Literature DB >> 11529274

The midbrain dopaminergic system: anatomy and genetic variation in dopamine neuron number of inbred mouse strains.

L Zaborszky1, C Vadasz.   

Abstract

The mesotelencephalic dopamine system is genetically variable and affects motor behavior, motivation, and learning. Here we examine the genetic variation of mesencephalic DA neuron number in a quasi-congenic RQI mouse strain and its background partner and in a recombinant inbred strain with different levels of mesencephalic tyrosine hydroxylase activity (TH/MES). We used B6.Cb4i5-alpha6/Vad, C57BL/6By, and CXBI, which are known to express high, intermediate, and low levels of TH/MES, respectively. Unbiased stereological sampling with optical disector counting methods were employed to estimate the number of TH-positive neurons in the A8-A9-A10 cell groups. Morphometric studies on the mesencephalic dopamine cell groups indicated that male mice of the B6.Cb4i5-alpha6/Vad strain were endowed with a significantly lower number of TH-positive cells than CXBI mice. In all strains studied, the right retrorubral field (A8 area) had a higher number of dopamine neurons compared to the left A8 area. The results suggest an inverse relationship between TH/MES and number of dopamine neurons in the A9-A10 cell groups and significant lateral asymmetry in the A8 cell group. A detailed anatomical atlas of the mesencephalic A8-A9-A10 dopaminergic cell groups in the mouse is also presented to facilitate the assignment of TH-positive neurons to specific cell groups.

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Year:  2001        PMID: 11529274     DOI: 10.1023/a:1010257808945

Source DB:  PubMed          Journal:  Behav Genet        ISSN: 0001-8244            Impact factor:   2.805


  19 in total

1.  A comparison of model-based (2D) and design-based (3D) stereological methods for estimating cell number in the substantia nigra pars compacta (SNpc) of the C57BL/6J mouse.

Authors:  Z C Baquet; D Williams; J Brody; R J Smeyne
Journal:  Neuroscience       Date:  2009-04-17       Impact factor: 3.590

2.  Otx-dependent expression of proneural bHLH genes establishes a neuronal bilateral asymmetry in C. elegans.

Authors:  Shunji Nakano; Ronald E Ellis; H Robert Horvitz
Journal:  Development       Date:  2010-11-01       Impact factor: 6.868

3.  Basal ganglia dopamine loss due to defect in purine recycling.

Authors:  Kiyoshi Egami; Silaja Yitta; Suhail Kasim; J Chris Lewers; Rosalinda C Roberts; Mohamed Lehar; H A Jinnah
Journal:  Neurobiol Dis       Date:  2007-02-08       Impact factor: 5.996

4.  HIV-1 Tat regulation of dopamine transmission and microglial reactivity is brain region specific.

Authors:  Douglas R Miller; Fatemeh Shaerzadeh; Leah Phan; Nesrin Sharif; Joyonna Gamble-George; Jay P McLaughlin; Wolfgang J Streit; Habibeh Khoshbouei
Journal:  Glia       Date:  2018-05-07       Impact factor: 7.452

5.  Clustering of large cell populations: method and application to the basal forebrain cholinergic system.

Authors:  Zoltan Nadasdy; Peter Varsanyi; Laszlo Zaborszky
Journal:  J Neurosci Methods       Date:  2010-04-14       Impact factor: 2.390

Review 6.  A guide to neurotoxic animal models of Parkinson's disease.

Authors:  Kim Tieu
Journal:  Cold Spring Harb Perspect Med       Date:  2011-09       Impact factor: 6.915

7.  Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia.

Authors:  Chang-Hyun Song; Xueliang Fan; Cicely J Exeter; Ellen J Hess; H A Jinnah
Journal:  Neurobiol Dis       Date:  2012-05-31       Impact factor: 5.996

Review 8.  HIV, Tat and dopamine transmission.

Authors:  Peter J Gaskill; Douglas R Miller; Joyonna Gamble-George; Hideaki Yano; Habibeh Khoshbouei
Journal:  Neurobiol Dis       Date:  2017-04-27       Impact factor: 5.996

9.  Oestrogen receptors enhance dopamine neurone survival in rat midbrain.

Authors:  M L Johnson; C C Ho; A E Day; Q D Walker; R Francis; C M Kuhn
Journal:  J Neuroendocrinol       Date:  2010-01-27       Impact factor: 3.627

10.  Neuropathological changes in the substantia nigra in schizophrenia but not depression.

Authors:  M R Williams; K Galvin; B O'Sullivan; C D MacDonald; E W K Ching; F Turkheimer; O D Howes; R K B Pearce; S R Hirsch; M Maier
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  2013-12-29       Impact factor: 5.270

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