“…This comparison revealed that the 1.5‐h delay in the expression of sox2 widened to a 5‐h delay for tnnt1 , and the overall rate was slowed to 73% of that at 28.5 °C. These results were remarkably similar to those previously reported using morphological milestones (Figure ).…”
Section: Resultssupporting
confidence: 92%
“…Open circles indicate mean onset of expression of sox2, shh, and tnnt1 at 24.5 °C ( n = 3). Solid lines indicate developmental rate at 28.5 °C and 24.5 °C as measured by Beasley et al .…”
Monitoring expression of the developmentally regulated genes shh, sox2, and tnnt1 by reverse transcriptase polymerase chain reaction (RT-PCR) allows determination of the rate of embryogenesis in zebrafish (Danio rerio) embryos without direct visual observation. The utility of combining this approach and morphological methods during toxicity studies was demonstrated with embryos developing at either 28.5 °C or 24.5 °C and with embryos exposed to sublethal doses of silver nanoparticles.
“…This comparison revealed that the 1.5‐h delay in the expression of sox2 widened to a 5‐h delay for tnnt1 , and the overall rate was slowed to 73% of that at 28.5 °C. These results were remarkably similar to those previously reported using morphological milestones (Figure ).…”
Section: Resultssupporting
confidence: 92%
“…Open circles indicate mean onset of expression of sox2, shh, and tnnt1 at 24.5 °C ( n = 3). Solid lines indicate developmental rate at 28.5 °C and 24.5 °C as measured by Beasley et al .…”
Monitoring expression of the developmentally regulated genes shh, sox2, and tnnt1 by reverse transcriptase polymerase chain reaction (RT-PCR) allows determination of the rate of embryogenesis in zebrafish (Danio rerio) embryos without direct visual observation. The utility of combining this approach and morphological methods during toxicity studies was demonstrated with embryos developing at either 28.5 °C or 24.5 °C and with embryos exposed to sublethal doses of silver nanoparticles.
“…Zebrafish can tolerate a temperature range of 24.5 to 28.5°C (Beasley et al. ). However, the growth speed of zebrafish embryos varies according to temperature (Kimmel et al.…”
Section: Temperaturementioning
confidence: 99%
“…When zebrafish embryos are raised at 24.5 to 28.5°C, they reach sphere stage at 4.1 or 3.8 hpf, and shield stage at 5.9 or 5.4 hpf (Beasley et al. ). These findings suggest that chemical exposure at a given time‐point may have different effects on embryonic development, depending on the ambient temperature.…”
With the high cost and the long-term assessment of developmental toxicity testing in mammals, the vertebrate zebrafish has become a useful alternative model organism for high-throughput developmental toxicity testing. Zebrafish is also very favorable for the 3R perspective in toxicology; however, the methodologies used by research groups vary greatly, posing considerable challenges to integrative analysis. In this review, we discuss zebrafish developmental toxicity testing, focusing on the methods of chemical exposure, the assessment of morphological abnormalities, housing conditions and their effects on the production of healthy embryos, and future directions. Zebrafish as a systems toxicology model has the potential to elucidate developmental toxicity pathways, and to provide a sound basis for human health risk assessments.
“…A temperature of 28 or 28.5 • C is used by several other research groups [2,[13][14][15]22]. The decision on optimal temperature is one of the most critical, as temperature has a direct impact on the development of the ZF embryo and its capacity to cover its developmental milestones, as development of ZF slows at lower temperatures [23]. In addition to its effect on ZF development rate, a higher temperature could also induce evaporation which could have a direct impact on the internal well concentration, and might therefore have a major impact on the study outcome for volatile test compounds.…”
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