• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

猫对致痒物质的反应。II. 具有无髓轴突的皮肤感受器群体。

Response to an itch-producing substance in cat. II. Cutaneous receptor populations with unmyelinated axons.

作者信息

Tuckett R P, Wei J Y

出版信息

Brain Res. 1987 Jun 9;413(1):95-103. doi: 10.1016/0006-8993(87)90157-0.

DOI:10.1016/0006-8993(87)90157-0
PMID:3594261
Abstract

Within the sampled population of cutaneous unmyelinated afferent neurons (n = 94), only the C-polymodal nociceptor population was reactive to the pruritogen cowhage. Of 62 C-polymodal neurons tested, 11 were unresponsive to cowhage. No C-polymodal neurons were more responsive to inactive, than to active, cowhage (n = 17) and all were responsive to mechanical (n = 62) stimuli and noxious heat (n = 24). The range of conduction velocities obtained by single-unit recording techniques was similar to that found by signal averaging the activity from larger strands of nerve. Hence, it is concluded that our recording technique was capable of recording from the smallest afferent fibers in a cutaneous nerve and it was unlikely that we would have missed finding a slowly conducting, pruritus-signaling neuron due to sampling bias. A search of slowly conducting afferents (n = 314) using electrocutaneous stimulation gave no evidence to suggest the existence of an unknown population of unmyelinated fibers that might signal pruritus. A number of alternative mechanisms by which the sensation of itch might be encoded were discussed, the most favored being the activation of a subset of the C-polymodal nociceptive population.

摘要

在采样的皮肤无髓传入神经元群体(n = 94)中,只有C类多模式伤害性感受器群体对致痒原刺蒴麻有反应。在测试的62个C类多模式神经元中,11个对刺蒴麻无反应。没有C类多模式神经元对失活的刺蒴麻比对活性刺蒴麻反应更强(n = 17),并且所有神经元都对机械刺激(n = 62)和有害热刺激(n = 24)有反应。通过单单位记录技术获得的传导速度范围与通过对较大神经束的活动进行信号平均所发现的范围相似。因此,可以得出结论,我们的记录技术能够记录皮肤神经中最小的传入纤维,并且由于采样偏差,我们不太可能错过发现一个传导缓慢的瘙痒信号神经元。使用皮肤电刺激对传导缓慢的传入纤维进行搜索(n = 314),没有证据表明存在可能发出瘙痒信号的未知无髓纤维群体。讨论了瘙痒感觉可能被编码的多种替代机制,最受青睐的是激活C类多模式伤害性感受器群体的一个子集。

相似文献

1
Response to an itch-producing substance in cat. II. Cutaneous receptor populations with unmyelinated axons.猫对致痒物质的反应。II. 具有无髓轴突的皮肤感受器群体。
Brain Res. 1987 Jun 9;413(1):95-103. doi: 10.1016/0006-8993(87)90157-0.
2
Response to an itch-producing substance in cat. I. Cutaneous receptor populations with myelinated axons.猫对致痒物质的反应。I. 具有有髓轴突的皮肤感受器群体。
Brain Res. 1987 Jun 9;413(1):87-94. doi: 10.1016/0006-8993(87)90156-9.
3
Sensory receptors with unmyelinated (C) fibers innervating the skin of the rabbit's ear.具有无髓鞘(C)纤维的感觉感受器支配着兔耳的皮肤。
J Neurophysiol. 1985 Sep;54(3):491-501. doi: 10.1152/jn.1985.54.3.491.
4
A role for nociceptive, myelinated nerve fibers in itch sensation.伤害感受性、有髓神经纤维在痒觉中的作用。
J Neurosci. 2011 Oct 19;31(42):14841-9. doi: 10.1523/JNEUROSCI.3005-11.2011.
5
Separate peripheral pathways for pruritus in man.人类瘙痒的独立外周通路。
J Neurophysiol. 2008 Oct;100(4):2062-9. doi: 10.1152/jn.90482.2008. Epub 2008 Jun 18.
6
A role for polymodal C-fiber afferents in nonhistaminergic itch.多模式C类纤维传入神经在非组胺能性瘙痒中的作用。
J Neurosci. 2008 Jul 23;28(30):7659-69. doi: 10.1523/JNEUROSCI.1760-08.2008.
7
The classification and properties of nociceptive afferent units from the skin of the anaesthetized pig.来自麻醉猪皮肤的伤害性传入神经单位的分类及特性
Eur J Neurosci. 1995 Mar 1;7(3):431-7. doi: 10.1111/j.1460-9568.1995.tb00339.x.
8
Microneurography of pruritus.瘙痒的微神经生理学研究
Neurosci Lett. 2010 Feb 19;470(3):193-6. doi: 10.1016/j.neulet.2009.06.092. Epub 2009 Jul 2.
9
Specific C-receptors for itch in human skin.人类皮肤中特异性的瘙痒C受体。
J Neurosci. 1997 Oct 15;17(20):8003-8. doi: 10.1523/JNEUROSCI.17-20-08003.1997.
10
Differential ability of human cutaneous nociceptors to signal mechanical pain and to produce vasodilatation.人类皮肤伤害感受器对机械性疼痛进行信号传导及产生血管舒张的差异能力。
J Neurosci. 1994 Mar;14(3 Pt 2):1756-65. doi: 10.1523/JNEUROSCI.14-03-01756.1994.

引用本文的文献

1
Electrically Evoked Itch in Human Subjects.人体受试者的电诱发瘙痒
Front Med (Lausanne). 2021 Jan 20;7:627617. doi: 10.3389/fmed.2020.627617. eCollection 2020.
2
Response characteristics of pruriceptive and nociceptive trigeminoparabrachial tract neurons in the rat.大鼠三叉神经脊束核内伤害性和瘙痒感受神经元的反应特征。
J Neurophysiol. 2015 Jan 1;113(1):58-70. doi: 10.1152/jn.00596.2014. Epub 2014 Oct 8.
3
A role for nociceptive, myelinated nerve fibers in itch sensation.伤害感受性、有髓神经纤维在痒觉中的作用。
J Neurosci. 2011 Oct 19;31(42):14841-9. doi: 10.1523/JNEUROSCI.3005-11.2011.
4
Responsiveness of C neurons in rat dorsal root ganglion to 5-hydroxytryptamine-induced pruritic stimuli in vivo.大鼠背根神经节 C 神经元对体内 5-羟色胺诱导瘙痒刺激的反应。
J Neurophysiol. 2010 Jul;104(1):271-9. doi: 10.1152/jn.00938.2009. Epub 2010 May 19.
5
Different forms of glycine- and GABA(A)-receptor mediated inhibitory synaptic transmission in mouse superficial and deep dorsal horn neurons.甘氨酸和 GABA(A)受体介导的抑制性突触传递在小鼠浅层和深层背角神经元中的不同形式。
Mol Pain. 2009 Nov 18;5:65. doi: 10.1186/1744-8069-5-65.
6
Pruritic and nociceptive sensations and dysesthesias from a spicule of cowhage.来自刺荨麻的瘙痒、伤害性感觉和感觉异常。
J Neurophysiol. 2009 Mar;101(3):1430-43. doi: 10.1152/jn.91268.2008. Epub 2009 Jan 14.
7
A role for polymodal C-fiber afferents in nonhistaminergic itch.多模式C类纤维传入神经在非组胺能性瘙痒中的作用。
J Neurosci. 2008 Jul 23;28(30):7659-69. doi: 10.1523/JNEUROSCI.1760-08.2008.
8
Separate peripheral pathways for pruritus in man.人类瘙痒的独立外周通路。
J Neurophysiol. 2008 Oct;100(4):2062-9. doi: 10.1152/jn.90482.2008. Epub 2008 Jun 18.
9
Cowhage-evoked itch is mediated by a novel cysteine protease: a ligand of protease-activated receptors.蒺藜草诱发的瘙痒由一种新型半胱氨酸蛋白酶介导:一种蛋白酶激活受体的配体。
J Neurosci. 2008 Apr 23;28(17):4331-5. doi: 10.1523/JNEUROSCI.0716-08.2008.
10
The itch-producing agents histamine and cowhage activate separate populations of primate spinothalamic tract neurons.产生瘙痒的介质组胺和刺蒴麻分别激活灵长类动物脊髓丘脑束神经元的不同群体。
J Neurosci. 2007 Sep 12;27(37):10007-14. doi: 10.1523/JNEUROSCI.2862-07.2007.