Literature DB >> 571007

Neuronal degeneration in the brain of the brindled mouse--a light microscope study.

K Yajima, K Suzuki.   

Abstract

The brindled mouse (Mobr) is a neurological mutant mouse with a deficiency in copper transport. This mutant has many clinical as well as biochemical features in common with Kinky hair syndrome (KHS) in humans (Tab. 1). Male hemizygotes (Mobr/Y) are characterized by the absence of fur pigment and curly whiskers. They become inactive, losing weight at around the 10th-12th post-natal day. They usually die in an emaciated state around the 15th-16th postnatal day. The brain weight is usually about three fourths of that of littermate controls. Microscopically, widespread neuronal degeneration was noted in the cerebral cortex and thalamic nuclei of male hemizygotes after the 12th post-natal day. The degeneration continued to increase until death. Scattered degenerated cells were also noted in the cerebellum. No such degenerative changes were observed in the brain of female heterozygotes (Mobr/+) or in normal or starved littermates. These degenerative changes of neurons in the brindled hemizygote mouse will be compared with the neuropathological changes observed in KHS and in experimental animals with copper deficiency, and the possible pathogenesis of these changes will be discussed.

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Year:  1979        PMID: 571007     DOI: 10.1097/00005072-197901000-00004

Source DB:  PubMed          Journal:  J Neuropathol Exp Neurol        ISSN: 0022-3069            Impact factor:   3.685


  12 in total

1.  Clinico-pathological study on macular mutant mouse.

Authors:  T Yamano; M Shimada; H Kawasaki; A Onaga; M Nishimura
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088

2.  Cerebellar changes of the female mice heterozygous for brindled gene.

Authors:  T Yamano; K Suzuki
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

3.  Neuronal degeneration in the brain of the brindled mouse. I. Chromological studies on the long-surviving group.

Authors:  K Yajima; K Suzuki
Journal:  Acta Neuropathol       Date:  1979-11       Impact factor: 17.088

4.  Decreased activity of cytochrome c oxidase in the macular mottled mouse: an immuno-electron microscopic study.

Authors:  K Seki; T Sato; Y Ishigaki; S Nakamura; Y Ishihara; T Ozawa
Journal:  Acta Neuropathol       Date:  1989       Impact factor: 17.088

5.  Neuropathologic study in the heterozygotes of X-linked brindled mutant mouse.

Authors:  H Matsushima; A Okuno; Y Eto; K Maekawa
Journal:  Acta Neuropathol       Date:  1985       Impact factor: 17.088

6.  Neuronal degeneration in the brain of the brindled mouse. An ultrastructural study of the cerebral cortical neurons.

Authors:  K Yajima; K Suzuki
Journal:  Acta Neuropathol       Date:  1979-01-12       Impact factor: 17.088

7.  Copper metabolism in mottled mouse mutants. Defective placental transfer of 64Cu to foetal brindled (Mobr) mice.

Authors:  J R Mann; J Camakaris; D M Danks
Journal:  Biochem J       Date:  1980-02-15       Impact factor: 3.857

8.  An ultrastructural study on the cerebellum of the brindled mouse.

Authors:  H Nagara; K Yajima; K Suzuki
Journal:  Acta Neuropathol       Date:  1980       Impact factor: 17.088

9.  Brindled mottled mouse: morphological changes of brain and visceral organs in hemizygous males following copper supplementation.

Authors:  K Suzuki; H Nagara
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

10.  Golgi study on brain of macular mutant mouse as a model of Menkes kinky hair disease.

Authors:  H Kawasaki; A Onaga; T Yamano; M Shimada; M Nishimura
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088

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