001     137908
005     20240321220334.0
024 7 _ |a 10.1111/jnc.13026
|2 doi
024 7 _ |a pmid:25581060
|2 pmid
024 7 _ |a 0022-3042
|2 ISSN
024 7 _ |a 1471-4159
|2 ISSN
024 7 _ |a altmetric:4191610
|2 altmetric
037 _ _ |a DZNE-2020-04230
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Depboylu, Candan
|0 P:(DE-HGF)0
|b 0
|e Corresponding author
245 _ _ |a Systemically administered neuregulin-1β1 rescues nigral dopaminergic neurons via the ErbB4 receptor tyrosine kinase in MPTP mouse models of Parkinson's disease.
260 _ _ |a Oxford
|c 2015
|b Wiley-Blackwell
264 _ 1 |3 online
|2 Crossref
|b Wiley
|c 2015-01-26
264 _ 1 |3 print
|2 Crossref
|b Wiley
|c 2015-05-01
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1588686872_1068
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336 7 _ |a ARTICLE
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336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a Previously, we demonstrated that systemically injected extracellular domain of neuregulin-1β1 (Nrg1β1), a nerve growth and differentiation factor, passes the blood-brain barrier and rescues dopaminergic neurons of substantia nigra in the 6-hydroxydopamine-mouse model of Parkinson's disease (PD). Here, we studied the effects of peripherally administered Nrg1β1 in another toxin-based mouse model of PD. For this purpose, (i) nigrostriatal pathway injury was induced by treatment of adult wild-type mice with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) in acute and subchronic paradigms; and (ii) Nrg1β1 or saline (control) were administered 1 h before each MPTP injection. We found that Nrg1β1 significantly reduced the loss of nigral dopaminergic neurons in both intoxication paradigms (7 days post-injection). However, Nrg1β1 did not reverse MPTP-induced decrease in dopamine levels and dopaminergic fibers in the striatum. We also show that MPTP conversion to its toxic metabolite 1-methyl-4-phenylpyridinium as well as levels of dopamine transporter, mediating intracellular uptake of 1-methyl-4-phenylpyridinium, are unaffected by Nrg1β1. Finally, neuroprotective properties of Nrg1β1 on nigral dopaminergic neurons are specifically mediated by ErbB4 as revealed through the study of ErbB4 knockout mice. In conclusion, systemically administered Nrg1β1 protects midbrain dopaminergic neurons against this PD-related toxic insult. Thus, Nrg1β1 may have a benefit in the treatment of PD patients. Previously, we demonstrated that systemically administered neuregulin-1β1 (Nrg1β1) passes the blood-brain barrier, phosphorylates ErbB4 receptors and elevates dopamine (DA) levels in the nigrostriatal system of healthy mice. Nrg1β1 protects nigral DAergic neurons in the 6-hydroxydopamine (6-OHDA) mouse model of Parkinson's disease (PD). Here, we show that Nrg1β1 rescues nigral DAergic neurons also against 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced cell death. ErbB4 expression is essential for the neuroprotective effect of Nrg1β1 on midbrain DAergic neurons. Nrg1β1 might be beneficial in PD treatment.
536 _ _ |a 344 - Clinical and Health Care Research (POF3-344)
|0 G:(DE-HGF)POF3-344
|c POF3-344
|f POF III
|x 0
542 _ _ |i 2015-09-01
|2 Crossref
|u http://doi.wiley.com/10.1002/tdm_license_1.1
588 _ _ |a Dataset connected to CrossRef, PubMed,
650 _ 7 |a Dopamine Agents
|2 NLM Chemicals
650 _ 7 |a Dopamine Plasma Membrane Transport Proteins
|2 NLM Chemicals
650 _ 7 |a Neuregulin-1
|2 NLM Chemicals
650 _ 7 |a Neuroprotective Agents
|2 NLM Chemicals
650 _ 7 |a neuregulin beta
|2 NLM Chemicals
650 _ 7 |a 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine
|0 9P21XSP91P
|2 NLM Chemicals
650 _ 7 |a Erbb4 protein, mouse
|0 EC 2.7.10.1
|2 NLM Chemicals
650 _ 7 |a Receptor, ErbB-4
|0 EC 2.7.10.1
|2 NLM Chemicals
650 _ 2 |a 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine: pharmacology
|2 MeSH
650 _ 2 |a Animals
|2 MeSH
650 _ 2 |a Animals, Genetically Modified
|2 MeSH
650 _ 2 |a Disease Models, Animal
|2 MeSH
650 _ 2 |a Dopamine Agents: pharmacology
|2 MeSH
650 _ 2 |a Dopamine Plasma Membrane Transport Proteins: metabolism
|2 MeSH
650 _ 2 |a Dopaminergic Neurons: drug effects
|2 MeSH
650 _ 2 |a MPTP Poisoning: chemically induced
|2 MeSH
650 _ 2 |a MPTP Poisoning: pathology
|2 MeSH
650 _ 2 |a Male
|2 MeSH
650 _ 2 |a Mice
|2 MeSH
650 _ 2 |a Mice, Inbred C57BL
|2 MeSH
650 _ 2 |a Neuregulin-1: pharmacology
|2 MeSH
650 _ 2 |a Neuregulin-1: therapeutic use
|2 MeSH
650 _ 2 |a Neuroprotective Agents: pharmacology
|2 MeSH
650 _ 2 |a Neuroprotective Agents: therapeutic use
|2 MeSH
650 _ 2 |a Receptor, ErbB-4: deficiency
|2 MeSH
650 _ 2 |a Receptor, ErbB-4: genetics
|2 MeSH
650 _ 2 |a Substantia Nigra: pathology
|2 MeSH
650 _ 2 |a Time Factors
|2 MeSH
700 1 _ |a Rösler, Thomas W
|0 P:(DE-2719)2810437
|b 1
|u dzne
700 1 _ |a de Andrade, Anderson
|0 P:(DE-HGF)0
|b 2
700 1 _ |a Oertel, Wolfgang H
|0 P:(DE-HGF)0
|b 3
700 1 _ |a Höglinger, Günter U
|0 P:(DE-2719)2811373
|b 4
|e Last author
|u dzne
773 1 8 |a 10.1111/jnc.13026
|b : Wiley, 2015-01-26
|n 4
|p 590-597
|3 journal-article
|2 Crossref
|t Journal of Neurochemistry
|v 133
|y 2015
|x 0022-3042
773 _ _ |a 10.1111/jnc.13026
|g Vol. 133, no. 4, p. 590 - 597
|0 PERI:(DE-600)2020528-4
|n 4
|q 133:4<590 - 597
|p 590-597
|t Journal of neurochemistry
|v 133
|y 2015
|x 0022-3042
909 C O |o oai:pub.dzne.de:137908
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910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
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910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
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|6 P:(DE-2719)2811373
913 1 _ |a DE-HGF
|b Forschungsbereich Gesundheit
|l Erkrankungen des Nervensystems
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