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神经激肽对成年纵向脊髓标本中胶状质神经元的作用。

Neurokinin actions on substantia gelatinosa neurones in an adult longitudinal spinal cord preparation.

作者信息

Bentley G N, Gent J P

机构信息

Department of Pharmacology, University of Leeds, UK.

出版信息

Brain Res. 1995 Feb 27;673(1):101-11. doi: 10.1016/0006-8993(94)01406-8.

Abstract

We have used an adult longitudinal spinal cord preparation to study the effects of a range of selective neurokinin analogues on single neurones located exclusively within the substantia gelatinosa. Since the preparation retained attached dorsal roots it was possible synaptically to activate the substantia gelatinosa neurones by electrical stimulation of their afferent fibres, thus providing a means of studying directly the role of neurokinins in mechanisms of primary afferent transmission. The actions of three agonists selective for the three NK receptor subtypes (NK1, GR73632; NK2, GR64349; NK3, senktide), and a highly selective antagonist at NK1 receptors (GR82334) were investigated. Experiments were performed on a total of 274 substantia gelatinosa neurones, estimates of conduction velocity for evoked responses suggested that the majority of these neurones were innervated by unmyelinated afferents. A large proportion responded to iontophoretically applied neurokinin agonists. The majority responded to NK1, fewer responded to NK2; some, although not all, of the neurones tested responded to both NK1 and NK2 agonists. In most cases the responses were excitatory, although inhibitory effects were observed in some neurones. None of the neurones tested responded to NK3 agonist. Excitatory and inhibitory actions could be demonstrated following abolition of synaptic transmission by removal of calcium, suggesting direct mechanisms for both effects. The antagonist alone failed to modify either spontaneous firing or firing in response to afferent stimulation in any of the neurones studied, even though the doses used were shown to be effective in selectively antagonising responses to the NK1 agonist, suggesting that neither relied on the endogenous release of neurokinins.

摘要

我们使用成年纵向脊髓标本,研究了一系列选择性神经激肽类似物对仅位于脊髓胶状质内的单个神经元的作用。由于该标本保留了附着的背根,通过电刺激其传入纤维在突触水平激活脊髓胶状质神经元成为可能,从而提供了一种直接研究神经激肽在初级传入传递机制中作用的方法。研究了三种对三种NK受体亚型具有选择性的激动剂(NK1,GR73632;NK2,GR64349;NK3,senktide)以及一种NK1受体的高选择性拮抗剂(GR82334)的作用。总共对274个脊髓胶状质神经元进行了实验,对诱发反应传导速度的估计表明,这些神经元中的大多数由无髓传入纤维支配。很大一部分神经元对离子导入的神经激肽激动剂有反应。大多数神经元对NK1有反应,对NK2有反应的较少;在测试的神经元中,一些(并非全部)对NK1和NK2激动剂都有反应。在大多数情况下,反应是兴奋性的,尽管在一些神经元中观察到了抑制作用。测试的神经元中没有一个对NK3激动剂有反应。去除钙消除突触传递后,可证明兴奋性和抑制性作用,提示两种作用均有直接机制。单独使用拮抗剂未能改变所研究的任何神经元的自发放电或对传入刺激的放电,尽管所使用的剂量已证明可有效选择性拮抗对NK1激动剂的反应,这表明两者均不依赖于神经激肽的内源性释放。

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