Title:Maternal Sodium Valproate Exposure Alters Neuroendocrine-Cytokines and Oxido-inflammatory Axes in Neonatal Albino Rats
Volume: 21
Issue: 8
Author(s): Neama A-G, El-bakry AM, Rasha EH and RG Ahmed*
Affiliation:
- Division of Anatomy and Embryology, Zoology Department, Faculty of Science, Beni-Suef University, Beni-Suef,Egypt
Keywords:
Sodium valproate, adrenal, brain, cytokines, dams, neonates.
Abstract:
Objective: The aim of the study was to determine the influence of maternal sodium valproate
(SVP) on neonatal neuroendocrine (hypothalamic-pituitary-adrenal; HPA)-cytokines and
oxido-inflammatory axes.
Methods: Pregnant rats (Rattus norvegicus) were orally administered (by gavage) SVP (50 mg/kg)
from gestation day (GD) 8 to lactation day (LD) 21.
Results: The elevation in serum corticotropin-releasing hormone (CRH), corticosterone, and
adrenocorticotropic hormone (ACTH) levels was highly significant at postnatal days (PNDs) 14
and 21 in both dams and neonates of the maternal SVP-treated group relative to those in the control
group. However, hypercortisolism (cortisolemia) was highly significant in neonates at both PNDs
14 and 21, while in dams, it was not significantly increased at LD 14 but was at LD 21. This disruption
caused adverse effects on maternal food consumption and maternal/neonatal body weight. The
maternal SVP treatment resulted in higher levels of neonatal serum adrenaline, noradrenaline, neuropeptide
Y (NPY), tumor necrosis factor-alpha (TNF-α), leptin, interleukins (IL-1β, IL-17, IL-4,
IL-6 & IL-2), transforming growth factor-beta (TGF-β), and prostaglandin E2 (PGE2), and lower
levels of neonatal serum growth hormone (GH), insulin growth factor-1 (IGF-1) and adiponectin at
both PNDs. This administration also induced the oxidative stress in neonatal cerebrum and cerebellum
at both tested PNDs via the production of free radicals (malondialdehyde; MDA & nitric
oxide; NO) and reduction of antioxidant parameters (glutathione; GSH, superoxide dismutase;
SOD & catalase; CAT).
Conclusion: Maternal SVP treatment stimulated the neonatal stress-brain (HPA) axis, resulted in
an oxido-inflammatory state, and disrupted the neuroendocrine-cytokines axis, and generally neonatal
health.
