Ohgaki T, Meguri H, Ogita K, Yoneda Y
Department of Pharmacology, Setsunan University, Osaka, Japan.
Brain Res. 1987 Nov 10;425(2):364-8. doi: 10.1016/0006-8993(87)90521-x.
The effect of systemic administration of grayanotoxin (GTX)-III, a constituent in leaves of Pieris japonica D. Don with an ability to activate the voltage-sensitive sodium channels in excitable tissues, on general behaviors of animals was studied using Std-ddy mice. Intraperitoneal administration of the toxin (0.1-0.25 mg/kg b. wt.) resulted in a dose-dependent manner in a significant and reversible muscle relaxation, and a profound and long lasting (greater than or equal to 60 min) depression of locomotor activity. Pretreatment with GTX-III caused a profound potentiation of the duration of loss of righting reflex by pentobarbital with a concomitant delay of the onset of convulsive seizures by various convulsants such as strychnine, picrotoxin and pentetrazol. Neither tetrodotoxin (1-5 micrograms/kg, i.p.) nor Ro15-1788 (1-5 mg/kg, i.p.) prevented the GTX-III-induced suppression of locomotor activity. These results suggest that GTX-III may elicit a central depressant action in mice through a molecular mechanism other than activation of the voltage-sensitive sodium channels in the brain.
用Std-ddy小鼠研究了日本马醉木(Pieris japonica D. Don)叶中一种能够激活可兴奋组织中电压敏感性钠通道的成分——灰毒素(GTX)-III全身给药对动物一般行为的影响。腹腔注射该毒素(0.1 - 0.25 mg/kg体重)会导致显著且可逆的肌肉松弛,并引起运动活动深度且持久(大于或等于60分钟)的抑制,呈剂量依赖性。预先用GTX-III处理会显著增强戊巴比妥致翻正反射消失的持续时间,同时延迟士的宁、印防己毒素和戊四氮等各种惊厥剂引发惊厥发作的起始时间。腹腔注射河豚毒素(1 - 5微克/千克)或Ro15 - 1788(1 - 5毫克/千克)均不能阻止GTX-III诱导的运动活动抑制。这些结果表明,GTX-III可能通过一种不同于激活脑中电压敏感性钠通道的分子机制在小鼠中引发中枢抑制作用。