Hirose A, Sasa M, Ohno Y, Takaori S
Department of Pharmacology, Faculty of Medicine, Kyoto University, Japan.
Jpn J Pharmacol. 1988 Dec;48(4):435-40. doi: 10.1254/jjp.48.435.
Electrophysiological studies using reserpine-treated cats were carried out to elucidate the effects of L-threo-3,4-dihydroxyphenylserine (L-threo-DOPS) on the noradrenergic pathway from the locus coeruleus (LC) to the caudate nucleus (CN) neurons, which were activated by iontophoretically applied bromocriptine, a dopamine D-2 receptor agonist. In the CN neurons, glutamate-induced firing was inhibited by iontophoretic application of noradrenaline, but not by repetitive stimulation of the LC or iontophoretically applied L-threo-DOPS. After intraventricular administration of L-threo-DOPS, however, LC stimulation inhibited the glutamate-induced firing. These results suggest that L-noradrenaline that was produced from the conversion of L-threo-DOPS inhibited the CN neurons which possess dopamine D-2 receptors.
使用利血平处理的猫进行电生理研究,以阐明L-苏式-3,4-二羟基苯丝氨酸(L-苏式-DOPS)对从蓝斑(LC)到尾状核(CN)神经元的去甲肾上腺素能通路的影响,这些神经元由离子电泳施加的多巴胺D-2受体激动剂溴隐亭激活。在CN神经元中,谷氨酸诱导的放电受到离子电泳施加去甲肾上腺素的抑制,但不受LC的重复刺激或离子电泳施加L-苏式-DOPS的抑制。然而,在脑室内给予L-苏式-DOPS后,LC刺激抑制了谷氨酸诱导的放电。这些结果表明,由L-苏式-DOPS转化产生的L-去甲肾上腺素抑制了具有多巴胺D-2受体的CN神经元。