ZFIN ID: ZDB-PUB-080602-11
Movement disorder and neuromuscular change in zebrafish embryos after exposure to caffeine
Chen, Y.H., Huang, Y.H., Wen, C.C., Wang, Y.H., Chen, W.L., Chen, L.C., and Tsay, H.J.
Date: 2008
Source: Neurotoxicology and teratology   30(5): 440-447 (Journal)
Registered Authors: Chen, Yau-Hung, Tsay, Huey-Jen
Keywords: Acetylcholine receptor, Caffeine, Embryonic development, Motor neuron, Muscle, Zebrafish
MeSH Terms:
  • Animals
  • Antibodies, Monoclonal
  • Caffeine/toxicity*
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Dyskinesia, Drug-Induced/pathology
  • Dyskinesia, Drug-Induced/physiopathology*
  • Embryo, Nonmammalian/abnormalities
  • Embryo, Nonmammalian/drug effects*
  • Embryonic Development/drug effects
  • Embryonic Development/physiology
  • Motor Neurons/drug effects*
  • Motor Neurons/pathology
  • Muscle Fibers, Skeletal/drug effects
  • Muscle Fibers, Skeletal/pathology
  • Muscle, Skeletal/abnormalities
  • Muscle, Skeletal/drug effects*
  • Muscle, Skeletal/innervation
  • Neuromuscular Junction/abnormalities
  • Neuromuscular Junction/drug effects
  • Neuromuscular Junction/physiopathology
  • Phosphodiesterase Inhibitors/toxicity
  • Sensation Disorders/chemically induced
  • Sensation Disorders/pathology
  • Sensation Disorders/physiopathology
  • Spinal Cord/abnormalities
  • Spinal Cord/drug effects*
  • Survival Rate
  • Time Factors
  • Toxicity Tests
  • Zebrafish
PubMed: 18508234 Full text @ Neurotoxicol. Teratol.
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ABSTRACT
Though caffeine is broadly distributed in many plants and foods, little is known about the teratogenic effects of caffeine during early embryonic development. Here, we used zebrafish as a model to test toxicity and teratogenicity since they have transparent eggs, making the organogenesis of zebrafish embryos easier to observe. When the exposure doses of caffeine were less than 150 ppm (17.5, 35, 50, 100 and 150 ppm), the zebrafish embryos exhibited no significant differences in survival rates after comparison with vehicle-control (0 ppm) group. As the exposure dosages increased, the survival rates decreased. No embryos survived after treatment with 300 ppm caffeine or higher dosages. The most evident change in embryos treated with caffeine was a shorter body length (vehicle-control: 3.26+/-0.01 mm, n=49; vs 150 ppm of caffeine: 2.67+/-0.03 mm, n=50). In addition, caffeine-treated embryos exhibited significantly reduced tactile sensitivity frequencies of touch-induced movement (vehicle-control: 9.93+/-0.77 vs 17.5-150 ppm caffeine: 5.37+/-0.52-0.10+/-0.06). Subtle changes are easily observed by staining with specific monoclonal antibodies F59, Znp1 and Zn5 to detect morphological changes in muscle fibers, primary motor axons and secondary motor axon projections, respectively. Our data show that the treatment of caffeine leads to misalignment of muscle fibers and motor neuron defects, especially secondary motor neuron axonal growth defects.
ADDITIONAL INFORMATION