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Updated: May 25, 2026

Modifying Levels of Maternal Dietary Folic Acid or Choline to Study the Impact of Deficiencies on Offspring Health Outcomes
Published on: June 28, 2024
Simultaneous folate intake may prevent adverse effect of valproic acid on neurulating nervous system
Ahmet Sukru Umur1, Mehmet Selcuki, Adem Bursali
1Faculty of Medicine, Department of Neurosurgery, Celal Bayar University, Manisa, Turkey. umuras@yahoo.com
Insights
Folic acid (FA) effectively prevents valproic acid (VA)-induced neural tube defects in chick embryos. FA halts apoptosis, safeguarding early embryonic development from VA
Area of Science:
- Developmental biology
- Teratology
- Neuroscience
Background:
- Valproic acid (VA) is a known teratogen, associated with neural tube defects.
- Folic acid (FA) is crucial for neural tube development.
- Understanding the interplay between FA and VA in early embryogenesis is vital.
Purpose of the Study:
- To investigate the preventive role of folic acid (FA) against valproic acid (VA)-induced teratogenicity.
- To examine the effects on neural tube development in early-stage chick embryos.
Main Methods:
- Chick embryos were divided into five groups: control, saline sham, VA-treated, FA-treated, and combined VA + FA treated.
- Histological analyses, TUNEL assay for apoptosis, and immunoperoxidase techniques for specific proteins (p53, bcl-2, caspases) were employed.
- Neural tube development and embryo viability were assessed after 72 hours.
Main Results:
- VA exposure led to significant embryo mortality and developmental retardation.
- Folic acid administration alone did not cause defects.
- Simultaneous administration of VA and FA significantly reduced mortality and maldevelopmental delays compared to VA alone.
Conclusions:
- Valproic acid (VA) appears to induce apoptosis, potentially independent of the p53 pathway.
- Folic acid (FA) effectively mitigates VA's teratogenic effects during neurulation.
- FA prevents VA-induced embryotoxicity by inhibiting the apoptotic cascade prior to caspase-3 activation.
Purpose:
The aim of this study is to elucidate the preventive effect of folic acid (FA) on teratogenic effects of valporic acid (VA) in early stage chick embryos on neural tube development.
Materials And Methods:
One hundred and fifty specific pathogen-free (SPF) chick eggs were used to investigate the neurulation in five groups. Group A was the control group. Group B was injected 0.02 ml of saline (0.9% NaCl) and was used for sham group. VA (0.72 mg) in 0.02 ml saline was injected in Group C, and 0.342 mcg of FA in 0.02 ml NaCl were administered to the embryos in Group D. VA (0.72 mg) + 0.342 mcg of FA in 0.02 ml saline were administered simultaneously to the eggs in Group E. At the end of 72 h, all embryos were extracted from eggs and were fixed, and for histological analyses hematoxylin and eosine was used, for detection of apoptotic cells terminal deoxyribonucleotide transferase-mediated dUTP-X nick end labeling (TUNEL) was used and for distribution of P53, bcl-2 and caspase-3, caspase-6, caspase-8 and caspase-9 immunoperoxidase techniques were used.
Results:
While there were no neural tube defects in the embryos of groups A, B and D, eight embryos died in group C and there were 12 embryos with retarded embryological development. In contrast to that, no death was observed in group E, but only eight embryos were detected with maldevelopmental delay stage.
Conclusion:
These results suggested that VA may induce apoptotic mechanisms but not through the p53 pathway. In addition, FA effectively prevents the teratogenic influence of VA on chick embryo at neurulation stages by stopping cascade of apoptosis before caspase 3 expression.
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