Literature DB >> 2594910

Infusions of cholecystokinin octapeptide into the ventral tegmental area potentiate amphetamine conditioned place preferences.

H O Pettit1, K Mueller.   

Abstract

Cholecystokinin (CCK) and dopamine (DA) coexist in both cell body and terminal areas of a mesolimbic pathway that projects from the ventral tegmental area (VTA) to the nucleus accumbens (N ACC). Autoradiography reveals extensive CCK binding sites in the N ACC, but not in the VTA. However, iontophoresis of CCK into the VTA results in activation or deactivation of DA neuronal firing rates, and bursting activity (depending on the dose of CCK administered). CCK could have neuromodulatory effects on mesolimbic DA neurons. In two studies, behavioral effects of infusions of CCK into the VTA were examined in the conditioned place preference (CPP) paradigm. The CPP paradigm is a behavioral test used to assess reinforcement induced by drug administration. Drugs with reinforcing properties can condition preferences for novel environments. CCK infusions into VTA (0.0, 0.04, 0.4, and 4.0 ng/cannula) potentiated amphetamine CPPs in a dose-dependent linear manner. CCK infusions by themselves did not have significant effects in the CPP paradigm. Results indicate a neuromodulatory role for CCK on the neuronal mechanisms that mediate the reinforcing effects of amphetamine. Results also implicate sites of action for CCK in the VTA.

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Year:  1989        PMID: 2594910     DOI: 10.1007/bf00445571

Source DB:  PubMed          Journal:  Psychopharmacology (Berl)        ISSN: 0033-3158            Impact factor:   4.530


  23 in total

1.  On the role of ascending catecholaminergic systems in intravenous self-administration of cocaine.

Authors:  D C Roberts; M E Corcoran; H C Fibiger
Journal:  Pharmacol Biochem Behav       Date:  1977-06       Impact factor: 3.533

2.  UNEQUAL INTERVALS AND UNEQUAL N IN TREND ANALYSES.

Authors:  J GAITO
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3.  Activity of A9 and A10 dopaminergic neurons in unrestrained rats: further characterization and effects of apomorphine and cholecystokinin.

Authors:  A S Freeman; B S Bunney
Journal:  Brain Res       Date:  1987-03-03       Impact factor: 3.252

Review 4.  Interactions between mesolimbic dopamine neurons, cholecystokinin, and neurotensin: evidence using in vivo voltammetry.

Authors:  A G Phillips; C D Blaha; H C Fibiger; R F Lane
Journal:  Ann N Y Acad Sci       Date:  1988       Impact factor: 5.691

5.  Peptide-monoamine coexistence: studies of the actions of cholecystokinin-like peptide on the electrical activity of midbrain dopamine neurons.

Authors:  L R Skirboll; A A Grace; D W Hommer; J Rehfeld; M Goldstein; T Hökfelt; B S Bunney
Journal:  Neuroscience       Date:  1981       Impact factor: 3.590

6.  Effects of cholecystokinin-like peptides on rearing activity and hexobarbital-induced sleep.

Authors:  G Zetler
Journal:  Eur J Pharmacol       Date:  1980-08-22       Impact factor: 4.432

7.  A subpopulation of mesencephalic dopamine neurons projecting to limbic areas contains a cholecystokinin-like peptide: evidence from immunohistochemistry combined with retrograde tracing.

Authors:  T Hökfelt; L Skirboll; J F Rehfeld; M Goldstein; K Markey; O Dann
Journal:  Neuroscience       Date:  1980       Impact factor: 3.590

8.  Destruction of dopaminergic nerve terminals in nucleus accumbens: effect on d-amphetamine self-administration.

Authors:  W H Lyness; N M Friedle; K E Moore
Journal:  Pharmacol Biochem Behav       Date:  1979-11       Impact factor: 3.533

9.  Neuropeptide modulation of apomorphine-induced stereotyped behavior.

Authors:  L K Blumstein; J N Crawley; L G Davis; F Baldino
Journal:  Brain Res       Date:  1987-02-24       Impact factor: 3.252

10.  The effects of cholecystokinin on dopaminergic mechanisms in rat striatum.

Authors:  R D Mashal; F Owen; J F Deakin; M Poulter
Journal:  Brain Res       Date:  1983-10-31       Impact factor: 3.252

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