Intracellular calcium increase in epileptiform activity: Modulation by levetiracetam and lamotrigine

Antonio Pisani, Paola Bonsi, Giuseppina Martella, Cristiano De Persis, Cinzia Costa, Francesco Pisani, Giorgio Bernardi, Paolo Calabresi

Research output: Contribution to journalArticle

102 Citations (Scopus)

Abstract

Purpose: Alterations in neuronal calcium (Ca2+) homeostasis are believed to play an essential role in the generation and propagation of epileptiform events. Levetiracetam (LEV) and lamotrigine (LTG), novel antiepileptic drugs (AEDs), were tested on epileptiform events and the corresponding elevations in intracellular Ca2+ concentration ([Ca2+]i) recorded from rat neocortical slices. Methods: Electrophysiological recordings were performed from single pyramidal neurons from a slice preparation. Spontaneous epileptiform events consisting of long-lasting, repetitive paroxysmal depolarization shifts (PDSs) and interictal spike activity were induced by reducing the magnesium concentration from the solution and by adding bicuculline and 4-aminopyridine. Simultaneously, microfluorimetric measurements of [Ca2+]i were performed. Optical imaging with Ca2+ indicators revealed a close correlation between Ca2+ transients and epileptiform events. Results: Both LEV and LTG were able to reduce both amplitude and duration of PDSs, as well as the concomitant elevation in [Ca2+]i, in a dose-dependent fashion. Whole-cell patch-clamp recordings from isolated neocortical neurons revealed that LEV significantly reduced N-, and partially P/Q-type high-voltage-activated (HVA) Ca2+ currents, whereas sodium currents were unaffected. Interestingly, the inhibitory effects of LEV were mimicked and occluded by LTG or by a combination of ω-conotoxin GVIA and ω-agatoxin IVA, selective blockers of N- and P/Q-type HVA channels, respectively, suggesting a common site of action for these AEDs. Conclusions: These results demonstrate that large, transient elevations in neuronal [Ca 2+]i correlate to epileptiform discharges. The antagonistic effects of LEV and LTG on [Ca2+]i overload might represent the basis for their anticonvulsant efficacy and could preserve neuronal viability.

Original languageEnglish
Pages (from-to)719-728
Number of pages10
JournalEpilepsia
Volume45
Issue number7
DOIs
Publication statusPublished - Jul 2004

Fingerprint

etiracetam
Calcium
Anticonvulsants
Agatoxins
Conotoxins
4-Aminopyridine
Bicuculline
Pyramidal Cells
Optical Imaging
Magnesium
Homeostasis
Sodium
lamotrigine
Neurons

Keywords

  • Antiepileptic drugs
  • Brain slice
  • Calcium
  • Epilepsy
  • Lamotrigine
  • Levetiracetam
  • Paroxysmal depolarizing shift

ASJC Scopus subject areas

  • Clinical Neurology
  • Neuroscience(all)

Cite this

Intracellular calcium increase in epileptiform activity : Modulation by levetiracetam and lamotrigine. / Pisani, Antonio; Bonsi, Paola; Martella, Giuseppina; De Persis, Cristiano; Costa, Cinzia; Pisani, Francesco; Bernardi, Giorgio; Calabresi, Paolo.

In: Epilepsia, Vol. 45, No. 7, 07.2004, p. 719-728.

Research output: Contribution to journalArticle

Pisani, Antonio ; Bonsi, Paola ; Martella, Giuseppina ; De Persis, Cristiano ; Costa, Cinzia ; Pisani, Francesco ; Bernardi, Giorgio ; Calabresi, Paolo. / Intracellular calcium increase in epileptiform activity : Modulation by levetiracetam and lamotrigine. In: Epilepsia. 2004 ; Vol. 45, No. 7. pp. 719-728.
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AU - De Persis, Cristiano

AU - Costa, Cinzia

AU - Pisani, Francesco

AU - Bernardi, Giorgio

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AB - Purpose: Alterations in neuronal calcium (Ca2+) homeostasis are believed to play an essential role in the generation and propagation of epileptiform events. Levetiracetam (LEV) and lamotrigine (LTG), novel antiepileptic drugs (AEDs), were tested on epileptiform events and the corresponding elevations in intracellular Ca2+ concentration ([Ca2+]i) recorded from rat neocortical slices. Methods: Electrophysiological recordings were performed from single pyramidal neurons from a slice preparation. Spontaneous epileptiform events consisting of long-lasting, repetitive paroxysmal depolarization shifts (PDSs) and interictal spike activity were induced by reducing the magnesium concentration from the solution and by adding bicuculline and 4-aminopyridine. Simultaneously, microfluorimetric measurements of [Ca2+]i were performed. Optical imaging with Ca2+ indicators revealed a close correlation between Ca2+ transients and epileptiform events. Results: Both LEV and LTG were able to reduce both amplitude and duration of PDSs, as well as the concomitant elevation in [Ca2+]i, in a dose-dependent fashion. Whole-cell patch-clamp recordings from isolated neocortical neurons revealed that LEV significantly reduced N-, and partially P/Q-type high-voltage-activated (HVA) Ca2+ currents, whereas sodium currents were unaffected. Interestingly, the inhibitory effects of LEV were mimicked and occluded by LTG or by a combination of ω-conotoxin GVIA and ω-agatoxin IVA, selective blockers of N- and P/Q-type HVA channels, respectively, suggesting a common site of action for these AEDs. Conclusions: These results demonstrate that large, transient elevations in neuronal [Ca 2+]i correlate to epileptiform discharges. The antagonistic effects of LEV and LTG on [Ca2+]i overload might represent the basis for their anticonvulsant efficacy and could preserve neuronal viability.

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