Altered hippocampal kynurenine pathway metabolism contribute to
hyperexcitability in mesial temporal lobe epilepsy-hippocampal sclerosis
Abstract
Background and Purpose Glutamate receptor mediated enhanced excitatory
neurotransmission is typically associated with mesial temporal lobe
epilepsy with hippocampal sclerosis (MTLE-HS). Kynurenic acid (KYNA) and
quinolinic acid (QUIN) are two important tryptophan-kynurenine pathway
(KP) metabolites that modulate glutamate receptor activity. This study
was designed to test the hypothesis that alteration in metabolism of KP
metabolites in the hippocampus of patients with MTLE-HS contributes to
abnormal glutamatergic transmission. Experimental Approach TKP
metabolites level were determined using HPLC and LC-MS/MS in the
hippocampal samples of patients with MTLE-HS compared to autopsy and
non-seizure control samples. mRNA and protein expression of TKP enzymes
were determined by qPCR and western blot. Spontaneous glutamatergic
activities were recorded from pyramidal neurons in presence of
kynurenine (KYN) and KYNA using whole cell patch clamp. Key Results We
observed significantly reduced KYNA and elevated QUIN levels in the
hippocampal samples, while KYN level remains unaltered. Spontaneous
glutamatergic activity in the hippocampal samples was higher compared to
that in non-seizure controls. Treatment with kynurenine inhibited the
glutamatergic activity in non-seizure control samples but not in case of
the hippocampal samples. However, exogenously applied KYNA inhibited
glutamatergic activity in both non-seizure control and hippocampal
samples. We also observed reduced levels of enzyme kynurenine
aminotransferase II and its co-factor pyridoxal phosphate in the
hippocampal samples. Conclusion Our findings indicate that altered
metabolism of TKP metabolites in hippocampus could contribute to
hyperglutamatergic tone in patients with MTLE-HS.