THE TRIAMINOPYRIDINE FLUPIRTINE PREVENTS CELL-DEATH IN RAT CORTICAL-CELLS INDUCED BY N-METHYL-D-ASPARTATE AND GP120 OF HIV-1

被引:55
作者
PEROVIC, S
SCHLEGER, C
PERGANDE, G
ISKRIC, S
USHIJIMA, H
RYTIK, P
MULLER, WEG
机构
[1] UNIV MAINZ, INST PHYS CHEM, ANGEW MOLEK BIOL ABT, D-55099 MAINZ, GERMANY
[2] ASTA MED AG, MED DEUTSCHLAND ABT, D-60314 FRANKFURT, GERMANY
[3] RUDJER BOSKOVIC INST, NEUROCHEM & MOLEC NEUROBIOL LAB, ZAGREB 41001, CROATIA
[4] INST PUBL HLTH, MINATO KU, TOKYO 108, JAPAN
[5] BYELORUSSIAN RES INST EPIDEMIOL & MICROBIOL, MINSK 220050, BELARUS
来源
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION | 1994年 / 288卷 / 01期
关键词
FLUPIRTINE; TRIAMINOPYRIDINE; NMDA (N-METHYL-D-ASPARTATE); NMDA RECEPTOR; NEURON; CELL DEATH; HIV-1; GP120;
D O I
10.1016/0922-4106(94)90006-X
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Flupirtine, a triaminopyridine derivative, is a non-opiate centrally acting analgesic agent with muscle relaxant properties. Now we show that this drug displays a potent cytoprotective effect on neurons (rat cortical cells) treated with (i) the excitatory amino acid N-methyl-D-aspartate (NMDA) or (ii) with the human immunodeficiency virus type 1 (HIV-1) coat protein gp120. In the absence of the drug the two agents cause a >90% reduction of cell viability after a 18 h incubation. During this period the DNA in the cells undergoes fragmentation and shows a pattern which is typical for cell death. If the neurons were preincubated with flupirtine for 2 h and subsequently exposed to the cytotoxic agents an almost complete protection was achieved. The cytoprotective effect of flupirtine in vitro was significant(above 10 mu M). Because flupirtine displays almost no clinical side effects and in light of the data presented here, flupirtine may be a promising drug also for the treatment of NMDA-mediated neurodegenerative disorders in general and for the treatment of AIDS-related encephalopathy in particular.
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页码:27 / 33
页数:7
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