{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,5]],"date-time":"2026-10-05T00:42:26Z","timestamp":1791160946195,"version":"4.1.0"},"reference-count":46,"publisher":"Wiley","issue":"s1","license":[{"start":{"date-parts":[[2012,5,21]],"date-time":"2012-05-21T00:00:00Z","timestamp":1337558400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Epilepsia"],"published-print":{"date-parts":[[2012,6]]},"abstract":"<jats:title>Summary<\/jats:title><jats:p>Treatments that modulate the size of the extracellular space (ECS) also block epileptiform activity in adult brain tissue. This includes the loop diuretics furosemide and bumetanide, and alterations of the osmolarity of the ECS. These treatments block epileptiform activity in a variety of laboratory adult seizure models regardless of the underlying synaptic and physiologic mechanisms generating the seizure activity. Optical imaging studies on adult hippocampal slices show that the blockade of epileptiform activity by these treatments is concomitant with their blockade of activity\u2010driven changes of the ECS. Here we develop and analyze the hypothesis that activity\u2010driven changes in the size of the ECS are <jats:italic>necessary<\/jats:italic> for the maintenance of hypersynchronous epileptiform activity. In support of this hypothesis is an accumulation of data from a number of studies suggesting that furosemide and bumetanide mediate antiepileptic effects through their blockade of cell swelling, dependent on their antagonism of the glial Na+\u2010K\u20102Cl cotransporter (NKCC1).<\/jats:p>","DOI":"10.1111\/j.1528-1167.2012.03471.x","type":"journal-article","created":{"date-parts":[[2012,5,21]],"date-time":"2012-05-21T20:20:45Z","timestamp":1337631645000},"page":"18-25","source":"Crossref","is-referenced-by-count":59,"title":["The extracellular space and epileptic activity in the adult brain: Explaining the antiepileptic effects of furosemide and bumetanide"],"prefix":"10.1111","volume":"53","author":[{"given":"Daryl W.","family":"Hochman","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2012,5,21]]},"reference":[{"key":"e_1_2_11_2_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2125.1976.tb04885.x"},{"key":"e_1_2_11_3_1","doi-asserted-by":"publisher","DOI":"10.1016\/0022-510X(91)90013-W"},{"key":"e_1_2_11_4_1","doi-asserted-by":"publisher","DOI":"10.1016\/0306-4522(94)90372-7"},{"key":"e_1_2_11_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/0306-4522(87)90029-7"},{"key":"e_1_2_11_6_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.neuron.2009.03.003"},{"key":"e_1_2_11_7_1","first-page":"331","volume-title":"Chloride channels and carriers in nerve, muscle and glial cells","author":"Cala PM","year":"1990"},{"key":"e_1_2_11_8_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0006-3495(00)76822-6"},{"key":"e_1_2_11_9_1","doi-asserted-by":"publisher","DOI":"10.1016\/0304-3940(90)90056-F"},{"key":"e_1_2_11_10_1","doi-asserted-by":"publisher","DOI":"10.1006\/cbir.1999.0397"},{"key":"e_1_2_11_11_1","doi-asserted-by":"publisher","DOI":"10.1038\/nm1301"},{"key":"e_1_2_11_12_1","doi-asserted-by":"publisher","DOI":"10.1523\/JNEUROSCI.20-10-03915.2000"},{"key":"e_1_2_11_13_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1749-6632.1985.tb14862.x"},{"key":"e_1_2_11_14_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0306-4522(98)00700-3"},{"key":"e_1_2_11_15_1","doi-asserted-by":"publisher","DOI":"10.1152\/jn.00944.2004"},{"key":"e_1_2_11_16_1","unstructured":"HaglundMM HochmanDW. 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