Effects of dexamethazone exposure on neural crest cells and primary and secondary neurulation during neurulation period in chick embryos


Uslu S., Tural Emon S., Alaca N. , Çalık Kocatürk D., Uslu U., Uysal A.

Turkish Neurosurgery, vol.21, no.2, pp.1-8, 2021 (Journal Indexed in SCI Expanded)

  • Publication Type: Article / Article
  • Volume: 21 Issue: 2
  • Publication Date: 2021
  • Doi Number: 10.5137/1019-5149.jtn.34904-21.2
  • Title of Journal : Turkish Neurosurgery
  • Page Numbers: pp.1-8

Abstract

Aim:The aim of this study was to evaluate the effects of dexamethasone (Dex) treatment on neural crest cells and primary and secondary neurulation in chick embryosMaterial and Methods:Sixty fertilized eggs with an average weight of 65 ± 2 g were incubated in 60%–70% humidity at 37.2°C ± 0.1°C. After 26 h of incubation, the control group (n = 12) received 0.1 mg/kg saline (S), group 1 (n = 12) received 0.1 mg/kg Dex, group 2 (n = 12) received 1 mg/kg Dex, and group 3 (n = 12) received 5 mg/kg Dex into each embryonic disc. The eggs were incubated until Hamburger–Hamilton stage (HH) 15, HH18, and HH20. Then, the embryos were dissected and evaluated both macroscopically and microscopically.Results:The mortality rate in the control group, group 1, and groups 2 and 3 was 27%, 48%, and 100%, respectively. The neural tube thicknesses in group 1 significantly increased in HH15 and HH20 (p < 0.05). The mitosis number in group 1 significantly decreased in each stage (p < 0.05). Wnt-1 expression was significantly lower in group 1 in HH15 (p < 0.05) and HH18 (p < 0.05), but there was no significant difference in HH20 (p > 0.05). Fibroblast growth factor (FGF) expression was significantly lower in group 1 in HH15 (p < 0.05). The expression of N-cadherin was significantly higher in group 1 in HH20 (p < 0.05). Fibronectin expression decreased in group 1 in HH18 (p < 0.01).Conclusion:Although the Dex treatment did not result in a neural tube closure defect, the mortality rates and neural tube thicknesses increased, whereas mitotic activation and Wnt-1 and FGF signal pathways reduced in some stages.