MIXED ACTIONS OF TMB-8 AS A CA2+ ANTAGONIST IN CULTURED MOUSE CORTICAL-NEURONS

被引:10
作者
GRIFFITHS, R [1 ]
GRIEVE, A [1 ]
FRANDSEN, A [1 ]
SCHOUSBOE, A [1 ]
机构
[1] ROYAL DANISH SCH PHARM,DEPT BIOL SCI,PHARMABIOTEC RES CTR,DK-2100 COPENHAGEN,DENMARK
关键词
CORTICAL NEURONS; GLUTAMATE; POTASSIUM; TMB-8; CALCIUM ANTAGONIST; INTRACELLULAR FREE CALCIUM;
D O I
10.1097/00001756-199401000-00018
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
THE action of TMB-8 [8-N,N-diethylamino)octy-3,4,5-trimethoxybenzoate] on glutamate (Glu)- and 55 mM KCl (K+)-induced increases in intracellular free calcium levels ([Ca2+](i)) was studied in cultured mouse cerebral cortical neurones. Glu-induced responses were mediated by two mechanisms, one independent of and the other dependent on extracellular Ca2+, both being inhibited by TMB-8 in a dose-dependent manner. TMB-8 had no effect on [H-3]dizocilpine binding kinetics in cortical membrane preparations. The transient and sustained phases of K+-induced increases in [Ca2+](i) were also inhibited by TMB-8 in a dose-dependent manner. The Ca2+ channel antagonist, verapamil, blocked K+-induced responses but had no effect on Glu-induced responses. Although TMB-8 displays multiple effects, its action at voltage-gated Ca2+ channels does not appear to contribute significantly to its inhibition of the Glu-induced increase in [Ca2+](i).
引用
收藏
页码:605 / 608
页数:4
相关论文
共 23 条
[1]   INHIBITION OF NA+/CA2+ EXCHANGE ENHANCES DELAYED NEURONAL DEATH ELICITED BY GLUTAMATE IN CEREBELLAR GRANULE CELL-CULTURES [J].
ANDREEVA, N ;
KHODOROV, B ;
STELMASHOOK, E ;
CRAGOE, E ;
VICTOROV, I .
BRAIN RESEARCH, 1991, 548 (1-2) :322-325
[2]  
BELHAGE B, 1993, NEUROSCIENCE, V53, P1019
[3]   INOSITOL PHOSPHATES AND CELL SIGNALING [J].
BERRIDGE, MJ ;
IRVINE, RF .
NATURE, 1989, 341 (6239) :197-205
[4]   STUDIES ON MECHANISM OF ACTION OF A NEW CA2+ ANTAGONIST, 8-(N,N-DIETHYLAMINO)OCTYL 3,4,5-TRIMETHOXYBENZOATE HYDROCHLORIDE IN SMOOTH AND SKELETAL-MUSCLES [J].
CHIOU, CY ;
MALAGODI, MH .
BRITISH JOURNAL OF PHARMACOLOGY, 1975, 53 (02) :279-285
[5]  
CHOI DW, 1988, J NEUROSCI, V8, P185
[6]  
FILL M, 1988, TRENDS NEUROSCI, V11, P543
[7]   BIOCHEMISTRY AND BIOPHYSICS OF EXCITATION-CONTRACTION COUPLING [J].
FLEISCHER, S ;
INUI, M .
ANNUAL REVIEW OF BIOPHYSICS AND BIOPHYSICAL CHEMISTRY, 1989, 18 :333-364
[8]   MOBILIZATION OF DANTROLENE-SENSITIVE INTRACELLULAR CALCIUM POOLS IS INVOLVED IN THE CYTOTOXICITY INDUCED BY QUISQUALATE AND N-METHYL-D-ASPARTATE BUT NOT BY 2-AMINO-3-(3-HYDROXY-5-METHYLISOXAZOL-4-YL)PROPIONATE AND KAINATE IN CULTURED CEREBRAL CORTICAL-NEURONS [J].
FRANDSEN, A ;
SCHOUSBOE, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (07) :2590-2594
[9]   DANTROLENE PREVENTS GLUTAMATE CYTOTOXICITY AND CA2+ RELEASE FROM INTRACELLULAR STORES IN CULTURED CEREBRAL CORTICAL-NEURONS [J].
FRANDSEN, A ;
SCHOUSBOE, A .
JOURNAL OF NEUROCHEMISTRY, 1991, 56 (03) :1075-1078
[10]   DIRECT EVIDENCE THAT EXCITOTOXICITY IN CULTURED NEURONS IS MEDIATED VIA N-METHYL-D-ASPARTATE (NMDA) AS WELL AS NON-NMDA RECEPTORS [J].
FRANDSEN, A ;
DREJER, J ;
SCHOUSBOE, A .
JOURNAL OF NEUROCHEMISTRY, 1989, 53 (01) :297-299