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Low-magnesium medium induces epileptiform activity in mouse olfactory bulb slices
Department of Physiology, University of Otago, Dunedin, New Zealand.ORCID iD: 0000-0002-1904-5554
Department of Physiology, University of Otago, Dunedin, New Zealand.
Department of Physiology, University of Otago, Dunedin, New Zealand.
2011 (English)In: Journal of Neurophysiology, ISSN 0022-3077, E-ISSN 1522-1598, Vol. 106, no 5, p. 2593-2605Article in journal (Refereed) Published
Abstract [en]

Magnesium-free medium can be used in brain slice studies to enhance glutamate receptor function, but this manipulation causes seizure-like activity in many cortical areas. The rodent olfactory bulb (OB) slice is a popular preparation, and potentially ictogenic ionic conditions have often been used to study odor processing. We studied low Mg2+-induced epileptiform discharges in mouse OB slices using extracellular and whole cell electrophysiological recordings. Low-Mg2+ medium induced two distinct types of epileptiform activity: an intraglomerular delta-frequency oscillation resembling slow sniff-induced activity and minute-long seizure-like events (SLEs) consisting of large negative-going field potentials accompanied by sustained depolarization of output neurons. SLEs were dependent on N-methyl-d-aspartate receptors and sodium currents and were facilitated by α-amino-3-hydroxy-5-methyl-4-isoxazole propionate receptors. The events were initiated in the glomerular layer and propagated laterally through the external plexiform layer at a slow time scale. Our findings confirm that low-Mg2+ medium should be used with caution in OB slices. Furthermore, the SLEs resembled the so-called slow direct current (DC) shift of clinical and experimental seizures, which has recently been recognized as being of great clinical importance. The OB slice may therefore provide a robust and unique in vitro model of acute seizures in which mechanisms of epileptiform DC shifts can be studied in isolation from fast oscillations.

Place, publisher, year, edition, pages
Rockville, MD, United States: American Physiological Society , 2011. Vol. 106, no 5, p. 2593-2605
National Category
Neurosciences
Identifiers
URN: urn:nbn:se:liu:diva-171571DOI: 10.1152/jn.00601.2011ISI: 000297690500040PubMedID: 21832029Scopus ID: 2-s2.0-80755169380OAI: oai:DiVA.org:liu-171571DiVA, id: diva2:1503238
Available from: 2020-11-23 Created: 2020-11-23 Last updated: 2020-12-01Bibliographically approved

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Igelström, Kajsa

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