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喹酸对小鼠中grayanotoxin诱导的运动活动抑制的预防作用。

Preventive action of quisqualic acid against grayanotoxin-induced suppression of locomotor activity in mice.

作者信息

Ohgaki T, Uchida S, Meguri H, Ogita K, Yoneda Y

机构信息

Department of Pharmacology, Setsunan University, Osaka, Japan.

出版信息

Neuropharmacology. 1988 Oct;27(10):1045-53. doi: 10.1016/0028-3908(88)90066-4.

Abstract

Grayanotoxin-III (GTX-III) is a constituent in leaves of Pieris japonica D. Don which exhibits, in vitro, the ability to open voltage-sensitive sodium channels in various excitable tissues. Effects of systemic administration of GTX-III were studied in vivo using Std-ddy mice. Salivation, vomiting and paralysis of the hind paws invariably occurred in mice injected intraperitoneally with 0.1 or 0.25 mg/kg of GTX-III. The writhing response to an intraperitoneal injection of acetic acid was considerably diminished by pretreatment of animals with the toxin. The grayanoid also caused a profound attenuation of the response to caudal compression, while inducing no significant alteration of that to thermal injury. Pretreatment with GTX-III resulted in a significant decrement of the time required for loss of the righting reflex induced by pentobarbital, with a concomitant delay in recovery. Mice injected with the toxin exhibited a significant and restorable suppression of coordination, and a long-lasting suppression of spontaneous locomotor activity in both horizontal and vertical directions. Neither tetrodotoxin (1-5 micrograms/kg, i.p.) nor Ro15-1788 (1-5 mg/kg, i.p.) prevented the GTX-III-induced suppression of locomotion. Atropine (5-10 mg/kg, i.p.) failed to antagonize the GTX-III-induced suppression but protected against salivation induced by the toxin without affecting other symptoms. Intracerebroventricular injection of quisqualic acid (0.5 microgram), one of the agonists for central glutamate receptors, but not that of tetrodotoxin (5 ng) prevented the GTX-III-induced suppression of horizontal movement. These results suggest that GTX-III may elicit its depressant action on horizontal locomotion possibly through interacting with central glutamatergic neurons rather than activating voltage-sensitive sodium channels in the brain. Possible involvement of muscarinic cholinergic neurons in the GTX-III-induced salivation is also suggested.

摘要

灰藜毒素III(GTX-III)是日本马醉木叶片中的一种成分,在体外实验中,它能够使各种可兴奋组织中的电压敏感性钠通道开放。利用Std-ddy小鼠在体内研究了GTX-III全身给药的效果。腹腔注射0.1或0.25mg/kg的GTX-III后,小鼠总是会出现流涎、呕吐和后爪麻痹的症状。用该毒素预处理动物后,腹腔注射醋酸引起的扭体反应明显减弱。该毒素也会使尾部压迫反应显著减弱,而对热损伤反应没有显著改变。用GTX-III预处理会导致戊巴比妥诱导的翻正反射消失所需时间显著缩短,同时恢复延迟。注射该毒素的小鼠表现出显著且可恢复的协调性抑制,以及在水平和垂直方向上对自发运动活动的长期抑制。河豚毒素(1-5微克/千克,腹腔注射)和Ro15-1788(1-5毫克/千克,腹腔注射)均不能预防GTX-III诱导的运动抑制。阿托品(5-10毫克/千克,腹腔注射)不能拮抗GTX-III诱导的抑制作用,但能预防毒素引起的流涎,且不影响其他症状。脑室内注射中枢谷氨酸受体激动剂之一的喹啉酸(0.5微克),而不是河豚毒素(5纳克),可以预防GTX-III诱导的水平运动抑制。这些结果表明,GTX-III可能通过与中枢谷氨酸能神经元相互作用,而非激活脑中的电压敏感性钠通道,从而对水平运动产生抑制作用。还提示了毒蕈碱胆碱能神经元可能参与了GTX-III诱导的流涎过程。

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