PUBLICATION
Role of nitric oxide in the behavioral and neurochemical effects of IB-MECA in zebrafish
- Authors
- Maximino, C., Gemaque, J., Benzecry, R., Lima, M.G., Batista, E.D., Picanço-Diniz, D.W., Oliveira, K.R., Herculano, A.M.
- ID
- ZDB-PUB-141114-9
- Date
- 2015
- Source
- Psychopharmacology 232(10): 1671-80 (Journal)
- Registered Authors
- Lima, Monica Gomes, Maximino, Caio
- Keywords
- none
- MeSH Terms
-
- Adenosine/analogs & derivatives*
- Adenosine/pharmacology
- Adenosine/therapeutic use
- Animals
- Anxiety/drug therapy
- Anxiety/metabolism*
- Dose-Response Relationship, Drug
- Male
- Motor Activity/drug effects*
- Motor Activity/physiology
- Nitric Oxide/physiology*
- Nitric Oxide Synthase/metabolism
- Serotonin/metabolism*
- Serotonin Plasma Membrane Transport Proteins/metabolism*
- Signal Transduction/drug effects
- Signal Transduction/physiology
- Zebrafish
- PubMed
- 25388291 Full text @ Psychpharma
Citation
Maximino, C., Gemaque, J., Benzecry, R., Lima, M.G., Batista, E.D., Picanço-Diniz, D.W., Oliveira, K.R., Herculano, A.M. (2015) Role of nitric oxide in the behavioral and neurochemical effects of IB-MECA in zebrafish. Psychopharmacology. 232(10):1671-80.
Abstract
Rationale The adenosine A3 receptor and the nitric oxide (NO) pathway regulate the function and localization of serotonin transporters (SERTs). These transporters regulate extracellular serotonin levels, which are correlated with defensive behavior.
Objective The purpose of this study was to understand the role of the A3AR on anxiety and arousal models in zebrafish, and whether this role is mediated by the nitrergic modulation of serotonin uptake.
Methods The effects of IB-MECA (0.01 and 0.1 mg/kg) were assessed in a series of behavioral tasks in adult zebrafish, as well as on extracellular serotonin levels in vivo and serotonin uptake in brain homogenates. Finally, the interaction between IB-MECA and drugs blocking voltage-dependent calcium channels (VDCCs), NO synthase, and SERT was analyzed.
Results At the lowest dose, IB-MECA decreased bottom dwelling and scototaxis, while at the highest dose, it also decreased shoaling, startle probability, and melanophore responses. These effects were accompanied by an increase in brain extracellular serotonin levels. IB-MECA also concentration-dependently increased serotonin uptake in vitro. The effects of IB-MECA on extracellular 5-HT, scototaxis, and geotaxis were blocked by L-NAME, while only the effects on 5-HT and scototaxis were blocked by verapamil. In vitro, the increase in 5-HT uptake was dependent on VDCCs and NO. Finally, fluoxetine blocked the effect of IB-MECA on scototaxis, but not geotaxis.
Conclusion These results suggest that the effect of IB-MECA on scototaxis are mediated by a VDCC-NO-SERT pathway. While NO seems to mediate the effects of IB-MECA on geotaxis, neither VDCCs nor SERT seems to be involved in this process.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping