2010
DOI: 10.1016/j.neuro.2010.05.008
|View full text |Cite
|
Sign up to set email alerts
|

Cuprizone neurotoxicity, copper deficiency and neurodegeneration

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

1
40
0
1

Year Published

2013
2013
2022
2022

Publication Types

Select...
7
2

Relationship

0
9

Authors

Journals

citations
Cited by 62 publications
(42 citation statements)
references
References 46 publications
1
40
0
1
Order By: Relevance
“…The exact mechanisms of general cuprizone toxicity are not fully understood so far. However, the neurotoxic effect of cuprizone is believed to be in part attributed to its capability of chelating copper, ultimately leading to chronic copper deficiency with subsequent inhibition of copper-dependent enzymes (Benetti et al 2010). Moreover, activity of monoamino oxidase B, an iron-dependent enzyme, has been detected in PAS-positive granules of SAMP8 mice (Nakamura et al 1995).…”
Section: Discussionmentioning
confidence: 99%
“…The exact mechanisms of general cuprizone toxicity are not fully understood so far. However, the neurotoxic effect of cuprizone is believed to be in part attributed to its capability of chelating copper, ultimately leading to chronic copper deficiency with subsequent inhibition of copper-dependent enzymes (Benetti et al 2010). Moreover, activity of monoamino oxidase B, an iron-dependent enzyme, has been detected in PAS-positive granules of SAMP8 mice (Nakamura et al 1995).…”
Section: Discussionmentioning
confidence: 99%
“…One study demonstrated that oligomers of CPZ-Cu 2+ precipitated in the gut, and this was proposed to result in a widespread deficiency of copper throughout the body, including the brain. 10 In contrast, chemical studies of the binding of CPZ to copper showed that upon copper binding, a 2CPZ-Cu 3+ species was formed and an extended feeding of low concentrations of CPZ resulted in increased levels of copper in the brain. 5 Recently, copper, iron, and manganese levels were measured in the brain after CPZ treatment for 6 weeks.…”
mentioning
confidence: 99%
“…A deficiency of copper has been proved to be related to microglial activation in the cerebral cortex and thalamus. Proinflammatory molecules such as radical oxygen species and cytokines which are secreted by activated microglia can ultimately damage oligodendrocytes and growth retardation [30]. Also myelination is a copper dependent process in CNS [29] and myelin is lost in the neuropathies of copper deficiency [31].…”
Section: Discussionmentioning
confidence: 99%