dc.creator | Villanueva, | |
dc.creator | Frenz, Patricia | |
dc.creator | Dragnic, Patricia | |
dc.creator | Orrego, Patricia | |
dc.date.accessioned | 2019-01-29T14:47:59Z | |
dc.date.available | 2019-01-29T14:47:59Z | |
dc.date.created | 2019-01-29T14:47:59Z | |
dc.date.issued | 1988 | |
dc.identifier | Brain Research, Volumen 461, Issue 2, 2018, Pages 377-380 | |
dc.identifier | 00068993 | |
dc.identifier | 10.1016/0006-8993(88)90271-5 | |
dc.identifier | http://repositorio.uchile.cl/handle/2250/160685 | |
dc.description.abstract | The efflux of endogenous glutamate from thin slices of rat brain cortex superfused in vitro with artificial cerebrospinal fluid (ACSF) was studied. Initially, glutamate efflux was very high (2.5 nmol/mg protein/min), possibly because of the cutting procedure, but declined sharply, and at 30 min of superfusion was 25 pmol/mg protein/min. In ACSF without added calcium, spontaneous glutamate efflux was always higher than that in calcium-containing medium, e.g. at 30 min it was 75 pmol/mg protein/min. Addition of 10 μM veratridine for 2 min, between 30 and 32 min of superfusion, led, in ACSF with calcium, to an increase in glutamate efflux of 288%, when the maximum efflux following veratridine is compared to the glutamate efflux that immediately preceded the application of this drug (from 25 to 97 pmol/mg protein/min), while in ACSF without added calcium, veratridine induced an increase of only 117% (from 75 to 163 pmol/mg protein/min). These results are interpreted as due to the dual effe | |
dc.language | en | |
dc.rights | http://creativecommons.org/licenses/by-nc-nd/3.0/cl/ | |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Chile | |
dc.source | Brain Research | |
dc.subject | Brain cortex | |
dc.subject | Calcium | |
dc.subject | Endogenous glutamate | |
dc.subject | Veratridine | |
dc.title | Veratridine-induced release of endogenous glutamate from rat brain cortex slices: a reappraisal of the role of calcium | |
dc.type | Artículos de revistas | |