• 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

一种改良的冲突回避检测方法揭示了两性之间疼痛敏感性的模态特异性差异。

An improved conflict avoidance assay reveals modality-specific differences in pain hypersensitivity across sexes.

机构信息

CERVO Brain Research Centre, Québec, QC, Canada.

Faculty of Dentistry, Université Laval, Québec, QC, Canada.

出版信息

Pain. 2024 Jun 1;165(6):1304-1316. doi: 10.1097/j.pain.0000000000003132. Epub 2024 Jan 26.

DOI:10.1097/j.pain.0000000000003132
PMID:38277178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11090034/
Abstract

Abnormal encoding of somatosensory modalities (ie, mechanical, cold, and heat) are a critical part of pathological pain states. Detailed phenotyping of patients' responses to these modalities have raised hopes that analgesic treatments could one day be tailored to a patient's phenotype. Such precise treatment would require a profound understanding of the underlying mechanisms of specific pain phenotypes at molecular, cellular, and circuitry levels. Although preclinical pain models have helped in that regard, the lack of a unified assay quantifying detailed mechanical, cold, and heat pain responses on the same scale precludes comparing how analgesic compounds act on different sensory phenotypes. The conflict avoidance assay is promising in that regard, but testing conditions require validation for its use with multiple modalities. In this study, we improve upon the conflict avoidance assay to provide a validated and detailed assessment of all 3 modalities within the same animal, in mice. We first optimized testing conditions to minimize the necessary amount of training and to reduce sex differences in performances. We then tested what range of stimuli produce dynamic stimulus-response relationships for different outcome measures in naive mice. We finally used this assay to show that nerve injury produces modality-specific sex differences in pain behavior. Our improved assay opens new avenues to study the basis of modality-specific abnormalities in pain behavior.

摘要

躯体感觉方式(即机械、冷和热)的异常编码是病理性疼痛状态的一个关键部分。对患者对这些方式的反应进行详细表型分析,使人们希望有朝一日可以根据患者的表型来定制镇痛治疗方法。这种精确的治疗方法需要在分子、细胞和电路水平上深刻理解特定疼痛表型的潜在机制。尽管临床前疼痛模型在这方面有所帮助,但缺乏一种统一的测定方法,无法在同一尺度上定量详细的机械、冷和热痛反应,这使得无法比较不同感觉表型的镇痛化合物的作用方式。回避冲突测定法在这方面很有前途,但测试条件需要验证其是否可以与多种方式一起使用。在这项研究中,我们改进了回避冲突测定法,以便在同一动物(即小鼠)中对所有 3 种方式进行验证和详细评估。我们首先优化了测试条件,以最大限度地减少所需的训练量,并减少了性能方面的性别差异。然后,我们测试了不同的结果测量标准在不同的刺激范围内产生动态刺激-反应关系的情况。最后,我们使用该测定法证明了神经损伤在疼痛行为中产生了特定于性别的感觉方式差异。我们改进的测定法为研究疼痛行为中特定于感觉方式的异常的基础开辟了新的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e082/11090034/77e9b5df54f7/jop-165-1304-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e082/11090034/382e7f59a3ba/jop-165-1304-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e082/11090034/cba604db2bb4/jop-165-1304-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e082/11090034/c684dd9085b4/jop-165-1304-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e082/11090034/4809a00d4b2e/jop-165-1304-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e082/11090034/8ae913beaadf/jop-165-1304-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e082/11090034/7ea621684ede/jop-165-1304-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e082/11090034/1d11f3dc65a0/jop-165-1304-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e082/11090034/77e9b5df54f7/jop-165-1304-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e082/11090034/382e7f59a3ba/jop-165-1304-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e082/11090034/cba604db2bb4/jop-165-1304-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e082/11090034/c684dd9085b4/jop-165-1304-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e082/11090034/4809a00d4b2e/jop-165-1304-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e082/11090034/8ae913beaadf/jop-165-1304-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e082/11090034/7ea621684ede/jop-165-1304-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e082/11090034/1d11f3dc65a0/jop-165-1304-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e082/11090034/77e9b5df54f7/jop-165-1304-g008.jpg

相似文献

1
An improved conflict avoidance assay reveals modality-specific differences in pain hypersensitivity across sexes.一种改良的冲突回避检测方法揭示了两性之间疼痛敏感性的模态特异性差异。
Pain. 2024 Jun 1;165(6):1304-1316. doi: 10.1097/j.pain.0000000000003132. Epub 2024 Jan 26.
2
Sex differences in thermal pain sensitivity and sympathetic reactivity for two strains of rat.两种品系大鼠热痛觉敏感性和交感反应性的性别差异。
J Pain. 2008 Aug;9(8):739-49. doi: 10.1016/j.jpain.2008.03.008. Epub 2008 May 16.
3
Measuring Pain Avoidance-Like Behavior in Drug-Dependent Rats.测量药物依赖大鼠的类似疼痛回避行为。
Curr Protoc Neurosci. 2018 Oct;85(1):e53. doi: 10.1002/cpns.53. Epub 2018 Sep 24.
4
Quantitative sensory testing in the German Research Network on Neuropathic Pain (DFNS): somatosensory abnormalities in 1236 patients with different neuropathic pain syndromes.定量感觉测试在德国神经病理性疼痛研究网络(DFNS)中的应用:1236 例不同神经病理性疼痛综合征患者的躯体感觉异常。
Pain. 2010 Sep;150(3):439-450. doi: 10.1016/j.pain.2010.05.002.
5
Learned avoidance from noxious mechanical simulation but not threshold semmes weinstein filament stimulation after nerve injury in rats.神经损伤后大鼠对有害机械模拟的学习性回避,但对阈值 semmes weinstein 纤维刺激无反应。
J Pain. 2010 Mar;11(3):280-6. doi: 10.1016/j.jpain.2009.07.011. Epub 2009 Nov 27.
6
Between Scylla and Charybdis: assessing the multidimensional aspects of pain behaviors in rats using a double avoidance place preference paradigm.处于两难境地:使用双回避位置偏爱范式评估大鼠疼痛行为的多维度方面。
Pain. 2025 Mar 1;166(3):587-595. doi: 10.1097/j.pain.0000000000003383. Epub 2024 Aug 20.
7
Pharmacological validation of voluntary gait and mechanical sensitivity assays associated with inflammatory and neuropathic pain in mice.用于验证与炎性和神经性疼痛相关的小鼠自发运动和机械敏感性检测的药理学方法。
Neuropharmacology. 2018 Mar 1;130:18-29. doi: 10.1016/j.neuropharm.2017.11.036. Epub 2017 Nov 27.
8
Modality of hyperalgesia tested, not type of nerve damage, predicts pharmacological sensitivity in rat models of neuropathic pain.所测试的痛觉过敏模态,而非神经损伤类型,可预测神经病理性疼痛大鼠模型中的药物敏感性。
Eur J Pain. 2010 May;14(5):503-9. doi: 10.1016/j.ejpain.2009.08.010. Epub 2009 Dec 5.
9
Comparison of three models of neuropathic pain in mice using a new method to assess cold allodynia: the double plate technique.使用一种评估冷觉异常性疼痛的新方法——双板技术,对小鼠三种神经性疼痛模型进行比较。
Neurosci Lett. 2006 May 22;399(3):240-4. doi: 10.1016/j.neulet.2006.01.058. Epub 2006 Feb 21.
10
Detection of cold pain, cold allodynia and cold hyperalgesia in freely behaving rats.在自由活动的大鼠中检测冷痛、冷觉异常和冷痛觉过敏。
Mol Pain. 2005 Dec 14;1:36. doi: 10.1186/1744-8069-1-36.

引用本文的文献

1
Painful Diabetic Neuropathy: Sex-Specific Mechanisms and Differences from Animal Models to Clinical Outcomes.疼痛性糖尿病神经病变:性别特异性机制以及从动物模型到临床结果的差异
Cells. 2024 Dec 7;13(23):2024. doi: 10.3390/cells13232024.
2
Anxiety-Like Behaviors in Mice Unmasked: Revealing Sex Differences in Anxiety Using a Novel Light-Heat Conflict Test.揭示小鼠的焦虑样行为:使用新型光热冲突试验揭示焦虑中的性别差异。
J Neurosci Res. 2024 Dec;102(12):e70002. doi: 10.1002/jnr.70002.
3
Modulating Neural Circuits of Pain in Preclinical Models: Recent Insights for Future Therapeutics.

本文引用的文献

1
The cellular coding of temperature in the mammalian cortex.哺乳动物大脑皮层中温度的细胞编码。
Nature. 2023 Feb;614(7949):725-731. doi: 10.1038/s41586-023-05705-5. Epub 2023 Feb 8.
2
Pregabalin Silences Oxaliplatin-Activated Sensory Neurons to Relieve Cold Allodynia.普瑞巴林沉默奥沙利铂激活的感觉神经元以缓解冷感觉异常。
eNeuro. 2023 Feb 21;10(2). doi: 10.1523/ENEURO.0395-22.2022. Print 2023 Feb.
3
Probing pain aversion in rats with the "Heat Escape Threshold" paradigm.用“热逃避阈值”范式探查大鼠的痛回避。
调节临床前模型中的疼痛神经回路:未来治疗的新见解。
Cells. 2024 Jun 7;13(12):997. doi: 10.3390/cells13120997.
Mol Pain. 2023 Jan-Dec;19:17448069231156657. doi: 10.1177/17448069231156657.
4
Maximizing treatment efficacy through patient stratification in neuropathic pain trials.在神经性疼痛试验中通过患者分层实现治疗效果最大化。
Nat Rev Neurol. 2023 Jan;19(1):53-64. doi: 10.1038/s41582-022-00741-7. Epub 2022 Nov 18.
5
Sex-specific effects of neuropathic pain on long-term pain behavior and mortality in mice.神经性疼痛对小鼠长期疼痛行为和死亡率的性别特异性影响。
Pain. 2023 Mar 1;164(3):577-586. doi: 10.1097/j.pain.0000000000002742. Epub 2022 Jul 29.
6
Thermal gradient ring reveals thermosensory changes in diabetic peripheral neuropathy in mice.热梯度环揭示了小鼠糖尿病周围神经病变中的热敏变化。
Sci Rep. 2022 Jun 13;12(1):9724. doi: 10.1038/s41598-022-14186-x.
7
Sex differences in choice-based thermal nociceptive tests in adult rats.成年大鼠基于选择的热痛觉测试中的性别差异。
Behav Brain Res. 2022 Jul 5;429:113919. doi: 10.1016/j.bbr.2022.113919. Epub 2022 May 4.
8
Sexual dimorphism in a neuronal mechanism of spinal hyperexcitability across rodent and human models of pathological pain.脊髓病理性疼痛啮齿动物和人类模型中神经元机制过度兴奋的性二态性。
Brain. 2022 Apr 29;145(3):1124-1138. doi: 10.1093/brain/awab408.
9
Predicting Treatment Response with Sensory Phenotyping in Post-Traumatic Neuropathic Pain.运用感觉表型预测创伤后神经病理性疼痛的治疗反应。
Pain Med. 2022 Sep 30;23(10):1726-1732. doi: 10.1093/pm/pnac045.
10
Sex Differences in a Rat Model of Peripheral Neuropathic Pain and Associated Levels of Endogenous Cannabinoid Ligands.外周神经性疼痛大鼠模型中的性别差异及内源性大麻素配体的相关水平
Front Pain Res (Lausanne). 2021 Jun 4;2:673638. doi: 10.3389/fpain.2021.673638. eCollection 2021.