Literature DB >> 7965819

Further studies on the relationship between dopamine cell density and haloperidol-induced catalepsy.

B Hitzemann1, K Dains, S Kanes, R Hitzemann.   

Abstract

Previous data have suggested that the genetic variability in the sensitivity to haloperidol-induced catalepsy is associated with the number of dopamine neurons in the substantia nigra zona compacta (SNZc). To further investigate this relationship, neuroleptic responsive (NR) and neuroleptic nonresponsive (NNR) lines were selected from the new heterogeneous stock/Northport (Np). At the fourth selected generation (S4), the NR/Np and NNR/Np lines differed more than 5-fold in their haloperidol ED50, but showed no difference in their ED50 to SCH 23390. Confirming the previous results, tyrosine hydroxylase (TH)-positive cell number in the SNZc was significantly higher in the NNR/Np as compared to the NR/Np line. The difference was most pronounced in the rostral SNZc, where TH cell number was increased 23%. Cell number also was increased significantly (38%) in the caudal ventral tegmental area (VTA). Fifty-two C57BL/6J:DBA/2J (B6D2)F2 hybrids were phenotyped for haloperidol response before determination of TH cell number. Paralleling the results in the selected lines, TH cell number in the SNZc was significantly (range, 10-28%) higher in the most nonresponsive F2 hybrids. TH cell number was determined in the SNZc and VTA of 10 standard inbred mouse strains for which the ED50 for haloperidol-induced catalepsy was known. TH cell number showed significant differences among inbred strains, with the largest difference (88%) noted between the 129/J and P/J strains in the rostral SNZc. In the VTA, differences as large as 95% were noted (AKR/crl vs. P/J). Among the inbred strains, there was no significant relationship between cell number and response except in the medial SNZc, where the most responsive strains had the highest cell number.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1994        PMID: 7965819

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  23 in total

1.  Gene networks and haloperidol-induced catalepsy.

Authors:  O D Iancu; P Darakjian; B Malmanger; N A R Walter; S McWeeney; R Hitzemann
Journal:  Genes Brain Behav       Date:  2011-11-11       Impact factor: 3.449

Review 2.  Systems genetics, bioinformatics and eQTL mapping.

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Journal:  Alcohol       Date:  2017-09-06       Impact factor: 2.405

4.  Progress in a replicated selection for elevated blood ethanol concentrations in HDID mice.

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Journal:  Genes Brain Behav       Date:  2013-12-06       Impact factor: 3.449

5.  Fear conditioning in mouse lines genetically selected for binge-like ethanol drinking.

Authors:  John C Crabbe; Jason P Schlumbohm; Wyatt Hack; Amanda M Barkley-Levenson; Pamela Metten; K Matthew Lattal
Journal:  Alcohol       Date:  2016-02-17       Impact factor: 2.405

6.  Selection for drinking in the dark alters brain gene coexpression networks.

Authors:  Ovidiu D Iancu; Denesa Oberbeck; Priscila Darakjian; Pamela Metten; Shannon McWeeney; John C Crabbe; Robert Hitzemann
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7.  Analysis of the mesotelencephalic dopamine system by quantitative-trait locus introgression.

Authors:  C Vadasz; I Sziraki; M Sasvari; P Kabai; L R Murthy; M Saito; I Laszlovszky
Journal:  Neurochem Res       Date:  1998-11       Impact factor: 3.996

8.  Shadoo (Sprn) and prion disease incubation time in mice.

Authors:  Sarah E Lloyd; Julia Grizenkova; Hirva Pota; John Collinge
Journal:  Mamm Genome       Date:  2009-06-10       Impact factor: 2.957

Review 9.  The value of animal models in predicting genetic susceptibility to complex diseases such as rheumatoid arthritis.

Authors:  Emma Ahlqvist; Malin Hultqvist; Rikard Holmdahl
Journal:  Arthritis Res Ther       Date:  2009-05-19       Impact factor: 5.156

10.  Sod1 deficiency reduces incubation time in mouse models of prion disease.

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Journal:  PLoS One       Date:  2013-01-22       Impact factor: 3.240

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