Inhibition of nitric oxide synthase prevents magnesium-free-induced epileptiform activity in guinea-pig piriform cortex neurones in vitro

被引:0
作者
V. Libri
Rosamaria Santarelli
Steven Nisticò
Gian Battista Azzena
机构
[1] Department of Pharmacology,
[2] The School of Pharmacy,undefined
[3] 29/39 Brunswick Square,undefined
[4] London WC1N 1AX,undefined
[5] UK,undefined
[6] Department of Biology,undefined
[7] University of Rome “Tor Vergata”,undefined
[8] Via della Ricerca Scientifica,undefined
[9] I-00173 Rome,undefined
[10] Italy,undefined
[11] Institute of Human Physiology,undefined
[12] Faculty of Medicine,undefined
[13] Catholic University of Sacred Heart,undefined
[14] Largo F. Vito1,undefined
[15] I-00168 Rome,undefined
[16] Italy,undefined
来源
Naunyn-Schmiedeberg's Archives of Pharmacology | 1997年 / 355卷
关键词
Key words Magnesium-free-induced epileptiform; activity; NMDA receptor; Nitric oxide synthase inhibitors; Synaptic transmission; Piriform cortex; Intracellular recording;
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摘要
The effects of N-nitro-L-arginine methyl ester (L-NAME), a nitric oxide (NO) synthase inhibitor, were examined on Mg2+-free-induced epileptiform activity, in guinea-pig piriform cortex slices in vitro. L-NAME (0.1-1mM) had no effect on neuronal membrane properties or electrically-evoked postsynaptic potentials (PSPs). In contrast, during superfusion of the slices with Mg2+-free solution neurones exhibited spontaneous and stimulus-evoked epileptiform potentials that were suppressed in the presence of L-NAME (100 μΜ) or the selective NMDA receptor antagonist DL-APV (100 μΜ). The inhibitory effects induced by L-NAME were reversibly reduced by L-arginine (1mM), but not D-arginine (1mM), the latter drug not being a substrate for NO formation. It was concluded that L-NAME can suppress epileptiform activity induced by Mg2+-free exposure primarily through a decrease in presynaptic transmitter release, although additional actions on the NMDA-receptor complex were also considered.
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页码:452 / 456
页数:4
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