Metallothionein proteins expression, copper and zinc concentrations, and lipid peroxidation level in a rodent model for amyotrophic lateral sclerosis

Eiichi Tokuda, Shin Ichi Ono, Kumiko Ishige, Akira Naganuma, Yoshihisa Ito, Takashi Suzuki

Research output: Contribution to journalArticle

63 Citations (Scopus)

Abstract

It has been hypothesized that copper-mediated oxidative stress contributes to the pathogenesis of familial amyotrophic lateral sclerosis (ALS), a fatal motor neuron disease in humans. To verify this hypothesis, we examined the copper and zinc concentrations and the amounts of lipid peroxides, together with that of the expression of metallothionein (MT) isoforms in a mouse model [superoxide dismutase1 transgenic (SOD1 Tg) mouse] of ALS. The expression of MT-I and MT-II (MT-I/II) isoforms were measured together with Western blotting, copper level, and lipid peroxides amounts increased in an age-dependent manner in the spinal cord, the region responsible for motor paralysis. A significant increase was already seen as early as 8-week-old SOD1 Tg mice, at which time the mice had not yet exhibited motor paralysis, and showed a further increase at 16 weeks of age, when paralysis was evident. Inversely, the spinal zinc level had significantly decreased at both 8 and 16 weeks of age. The third isoform, the MT-III level, remained at the same level as an 8-week-old wild-type mouse, finally increasing to a significant level at 16 weeks of age. It has been believed that a mutant SOD1 protein, encoded by a mutant SOD1, gains a novel cytotoxic function while maintaining its original enzymatic activity, and causes motor neuron death (gain-of-toxic function). Copper-mediated oxidative stress seems to be a probable underlying pathogenesis of gain-of-toxic function. Taking the above current concepts and the classic functions of MT into account, MTs could have a disease modifying property: the MT-I/II isoform for attenuating the gain-of-toxic function at the early stage of the disease, and the MT-III isoform at an advanced stage.

Original languageEnglish
Pages (from-to)33-41
Number of pages9
JournalToxicology
Volume229
Issue number1-2
DOIs
Publication statusPublished - 2007 Jan 5
Externally publishedYes

Fingerprint

Metallothionein
Amyotrophic Lateral Sclerosis
Lipid Peroxidation
Zinc
Copper
Rodentia
Protein Isoforms
Poisons
Lipids
Paralysis
Oxidative stress
Lipid Peroxides
Proteins
Superoxides
Transgenic Mice
Neurons
Oxidative Stress
Motor Neuron Disease
Motor Neurons
Mutant Proteins

Keywords

  • Amyotrophic lateral sclerosis
  • Copper
  • Metallothionein
  • Oxidative stress
  • Superoxide dismutase1
  • Zinc

ASJC Scopus subject areas

  • Toxicology

Cite this

Metallothionein proteins expression, copper and zinc concentrations, and lipid peroxidation level in a rodent model for amyotrophic lateral sclerosis. / Tokuda, Eiichi; Ono, Shin Ichi; Ishige, Kumiko; Naganuma, Akira; Ito, Yoshihisa; Suzuki, Takashi.

In: Toxicology, Vol. 229, No. 1-2, 05.01.2007, p. 33-41.

Research output: Contribution to journalArticle

Tokuda, Eiichi ; Ono, Shin Ichi ; Ishige, Kumiko ; Naganuma, Akira ; Ito, Yoshihisa ; Suzuki, Takashi. / Metallothionein proteins expression, copper and zinc concentrations, and lipid peroxidation level in a rodent model for amyotrophic lateral sclerosis. In: Toxicology. 2007 ; Vol. 229, No. 1-2. pp. 33-41.
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