Chemogenetic ablation of dopaminergic neurons leads to transient locomotor impairments in zebrafish larvae.
Identifieur interne : 000800 ( Main/Curation ); précédent : 000799; suivant : 000801Chemogenetic ablation of dopaminergic neurons leads to transient locomotor impairments in zebrafish larvae.
Auteurs : Rafael Godoy [Canada] ; Sandra Noble [Canada] ; Kevin Yoon [Canada] ; Hymie Anisman [Canada] ; Marc Ekker [Canada]Source :
- Journal of neurochemistry [ 1471-4159 ] ; 2015.
English descriptors
- KwdEn :
- Animals, Animals, Genetically Modified, Brain (cytology), Brain (growth & development), Dopaminergic Neurons (drug effects), Dyskinesia, Drug-Induced (genetics), Dyskinesia, Drug-Induced (physiopathology), Green Fluorescent Proteins, Humans, Larva (growth & development), Locomotion (drug effects), MPTP Poisoning (pathology), Metronidazole (pharmacology), Nerve Regeneration, Swimming, Zebrafish.
- MESH :
- chemical , pharmacology : Metronidazole.
- chemical : Green Fluorescent Proteins.
- cytology : Brain.
- drug effects : Dopaminergic Neurons, Locomotion.
- genetics : Dyskinesia, Drug-Induced.
- growth & development : Brain, Larva.
- pathology : MPTP Poisoning.
- physiopathology : Dyskinesia, Drug-Induced.
- Animals, Animals, Genetically Modified, Humans, Nerve Regeneration, Swimming, Zebrafish.
Abstract
To determine the impact of a controlled loss of dopaminergic neurons on locomotor function, we generated transgenic zebrafish, Tg(dat:CFP-NTR), expressing a cyan fluorescent protein-nitroreductase fusion protein (CFP-NTR) under the control of dopamine transporter (dat) cis-regulatory elements. Embryonic and larval zebrafish express the transgene in several groups of dopaminergic neurons, notably in the olfactory bulb, telencephalon, diencephalon and caudal hypothalamus. Administration of the pro-drug metronidazole (Mtz) resulted in activation of caspase 3 in CFP-positive neurons and in a reduction in dat-positive cells by 5 days post-fertilization (dpf). Loss of neurons coincided with impairments in global locomotor parameters such as swimming distance, percentage of time spent moving, as well as changes in tail bend parameters such as time to maximal bend and angular velocity. Dopamine levels were transiently decreased following Mtz administration. Recovery of some of the locomotor parameters was observed by 7 dpf. However, the total numbers of dat-expressing neurons were still decreased at 7, 12, or 14 dpf, even though there was evidence for production of new dat-expressing cells. Tg(dat:CFP-NTR) zebrafish provide a model to correlate altered dopaminergic neuron numbers with locomotor function and to investigate factors influencing regeneration of dopaminergic neurons.
DOI: 10.1111/jnc.13214
PubMed: 26118896
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pubmed:26118896Le document en format XML
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<front><div type="abstract" xml:lang="en">To determine the impact of a controlled loss of dopaminergic neurons on locomotor function, we generated transgenic zebrafish, Tg(dat:CFP-NTR), expressing a cyan fluorescent protein-nitroreductase fusion protein (CFP-NTR) under the control of dopamine transporter (dat) cis-regulatory elements. Embryonic and larval zebrafish express the transgene in several groups of dopaminergic neurons, notably in the olfactory bulb, telencephalon, diencephalon and caudal hypothalamus. Administration of the pro-drug metronidazole (Mtz) resulted in activation of caspase 3 in CFP-positive neurons and in a reduction in dat-positive cells by 5 days post-fertilization (dpf). Loss of neurons coincided with impairments in global locomotor parameters such as swimming distance, percentage of time spent moving, as well as changes in tail bend parameters such as time to maximal bend and angular velocity. Dopamine levels were transiently decreased following Mtz administration. Recovery of some of the locomotor parameters was observed by 7 dpf. However, the total numbers of dat-expressing neurons were still decreased at 7, 12, or 14 dpf, even though there was evidence for production of new dat-expressing cells. Tg(dat:CFP-NTR) zebrafish provide a model to correlate altered dopaminergic neuron numbers with locomotor function and to investigate factors influencing regeneration of dopaminergic neurons.</div>
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