Suppr超能文献

龟脊髓切片制备中背角神经元平台特性的调制。

Modulation of plateau properties in dorsal horn neurones in a slice preparation of the turtle spinal cord.

作者信息

Russo R E, Nagy F, Hounsgaard J

机构信息

Department of Medical Physiology, Panum Institute, University of Copenhagen, Denmark.

出版信息

J Physiol. 1997 Mar 1;499 ( Pt 2)(Pt 2):459-74. doi: 10.1113/jphysiol.1997.sp021941.

Abstract
  1. Modulation of plateau properties in dorsal horn neurones was studied in a transverse slice preparation of the spinal cord of the turtle. In plateau-generating neurones high frequency stimulation of the ipsilateral dorsal root (10-20 Hz, 0.5-2 min) produced a slow depolarization (2.9 +/- 0.6 mV, mean +/- S.E.M.; n = 6) and enhanced the properties mediated by dihydropyridine-sensitive Ca2+ channels. The tetanic stimulus facilitated wind-up and after-discharges even when fast synaptic transmission was blocked by 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX, 10-20 microM), (+/-)-2-amino-5-phosphonopentanoic acid (AP5, 100 microM), bicuculline (10-20 microM) and strychnine (5-20 microM). 2. Application of cis-(+/-)-1-aminocyclopentane-1,3-dicarboxylic acid (ACPD, 10-50 microM) produced a slow depolarization (5.9 +/- 0.5 mV, n = 21) accompanied by an increase in input resistance (28.8 +/- 5.1%, n = 12). 3. ACPD increased the excitability by facilitating the plateau properties. In the presence of tetrodotoxin (TTX, 1 microM) a lower threshold and a slower decay of the plateau potential were observed. These effects resulted in facilitation of wind-up and prolonged after-discharges. 4. All ACPD-induced effects were blocked by alpha-methyl-4-carboxyphenylglycine (MCPG, 0.5-1 mM), a selective antagonist of metabotropic glutamate receptors. The selective agonist for the type I metabotropic glutamate receptor ((RS)-3,5-dihydrophenylglycine (DHPG, 50 microM)) reproduced all the effects of ACPD. 5. Application of a supposed neuromodulator, substance P (1-2 microM) produced a transient depolarization (4 +/- 0.6 mV) lasting 4-6 min during continued application of substance P. Variable effects on the input resistance were observed, a slight increase (12 +/- 2%) being the most frequent. In 61% of the cells, substance P induced a clear increase in excitability with no detectable change in input resistance or membrane potential. 6. The effects of substance P on plateau properties were indistinguishable from those produced by ACPD. Unlike the transient depolarization, the facilitation of the plateau properties persisted in the presence of the agonist. 7. The substance P-induced facilitation of the plateau potential was blocked by GR 82334 (5-10 microM), a selective NK-1 tachykinin-receptor antagonist, and was not affected by MEN 10376 (2 microM), a selective NK-2 antagonist. 8. The facilitation of plateau properties produced by dorsal root stimulation was also reduced by antagonists of metabotropic glutamate receptors and NK-1 tachykinin receptors. 9. We propose that modulation of postsynaptic plateau properties in dorsal horn neurones by activation of type I metabotropic glutamate receptors and NK-1 tachykinin receptors is involved in processing nociceptive information.
摘要
  1. 在乌龟脊髓的横向切片标本中研究了背角神经元平台特性的调制。在产生平台电位的神经元中,高频刺激同侧背根(10 - 20 Hz,0.5 - 2分钟)产生缓慢去极化(2.9±0.6 mV,平均值±标准误;n = 6),并增强了由二氢吡啶敏感的Ca2 +通道介导的特性。即使快速突触传递被6 - 氰基 - 7 - 硝基喹喔啉 - 2,3 - 二酮(CNQX,10 - 20 μM)、(±) - 2 - 氨基 - 5 - 膦酰基戊酸(AP5,100 μM)、荷包牡丹碱(10 - 20 μM)和士的宁(5 - 20 μM)阻断,强直刺激仍促进了wind - up和后放电。2. 应用顺式(±) - 1 - 氨基环戊烷 - 1,3 - 二羧酸(ACPD,10 - 50 μM)产生缓慢去极化(5.9±0.5 mV,n = 21),同时输入电阻增加(28.8±5.1%,n = 12)。3. ACPD通过促进平台特性增加了兴奋性。在存在河豚毒素(TTX,1 μM)的情况下,观察到平台电位的阈值降低和衰减减慢。这些效应导致wind - up的促进和后放电延长。4. 所有ACPD诱导的效应均被α - 甲基 - 4 - 羧基苯基甘氨酸(MCPG,0.5 - 1 mM)阻断,MCPG是代谢型谷氨酸受体的选择性拮抗剂。I型代谢型谷氨酸受体的选择性激动剂((RS) - 3,5 - 二氢苯基甘氨酸(DHPG,50 μM))重现了ACPD的所有效应。5. 应用一种假定的神经调节剂P物质(1 - 2 μM)在持续应用P物质期间产生了持续4 - 6分钟的短暂去极化(4±0.6 mV)。观察到对输入电阻的可变效应,最常见的是轻微增加(12±2%)。在61%的细胞中,P物质诱导兴奋性明显增加,而输入电阻或膜电位无可检测到的变化。6. P物质对平台特性的影响与ACPD产生的影响无法区分。与短暂去极化不同,在激动剂存在的情况下,平台特性的促进持续存在。7. P物质诱导的平台电位促进被GR 82334(5 - 10 μM)阻断,GR 82334是一种选择性NK - 1速激肽受体拮抗剂,并且不受MEN 10376(2 μM)的影响,MEN 10376是一种选择性NK - 2拮抗剂。8. 代谢型谷氨酸受体和NK - 1速激肽受体的拮抗剂也降低了背根刺激产生的平台特性促进。9. 我们提出,通过激活I型代谢型谷氨酸受体和NK - 1速激肽受体对背角神经元突触后平台特性的调制参与了伤害性信息的处理。

相似文献

引用本文的文献

本文引用的文献

3
The pharmacology of pain signalling.疼痛信号传导的药理学
Curr Opin Neurobiol. 1993 Aug;3(4):611-8. doi: 10.1016/0959-4388(93)90063-5.
4
Central hyperexcitability triggered by noxious inputs.由有害输入触发的中枢性过度兴奋。
Curr Opin Neurobiol. 1993 Aug;3(4):602-10. doi: 10.1016/0959-4388(93)90062-4.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验