Literature DB >> 25929815

Implementation of a manual for working with wobbler mice and criteria for discontinuation of the experiment.

Bastian Ott1, Carolin Dahlke1, Karl Meller1, Markus Napirei2, Thomas Schmitt-John3, Beate Brand-Saberi2, Carsten Theiss4, Darius Saberi1.   

Abstract

Mouse breeding is of importance to a whole range of medical and biological research. There are many known mouse models for motor neuron diseases. However, it must be kept in mind that especially mouse models for amyotrophic lateral sclerosis develop severe symptoms causing intense stress. This article is designed to summarize conscientious work with the wobbler mouse, a model for the sporadic form of amyotrophic lateral sclerosis. This mouse model is characterized by a degeneration of α-motor-neurons leading to head tremor, loss of body weight and rapidly progressive paralysis. Although this mouse model has been known since 1956, there are no guidelines for breeding wobbler mice. Due to the lack of such guidelines the present study tries to close this gap and implements a manual for further studies. It includes the whole workflow in regard to wobbler mice from breeding and animal care taking, genotyping and phenotype analysis, but also gives some examples for the use of various neuronal tissues for histological investigation. Beside the progress in research a second aim should always be the enhancement of mouse welfare and reduction of stress for the laboratory animals.
Copyright © 2015 Elsevier GmbH. All rights reserved.

Entities:  

Keywords:  Amyotrophic lateral sclerosis; Animal care; Criteria for discontinuation; PCR; Wobbler

Mesh:

Year:  2015        PMID: 25929815     DOI: 10.1016/j.aanat.2015.03.007

Source DB:  PubMed          Journal:  Ann Anat        ISSN: 0940-9602            Impact factor:   2.698


  7 in total

1.  Dysregulated expression and distribution of Kif5α in neurites of wobbler motor neurons.

Authors:  Kilian Kürten; Anne-Christin Gude; Aimo Samuel Christian Epplen; Jan Stein; Carsten Theiss; Veronika Matschke
Journal:  Neural Regen Res       Date:  2023-01       Impact factor: 6.058

2.  Increased ROS Level in Spinal Cord of Wobbler Mice due to Nmnat2 Downregulation.

Authors:  Pascal Röderer; Lara Klatt; Felix John; Verena Theis; Konstanze F Winklhofer; Carsten Theiss; Veronika Matschke
Journal:  Mol Neurobiol       Date:  2018-03-16       Impact factor: 5.590

3.  ROS scavengers decrease γH2ax spots in motor neuronal nuclei of ALS model mice in vitro.

Authors:  Maya Junghans; Felix John; Hilal Cihankaya; Daniel Schliebs; Konstanze F Winklhofer; Verian Bader; Johann Matschke; Carsten Theiss; Veronika Matschke
Journal:  Front Cell Neurosci       Date:  2022-08-31       Impact factor: 6.147

4.  Inflammation and neuronal death in the motor cortex of the wobbler mouse, an ALS animal model.

Authors:  Carolin Dahlke; Darius Saberi; Bastian Ott; Beate Brand-Saberi; Thomas Schmitt-John; Carsten Theiss
Journal:  J Neuroinflammation       Date:  2015-11-24       Impact factor: 8.322

Review 5.  VPS54 and the wobbler mouse.

Authors:  Thomas Schmitt-John
Journal:  Front Neurosci       Date:  2015-10-21       Impact factor: 4.677

6.  Deregulated miR-29b-3p Correlates with Tissue-Specific Activation of Intrinsic Apoptosis in An Animal Model of Amyotrophic Lateral Sclerosis.

Authors:  Christina L Klatt; Verena Theis; Stephan Hahn; Carsten Theiss; Veronika Matschke
Journal:  Cells       Date:  2019-09-12       Impact factor: 6.600

7.  Increased ROS-Dependent Fission of Mitochondria Causes Abnormal Morphology of the Cell Powerhouses in a Murine Model of Amyotrophic Lateral Sclerosis.

Authors:  Jan Stein; Bernd Walkenfort; Hilal Cihankaya; Mike Hasenberg; Verian Bader; Konstanze F Winklhofer; Pascal Röderer; Johann Matschke; Carsten Theiss; Veronika Matschke
Journal:  Oxid Med Cell Longev       Date:  2021-10-14       Impact factor: 6.543

  7 in total

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