Investigation of the Effect of Tenoxicam on Neural Tube Defect Using Chick Embryo Model.

AIM

To evaluate tenoxicam's effects on embryonic neural tube formation to identify potential teratogenicity and determine the underlying mechanisms leading to neural tube defects (NTDs).

MATERIAL AND METHODS

This study was conducted at our University's Neuro-embryology Laboratory. A total of 100 fertile chicken eggs were opened using the windowing method after 24 hours of incubation. The embryo models were divided into four groups based on tenoxicam dosage: 0.01, 0.02, 0.10 μg, and control group (0.9% SF was administered). The tenoxicam groups were administered 20 μL volume sub-blastodermally. The eggs were incubated for another 24 hours after being covered with sterile draping. All the eggs were opened at the 48th hour, and the embryos were evaluated.

RESULTS

Each group consisted of 25 chicken embryos. Normal neural tube development was observed in Group 1 (0.01μg) with 23 out of 25 embryos, Group 2 (0.02 μg) with 20 out of 25 embryos, Group 3 (0.10μg) with 16 out of 25 embryos, and Group 4 (control group) with 24 out of 25 embryos. Additionally, the rates of absence of embryo development were 8%, 8%, 12%, and 4% in Groups 1, 2, and 3 and the control group, respectively.

CONCLUSION

We observed that tenoxicam use caused midline closure defects in early chicken embryos in a dose-dependent manner. Further studies are required to determine the mechanisms underlying the embryonic damage and teratogenic effects due to genetic and environmental factors and minimize the development of congenital defects.