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Journal of Neurochemistry
Article . 2015 . Peer-reviewed
License: Wiley Online Library User Agreement
Data sources: Crossref
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
DZNE Pub
Article . 2015
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Systemically administered neuregulin‐1β1 rescues nigral dopaminergic neurons via the ErbB4 receptor tyrosine kinase in MPTP mouse models of Parkinson's disease

Authors: Günter U. Höglinger; Günter U. Höglinger; Günter U. Höglinger; Wolfgang H. Oertel; Thomas W. Rösler; Thomas W. Rösler; Anderson de Andrade; +1 Authors

Systemically administered neuregulin‐1β1 rescues nigral dopaminergic neurons via the ErbB4 receptor tyrosine kinase in MPTP mouse models of Parkinson's disease

Abstract

AbstractPreviously, 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. image 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.

Country
Germany
Keywords

therapeutic use [Neuregulin-1], Male, Receptor, ErbB-4, Time Factors, pharmacology [Neuregulin-1], Neuregulin-1, Dopamine Agents, drug effects [Dopaminergic Neurons], genetics [Receptor, ErbB-4], pathology [MPTP Poisoning], Animals, Genetically Modified, Mice, Animals, pharmacology [1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine], pathology [Substantia Nigra], chemically induced [MPTP Poisoning], Dopamine Plasma Membrane Transport Proteins, neuregulin beta, pharmacology [Neuroprotective Agents], deficiency [Receptor, ErbB-4], Dopaminergic Neurons, MPTP Poisoning, therapeutic use [Neuroprotective Agents], Erbb4 protein, mouse, Mice, Inbred C57BL, Substantia Nigra, pharmacology [Dopamine Agents], Disease Models, Animal, Neuroprotective Agents, 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine, metabolism [Dopamine Plasma Membrane Transport Proteins], ddc: ddc:610

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
25
Top 10%
Average
Top 10%
bronze