Run down of GABAergic depolarization during metabolic inhibition of rat hippocampal CA1 neurons

被引:1
作者
Matsumoto, Nozomu [1 ]
Noda, Eiichiro [1 ]
Nabekura, Junichi [1 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Otorhinolaryngol, Higashi Ku, Fukuoka 8128582, Japan
关键词
metabolic poisoning; chloride; NaCN; muscimol;
D O I
10.1016/j.lfs.2006.03.012
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
We investigated the effects of metabolic inhibition on both the shift in the equilibrium potential for Cl- (Ecl) and the run down of GABA(A) receptor responses, using nystatin- and gramicidin-perforated patch-clamp recordings from rat hippocampal CA1 neurons. Metabolic inhibition with NaCN decreased outward GABAergic currents while increasing inward GABAergic currents. E-Cl showed a positive shift almost immediately after metabolic poisoning. This shift always occurred prior to GABA receptor run down, which was observed as decreases in whole cell conductance during application of a GABA(A) receptor agonist. The results indicate that GABAergic responses tend to become depolarizing during metabolic inhibition and the run down of the GABAergic response may therefore be neuroprotective against excitotoxicity. Furthermore the results illustrate the importance of considering both changes in receptor function and current driving force, and their temporal relationship, in order to understand the physiological response of the GABAergic system during metabolic stress. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1021 / 1026
页数:6
相关论文
共 33 条
[1]   ELEVATED GAMMA-AMINOBUTYRIC-ACID LEVELS ATTENUATE THE METABOLIC RESPONSE TO BILATERAL ISCHEMIA [J].
ABEL, MS ;
MCCANDLESS, DW .
JOURNAL OF NEUROCHEMISTRY, 1992, 58 (02) :740-744
[2]   Techniques: Applications of the nerve-bouton preparation in neuropharmacology [J].
Akaike, N ;
Moorhouse, AJ .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2003, 24 (01) :44-47
[3]   NYSTATIN PERFORATED-PATCH RECORDING AND ITS APPLICATIONS TO ANALYSES OF INTRACELLULAR MECHANISMS [J].
AKAIKE, N ;
HARATA, N .
JAPANESE JOURNAL OF PHYSIOLOGY, 1994, 44 (05) :433-473
[4]   Gramicidin perforated patch recording and intracellular chloride activity in excitable cells [J].
Akaike, N .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 1996, 65 (03) :251-264
[5]   Modulation of the excitability of cholinergic basal forebrain neurones by KATp channels [J].
Allen, TGJ ;
Brown, DA .
JOURNAL OF PHYSIOLOGY-LONDON, 2004, 554 (02) :353-370
[6]   Involvement of phosphatase activities in the run-down of GABAA receptor function in rat cerebellar granule cells in culture [J].
Amico, C ;
Cupello, A ;
Fossati, C ;
Robello, M .
NEUROSCIENCE, 1998, 84 (02) :529-535
[7]   An electron spin resonance spin-trapping investigation of the free radicals formed by the reaction of mitochondrial cytochrome c oxidase with H2O2 [J].
Chen, YR ;
Gunther, MR ;
Mason, RP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (06) :3308-3314
[8]   GABA - AN EXCITATORY TRANSMITTER IN EARLY POSTNATAL LIFE [J].
CHERUBINI, E ;
GAIARSA, JL ;
BENARI, Y .
TRENDS IN NEUROSCIENCES, 1991, 14 (12) :515-519
[9]   Anoxia-induced neuronal injury: Role of Na+ entry and Na+-dependent transport [J].
Chidekel, AS ;
Friedman, JE ;
Haddad, GG .
EXPERIMENTAL NEUROLOGY, 1997, 146 (02) :403-413
[10]   GABA DOES NOT PROTECT CEREBROCORTICAL CULTURES AGAINST EXCITOTOXIC CELL-DEATH [J].
ERDO, SL ;
MICHLER, A .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1990, 182 (01) :203-206