Kawabata A, Sasa M, Kishimoto T, Takaori S
Department of Pharmacology, Faculty of Medicine, Kyoto University, Japan.
Jpn J Pharmacol. 1991 Jan;55(1):101-6. doi: 10.1254/jjp.55.101.
The effects of anti-vertigo drugs on medial vestibular nucleus (MVN) neurons were examined to assess the site and mode of action using cats anesthetized with alpha-chloralose. Single neuron activity in the MVN was extracellularly recorded using a silver wire microelectrode attached along a seven-barreled micropipette, each of which was filled with diphenhydramine, diphenidol, betahistine, glutamate or NaCl. Type I of the MVN neurons were identified according to the responses obtained when the animal placed on a turn-table was rotated sinusoidally. The effects of the drugs were examined on type I neurons which received impulses primarily from the labyrinth and sent them to the oculomotor nuclei. The microiontophoretic application of diphenhydramine, diphenidol and betahistine inhibited rotation-induced firing of type I MVN neurons. Diphenhydramine and diphenidol were more potent than betahistine. These results suggest that these drugs directly act on MVN neurons to reduce the responsiveness to rotatory stimulation.
使用α-氯醛糖麻醉的猫,研究抗眩晕药物对内侧前庭核(MVN)神经元的影响,以评估其作用部位和作用方式。使用沿着七管微量移液器附着的银丝微电极,在MVN中细胞外记录单个神经元活动,每个微量移液器中填充有苯海拉明、地芬尼多、倍他司汀、谷氨酸或氯化钠。根据将置于转台上的动物进行正弦旋转时获得的反应,识别MVN神经元的I型。研究了这些药物对主要从迷路接收冲动并将其发送到动眼神经核的I型神经元的影响。苯海拉明、地芬尼多和倍他司汀的微量离子电泳应用抑制了I型MVN神经元的旋转诱导放电。苯海拉明和地芬尼多比倍他司汀更有效。这些结果表明,这些药物直接作用于MVN神经元,以降低对旋转刺激的反应性。