pharmacol Exp Ther. 1983 Mar;224(3):662-73 PMID: 6402587
  12. Drug self-administration by laboratory animals: control by schedules of reinforcement.
    Annu Rev Pharmacol Toxicol. 1978;18:313-39 PMID: 348062
  13. Relationship between reward-enhancing and stereotypical effects of psychomotor stimulant drugs.
    Nature. 1976 Nov 4;264(5581):57-9 PMID: 12471
  14. Functional studies of the central catecholamines.
    Int Rev Neurobiol. 1982;23:303-65 PMID: 6749738
  15. Limbic lesions and the problem of stimulus--reinforcement associations.
    Exp Neurol. 1972 Aug;36(2):362-77 PMID: 4626489
  16. Pharmacologic studies on a new central stimulant, alpha-(2-piperidyl) benzhydrol hydrochloride (MRD-108).
    J Pharmacol Exp Ther. 1954 Feb;110(2):180-7 PMID: 13118492
  17. Reinstatement of cocaine-reinforced responding in the rat.
    Psychopharmacology (Berl). 1981;75(2):134-43 PMID: 6798603
  18. Dopaminergic substrates of amphetamine-induced place preference conditioning.
    Brain Res. 1982 Dec 16;253(1-2):185-93 PMID: 6817850
  19. The distribution of the projection from the hippocampal formation to the nucleus accumbens in the rat: an anterograde- and retrograde-horseradish peroxidase study.
    Neuroscience. 1982 Oct;7(10):2321-35 PMID: 6817161
Article Info
Journal
Psychopharmacology
Abbr.
Psychopharmacology (Berl)
ISSN
0033-3158
Published
1984-00-00
Pages
405-12
Language
English
Region
Germany
NLM ID
7608025
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]