Altered inhibition in the hippocampal neural networks after spreading depression. (24th September 2015)

• Record Type: Journal Article
• Authors: Mesgari, M.; Ghaffarian, N.; Khaleghi Ghadiri, M.; Sadeghian, H.; Speckmann, E.-J.; Stummer, W.; Gorji, A.
• Is Part Of: Neuroscience. Volume 304(2015)
• Page Start: 190
• Page End: 197
• Publication Date: 2015-09-24
• Subjects: SD spreading depression -- PPD paired-pulse depression -- IPSPs inhibitory post synaptic potentials -- ACSF artificial cerebrospinal fluid; spreading depolarization -- epilepsy -- migraine -- stroke -- hippocampus -- disinhibition; Neurochemistry -- Periodicals; Neurophysiology -- Periodicals; Neurology -- Periodicals; Neurochimie -- Périodiques; Neurophysiologie -- Périodiques; Neurochemistry; Neurophysiology; Electronic journals; Periodicals; Electronic journals; 612.8
• DOI: 10.1016/j.neuroscience.2015.07.035
• Languages: English
• ISSNs: 0306-4522

Abstract

Highlights: Delayed neuronal hyperexcitability occurred after spreading depression (SD). Hyperexcitability after SD may play a role in the mechanism of SD-related disorders. SD enhanced the number and duration of bicuculline-induced afterdischarges. Paired-pulse inhibition and inhibitory post synaptic potentials were reduced by SD. GABA-mediated inhibition contributes to SD-induced delayed hyperexcitability. Abstract: Prolonged neuronal depression after spreading depression (SD) is followed by a late cellular and synaptic hyperexcitability. Intra- and extracellular recordings of bioelectrical activities were performed in the rodent hippocampus to investigate the role of γ-aminobutyric acid (GABA)-mediated inhibition in the late hyperexcitable state of SD. The effect of KCl-induced negative DC potential shifts was investigated on extracellularly recorded paired-pulse depression (PPD) and bicuculline-induced afterdischarges as well as intracellularly recorded inhibitory post synaptic potentials (IPSPs) in the hippocampal CA1 area. The results revealed that SD decreased the degree of PPD, enhanced the number and duration of bicuculline-induced afterdischarges, and reduced the amplitude and duration of IPSPs. Application of low concentrations of bicuculline before the induction of SD enhanced the inhibitory effect of SD on IPSPs. Data indicate the contribution of GABA-mediated inhibition to SD-induced delayed hyperexcitability. Modulation of GABA function in the late hyperexcitability phase of SD may play a role in therapeutic management of SD-related neurological disorders.