PUBLICATION

The alcohol-sensitive period during early octavolateral organ development in zebrafish (Danio rerio)

Authors
Zamora, L.Y., Miguel, K.C., Lu, Z.
ID
ZDB-PUB-170121-5
Date
2017
Source
Journal of neuroscience research   95(5): 1194-1203 (Journal)
Registered Authors
Keywords
hair cell, hearing, lateral line neuromast, otic vesicle, otolith
MeSH Terms
  • Age Factors
  • Analysis of Variance
  • Animals
  • Animals, Genetically Modified
  • Central Nervous System Depressants/toxicity*
  • Ear, Inner/drug effects*
  • Ear, Inner/embryology
  • Embryo, Nonmammalian
  • Ethanol/toxicity*
  • Green Fluorescent Proteins/genetics
  • Green Fluorescent Proteins/metabolism
  • Hair Cells, Auditory/drug effects*
  • Hearing/drug effects*
  • Hearing/physiology
  • Hearing Loss/chemically induced
  • Keratin-4/genetics
  • Keratin-4/metabolism
  • Larva/drug effects
  • Lateral Line System/drug effects
  • Lateral Line System/embryology
  • Zebrafish
PubMed
28105691 Full text @ J. Neurosci. Res.
Abstract
Fetal alcohol exposure can cause Fetal Alcohol Spectrum Disorders (FASD), completely preventable developmental disabilities characterized by permanent birth defects. However, specific gestational timing when developing organs are most sensitive to alcohol exposure is unclear. In this study, we examined the temporal effects of embryonic alcohol exposure on octavolateral organs in zebrafish (Danio rerio), including inner ears and lateral line neuromasts that function in hearing, balance, and hydrodynamic detection, respectively. To determine an alcohol-sensitive period in the first 24 hours post fertilization (hpf), Et(krt4:EGFP)sqet4 zebrafish that express green fluorescent protein in sensory hair cells were treated in 2% alcohol for 2, 3, and 5-hours. Octavolateral organs of control and alcohol-exposed larvae were examined at 3, 5, and 7 days post fertilization (dpf). Using confocal and light microscopy, we found that alcohol-exposed larvae had significantly smaller otic vesicles and saccular otoliths than control larvae at 3 dpf. Only alcohol-exposed larvae from 12-17 hpf had smaller otic vesicles at 5 dpf, smaller saccular otoliths at 7 dpf and fewer saccular hair cells, neuromasts and hair cells per neuromast at 3 dpf. In addition, auditory function was assessed by microphonic potential recordings from inner ear hair cells in response to 200-Hz stimulation. Hearing sensitivity was reduced for alcohol-exposed larvae from 7-12 and 12-17 hpf. Our results show that 12-17 hpf is an alcohol-sensitive time window when morphology and function of zebrafish octavolateral organs are most vulnerable to alcohol exposure. This study implies that embryonic alcohol exposure timing during early development can influence severity of hearing deficits. © 2017 Wiley Periodicals, Inc.
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