ZFIN ID: ZDB-PUB-080826-9
Uncoupling nicotine mediated motoneuron axonal pathfinding errors and muscle degeneration in zebrafish
Welsh, L., Tanguay, R.L., and Svoboda, K.R.
Date: 2009
Source: Toxicol. Appl. Pharmacol. 237(1): 29-40 (Journal)
Registered Authors: Svoboda, Kurt, Tanguay, Robert L.
Keywords: Motoneuron, Axonal pathfinding, Muscle degeneration, Sofa potato
MeSH Terms: Animals; Animals, Genetically Modified; Cell Movement; Embryo, Nonmammalian/cytology; Embryo, Nonmammalian/drug effects (all 29) expand
PubMed: 18694773 Full text @ Toxicol. Appl. Pharmacol.
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ABSTRACT
Zebrafish embryos offer a unique opportunity to investigate the mechanisms by which nicotine exposure impacts early vertebrate development. Embryos exposed to nicotine become functionally paralyzed by 42 hpf suggesting that the neuromuscular system is compromised in exposed embryos. We previously demonstrated that secondary spinal motoneurons in nicotine-exposed embryos were delayed in development and that their axons made pathfinding errors (Svoboda et al., 2002). In that study, we did not consider the potential role that altered skeletal muscle development caused by nicotine exposure could play in contributing to the errors in spinal motoneuron axon pathfinding. In this study, we show that an alteration in skeletal muscle development occurs in tandem with alterations in spinal motoneuron development upon exposure to nicotine. The alteration in the muscle involves the binding of nicotine to the muscle-specific AChRs. The nicotine-induced alteration in muscle development does not occur in the zebrafish mutant (Sofa Potato, [sop]), which lacks functional muscle-specific AChRs. Even though muscle development is unaffected by nicotine exposure in sop mutants, motoneuron axonal pathfinding errors still occur in these mutants, indicating a direct effect of nicotine exposure on nervous system development.
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