PUBLICATION

Sustained behavioral effects of lithium exposure during early development in zebrafish: Involvement of the Wnt-β-catenin signaling pathway

Authors
Nery, L.R., Eltz, N.S., Martins, L., Guerim, L.D., Pereira, T.C., Bogo, M.R., Vianna, M.R.
ID
ZDB-PUB-140513-7
Date
2014
Source
Progress in neuro-psychopharmacology & biological psychiatry   55: 101-8 (Journal)
Registered Authors
Keywords
Lithium, N-Cadherin, Neurobehavioral effects, Wnt, Zebrafish, β-Catenin
MeSH Terms
  • Animals
  • Antimanic Agents/toxicity*
  • Blotting, Western
  • Cadherins/metabolism
  • Dose-Response Relationship, Drug
  • Heart Defects, Congenital/chemically induced
  • Kaplan-Meier Estimate
  • Lithium Chloride/toxicity*
  • Motor Activity/physiology
  • RNA, Messenger
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tail/abnormalities
  • Wnt3A Protein/metabolism*
  • Zebrafish/growth & development*
  • Zebrafish/physiology
  • Zebrafish Proteins/metabolism*
  • beta Catenin/metabolism*
PubMed
24813569 Full text @ Prog. Neuropsychopharmacol. Biol. Psychiatry
Abstract
Lithium has been the paradigmatic treatment for bipolar disorder since 1950s, offering prophylactic and acute efficacy against maniac and depressive episodes. Its use during early pregnancy and the perinatal period remains controversial due to reports of negative consequences on the newborn including teratogenic and neurobehavioral effects generally referred as Floppy baby syndrome. The mechanisms underlying lithium therapeutic action are still elusive but exacerbation of Wnt signaling pathway due to GSK-3 inhibition is believed to represent its main effect. In this study we evaluated the impact of lithium exposure during zebrafish embryonic and early development including behavioral and molecular characterization of Wnt-β-catenin pathway components. Wild-type zebrafish embryos were individually treated for 72 hpf with LiCl at 0.05, 0.5 and 5mM. No significant teratogenic and embryotoxic effects were observed. At the end of treatment period western blot analysis of selected Wnt-β-catenin system components showed increased β-catenin and decreased N-cadherin protein levels, without significant changes in Wnt3a, supporting GSK-3 inhibition as lithium's main target. At 10 dpf 0.5 and 5mM lithium-treated larvae showed a dose-dependent decrease in locomotion among other exploratory parameters, resembling lithium-induced Floppy baby syndrome neurobehavioral symptoms in humans. At this later period previously altered proteins returned to control levels in treated groups, suggesting that the neurobehavioral effects are a lasting consequence of lithium exposure during early development. qRT-PCR analysis of β-catenin and N-cadherin gene expression showed no effects of lithium at 3 or 10 dpf, suggesting that protein fluctuations were likely due to post-transcriptional events. Other Wnt target genes were evaluated and only discrete alterations were observed. These results suggest that zebrafish may be a valuable model for investigation of early effects of lithium that may be mediated by effects on the Wnt signaling pathway.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping