Suppr超能文献

传递疼痛和瘙痒信息:产生门控的脊髓环路的现代观点。

Transmitting pain and itch messages: a contemporary view of the spinal cord circuits that generate gate control.

机构信息

Department of Anatomy, University California, San Francisco, San Francisco, CA 94158, USA.

Department of Anatomy, University California, San Francisco, San Francisco, CA 94158, USA.

出版信息

Neuron. 2014 May 7;82(3):522-36. doi: 10.1016/j.neuron.2014.01.018.

Abstract

The original formulation of Gate Control Theory (GCT) proposed that the perception of pain produced by spinal cord signaling to the brain depends on a balance of activity generated in large (nonnociceptive)- and small (nociceptive)-diameter primary afferent fibers. The theory proposed that activation of the large-diameter afferent "closes" the gate by engaging a superficial dorsal horn interneuron that inhibits the firing of projection neurons. Activation of the nociceptors "opens" the gate through concomitant excitation of projection neurons and inhibition of the inhibitory interneurons. Sixty years after publication of the GCT, we are faced with an ever-growing list of morphologically and neurochemically distinct spinal cord interneurons. The present Review highlights the complexity of superficial dorsal horn circuitry and addresses the question whether the premises outlined in GCT still have relevance today. By examining the dorsal horn circuits that underlie the transmission of "pain" and "itch" messages, we also address the extent to which labeled lines can be incorporated into a contemporary view of GCT.

摘要

门控控制理论(GCT)的原始表述提出,脊髓向大脑发出的信号所产生的疼痛感知取决于大(非伤害性)和小(伤害性)直径初级传入纤维产生的活动之间的平衡。该理论提出,大直径传入纤维的激活通过激活浅层背角中间神经元来“关闭”门,该中间神经元抑制投射神经元的放电。伤害感受器的激活通过同时兴奋投射神经元和抑制抑制性中间神经元来“打开”门。GCT 发表 60 年后,我们面临着越来越多形态和神经化学上不同的脊髓中间神经元。本综述强调了浅层背角回路的复杂性,并探讨了 GCT 中概述的前提在今天是否仍然具有相关性。通过检查背角回路,我们还探讨了在多大程度上可以将标记线纳入 GCT 的当代观点。这些回路是“疼痛”和“瘙痒”信息传递的基础。

相似文献

2
Spinal Circuits Transmitting Mechanical Pain and Itch.
Neurosci Bull. 2018 Feb;34(1):186-193. doi: 10.1007/s12264-017-0136-z. Epub 2017 May 8.
4
Spinal presynaptic inhibition in pain control.
Neuroscience. 2014 Dec 26;283:95-106. doi: 10.1016/j.neuroscience.2014.09.032. Epub 2014 Sep 22.
5
Neonatal Injury Evokes Persistent Deficits in Dynorphin Inhibitory Circuits within the Adult Mouse Superficial Dorsal Horn.
J Neurosci. 2020 May 13;40(20):3882-3895. doi: 10.1523/JNEUROSCI.0029-20.2020. Epub 2020 Apr 14.
6
Spinal Circuits for Touch, Pain, and Itch.
Annu Rev Physiol. 2018 Feb 10;80:189-217. doi: 10.1146/annurev-physiol-022516-034303. Epub 2017 Sep 27.
9
Aberrant synaptic integration in adult lamina I projection neurons following neonatal tissue damage.
J Neurosci. 2015 Feb 11;35(6):2438-51. doi: 10.1523/JNEUROSCI.3585-14.2015.
10
Identifying functional populations among the interneurons in laminae I-III of the spinal dorsal horn.
Mol Pain. 2017 Jan;13:1744806917693003. doi: 10.1177/1744806917693003.

引用本文的文献

1
Targeted-Produced Dirhamnolipids from Induce Antinociception in Mice.
ACS Omega. 2025 Aug 7;10(32):36056-36067. doi: 10.1021/acsomega.5c03648. eCollection 2025 Aug 19.
3
Sensory-spinal neuron co-culture platform enables analysis of sensory-driven spinal activation.
Front Neurosci. 2025 Jul 7;19:1619340. doi: 10.3389/fnins.2025.1619340. eCollection 2025.
5
Arrestin-biased allosteric modulator of neurotensin receptor 1 alleviates acute and chronic pain.
Cell. 2025 Aug 7;188(16):4332-4349.e21. doi: 10.1016/j.cell.2025.04.038. Epub 2025 May 19.
6
Neurocircuitry basis of motor cortex-related analgesia as an emerging approach for chronic pain management.
Nat Ment Health. 2024 May;2(5):496-513. doi: 10.1038/s44220-024-00235-z. Epub 2024 May 13.
7
Spinal cord stimulation using time-dynamic pulses achieves longer reversal of allodynia compared to tonic pulses in a rat model of neuropathic pain.
Front Pain Res (Lausanne). 2025 Apr 9;6:1541078. doi: 10.3389/fpain.2025.1541078. eCollection 2025.
9
Non-invasive in vivo bidirectional magnetogenetic modulation of pain circuits.
bioRxiv. 2025 Mar 19:2025.03.18.644041. doi: 10.1101/2025.03.18.644041.

本文引用的文献

1
Chronic itch development in sensory neurons requires BRAF signaling pathways.
J Clin Invest. 2013 Nov;123(11):4769-80. doi: 10.1172/JCI70528.
2
Ontogeny of excitatory spinal neurons processing distinct somatic sensory modalities.
J Neurosci. 2013 Sep 11;33(37):14738-48. doi: 10.1523/JNEUROSCI.5512-12.2013.
3
The sensory neurons of touch.
Neuron. 2013 Aug 21;79(4):618-39. doi: 10.1016/j.neuron.2013.07.051.
4
Pain hypersensitivity mechanisms at a glance.
Dis Model Mech. 2013 Jul;6(4):889-95. doi: 10.1242/dmm.011502.
5
Functional differences between neurochemically defined populations of inhibitory interneurons in the rat spinal dorsal horn.
Pain. 2013 Dec;154(12):2606-2615. doi: 10.1016/j.pain.2013.05.001. Epub 2013 May 7.
6
The cells and circuitry for itch responses in mice.
Science. 2013 May 24;340(6135):968-71. doi: 10.1126/science.1233765.
9
Peptidergic CGRPα primary sensory neurons encode heat and itch and tonically suppress sensitivity to cold.
Neuron. 2013 Apr 10;78(1):138-51. doi: 10.1016/j.neuron.2013.01.030. Epub 2013 Mar 21.

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