Heart malformation is an early response to valproic acid in developing zebrafish

• Published in: Naunyn-Schmiedeberg's archives of pharmacology Vol. 393; no. 12; pp. 2387 - 2409
• Main Authors: Rajesh, Venugopalan, Deepan, Natarajan, Anitha, Vijayakumar, Kalaiselvan, Duraisamy, Jayaseelan, Subramanian, Sivakumar, Palanivel, Ganesan, Vellaiyachamy
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.12.2020; Springer Nature B.V
• Subjects: Acetylation; Biomedical and Life Sciences; Biomedicine; Bipolar disorder; Body length; Body size; Bradycardia; Danio rerio; Developmental stages; Embryogenesis; Epilepsy; Experiments; Fertilization; Gene expression; Hatching; Headache; Heart; Heart diseases; Histone deacetylase; Histones; Migraine; Neurosciences; Notochord; Original Article; Pericardium; Pharmacology/Toxicology; Psychosis; Spawning; Teratogenicity; Valproic acid; Heart rate; Embryonic development; Zebrafish; Cardiac malformation; Valproic acid
• ISSN: 0028-1298; 1432-1912
• DOI: 10.1007/s00210-020-01949-4

Valproic acid (VPA) is a branched short-chain fatty acid primarily used in epilepsy, but is also used in bipolar disorder, migraine, and psychotic disorders. Despite its wide range of use, it is a teratogen resulting in various congenital abnormalities. Although a large number of scientific studies evidenced the teratogenic effects, there are limited data on embryonic exposure to VPA at specific or different stages of early embryogenesis. Based on this, the present study was planned to investigate the embryonic exposure to VPA at specific and different hours post fertilization (hpf) in zebrafish embryonic model. In first set of experiments, embryos from spawning groups of adult zebrafish were exposed to different molar concentrations of VPA at 2.5 hpf, and in the second set of experiments, embryos were exposed to VPA 100 μM at 24 hpf, 36 hpf, 48 hpf, 72 hpf, and 96 hpf. The parameters examined were hatching rate, mortality, morphology, body length, pericardial sac size, heartrate, anatomical changes in heart, skeletal and notochord till 120 hpf. It was observed that the embryos exposed to VPA at 2.5 hpf suffered from cardiac abnormalities including heart malformation, bradycardia, circulatory failure, and pericardial sac enlargement which was more apparent in embryos exposed to 100 μM VPA. In the second set of experiments, embryos exposed to VPA 100 μM at 24 hpf and 36 hpf suffered from heart malformations, but there was no incidence of cardiac malformation in embryos exposed to VPA at 48 hpf, 72 hpf, and 96 hpf. From the results, it was evident that exposure to VPA at early developmental stage of embryogenesis produced congenital cardiac abnormalities. Since VPA is a selective HDAC inhibitor, histone acetylation with aberrant gene expression during cardiogenesis might be the underlying cause of cardiac malformation.