Українська English

ISSN 2522-9028 (Print)
ISSN 2522-9036 (Online)
DOI: https://doi.org/10.15407/fz

Fiziologichnyi Zhurnal

is a scientific journal issued by the

Bogomoletz Institute of Physiology
National Academy of Sciences of Ukraine

Editor-in-chief: V.F. Sagach

The journal was founded in 1955 as
1955 – 1977 "Fiziolohichnyi zhurnal" (ISSN 0015 – 3311)
1978 – 1993 "Fiziologicheskii zhurnal" (ISSN 0201 – 8489)
1994 – 2016 "Fiziolohichnyi zhurnal" (ISSN 0201 – 8489)
2017 – "Fiziolohichnyi zhurnal" (ISSN 2522-9028)

Fiziol. Zh. 2017; 63(2): 10-16


Effect of altered extracellular magnesium concentration on the neuronal activity in different hippocampal regions of immature rats

A.Vlasiuk, A. Romanov, D. Isaev, E. Isaeva

    O.O.Bogomoletz Institute of Physiology of National Academy of Science of Ukraine, Kyiv
DOI: https://doi.org/10.15407/fz63.02.010


Abstract

Using acute hippocampal slice preparation dissected from immature rats, we investigated the effect of lowering Mg2+ concentration in the extracellular solution on the probability to evoke epileptiform activity in different regions of hippocampus. Electrophysiological recordings revealed different patterns of such activity in hippocampal CA1 region. In agreement with studies on the adult rat hippocampus probability to induce epileptiform activity by means of lowering Mg2+ concentration was increased in the ventral part of hippocampus (VH) compared to dorsal part (DH). We also found a significant increase in probability to induce ictal-like activity (ILE) in both hippocampal regions compared to results obtained in adult rats with a higher rate of ILE incidence in VH (90 %) compared to DH (50 %). Our experiments with cuts of hippocampal fiber pathways showed that in VH, ILE originated in CA1 region and propagated to CA3 region and dentate gyrus, while interictal-like activity originated in CA3 region. Possible mechanisms of the region specificity of the development of epileptiform activity in the immature hippocampus discussed.

Keywords: epileptiform activity; dorsal and ventral hippocampus; immature rat

References

  1. Téllez-Zenteno JF and Hernández-Ronquillo L. A Review of the Epidemiology of Temporal Lobe Epilepsy. Epilepsy Res Treat. 2012; 1–5. CrossRef PubMed PubMedCentral
  2.  
  3. Curia G, Lucchi C, Vinet J, Gualtieri F, Marinelli C, Torsello A, Costantino L, and Biagini G. Pathophysiogenesis of mesial temporal lobe epilepsy: is prevention of damage antiepileptogenic? Curr Med Chem. 2014; 21: 663–88. CrossRef PubMed PubMedCentral
  4.  
  5. McNamara JO. Cellular and molecular basis of epilepsy. J Neurosci. 1994; 14: 3413–25. PubMed
  6.  
  7. Fanselow MS and Dong HW. Are the dorsal and ventral hippocampus functionally distinct structures? Neuron. 2010; 65: 7–19. CrossRef PubMed PubMedCentral
  8.  
  9. Papatheodoropoulos C, Moschovos C, and Kostopoulos G. Greater contribution of N-methyl-D-aspartic acid receptors in ventral compared to dorsal hippocampal slices in the expression and long-term maintenance of epileptiform activity. Neuroscience. 2005; 135: 765–79. CrossRef PubMed
  10.  
  11. Ekstrand J, Pouliot W, Scheerlinck P, and Dudek FE. Lithium pilocarpine-induced status epilepticus in postnatal day 20 rats results in greater neuronal injury in ventral versus dorsal hippocampus. Neuroscience. 2011; 192:699–707. CrossRef PubMed PubMedCentral
  12.  
  13. Isaeva E, Romanov A, Holmes GL, and Isaev D. Status epilepticus results in region-specific alterations in seizure susceptibility along the hippocampal longitudinal axis. Epilepsy Res. 2015; 110: 166–70. CrossRef PubMed PubMedCentral
  14.  
  15. Papatheodoropoulos C, Asprodini E, Nikita I, and Koutsona C. W eaker synaptic inhibition in CA1 region of ventral compared to dorsal rat hippocampal slices. 2002; 117–21.
  16.  
  17. Gilbert M, Racine RJ, and Smith GK. Epileptiform burst responses in ventral vs dorsal hippocampal slices. Brain Res.1985; 361: 389–91. CrossRef  
  18. Pandis C, Sotiriou E, Kouvaras E, Asprodini E, Papatheodoropoulos C, and Angelatou F. Differential expression of NMDA and AMPA receptor subunits in rat dorsal and ventral hippocampus. Neuroscience. 2006; 140: 163–75. CrossRef PubMed
  19.  
  20. Walther H, Lambert JD, Jones RS, Heinemann U, and Hamon B. Epileptiform activity in combined slices of the hippocampus, subiculum and entorhinal cortex during perfusion with low magnesium medium. Neurosci Lett. 1986; 69: 156–61. CrossRef  
  21. Mody I, Lambert JD, and Heinemann U. Low extracellular magnesium induces epileptiform activity and spreading depression in rat hippocampal slices. J Neurophysiol. 1987; 57: 869–88. PubMed
  22.  
  23. Jones RS and Heinemann U. Pre- and postsynaptic K+ and Ca2+ fluxes in area CA1 of the rat hippocampus in vitro: effects of Ni2+, TEA and 4-AP. Exp Brain Res. 1987; 68: 205–09. CrossRef PubMed
  24.  
  25. Monyer H, Burnashev N, Laurie DJ, Sakmann B, and Seeburg PH, Developmental and regional expression in the rat brain and functional properties of four NMDA receptors. Neuron. 1994; 12: 529–40. CrossRef  
  26. Sanchez RM and Jensen FE.Maturational Aspects of Epilepsy Mechanisms and Consequences for the Immature Brain. 2001; 577–85.
  27.  
  28. Weissinger F, Buchheim K, Siegmund H, Heinemann U, and Meierkord H.Optical imaging reveals characteristic seizure onsets, spread patterns, and propagation velocities in hippocampal-entorhinal cortex slices of juvenile rats. Neurobiol Dis. 2000; 7: 286–98. CrossRef PubMed
  29.  
  30. Lewis DV, Jones LS, and Mott DD. Hippocampal epileptiform activity induced by magnesium-free medium: 1900; 6: 95–101.
  31.  
  32. Quilichini PP, Diabira D, Chiron C, Ben-Ari Y, and Gozlan H. Persistent epileptiform activity induced by low Mg2+ in intact immature brain structures. Eur J Neurosci. 2002; 16: 850–60. CrossRef PubMed
  33.  
  34. Coultrap SJ, Nixon KM, Alvestad RM, Valenzuela CF, and Browning MD, Differential expression of NMDA receptor subunits and splice variants among the CA1, CA3 and dentate gyrus of the adult rat. Brain Res Mol Brain Res.2005; 135: 104–11. CrossRef PubMed
  35.  
  36. Dingledine R, Borges K, Bowie D, and Traynelis S. The glutamate receptor ion channels. Pharmacol Rev. 1999; 51: 7–61. PubMed

© National Academy of Sciences of Ukraine, Bogomoletz Institute of Physiology, 2014-2024.