Mutant mice lacking the cholecystokinin2 receptor show a dopamine-dependent hyperactivity and a behavioral sensitization to morphine

Cholecystokinin2 (CCK2) receptor-deficient mice were used to analyze the in vivo function of CCK2 receptor and especially the incidence of this gene invalidation on enkephalinergic and dopaminergic systems. Hyperlocomotor activity of CCK2 receptor-deficient mice was suppressed by a selective D2 anta...

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Published inNeuroscience letters Vol. 306; no. 1-2; pp. 41 - 44
Main Authors DAUGE, Valérie, BESLOT, Francoise, MATSUI, Toshimitsu, ROQUES, Bernard Pierre
Format Journal Article
LanguageEnglish
Published Shannon Elsevier 22.06.2001
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Abstract Cholecystokinin2 (CCK2) receptor-deficient mice were used to analyze the in vivo function of CCK2 receptor and especially the incidence of this gene invalidation on enkephalinergic and dopaminergic systems. Hyperlocomotor activity of CCK2 receptor-deficient mice was suppressed by a selective D2 antagonist but not by a D1 antagonist. Injection of amphetamine induced a hyperlocomotor activity in both groups of mice while mutant mice were less sensitive to cocaine. Administration of 6 mg/kg of morphine once every 2 days for 5 days significantly (P<0.05) enhanced motor activity the last day compared to the first day, only in CCK2 receptor-deficient mice. These results emphasize the role of CCK2 receptors in counteracting the effects of dopaminergic systems and suggest that CCK2 receptor invalidation could lead to a slight behavioral sensitization.
AbstractList Cholecystokinin2 (CCK2) receptor-deficient mice were used to analyze the in vivo function of CCK2 receptor and especially the incidence of this gene invalidation on enkephalinergic and dopaminergic systems. Hyperlocomotor activity of CCK2 receptor-deficient mice was suppressed by a selective D2 antagonist but not by a D1 antagonist. Injection of amphetamine induced a hyperlocomotor activity in both groups of mice while mutant mice were less sensitive to cocaine. Administration of 6 mg/kg of morphine once every 2 days for 5 days significantly (P<0.05) enhanced motor activity the last day compared to the first day, only in CCK2 receptor-deficient mice. These results emphasize the role of CCK2 receptors in counteracting the effects of dopaminergic systems and suggest that CCK2 receptor invalidation could lead to a slight behavioral sensitization.
Author MATSUI, Toshimitsu
ROQUES, Bernard Pierre
BESLOT, Francoise
DAUGE, Valérie
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  givenname: Toshimitsu
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Issue 1-2
Keywords Dopamine
Hyperactivity
Rodentia
Morphine
Opiates
Catecholamine
Narcotic analgesic
Cholecystokinin receptor
Vertebrata
Mammalia
Mouse
Animal
Neurotransmitter
Sensitization
Behavior
Mutation
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Snippet Cholecystokinin2 (CCK2) receptor-deficient mice were used to analyze the in vivo function of CCK2 receptor and especially the incidence of this gene...
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SubjectTerms Analgesics
Analgesics, Opioid - pharmacology
Animals
Behavior, Animal - drug effects
Behavior, Animal - physiology
Biological and medical sciences
Brain - drug effects
Brain - metabolism
Brain - physiopathology
Cholecystokinin - metabolism
Dopamine - metabolism
Dopamine Agonists - pharmacology
Dopamine Antagonists - pharmacology
Dopamine D2 Receptor Antagonists
Enkephalins - metabolism
Female
Hyperkinesis - chemically induced
Hyperkinesis - metabolism
Hyperkinesis - physiopathology
Male
Medical sciences
Mice
Mice, Mutant Strains - genetics
Mice, Mutant Strains - metabolism
Morphine - pharmacology
Neural Pathways - drug effects
Neural Pathways - metabolism
Neural Pathways - physiopathology
Neurons - drug effects
Neurons - metabolism
Neuropharmacology
Pharmacology. Drug treatments
Receptors, Cholecystokinin - deficiency
Receptors, Cholecystokinin - drug effects
Receptors, Cholecystokinin - genetics
Receptors, Dopamine D1 - antagonists & inhibitors
Receptors, Dopamine D1 - metabolism
Receptors, Dopamine D2 - metabolism
Title Mutant mice lacking the cholecystokinin2 receptor show a dopamine-dependent hyperactivity and a behavioral sensitization to morphine
URI https://www.ncbi.nlm.nih.gov/pubmed/11403953
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