Folate homeostasis in epileptic rats

Epilepsy Res. 2018 May:142:64-72. doi: 10.1016/j.eplepsyres.2018.03.014. Epub 2018 Mar 16.

Abstract

Folate is involved in metabolic processes and it has been implicated in both aggravation and amelioration of seizures. The aim of the current work was to study the effect of chronic temporal lobe epilepsy (TLE) on the plasma and brain concentrations of folate and on its uptake carriers in the brain - the reduced folate carrier (RFC), folate receptor α (FRα) and proton coupled folate transporter (PCFT). We utilized the rat lithium pilocarpine model for TLE. Approximately two months following status epilepticus, rats with spontaneous recurrent seizures (SRS) were sacrificed for brain and plasma folate concentration analyses and folate uptake carrier expression studies. RT-PCR and western blot analyses were utilized for quantification of folate carriers' mRNAs and proteins, respectively. The distribution of folate carriers in the brain was studied using immunohistochemistry. In the SRS rats we found lower plasma concentrations (10 ± 0.9 in control vs. 6.6 ± 1.6 ng/ml in SRS, P < 0.05), but preserved cortical and increased hippocampal levels of folate (0.5 ± 0.1 in control vs. 0.9 ± 0.2 ng/mg in SRS, P = 0.055). Hippocampus - to - plasma ratio of folate concentration was 3-fold higher in the SRS group, compared with the controls (0.13 ± 0.03 vs. 0.04 ± 0.02, respectively; P < 0.01). mRNA and protein levels of the folate uptake carriers did not differ between SRS rats and controls. However, immunofluorescent staining quantification revealed that the emission intensity of both RFC and FRα was elevated 8-fold and 4-fold, respectively, in hippocampal CA1 neurons of SRS rats, compared to controls (P < 0.01). PCFT was unquantifiable. If corroborated by complementary research in humans, the findings of this study may be utilized clinically for supplemental therapy planning, in imaging the epileptic focus, and for drug delivery into the epileptic brain. Further studies are required for better elucidating the clinical and mechanistic significance of altered folate balances in the epileptic brain.

Keywords: Cornu Ammonis 1 (CA1); Folate receptor alpha; Folic acid; Reduced folate carrier; Spontaneous recurrent seizures; Temporal lobe epilepsy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / metabolism*
  • CD11b Antigen / metabolism
  • Convulsants / toxicity
  • Disease Models, Animal
  • Folate Receptor 1 / genetics
  • Folate Receptor 1 / metabolism
  • Folic Acid / genetics
  • Folic Acid / metabolism*
  • Glial Fibrillary Acidic Protein / metabolism
  • Hippocampus / metabolism
  • Homeostasis / drug effects
  • Homeostasis / physiology*
  • Lithium / toxicity
  • Male
  • Phosphopyruvate Hydratase / metabolism
  • Pilocarpine / toxicity
  • Proton-Coupled Folate Transporter / genetics
  • Proton-Coupled Folate Transporter / metabolism
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Reduced Folate Carrier Protein / genetics
  • Reduced Folate Carrier Protein / metabolism
  • Statistics, Nonparametric
  • Status Epilepticus / chemically induced
  • Status Epilepticus / metabolism*
  • Status Epilepticus / pathology

Substances

  • CD11b Antigen
  • Convulsants
  • Folate Receptor 1
  • Glial Fibrillary Acidic Protein
  • Proton-Coupled Folate Transporter
  • RNA, Messenger
  • Reduced Folate Carrier Protein
  • Pilocarpine
  • Folic Acid
  • Lithium
  • Phosphopyruvate Hydratase