Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
28
pubmed:dateCreated
2005-7-14
pubmed:abstractText
Parkinson's disease (PD) is characterized by a loss of ventral midbrain dopaminergic neurons, which can be modeled by the neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). Inflammatory oxidants have emerged as key contributors to PD- and MPTP-related neurodegeneration. Here, we show that myeloperoxidase (MPO), a key oxidant-producing enzyme during inflammation, is upregulated in the ventral midbrain of human PD and MPTP mice. We also show that ventral midbrain dopaminergic neurons of mutant mice deficient in MPO are more resistant to MPTP-induced cytotoxicity than their wild-type littermates. Supporting the oxidative damaging role of MPO in this PD model are the demonstrations that MPO-specific biomarkers 3-chlorotyrosine and hypochlorous acid-modified proteins increase in the brains of MPTP-injected mice. This study demonstrates that MPO participates in the MPTP neurotoxic process and suggests that inhibitors of MPO may provide a protective benefit in PD.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1529-2401
pubmed:author
pubmed:issnType
Electronic
pubmed:day
13
pubmed:volume
25
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
6594-600
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:16014720-1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine, pubmed-meshheading:16014720-Amyotrophic Lateral Sclerosis, pubmed-meshheading:16014720-Animals, pubmed-meshheading:16014720-Brain, pubmed-meshheading:16014720-Corpus Striatum, pubmed-meshheading:16014720-Dopamine, pubmed-meshheading:16014720-Drug Evaluation, Preclinical, pubmed-meshheading:16014720-Enzyme Induction, pubmed-meshheading:16014720-Humans, pubmed-meshheading:16014720-Huntington Disease, pubmed-meshheading:16014720-Hypochlorous Acid, pubmed-meshheading:16014720-Male, pubmed-meshheading:16014720-Mesencephalon, pubmed-meshheading:16014720-Mice, pubmed-meshheading:16014720-Mice, Inbred C57BL, pubmed-meshheading:16014720-Mice, Knockout, pubmed-meshheading:16014720-Nerve Tissue Proteins, pubmed-meshheading:16014720-Neurons, pubmed-meshheading:16014720-Oxidative Stress, pubmed-meshheading:16014720-Parkinson Disease, pubmed-meshheading:16014720-Parkinsonian Disorders, pubmed-meshheading:16014720-Peroxidase, pubmed-meshheading:16014720-RNA, Messenger, pubmed-meshheading:16014720-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:16014720-Tyrosine
pubmed:year
2005
pubmed:articleTitle
Ablation of the inflammatory enzyme myeloperoxidase mitigates features of Parkinson's disease in mice.
pubmed:affiliation
Department of Neurology, Columbia University, New York, New York 10032, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural