• 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

大鼠巨细胞网状核和巨细胞α部对脊髓伤害性信息传递下行易化和抑制的特征

Characterization of descending facilitation and inhibition of spinal nociceptive transmission from the nuclei reticularis gigantocellularis and gigantocellularis pars alpha in the rat.

作者信息

Zhuo M, Gebhart G F

机构信息

Department of Pharmacology, College of Medicine, University of Iowa, Iowa City 52242.

出版信息

J Neurophysiol. 1992 Jun;67(6):1599-614. doi: 10.1152/jn.1992.67.6.1599.

DOI:10.1152/jn.1992.67.6.1599
PMID:1352804
Abstract
  1. Descending influences produced by focal electrical stimulation in the nuclei reticularis gigantocellularis (NGC) and gigantocellularis pars alpha (NGC alpha) on spinal nociceptive transmission and the dorsoventral region of spinal white matter mediating stimulation-produced modulation were examined in pentobarbital sodium-anesthetized, paralyzed rats. Spinal units studied responded to mechanical stimuli and noxious heating (50 degrees C) of cutaneous receptive fields confined to the glabrous skin of the ipsilateral hind foot. Recording sites were located in laminae I-VI of the L3-L5 spinal segments. 2. Electrical stimulation in the NGC or NGC alpha produced both facilitation and inhibition of responses of spinal units to noxious heating of the skin. At 33 of 57 stimulation sites in the NGC and NGC alpha, electrical stimulation produced biphasic effects, facilitating responses at lesser intensities (5-25 microA) and inhibiting responses at greater intensities (50-100 microA). At 21 other sites in the NGC and NGC alpha, electrical stimulation (5-100 microA) only inhibited, and at 3 sites stimulation (5-100 microA) only facilitated responses of spinal units to noxious heating of the skin. 3. Electrical stimulation in the NGC or NGC alpha contralateral to the spinal recording site produced the same magnitude of facilitation/inhibition or inhibition of spinal nociceptive transmission as did stimulation in the ipsilateral NGC and NGC alpha. 4. The latencies to descending facilitation and inhibition of spinal nociceptive transmission from the NGC and NGC alpha were estimated by a cumulative sum technique to be 232 and 80 ms, respectively. 5. Responses of spinal units to graded heating (42-50 degrees C) of the skin exhibited positively accelerating stimulus-response functions (SRF) throughout the temperature range tested. Electrical stimulation at lesser, "facilitating" intensities produced a parallel, leftward shift of the SRF, whereas stimulation at greater, "inhibitory" intensities significantly decreased the slope of the SRF without affecting the threshold for response. 6. To determine whether activation of cell bodies in the NGC or NGC alpha were capable of replicating the effects of electrical stimulation, L-glutamate was microinjected into sites where electrical stimulation facilitated at lesser and inhibited at greater intensities the responses of spinal units to 50 degrees C heating of the skin. L-Glutamate (5 nmol) produced a rapid onset, short-lasting and reproducible facilitation of nociceptive transmission; glutamate microinjection into the same site at a greater dosage (50 nmol) inhibited responses of the same spinal units.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 在戊巴比妥钠麻醉、麻痹的大鼠中,研究了网状巨细胞核(NGC)和巨细胞α部(NGCα)的局灶性电刺激对脊髓伤害性传递以及介导刺激产生调制的脊髓白质背腹区域的下行影响。所研究的脊髓神经元对局限于同侧后足无毛皮肤的机械刺激和有害热刺激(50℃)有反应。记录部位位于L3 - L5脊髓节段的Ⅰ - Ⅵ层。2. NGC或NGCα中的电刺激对脊髓神经元对皮肤有害热刺激的反应既有易化作用,也有抑制作用。在NGC和NGCα的57个刺激部位中的33个,电刺激产生双相效应,在较小强度(5 - 25微安)时易化反应,在较大强度(50 - 100微安)时抑制反应。在NGC和NGCα的另外21个部位,电刺激(5 - 100微安)仅产生抑制作用,在3个部位刺激(5 - 100微安)仅易化脊髓神经元对皮肤有害热刺激的反应。3. 与脊髓记录部位对侧的NGC或NGCα中的电刺激,对脊髓伤害性传递产生的易化/抑制或抑制作用的幅度,与同侧NGC和NGCα中的刺激相同。4. 采用累积总和技术估计,来自NGC和NGCα的脊髓伤害性传递下行易化和抑制的潜伏期分别为232毫秒和80毫秒。5. 在整个测试温度范围内,脊髓神经元对皮肤分级加热(42 - 50℃)的反应表现出正加速的刺激 - 反应函数(SRF)。较小的、“易化”强度的电刺激使SRF产生平行的、向左的移位,而较大的、“抑制”强度的刺激显著降低SRF的斜率,而不影响反应阈值。6. 为了确定NGC或NGCα中细胞体的激活是否能够复制电刺激的效应,将L - 谷氨酸微量注射到电刺激在较小强度时易化、在较大强度时抑制脊髓神经元对50℃皮肤加热反应的部位。L - 谷氨酸(5纳摩尔)迅速产生、持续时间短且可重复的伤害性传递易化作用;以更大剂量(50纳摩尔)将谷氨酸微量注射到同一部位则抑制相同脊髓神经元的反应。(摘要截短于400字)

相似文献

1
Characterization of descending facilitation and inhibition of spinal nociceptive transmission from the nuclei reticularis gigantocellularis and gigantocellularis pars alpha in the rat.大鼠巨细胞网状核和巨细胞α部对脊髓伤害性信息传递下行易化和抑制的特征
J Neurophysiol. 1992 Jun;67(6):1599-614. doi: 10.1152/jn.1992.67.6.1599.
2
Modulation of spinal nociceptive transmission from nuclei tractus solitarii: a relay for effects of vagal afferent stimulation.孤束核介导的脊髓伤害性信息传递的调制:迷走神经传入刺激效应的一个中继环节
J Neurophysiol. 1990 May;63(5):971-86. doi: 10.1152/jn.1990.63.5.971.
3
Quantitative characterization and spinal pathway mediating inhibition of spinal nociceptive transmission from the lateral reticular nucleus in the rat.大鼠外侧网状核介导脊髓伤害性信息传递抑制的定量特征及脊髓通路
J Neurophysiol. 1988 Jan;59(1):226-47. doi: 10.1152/jn.1988.59.1.226.
4
Characterization of descending inhibition and facilitation from the nuclei reticularis gigantocellularis and gigantocellularis pars alpha in the rat.大鼠巨细胞网状核和巨细胞α部下行抑制与易化作用的特征分析
Pain. 1990 Sep;42(3):337-350. doi: 10.1016/0304-3959(90)91147-B.
5
Effects of neonatal capsaicin treatment on descending modulation of spinal nociception from the rostral, medial medulla in adult rat.新生期辣椒素处理对成年大鼠延髓头端内侧脊髓伤害性感受下行调制的影响。
Brain Res. 1994 May 9;645(1-2):164-78. doi: 10.1016/0006-8993(94)91650-0.
6
Vagal afferent modulation of spinal nociceptive transmission in the rat.
J Neurophysiol. 1989 Aug;62(2):401-15. doi: 10.1152/jn.1989.62.2.401.
7
Spinal serotonin receptors mediate descending facilitation of a nociceptive reflex from the nuclei reticularis gigantocellularis and gigantocellularis pars alpha in the rat.脊髓5-羟色胺受体介导大鼠巨细胞网状核和α部巨细胞网状核对伤害性反射的下行易化作用。
Brain Res. 1991 May 31;550(1):35-48. doi: 10.1016/0006-8993(91)90402-h.
8
Quantitative comparison of inhibition in spinal cord of nociceptive information by stimulation in periaqueductal gray or nucleus raphe magnus of the cat.猫中脑导水管周围灰质或中缝大核刺激对脊髓伤害性信息抑制作用的定量比较
J Neurophysiol. 1983 Dec;50(6):1433-45. doi: 10.1152/jn.1983.50.6.1433.
9
Spinal cholinergic and monoaminergic receptors mediate descending inhibition from the nuclei reticularis gigantocellularis and gigantocellularis pars alpha in the rat.脊髓胆碱能和单胺能受体介导大鼠巨细胞网状核和巨细胞α部的下行抑制。
Brain Res. 1990 Dec 3;535(1):67-78. doi: 10.1016/0006-8993(90)91825-2.
10
Biphasic modulation of spinal visceral nociceptive transmission from the rostroventral medial medulla in the rat.大鼠延髓头端腹内侧区对脊髓内脏伤害性信息传递的双相调制
J Neurophysiol. 2002 May;87(5):2225-36. doi: 10.1152/jn.2002.87.5.2225.

引用本文的文献

1
Adult zymosan re-exposure exacerbates the molecular alterations in the brainstem rostral ventromedial medulla of rats with early life zymosan-induced cystitis.成年大鼠再次接触酵母聚糖会加剧早年因酵母聚糖诱导膀胱炎的大鼠脑干头端腹内侧延髓的分子改变。
Neurobiol Pain. 2024 Jul 24;16:100160. doi: 10.1016/j.ynpai.2024.100160. eCollection 2024 Jul-Dec.
2
NMDARs mediate peripheral and central sensitization contributing to chronic orofacial pain.N-甲基-D-天冬氨酸受体介导外周和中枢敏化,导致慢性口面部疼痛。
Front Cell Neurosci. 2022 Sep 27;16:999509. doi: 10.3389/fncel.2022.999509. eCollection 2022.
3
Brainstem Pain-Modulation Circuitry and Its Plasticity in Neuropathic Pain: Insights From Human Brain Imaging Investigations.
脑干疼痛调制回路及其在神经性疼痛中的可塑性:来自人脑成像研究的见解
Front Pain Res (Lausanne). 2021 Jul 30;2:705345. doi: 10.3389/fpain.2021.705345. eCollection 2021.
4
Role of Descending Serotonergic Fibers in the Development of Pathophysiology after Spinal Cord Injury (SCI): Contribution to Chronic Pain, Spasticity, and Autonomic Dysreflexia.下行5-羟色胺能纤维在脊髓损伤(SCI)后病理生理学发展中的作用:对慢性疼痛、痉挛和自主神经反射异常的影响
Biology (Basel). 2022 Feb 1;11(2):234. doi: 10.3390/biology11020234.
5
Neuronal Adenylyl Cyclase Targeting Central Plasticity for the Treatment of Chronic Pain.靶向神经元腺苷酸环化酶治疗慢性疼痛的中枢可塑性。
Neurotherapeutics. 2020 Jul;17(3):861-873. doi: 10.1007/s13311-020-00927-1. Epub 2020 Sep 15.
6
Activating an anterior nucleus gigantocellularis subpopulation triggers emergence from pharmacologically-induced coma in rodents.激活巨细胞前核亚群可触发啮齿动物从药物诱导的昏迷中苏醒。
Nat Commun. 2019 Jul 1;10(1):2897. doi: 10.1038/s41467-019-10797-7.
7
Supraspinal Mechanisms of Spinal Cord Stimulation for Modulation of Pain: Five Decades of Research and Prospects for the Future.脊髓刺激调制疼痛的脊髓上机制:五十年的研究与未来展望。
Anesthesiology. 2019 Apr;130(4):651-665. doi: 10.1097/ALN.0000000000002353.
8
Modality selective roles of pro-nociceptive spinal 5-HT and 5-HT receptors in normal and neuropathic states.在正常和病态状态下,脊髓促伤害性 5-HT 及其受体的模式选择性作用。
Neuropharmacology. 2018 Dec;143:29-37. doi: 10.1016/j.neuropharm.2018.09.028. Epub 2018 Sep 18.
9
Heterosynaptic long-term potentiation from the anterior cingulate cortex to spinal cord in adult rats.成年大鼠扣带回前部皮质到脊髓的异突触长时程增强。
Mol Pain. 2018 Jan-Dec;14:1744806918798406. doi: 10.1177/1744806918798406. Epub 2018 Aug 14.
10
Top-down descending facilitation of spinal sensory excitatory transmission from the anterior cingulate cortex.来自前扣带皮层的脊髓感觉传入的自上而下的易化。
Nat Commun. 2018 May 14;9(1):1886. doi: 10.1038/s41467-018-04309-2.