PUBLICATION

Effects of embryonic cyclosporine exposures on brain development and behavior

Authors
Clift, D.E., Thorn, R.J., Passarelli, E.A., Kapoor, M., LoPiccolo, M.K., Richendrfer, H.A., Colwill, R.M., Creton, R.
ID
ZDB-PUB-150117-7
Date
2015
Source
Behavioural brain research   282: 117-24 (Journal)
Registered Authors
Creton, Robbert
Keywords
Zebrafish, behavior, brain, calcineurin, cyclosporin, cyclosporine
MeSH Terms
  • Animals
  • Behavior, Animal/drug effects*
  • Brain/drug effects*
  • Brain/growth & development*
  • Calcineurin Inhibitors/pharmacology*
  • Cyclosporine/pharmacology*
  • Eye/drug effects
  • Eye/growth & development
  • Female
  • Immunosuppressive Agents/pharmacology
  • Larva/drug effects
  • Larva/growth & development
  • Male
  • Pregnancy
  • Tacrolimus/pharmacology
  • Time Factors
  • Vision, Ocular/drug effects
  • Zebrafish/growth & development
PubMed
25591474 Full text @ Behav. Brain Res.
Abstract
Cyclosporine, a calcineurin inhibitor, is successfully used as an immunosuppressant in transplant medicine. However, the use of this pharmaceutical during pregnancy is concerning, since calcineurin is thought to play a role in neural development. The risk for human brain development is difficult to evaluate, because of a lack of basic information on the sensitive developmental times and the potentially pleiotropic effects on brain development and behavior. In the present study, we use zebrafish as a model system to examine the effects of embryonic cyclosporine exposures. Early embryonic exposures reduced the size of the eyes and brain. Late embryonic exposures did not affect the size of the eyes or brain, but did lead to substantial behavioral defects at the larval stages. The cyclosporine-exposed larvae displayed a reduced avoidance response to visual stimuli, low swim speeds, increased resting, an increase in thigmotaxis, and changes in the average distance between larvae. Similar results were obtained with the calcineurin inhibitor FK506, suggesting that most, but not all, effects on brain development and behavior are mediated by calcineurin inhibition. Overall, the results show that cyclosporine can induce either structural or functional brain defects, depending on the exposure window. The observed functional brain defects highlight the importance of quantitative behavioral assays when evaluating the risk of developmental exposures.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping