Cargando…

Dopamine Modulates Serotonin Innervation in the Drosophila Brain

Parkinson’s disease (PD) results from a progressive degeneration of the dopaminergic nigrostriatal system leading to a decline in movement control, with resting tremor, rigidity and postural instability. Several aspects of PD can be modeled in the fruit fly, Drosophila melanogaster, including α-synu...

Descripción completa

Detalles Bibliográficos
Autores principales: Niens, Janna, Reh, Fabienne, Çoban, Büşra, Cichewicz, Karol, Eckardt, Julia, Liu, Yi-Ting, Hirsh, Jay, Riemensperger, Thomas D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650618/
https://www.ncbi.nlm.nih.gov/pubmed/29085286
http://dx.doi.org/10.3389/fnsys.2017.00076
_version_ 1783272734851072000
author Niens, Janna
Reh, Fabienne
Çoban, Büşra
Cichewicz, Karol
Eckardt, Julia
Liu, Yi-Ting
Hirsh, Jay
Riemensperger, Thomas D.
author_facet Niens, Janna
Reh, Fabienne
Çoban, Büşra
Cichewicz, Karol
Eckardt, Julia
Liu, Yi-Ting
Hirsh, Jay
Riemensperger, Thomas D.
author_sort Niens, Janna
collection PubMed
description Parkinson’s disease (PD) results from a progressive degeneration of the dopaminergic nigrostriatal system leading to a decline in movement control, with resting tremor, rigidity and postural instability. Several aspects of PD can be modeled in the fruit fly, Drosophila melanogaster, including α-synuclein-induced degeneration of dopaminergic neurons, or dopamine (DA) loss by genetic elimination of neural DA synthesis. Defective behaviors in this latter model can be ameliorated by feeding the DA precursor L-DOPA, analogous to the treatment paradigm for PD. Secondary complication from L-DOPA treatment in PD patients are associated with ectopic synthesis of DA in serotonin (5-HT)-releasing neurons, leading to DA/5-HT imbalance. Here we examined the neuro-anatomical adaptations resulting from imbalanced DA/5-HT signaling in Drosophila mutants lacking neural DA. We find that, similar to rodent models of PD, lack of DA leads to increased 5-HT levels and arborizations in specific brain regions. Conversely, increased DA levels by L-DOPA feeding leads to reduced connectivity of 5-HT neurons to their target neurons in the mushroom body (MB). The observed alterations of 5-HT neuron plasticity indicate that loss of DA signaling is not solely responsible for the behavioral disorders observed in Drosophila models of PD, but rather a combination of the latter with alterations of 5-HT circuitry.
format Online
Article
Text
id pubmed-5650618
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-56506182017-10-30 Dopamine Modulates Serotonin Innervation in the Drosophila Brain Niens, Janna Reh, Fabienne Çoban, Büşra Cichewicz, Karol Eckardt, Julia Liu, Yi-Ting Hirsh, Jay Riemensperger, Thomas D. Front Syst Neurosci Neuroscience Parkinson’s disease (PD) results from a progressive degeneration of the dopaminergic nigrostriatal system leading to a decline in movement control, with resting tremor, rigidity and postural instability. Several aspects of PD can be modeled in the fruit fly, Drosophila melanogaster, including α-synuclein-induced degeneration of dopaminergic neurons, or dopamine (DA) loss by genetic elimination of neural DA synthesis. Defective behaviors in this latter model can be ameliorated by feeding the DA precursor L-DOPA, analogous to the treatment paradigm for PD. Secondary complication from L-DOPA treatment in PD patients are associated with ectopic synthesis of DA in serotonin (5-HT)-releasing neurons, leading to DA/5-HT imbalance. Here we examined the neuro-anatomical adaptations resulting from imbalanced DA/5-HT signaling in Drosophila mutants lacking neural DA. We find that, similar to rodent models of PD, lack of DA leads to increased 5-HT levels and arborizations in specific brain regions. Conversely, increased DA levels by L-DOPA feeding leads to reduced connectivity of 5-HT neurons to their target neurons in the mushroom body (MB). The observed alterations of 5-HT neuron plasticity indicate that loss of DA signaling is not solely responsible for the behavioral disorders observed in Drosophila models of PD, but rather a combination of the latter with alterations of 5-HT circuitry. Frontiers Media S.A. 2017-10-16 /pmc/articles/PMC5650618/ /pubmed/29085286 http://dx.doi.org/10.3389/fnsys.2017.00076 Text en Copyright © 2017 Niens, Reh, Çoban, Cichewicz, Eckardt, Liu, Hirsh and Riemensperger. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Niens, Janna
Reh, Fabienne
Çoban, Büşra
Cichewicz, Karol
Eckardt, Julia
Liu, Yi-Ting
Hirsh, Jay
Riemensperger, Thomas D.
Dopamine Modulates Serotonin Innervation in the Drosophila Brain
title Dopamine Modulates Serotonin Innervation in the Drosophila Brain
title_full Dopamine Modulates Serotonin Innervation in the Drosophila Brain
title_fullStr Dopamine Modulates Serotonin Innervation in the Drosophila Brain
title_full_unstemmed Dopamine Modulates Serotonin Innervation in the Drosophila Brain
title_short Dopamine Modulates Serotonin Innervation in the Drosophila Brain
title_sort dopamine modulates serotonin innervation in the drosophila brain
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650618/
https://www.ncbi.nlm.nih.gov/pubmed/29085286
http://dx.doi.org/10.3389/fnsys.2017.00076
work_keys_str_mv AT niensjanna dopaminemodulatesserotonininnervationinthedrosophilabrain
AT rehfabienne dopaminemodulatesserotonininnervationinthedrosophilabrain
AT cobanbusra dopaminemodulatesserotonininnervationinthedrosophilabrain
AT cichewiczkarol dopaminemodulatesserotonininnervationinthedrosophilabrain
AT eckardtjulia dopaminemodulatesserotonininnervationinthedrosophilabrain
AT liuyiting dopaminemodulatesserotonininnervationinthedrosophilabrain
AT hirshjay dopaminemodulatesserotonininnervationinthedrosophilabrain
AT riemenspergerthomasd dopaminemodulatesserotonininnervationinthedrosophilabrain