PUBLICATION

Vincristine and bortezomib cause axon outgrowth and behavioral defects in larval zebrafish

Authors
Khan, T.M., Benaich, N., Malone, C.F., Bernardos, R.L., Russell, A.R., Downes, G.B., Barresi, M.J., and Hutson, L.D.
ID
ZDB-PUB-120404-12
Date
2012
Source
Journal of the peripheral nervous system : JPNS   17(1): 76-89 (Journal)
Registered Authors
Barresi, Michael J. F., Bernardos, Rebecca, Downes, Gerald, Hutson, Lara
Keywords
behavior, chemotherapy, development, neuropathy, proteasome inhibitor
MeSH Terms
  • Animals
  • Antineoplastic Agents/adverse effects*
  • Axons/drug effects*
  • Axons/pathology
  • Behavior, Animal/drug effects*
  • Boronic Acids/adverse effects*
  • Bortezomib
  • Immunohistochemistry
  • Larva/drug effects
  • Pyrazines/adverse effects*
  • Vincristine/adverse effects*
  • Zebrafish
PubMed
22462669 Full text @ J. Peripher. Nerv. Syst.
Abstract

Peripheral neuropathy is a common side effect of a number of pharmaceutical compounds, including several chemotherapy drugs. Among these are vincristine sulfate, a mitotic inhibitor used to treat a variety of leukemias, lymphomas, and other cancers, and bortezomib, a 26S proteasome inhibitor used primarily to treat relapsed multiple myeloma and mantle cell lymphoma. To gain insight into the mechanisms by which these compounds act, we tested their effects in zebrafish. Vincristine or bortezomib given during late embryonic development caused significant defects at both behavioral and cellular levels. Intriguingly, the effects of the two drugs appear to be distinct. Vincristine causes uncoordinated swimming behavior, which is coupled with a reduction in the density of sensory innervation and overall size of motor axon arbors. Bortezomib, in contrast, increases the duration and amplitude of muscle contractions associated with escape swimming, which is coupled with a preferential reduction in fine processes and branches of sensory and motor axons. These results demonstrate that zebrafish is a convenient in vivo assay system for screening potential pharmaceutical compounds for neurotoxic side effects, and they provide an important step toward understanding how vincristine and bortezomib cause peripheral neuropathy.

Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping