• 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

神经性疼痛:强啡肽的矛盾之处。

Neuropathic pain: the paradox of dynorphin.

作者信息

Lai J, Ossipov M H, Vanderah T W, Malan T P, Porreca F

机构信息

Department of Pharmacology, University of Arizona Health Sciences Center, Tucson 85724, USA.

出版信息

Mol Interv. 2001 Aug;1(3):160-7.

PMID:14993349
Abstract

One of the curious but common consequences of opioid administration in the clinical setting is the induction, at sites uninvolved in the original presentation of discomfort, of pain itself. The induction of pain is also a reliable, measurable phenomenon in animals receiving continuous delivery of opioid. Such pain induction is associated with the expression of spinal dynorphin, a finding that is especially intriguing in light of dynorphin's ability to recapitulate many of the characteristics of chronic, neuropathic pain when administered intrathecally (i.e., into the spine). The effective treatment of chronic pain syndromes-and of tolerance to antinociceptive therapies-may thus rest on an understanding of the biological roles of dynorphin in neurotransmission.

摘要

在临床环境中,使用阿片类药物会产生一种奇特但常见的后果,即在最初未出现不适的部位诱发疼痛本身。在持续接受阿片类药物的动物中,疼痛的诱发也是一种可靠的、可测量的现象。这种疼痛诱发与脊髓强啡肽的表达有关,鉴于强啡肽鞘内注射(即注入脊髓)时能够重现许多慢性神经性疼痛的特征,这一发现尤其引人关注。因此,慢性疼痛综合征以及对抗痛觉疗法耐受性的有效治疗可能取决于对强啡肽在神经传递中的生物学作用的理解。

相似文献

1
Neuropathic pain: the paradox of dynorphin.神经性疼痛:强啡肽的矛盾之处。
Mol Interv. 2001 Aug;1(3):160-7.
2
Opioid induced hyperalgesia: clinical implications for the pain practitioner.阿片类药物诱导的痛觉过敏:对疼痛治疗从业者的临床意义。
Pain Physician. 2009 May-Jun;12(3):679-84.
3
Dynorphin promotes abnormal pain and spinal opioid antinociceptive tolerance.强啡肽会加剧异常疼痛并导致脊髓阿片类药物抗伤害感受耐受性。
J Neurosci. 2000 Sep 15;20(18):7074-9. doi: 10.1523/JNEUROSCI.20-18-07074.2000.
4
Nociceptive behavior induced by the endogenous opioid peptides dynorphins in uninjured mice: evidence with intrathecal N-ethylmaleimide inhibiting dynorphin degradation.内源性阿片肽强啡肽在未受伤小鼠中诱导的伤害感受行为:鞘内注射N-乙基马来酰亚胺抑制强啡肽降解的证据
Int Rev Neurobiol. 2009;85:191-205. doi: 10.1016/S0074-7742(09)85015-0.
5
Intrathecal injection of the sigma(1) receptor antagonist BD1047 blocks both mechanical allodynia and increases in spinal NR1 expression during the induction phase of rodent neuropathic pain.鞘内注射σ1受体拮抗剂BD1047可在啮齿动物神经性疼痛的诱导期阻断机械性异常性疼痛并抑制脊髓NR1表达增加。
Anesthesiology. 2008 Nov;109(5):879-89. doi: 10.1097/ALN.0b013e3181895a83.
6
Ketorolac prevents recurrent withdrawal induced hyperalgesia but does not inhibit tolerance to spinal morphine in the rat.酮咯酸可预防复发性戒断诱导的痛觉过敏,但不抑制大鼠对脊髓吗啡的耐受性。
Eur J Pain. 2007 Jan;11(1):1-6. doi: 10.1016/j.ejpain.2005.12.007. Epub 2006 Jan 30.
7
Mechanisms of induction of persistent nociception by dynorphin.强啡肽诱导持续性伤害性感受的机制。
J Pharmacol Exp Ther. 2001 Oct;299(1):6-11.
8
An antisense oligonucleotide to the N-methyl-D-aspartate (NMDA) subunit NMDAR1 attenuates NMDA-induced nociception, hyperalgesia, and morphine tolerance.一种针对N-甲基-D-天冬氨酸(NMDA)亚基NMDAR1的反义寡核苷酸可减轻NMDA诱导的伤害感受、痛觉过敏和吗啡耐受性。
J Pharmacol Exp Ther. 2005 Feb;312(2):834-40. doi: 10.1124/jpet.104.074856. Epub 2004 Sep 23.
9
Mechanisms of opioid-induced pain and antinociceptive tolerance: descending facilitation and spinal dynorphin.阿片类药物诱导的疼痛和抗伤害感受耐受的机制:下行易化和脊髓强啡肽
Pain. 2001 May;92(1-2):5-9. doi: 10.1016/s0304-3959(01)00311-6.
10
Changes in G proteins genes expression in rat lumbar spinal cord support the inhibitory effect of chronic pain on the development of tolerance to morphine analgesia.大鼠腰段脊髓中G蛋白基因表达的变化支持慢性疼痛对吗啡镇痛耐受性发展的抑制作用。
Neurosci Res. 2005 Nov;53(3):250-6. doi: 10.1016/j.neures.2005.06.020. Epub 2005 Aug 1.

引用本文的文献

1
Microiontophoretic Application of Dynorphin in Dental Pain: Excitatory or Inhibitory Effects.强啡肽的微量离子导入在牙科疼痛中的应用:兴奋还是抑制作用。
J Pain Res. 2025 Jan 25;18:455-464. doi: 10.2147/JPR.S499040. eCollection 2025.
2
Epigenetic and Transcriptional Control of the Opioid Prodynorphine Gene: In-Depth Analysis in the Human Brain.阿片样物质前原啡肽基因的表观遗传和转录控制:人脑的深入分析。
Molecules. 2021 Jun 7;26(11):3458. doi: 10.3390/molecules26113458.
3
Estrogens as arbiters of sex-specific and reproductive cycle-dependent opioid analgesic mechanisms.
雌激素作为性别特异性和生殖周期依赖性阿片类药物镇痛机制的裁决者。
Vitam Horm. 2019;111:227-246. doi: 10.1016/bs.vh.2019.06.002. Epub 2019 Jul 2.
4
Dynorphinergic system alterations in the corticostriatal circuitry of neuropathic mice support its role in the negative affective component of pain.神经病理性疼痛小鼠皮质纹状体回路中的强啡肽能系统改变支持其在疼痛负性情感成分中的作用。
Genes Brain Behav. 2019 Jul;18(6):e12467. doi: 10.1111/gbb.12467. Epub 2018 Mar 15.
5
Opioid precursor protein isoform is targeted to the cell nuclei in the human brain.阿片样物质前体蛋白同工型定位于人脑的细胞核中。
Biochim Biophys Acta Gen Subj. 2017 Feb;1861(2):246-255. doi: 10.1016/j.bbagen.2016.11.002. Epub 2016 Nov 10.
6
Cyclic non-opioid dynorphin A analogues for the bradykinin receptors.用于缓激肽受体的环状非阿片类强啡肽A类似物。
Bioorg Med Chem Lett. 2016 Nov 15;26(22):5513-5516. doi: 10.1016/j.bmcl.2016.10.010. Epub 2016 Oct 6.
7
Various modifications of the amphipathic dynorphin A pharmacophore for rat brain bradykinin receptors.用于大鼠脑缓激肽受体的两亲性强啡肽A药效基团的各种修饰。
Chem Biol Drug Des. 2016 Oct;88(4):615-9. doi: 10.1111/cbdd.12789. Epub 2016 Jun 6.
8
Separation of dynorphin peptides by capillary electrochromatography using a polydiallyldimethylammonium chloride gold nanoparticle-modified capillary.使用聚二烯丙基二甲基氯化铵金纳米颗粒修饰的毛细管通过毛细管电色谱法分离强啡肽肽段。
Electrophoresis. 2016 Sep;37(17-18):2297-304. doi: 10.1002/elps.201600006. Epub 2016 Jun 16.
9
Sustained Suppression of Hyperalgesia during Latent Sensitization by μ-, δ-, and κ-opioid receptors and α2A Adrenergic Receptors: Role of Constitutive Activity.μ-、δ-和κ-阿片受体以及α2A肾上腺素能受体在潜在致敏过程中对痛觉过敏的持续抑制作用:组成性活性的作用
J Neurosci. 2016 Jan 6;36(1):204-21. doi: 10.1523/JNEUROSCI.1751-15.2016.
10
Targeting Opioid-Induced Hyperalgesia in Clinical Treatment: Neurobiological Considerations.靶向治疗阿片类药物诱导的痛觉过敏:神经生物学方面的考虑。
CNS Drugs. 2015 Jun;29(6):465-86. doi: 10.1007/s40263-015-0255-x.