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Cited by 508

The DOI matches its Crossref record; 88 of the 88 references it cites were found in a registry or an index.

Parkin gene inactivation alters behaviour and dopamine neurotransmission in the mouse

Itier, J.-M.·2003·Human Molecular Genetics

Abstract

Mutations of the parkin gene are the most frequent cause of early onset autosomal recessive parkinsonism (EO-AR). Here we show that inactivation of the parkin gene in mice results in motor and cognitive deficits, inhibition of amphetamine-induced dopamine release and inhibition of glutamate neurotransmission. The levels of dopamine are increased in the limbic brain areas of parkin mutant mice and there is a shift towards increased metabolism of dopamine by MAO. Although there was no evidence for a reduction of nigrostriatal dopamine neurons in the parkin mutant mice, the level of dopamine transporter protein was reduced in these animals, suggesting a decreased density of dopamine terminals, or adaptative changes in the nigrostriatal dopamine system. GSH levels were increased in the striatum and fetal mesencephalic neurons from parkin mutant mice, suggesting that a compensatory mechanism may protect dopamine neurons from neuronal death. These parkin mutant mice provide a valuable tool to better understand the preclinical deficits observed in patients with PD and to characterize the mechanisms leading to the degeneration of dopamine neurons that could provide new strategies for neuroprotection.

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Metadata

Authors
Itier, J.-M.
Venue
Human Molecular Genetics
Published
2003-07-15
Volume
12
Issue
18
Pages
2277-2291
ISSN
  • 0964-6906 (ISSN-L)
  • 1460-2083
OpenAlex
W2158259597
Cited by
508
References
88
FWCI
21.33
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Parkin gene inactivation alters behaviour and dopamine neurotransmission in the mouse. https://app.cochat.ai/papers/10.1093/hmg/ddg239
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Itier, J.-M. (2003). Parkin gene inactivation alters behaviour and dopamine neurotransmission in the mouse. Human Molecular Genetics. https://doi.org/10.1093/hmg/ddg239

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