Literature DB >> 18053966

Rats selectively-bred for behavior related to affective disorders: proclivity for intake of alcohol and drugs of abuse, and measures of brain monoamines.

J M Weiss1, C H K West, M S Emery, R W Bonsall, J P Moore, K A Boss-Williams.   

Abstract

Several lines of rats potentially useful for studying affective disorders have been developed in our laboratory though selective breeding for behavioral characteristics. The propensity of these lines to consume alcohol and other drugs of abuse (amphetamine and cocaine) was examined. Also, measurement of the concentration of brain monoamines - norepinephrine, dopamine, and serotonin - as well as estimation of their metabolism by measurement of the major extracellular metabolites of these monoamines was carried out to examine possible relationships of brain chemistry to the behavioral characteristics shown by these lines, as well as to their propensity for drug usage. The lines of rats are: Swim Low-active (SwLo) and Swim High-active (SwHi), which show either very low (SwLo) or very high (SwHi) amounts of motor activity in a swim test; Swim-test Susceptible (Susceptible or SUS) and Swim-test Resistant (Resistant or RES), which are highly susceptible (SUS) or highly resistant (RES) to having their swim-test activity depressed by being exposed to a stressful condition prior to the swim test; and Hyperactive (HYPER), which show spontaneous nocturnal hyperactivity compared to non-selectively bred (i.e., normal) rats as well as both extreme hyperactivity and behavioral depression after being exposed to a stressful condition. Regarding alcohol and drug usage, SUS rats readily consume alcohol while all other lines including non-selected, normal rats do not, and SwLo rats show a strong tendency to consume amphetamine and cocaine. Marked differences in brain monoamines were found between the various lines and normal rats, with salient differences seen in norepinephrine, particularly in the hippocampus, and in dopamine in forebrain regions (striatum and nucleus accumbens).

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Year:  2007        PMID: 18053966     DOI: 10.1016/j.bcp.2007.09.027

Source DB:  PubMed          Journal:  Biochem Pharmacol        ISSN: 0006-2952            Impact factor:   5.858


  17 in total

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Review 2.  Rat animal models for screening medications to treat alcohol use disorders.

Authors:  Richard L Bell; Sheketha R Hauser; Tiebing Liang; Youssef Sari; Antoniette Maldonado-Devincci; Zachary A Rodd
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3.  Several stressors fail to reduce adult hippocampal neurogenesis.

Authors:  Nicola D Hanson; Michael J Owens; Katherine A Boss-Williams; Jay M Weiss; Charles B Nemeroff
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Review 4.  Modeling treatment-resistant depression.

Authors:  Benjamin Adam Samuels; Eduardo David Leonardo; Reto Gadient; Amanda Williams; Jin Zhou; Denis J David; Alain Michel Gardier; Erik H F Wong; René Hen
Journal:  Neuropharmacology       Date:  2011-02-26       Impact factor: 5.250

Review 5.  Effects of stress on alcohol drinking: a review of animal studies.

Authors:  Howard C Becker; Marcelo F Lopez; Tamara L Doremus-Fitzwater
Journal:  Psychopharmacology (Berl)       Date:  2011-08-18       Impact factor: 4.530

6.  Operant psychostimulant self-administration in a rat model of depression.

Authors:  Sharon J Lin; S Alisha Epps; Charles H West; Katherine A Boss-Williams; Jay M Weiss; David Weinshenker
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7.  Sex and lineage interact to predict behavioral effects of chronic adolescent stress in rats.

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8.  Locus coeruleus neuronal activity determines proclivity to consume alcohol in a selectively-bred line of rats that readily consumes alcohol.

Authors:  Charles H K West; Katherine A Boss-Williams; James C Ritchie; Jay M Weiss
Journal:  Alcohol       Date:  2015-09-25       Impact factor: 2.405

Review 9.  The role of 5-HT3 receptors in drug abuse and as a target for pharmacotherapy.

Authors:  E A Engleman; Z A Rodd; R L Bell; J M Murphy
Journal:  CNS Neurol Disord Drug Targets       Date:  2008-11       Impact factor: 4.388

10.  Adenoviral vectors for highly selective gene expression in central serotonergic neurons reveal quantal characteristics of serotonin release in the rat brain.

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Journal:  BMC Biotechnol       Date:  2009-03-19       Impact factor: 2.563

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