Medical Journals

Impulsivity-anxiety-related Behavior and Profiles of Morphine-induced Analgesia in Heterozygous Reeler Mice.

Authors:
  • Ognibene Elisa
  • Adriani Walter
  • Granstrem Oleg
  • Pieretti Stefano
  • Laviola Giovanni

From: Behavioral Neuroscience Section, Dept. Cell Biology and Neuroscience, Istituto Superiore di Sanità, Roma, Italy.

Brain research

  • Publish Date: Feb 2007
  • ISSN: 0006-8993
  • Volume: 1131
  • Issue: 1
  • Pages: 173-80
  • Medium: Print
  • Language: English
  • Citation (JAMA): Ognibene Elisa, Adriani Walter, Granstrem Oleg, et al. Impulsivity-anxiety-related Behavior and Profiles of Morphine-induced Analgesia in Heterozygous Reeler Mice.. Brain Res. Feb 2007;1131:173-80

Abstract

Reelin is an extracellular matrix protein, secreted by GABAergic interneurons, that provides a signal for neural plasticity. A downregulation of reelin may be a factor to be considered in the study of major psychiatric disorders. The heterozygous reeler mouse model, thus, may be important to reveal those alterations in behavioral phenotype produced by reduced neural plasticity. Heterozygous (HZ) and wild-type (WT) mice were tested for anxiety-related behavior, motor impulsivity, and morphine-induced analgesia. Heterozygous mice showed significantly lower levels of anxiety- and risk-assessment-related behaviors in the elevated plus-maze during adolescence, in the absence of basal changes in general locomotion. Adult mice were assessed for profiles of impulsive behavior in operant chambers, and HZ mice exhibited elevated levels of motor impulsivity. When mice were assessed in nociception tests, a genotype difference in morphine-induced analgesia was found, and these results were confirmed by measurement of mu-receptors in the midbrain. The basal behavioral profile of the HZ genotype reveals important differences, consistent with decreased behavioral inhibition and emotionality, which can be revealed as early as in adolescence, together with slight increment of impulsive behavior and altered pain threshold and at the adult age. The HZ genotype can thus represent a useful animal model for the study of behavioral disorders consequent to reduced neural plasticity.

Mesh Headings (Keywords): Analgesics, Opioid, Animals, Anxiety Disorders, Brain Chemistry, Cell Adhesion Molecules, Neuronal, Disease Models, Animal, Drug Resistance, Drug Tolerance, Emotions, Extracellular Matrix Proteins, Female, Genetic Predisposition to Disease, Heterozygote, Impulsive Behavior, Male, Maze Learning, Mesencephalon, Mice, Mice, Neurologic Mutants, Morphine, Motor Activity, Nerve Tissue Proteins, Neuronal Plasticity, Pain, Pain Threshold, Receptors, Opioid, mu, Serine Endopeptidases


Check for Full Text / PubMed Unique Identifier (PMID): 17174287


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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