Epileptiform discharges induced by altering extracellular potassium and calcium in the rat hippocampal slice
- PMID: 3391256
- DOI: 10.1016/0014-4886(88)90071-4
Epileptiform discharges induced by altering extracellular potassium and calcium in the rat hippocampal slice
Abstract
During and after intense neuronal activity the concentration of extracellular potassium ([K+]o) increases while the concentration of calcium ([Ca2+]o) decreases. The present study examined the effect of increased [K+]o alone, and with a parallel decrease in [Ca2+]o, on overall excitability, long-term potentiation (LTP), and the appearance of epileptiform discharges. [K+]o and [Ca2+]o were varied over the range in which they fluctuate in vivo. Hippocampal slices were first equilibrated in a control artificial CSF containing 3.1 mM K+ and 1.5 mM Ca2+ and then reequilibrated in an identical solution except that the K+ was increased to 3.55, 4, 5, 6, or 8 mM with and without a decrease in Ca2+ to 1.0 mM. Raising [K+]o caused a leftward shift of input-output curves. Lowering [Ca2+]o to 1.0 mM had no effect on the ability of [K+]o to shift the input-output curve to the left. LTP was not changed by increasing [K+]o. Lowering [Ca2+]o to 1.0 mM blocked LTP and increasing the [K+]o did not overcome this blockade. When [K+]o alone was altered, the [K+]oS at which epileptiform bursts occurred 50% of the time were 5.6 and 7.6 mM for stimulus-locked and spontaneous bursting, respectively. The combination of decreased [Ca2+]o and increased [K+]o made slices considerably more prone to epileptiform activity. In 1.0 mM [Ca2+]o, the [K+]o at which 50% of the slices showed stimulus-locked bursting was decreased to 3.6 mM while that for spontaneous discharges was 5.4 mM. The sensitivity of hippocampal slices to [K+]o and [Ca2+]o, and the synergistic actions of alterations of these ions, indicates that even small changes in the aggregate extracellular ionic milieu may be important in epileptogenesis.
Similar articles
-
Cesium induces spontaneous epileptiform activity without changing extracellular potassium regulation in rat hippocampus.J Neurophysiol. 1999 Dec;82(6):3339-46. doi: 10.1152/jn.1999.82.6.3339. J Neurophysiol. 1999. PMID: 10601465
-
In vitro effects of extracellular calcium concentrations on hippocampal pyramidal cell responses.Exp Neurol. 1988 Jul;101(1):132-46. doi: 10.1016/0014-4886(88)90070-2. Exp Neurol. 1988. PMID: 3391255
-
Hippocampal slices from kindled rats show an increased sensitivity for induction of epileptiform activity by changes in extracellular ion concentrations.Neurosci Lett. 1988 Jun 17;89(1):43-8. doi: 10.1016/0304-3940(88)90478-8. Neurosci Lett. 1988. PMID: 3399140
-
Extracellular calcium and potassium concentration changes in chronic epileptic brain tissue.Adv Neurol. 1986;44:641-61. Adv Neurol. 1986. PMID: 3518350 Review.
-
Ionic changes and alterations in the size of the extracellular space during epileptic activity.Adv Neurol. 1986;44:619-39. Adv Neurol. 1986. PMID: 3518349 Review.
Cited by
-
Progressive, potassium-sensitive epileptiform activity in hippocampal area CA3 of pilocarpine-treated rats with recurrent seizures.Epilepsy Res. 2011 Nov;97(1-2):92-102. doi: 10.1016/j.eplepsyres.2011.07.008. Epub 2011 Aug 30. Epilepsy Res. 2011. PMID: 21880468 Free PMC article.
-
Glycolysis regulates neuronal excitability via lactate receptor, HCA1R.Brain. 2023 May 2;146(5):1888-1902. doi: 10.1093/brain/awac419. Brain. 2023. PMID: 36346130 Free PMC article.
-
Multifunctional hydrogel electronics for closed-loop antiepileptic treatment.Sci Adv. 2024 Nov 22;10(47):eadq9207. doi: 10.1126/sciadv.adq9207. Epub 2024 Nov 22. Sci Adv. 2024. PMID: 39576849 Free PMC article.
-
Glycolytic lactate production supports status epilepticus in experimental animals.Ann Clin Transl Neurol. 2023 Oct;10(10):1873-1884. doi: 10.1002/acn3.51881. Epub 2023 Aug 25. Ann Clin Transl Neurol. 2023. PMID: 37632130 Free PMC article.
-
Electrophoretic drug delivery for seizure control.Sci Adv. 2018 Aug 29;4(8):eaau1291. doi: 10.1126/sciadv.aau1291. eCollection 2018 Aug. Sci Adv. 2018. PMID: 30167463 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous