Effects of neuromuscular blocking agents on excitatory transmission and γ-aminobutyric acidA-mediated inhibition in the rat hippocampal slice

被引:11
作者
Chiodini, FC
Tassonyi, E
Fuchs-Buder, T
Fathi, M
Bertrand, D
Muller, D
机构
[1] Ctr Med Univ Geneva, Dept Anesthesiol, Pharmacol & Intens Care Unit, CH-1211 Geneva 4, Switzerland
[2] Ctr Med Univ Geneva, Dept Physiol, CH-1211 Geneva, Switzerland
关键词
atracurium; CA1; excitatory postsynaptic field potentials; inhibitory postsynaptic potentials; laudanosine;
D O I
10.1097/00000542-199804000-00021
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: Although neuromuscular blocking agents do not cross the blood-brain barrier, they may penetrate the central nervous system under particular circumstances and eventually cause neurotoxic consequences. Methods: The effects of neuromuscular blocking agents on excitatory and inhibitory transmission in area CA1 of rat hippocampal slices were investigated using extracellular and intracellular recording techniques. Results: Application of atracurium in the perfusion medium resulted in a dose-dependent enhancement of excitatory synaptic responses averaging 48.7 +/- 4.3% at a concentration of 10 nM. This effect was correlated with an increase in the size of the presynaptic fiber volley. Laudanosine, but not pancuronium bromide or vecuronium bromide, produced similar changes. In addition, atracurium and laudanosine blocked inhibitory transmission and reduced intracellularly recorded gamma-aminobutyric acid(A) receptor-mediated potentials. These effects were observed only at concentrations >1 mu M and were not reproduced by pancuronium bromide and vecuronium bromide. Conclusions: Atracurium and its metabolite, laudanosine, contrary to pancuronium bromide and vecuronium bromide, produce two distinct effects on hippocampal slices. They enhance excitatory transmission and neuronal excitability and they block inhibitory gamma-aminobutyric acid(A)-mediated synaptic responses.
引用
收藏
页码:1003 / 1013
页数:11
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