Format

Send to

Choose Destination
Prog Neuropsychopharmacol Biol Psychiatry. 2018 Jun 8;84(Pt A):181-189. doi: 10.1016/j.pnpbp.2018.02.010. Epub 2018 Feb 26.

Pharmacological analysis of zebrafish lphn3.1 morphant larvae suggests that saturated dopaminergic signaling could underlie the ADHD-like locomotor hyperactivity.

Author information

1
Paris-Saclay Institute for Neuroscience (Neuro-PSI), UMR 9197, CNRS - Université Paris-Sud, Team Zebrafish Neurogenetics, Avenue de la Terrasse, F-91190 Gif-sur-Yvette, France; Laboratory for Developmental Gene Regulation, RIKEN Brain Science Institute, Saitama 351-0198, Japan. Electronic address: merlin.lange@riken.jp.
2
Paris-Saclay Institute for Neuroscience (Neuro-PSI), UMR 9197, CNRS - Université Paris-Sud, Team Zebrafish Neurogenetics, Avenue de la Terrasse, F-91190 Gif-sur-Yvette, France.
3
Paris-Saclay Institute for Neuroscience (Neuro-PSI), UMR 9197, CNRS - Université Paris-Sud, Team Zebrafish Neurogenetics, Avenue de la Terrasse, F-91190 Gif-sur-Yvette, France; Dept. Neuroscience, Psychology and Behaviour, University of Leicester, Leicester LE1 7RH, UK.
4
Paris-Saclay Institute for Neuroscience (Neuro-PSI), UMR 9197, CNRS - Université Paris-Sud, Team Zebrafish Neurogenetics, Avenue de la Terrasse, F-91190 Gif-sur-Yvette, France; Unit Zebrafish Neurogenetics, Department of Developmental and Stem Cell Biology, Institut Pasteur and CNRS UMR3738, 25 rue du Dr Roux, 75015 Paris, France. Electronic address: laure.bally-cuif@pasteur.fr.

Abstract

Polymorphisms in the gene coding for the adhesion G-protein coupled receptor LPHN3 are a risk factor for attention-deficit/hyperactivity disorder (ADHD). Transient down-regulation of latrophilin3.1 (lphn3.1), the zebrafish LPHN3 homologue, causes hyperactivity. Zebrafish injected with a lphn3.1-specific morpholino are hyperactive and display an impairment in dopaminergic neuron development. In the present study we used lphn3.1 morphants to further characterize the changes to dopaminergic signaling that trigger hyperactivity. We applied dopamine agonists (Apomorphine, Quinpirole, SKF-38393) and antagonists (Haloperidol, Eticlopride, SCH-23390) to Lphn3.1 morpholino-injected or control-injected animals. The percentage of change in locomotor activity was then determined at three different time periods (10-20 min, 30-40 min and 60-70 min). Our results show that drugs targeting dopamine receptors appear to elicit similar effects on locomotion in zebrafish larvae and mammals. In addition, we observed that lphn3.1 morphants have an overall hyposensitivity to dopamine agonists and antagonists compared to control fish. These results are compatible with a model whereby dopaminergic neurotransmission is saturated in lphn3.1 morphants.

KEYWORDS:

Behavior; Dopamine; Latrophilin 3; Locomotion; Zebrafish

Supplemental Content

Full text links

Icon for Elsevier Science Icon for PubMed Central
Loading ...
Support Center