Differential effects of the serotonin receptors on cultured rat cerebral cortical neurons

被引:0
|
作者
T. Matsuoka
T. Nishizaki
Y. Ikeuchi
Y. Okada
K. Sumino
机构
[1] Department of Public Health,
[2] Kobe University School of Medicine,undefined
[3] 7-5-1 Kusunoki-cho,undefined
[4] Chuo-ku,undefined
[5] Kobe 650 (Japan),undefined
[6] Department of Physiology,undefined
[7] Kobe University School of Medicine,undefined
[8] 7-5-1 Kusunoki-cho,undefined
[9] Chuo-ku,undefined
[10] Kobe 650 (Japan),undefined
[11] Fax +81 78 341 5732,undefined
关键词
Key words. Serotonin; ligand-gated receptor; G-protein-coupled receptor; patch-clamp; cerebral cortical neuron.;
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摘要
Effects of serotonin (5-HT) on cerebral cortical neurons were examined by patch clamp techniques. 5-HT produced a variety of responses such as outward (19/73 patches/neurons), slow inward (15/73 patches/neurons), fast inward (8/73 patches/neurons), and mixed currents (initially fast inward deflection followed by an outward response: 2/73 patches/neurons), with a latency of 12 sec, 15 sec, 0 sec, and 0 sec respectively, at a holding potential of −60 mV in whole-cell patches. The fast inward currents were again evoked by a selective 5-HT3 receptor agonist, 1-(m-chlorophenyl)-biguanide hydrochloride (CPBG). In the cell-attached patch clamp configuration, 5-HT inside the patch pipette elicited single channel currents with slope conductances of 42 pS and 132 pS (4/42 patches/neurons). CPBG inside the patch pipette evoked inward single channel currents with a lower slope conductance of 41 pS (3/23 patches/neurons). In contrast, application of 5-HT or a 5-HT2 receptor agonist, α-methyl-5-hydroxytryptamine-maleate, outside the patch pipette induced outward single channel currents with a major slope conductance of 140 pS (8/30 patches/neurons) or 135 pS (6/20 patches/neurons), respectively. These results indicate that the outward and fast inward currents may be mediated respectively by the 5-HT2 receptor, which is coupled to a G-protein, and by the 5-HT3 receptor, which contains the non-selective cation channel, and that the mixed type may be caused by both the 5-HT2 and 5-HT3 receptors.
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页码:233 / 236
页数:3
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