Effects of neutral ionophores on membrane electrical characteristics of NG108-15 cells

被引:26
作者
Doebler, JA [1 ]
机构
[1] USA, Med Res Inst Chem Def, Div Pharmacol, Neurotoxicol Branch, Aberdeen Proving Ground, MD 21010 USA
关键词
action potential; CCCP; enniatin; in vitro model; membrane potential; membrane resistance; NG108-15 (neuroblastoma X glioma) hybrid cells; nonactin; valinomycin;
D O I
10.1016/S0378-4274(99)00193-9
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The effects of several K+-selective neutral ionophores on membrane electrical characteristics of differentiated NG108-15 (neuroblastoma X glioma hybrid) cells were examined. Specifically, alterations in membrane resting potential (V-m), input resistance (R-in) and electrically-induced action potential generation were determined upon bath application of enniatin (0.1-10 mu g/ml), nonactin (0.1-10 mu M) and valinomycin (0.1-10 mu M). Although some cells exhibited a slight hyperpolarization and/or reduced R-in, i.e. membrane electrical correlates of enhanced K+ loss, neither V-m nor R-in were significantly altered by any of the ionophores. However, valinomycin and especially nonactin affected action potentials induced by electrical stimulation. This was apparent in the ablation of action potentials in some cells and in the occurrence of degenerative changes in action potential shape in others. The simultaneous administration of the neutral ionophores and the protonophore CCCP or the superfusion of enniatin, nonactin or valinomycin in high (50 mM) glucose-containing physiological solution did not yield more extensive alterations in V-m or R-in. These data suggest that the neutral ionophores are unable to materially enhance K+ flux above the relatively high resting level in NG108-15 cells. Thus, alterations in action potentials appear to be unrelated to K+ transport activity. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:27 / 38
页数:12
相关论文
共 36 条
[1]  
ALONSO MA, 1982, EUR J BIOCHEM, V127, P567
[2]   INCREASE OF POTASSIUM FLUX BY VALINOMYCIN IN EMBRYONIC CHICK HEART [J].
CARMELIET, EE ;
LIEBERMAN, M .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1975, 358 (03) :243-257
[3]   Membrane potential and resistance changes in NG108-15 cells: An in vitro model to study membrane-active compounds [J].
Doebler, JA .
TOXICOLOGY METHODS, 1999, 9 (01) :35-45
[4]   Effects of protonophores on membrane electrical characteristics in NG108-15 cells [J].
Doebler, JA .
NEUROCHEMICAL RESEARCH, 2000, 25 (02) :263-268
[5]  
DOEBLER JA, 2000, IN PRESS TOXICOL VIT
[6]  
FAHIM M, 1983, J EXP BIOL, V107, P491
[7]   SIMULTANEOUS IMAGING OF CELL AND MITOCHONDRIAL-MEMBRANE POTENTIALS [J].
FARKAS, DL ;
WEI, MD ;
FEBBRORIELLO, P ;
CARSON, JH ;
LOEW, LM .
BIOPHYSICAL JOURNAL, 1989, 56 (06) :1053-1069
[8]   EFFECTS OF ALTERATIONS OF TRANSMEMBRANE NA+ AND K+ GRADIENTS BY IONOPHORES (NIGERICIN, MONENSIN) ON SEROTONIN TRANSPORT IN HUMAN-BLOOD PLATELETS [J].
FEINSTEIN, MB ;
HENDERSON, EG ;
SHAAFI, RI .
BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 468 (02) :284-295
[9]   13 CATIONIC IONOPHORES - THEIR ACUTE TOXICITY, NEUROBEHAVIORAL AND MEMBRANE EFFECTS [J].
GAD, SC ;
REILLY, C ;
SIINO, K ;
GAVIGAN, FA ;
WITZ, G .
DRUG AND CHEMICAL TOXICOLOGY, 1985, 8 (06) :451-468
[10]   DEPENDENCY OF DELTA-PH-RELAXATION ACROSS VESICULAR MEMBRANES ON THE BUFFERING POWER OF BULK SOLUTIONS AND LIPIDS [J].
GRZESIEK, S ;
DENCHER, NA .
BIOPHYSICAL JOURNAL, 1986, 50 (02) :265-276