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在不改变自发或诱发神经活动的浓度下,银环蛇毒素-636可阻断N-甲基-D-天冬氨酸对非洲爪蟾侧线的作用。

Argiotoxin-636 blocks effects of N-methyl-D-aspartate on lateral line of Xenopus laevis at concentrations which do not alter spontaneous or evoked neural activity.

作者信息

Guth S L, Scapini D A, Drescher M J, Drescher D G

机构信息

Department of Otolaryngology, Wayne State University School of Medicine, Detroit, Michigan 48201.

出版信息

Life Sci. 1990;47(16):1437-45. doi: 10.1016/0024-3205(90)90522-s.

DOI:10.1016/0024-3205(90)90522-s
PMID:2250561
Abstract

Activity of primary afferent neurons in acousticolateralis organs can be modulated by excitatory amino acids (EAA) and their antagonists, and EAA are among the better candidates for the transmitter(s) between hair cells and afferent neurons. Argiotoxin-636 (ATX) is a spider venom toxin that is a selective antagonist of the N-methyl-D-aspartate (NMDA) subtype of excitatory amino acid receptors in vertebrates. In the present study, the effects of NMDA alone and in combination with ATX on resting firing rate (spontaneous activity) and mechanically stimulated activity of lateral line afferent neurons of post-metamorphic Xenopus laevis were compared. Perfusion of NMDA (100 or 200 microM) typically produced a biphasic effect on spontaneous activity consisting of a transient increase followed by a decrease in firing rate. Mechanical stimulation applied after the initial response to NMDA produced an increase in firing activity that was not significantly different from the increase in firing activity evoked in the absence of NMDA. ATX at 1-2 microM did not alter either spontaneous or evoked activity, but blocked in a reversible manner both the excitatory and inhibitory actions of NMDA on spontaneous activity. These results suggest the presence of an NMDA receptor in the lateral line but do not support the hypothesis that the generation of action potentials by the afferent transmitter is solely dependent on activation of postsynaptic NMDA receptor-ion channels.

摘要

听侧线器官中初级传入神经元的活动可被兴奋性氨基酸(EAA)及其拮抗剂调节,并且EAA是毛细胞与传入神经元之间递质的较好候选者之一。Argiotoxin - 636(ATX)是一种蜘蛛毒液毒素,是脊椎动物中兴奋性氨基酸受体的N - 甲基 - D - 天冬氨酸(NMDA)亚型的选择性拮抗剂。在本研究中,比较了单独使用NMDA以及NMDA与ATX联合使用对变态后非洲爪蟾侧线传入神经元静息放电率(自发活动)和机械刺激活动的影响。灌注NMDA(100或200微摩尔)通常对自发活动产生双相效应,包括放电率先短暂增加然后降低。在对NMDA的初始反应之后施加的机械刺激使放电活动增加,这与在无NMDA时诱发的放电活动增加没有显著差异。1 - 2微摩尔的ATX既不改变自发活动也不改变诱发活动,但以可逆方式阻断了NMDA对自发活动的兴奋和抑制作用。这些结果表明侧线中存在NMDA受体,但不支持传入递质产生动作电位仅依赖于突触后NMDA受体离子通道激活的假说。

相似文献

1
Argiotoxin-636 blocks effects of N-methyl-D-aspartate on lateral line of Xenopus laevis at concentrations which do not alter spontaneous or evoked neural activity.在不改变自发或诱发神经活动的浓度下,银环蛇毒素-636可阻断N-甲基-D-天冬氨酸对非洲爪蟾侧线的作用。
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Primary afferents evoke excitatory amino acid receptor-mediated EPSPs that are modulated by presynaptic GABAB receptors in lamprey.初级传入神经在七鳃鳗中引发由兴奋性氨基酸受体介导的兴奋性突触后电位(EPSP),这些电位受到突触前GABAB受体的调节。
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