• 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

损伤后疼痛状态下高阈值传入输入诱发的传入处理促进的脊髓药理学。

The spinal pharmacology of facilitation of afferent processing evoked by high-threshold afferent input of the postinjury pain state.

作者信息

Yaksh T L

机构信息

Department of Anesthesiology, University of California, San Diego, La Jolla 92093.

出版信息

Curr Opin Neurol Neurosurg. 1993 Apr;6(2):250-6.

PMID:8097639
Abstract

Repetitive C afferent input evokes a facilitated state of processing that results in increased receptive fields and exaggerated responses to afferent input ("wind-up"). These phenomena underlie the behavioral phenomena of secondary hyperalgesia and this in turn is an important component of postoperative pain. The initiation of this facilitated component is not well blocked by even higher concentrations of volatile anesthetics, but it can be prevented by pretreatment with agents known to block afferent input (local anesthetics) or C-fiber transmitter release (opiates) or to act at one of several links to block a complex spinal cascade involving the N-methyl-D-aspartate receptor, nitric oxide synthase, and cyclooxygenase. These fundamental mechanisms promise to have an impact on the management of postoperative pain.

摘要

重复的C类传入输入引发一种促进性的处理状态,导致感受野增加以及对传入输入的反应增强(“wind-up”)。这些现象是继发性痛觉过敏行为现象的基础,而继发性痛觉过敏又是术后疼痛的一个重要组成部分。即使是更高浓度的挥发性麻醉剂也不能很好地阻断这种促进性成分的起始,但可以通过用已知能阻断传入输入的药物(局部麻醉剂)、C纤维递质释放的药物(阿片类药物)或作用于几个环节之一以阻断涉及N-甲基-D-天冬氨酸受体、一氧化氮合酶和环氧化酶的复杂脊髓级联反应的药物进行预处理来预防。这些基本机制有望对术后疼痛的管理产生影响。

相似文献

1
The spinal pharmacology of facilitation of afferent processing evoked by high-threshold afferent input of the postinjury pain state.损伤后疼痛状态下高阈值传入输入诱发的传入处理促进的脊髓药理学。
Curr Opin Neurol Neurosurg. 1993 Apr;6(2):250-6.
2
[Pharmacology of spinal facilitation: the basis for preventive analgesia].[脊髓易化的药理学:预防性镇痛的基础]
Rev Esp Anestesiol Reanim. 1998 Jan;45(1):17-23.
3
Depression of NMDA-receptor-mediated segmental transmission by ketamine and ketoprofen, but not L-NAME, on the in vitro neonatal rat spinal cord preparation.氯胺酮和酮洛芬而非左旋精氨酸甲酯对体外培养的新生大鼠脊髓标本中NMDA受体介导的节段性传递的抑制作用。
Brain Res. 2006 Jun 13;1094(1):57-64. doi: 10.1016/j.brainres.2006.03.117. Epub 2006 May 23.
4
Pre-emptive analgesia and surgical pain.超前镇痛与手术疼痛
Prog Brain Res. 2000;129:505-24. doi: 10.1016/S0079-6123(00)29037-7.
5
Pain after injury: some basic mechanisms.
J Fla Med Assoc. 1997 Jan;84(1):16-9.
6
Oxytocin actions on afferent evoked spinal cord neuronal activities in neuropathic but not in normal rats.催产素对神经性大鼠而非正常大鼠的传入神经诱发脊髓神经元活动有影响。
Brain Res. 2005 May 31;1045(1-2):124-33. doi: 10.1016/j.brainres.2005.03.020. Epub 2005 Apr 21.
7
Wind-up of spinal cord neurones and pain sensation: much ado about something?脊髓神经元的wind-up与痛觉:小题大做? (注:“wind-up”在此语境可能需结合专业知识准确理解其含义,比如可能是指脊髓神经元的某种特性或现象等,这里直接保留英文以便读者根据专业背景准确把握,同时整体翻译了句子大意)
Prog Neurobiol. 2000 Jun;61(2):169-203. doi: 10.1016/s0301-0082(99)00051-9.
8
"Pre-emptive analgesia" may follow epidural anaesthesia.“超前镇痛”可能在硬膜外麻醉后出现。
Can J Anaesth. 1993 Oct;40(10):1002-3. doi: 10.1007/BF03010109.
9
The effects of microinjection of morphine into thalamic nucleus submedius on formalin-evoked nociceptive responses of neurons in the rat spinal dorsal horn.向大鼠丘脑正中核微量注射吗啡对福尔马林诱发的脊髓背角神经元伤害性反应的影响。
Neurosci Lett. 2006 Jun 19;401(1-2):103-7. doi: 10.1016/j.neulet.2006.02.075. Epub 2006 Mar 23.
10
GABA(A) receptor facilitation of neurokinin release from primary afferent terminals in the rat spinal cord.γ-氨基丁酸A型(GABA(A))受体促进大鼠脊髓初级传入终末释放神经激肽
Neuroscience. 2005;130(4):1013-27. doi: 10.1016/j.neuroscience.2004.10.019.

引用本文的文献

1
Differential effects of ketamine and MK-801 on A-fiber and C-fiber responses of spinal wide dynamic range neurons in the cat.氯胺酮和MK-801对猫脊髓广动力范围神经元A纤维和C纤维反应的不同影响。
J Anesth. 1997 Sep;11(3):184-192. doi: 10.1007/BF02480035.
2
Effects of general anesthetics on substance P release and c-Fos expression in the spinal dorsal horn.全麻药物对脊髓背角 P 物质释放和 c-Fos 表达的影响。
Anesthesiology. 2013 Aug;119(2):433-42. doi: 10.1097/ALN.0b013e31829996b6.
3
N-methyl-D-aspartate receptors and large conductance calcium-sensitive potassium channels inhibit the release of opioid peptides that induce mu-opioid receptor internalization in the rat spinal cord.
N-甲基-D-天冬氨酸受体和大电导钙敏感钾通道抑制阿片肽的释放,这些阿片肽会诱导大鼠脊髓中的μ-阿片受体内化。
Neuroscience. 2005;136(2):549-62. doi: 10.1016/j.neuroscience.2005.08.032. Epub 2005 Oct 3.
4
Antinociceptive interactions between intrathecal gabapentin and MK801 or NBQX in rat formalin test.鞘内注射加巴喷丁与MK801或NBQX在大鼠福尔马林试验中的抗伤害感受相互作用
J Korean Med Sci. 2005 Apr;20(2):307-12. doi: 10.3346/jkms.2005.20.2.307.
5
ACEA 1021: flip or flop?ACEA 1021:成功还是失败?
CNS Drug Rev. 2004 Winter;10(4):337-48. doi: 10.1111/j.1527-3458.2004.tb00031.x.
6
Interaction between intrathecal gabapentin and adenosine in the formalin test of rats.大鼠福尔马林试验中鞘内注射加巴喷丁与腺苷之间的相互作用。
J Korean Med Sci. 2004 Aug;19(4):581-5. doi: 10.3346/jkms.2004.19.4.581.
7
Locus-specific rescue of GluRepsilon1 NMDA receptors in mutant mice identifies the brain regions important for morphine tolerance and dependence.在突变小鼠中对GluRepsilon1 N-甲基-D-天冬氨酸受体进行基因座特异性拯救,确定了对吗啡耐受性和依赖性重要的脑区。
J Neurosci. 2003 Jul 23;23(16):6529-36. doi: 10.1523/JNEUROSCI.23-16-06529.2003.
8
Pain in terminally ill patients: guidelines for pharmacological management.晚期患者的疼痛:药物治疗指南
CNS Drugs. 2003;17(9):621-31. doi: 10.2165/00023210-200317090-00002.
9
The epidural and intrathecal administration of somatotrophin-release inhibiting factor: native and synthetic analogues.生长激素释放抑制因子的硬膜外和鞘内给药:天然及合成类似物
Curr Rev Pain. 2000;4(1):82-90. doi: 10.1007/s11916-000-0013-7.
10
Neurokinin 1 receptor internalization in spinal cord slices induced by dorsal root stimulation is mediated by NMDA receptors.背根刺激诱导的脊髓切片中神经激肽1受体的内化由NMDA受体介导。
J Neurosci. 1997 Nov 1;17(21):8129-36. doi: 10.1523/JNEUROSCI.17-21-08129.1997.