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内源性三磷酸腺苷参与芥子油诱导的三叉神经尾侧亚核(延髓背角)中枢敏化。

Endogenous ATP involvement in mustard-oil-induced central sensitization in trigeminal subnucleus caudalis (medullary dorsal horn).

作者信息

Chiang C Y, Zhang S, Xie Y F, Hu J W, Dostrovsky J O, Salter M W, Sessle B J

机构信息

Faculty of Dentistry, University of Toronto, 124 Edward St., Toronto, ON M5G 1G6, Canada.

出版信息

J Neurophysiol. 2005 Sep;94(3):1751-60. doi: 10.1152/jn.00223.2005. Epub 2005 May 18.

Abstract

Central sensitization represents a sustained hypersensitive state of dorsal horn nociceptive neurons that can be evoked by peripheral inflammation or injury to nerves and tissues. It reflects neuroplastic changes such as increases in neuronal spontaneous activity, receptive field size, and responses to suprathreshold stimuli and a decrease in activation threshold. We recently demonstrated that purinergic receptor mechanisms in trigeminal subnucleus caudalis (Vc; medullary dorsal horn) are also involved in the initiation and maintenance of central sensitization in brain stem nociceptive neurons of trigeminal subnucleus oralis. The aim of the present study was to investigate whether endogenous ATP is involved in the development of central sensitization in Vc itself. The experiments were carried out on urethan/alpha-chloralose anesthetized and immobilized rats. Single neurons were recorded and identified as nociceptive-specific (NS) in the deep laminae of Vc. During continuous saline superfusion (0.6 ml/h it) over the caudal medulla, Vc neuronal central sensitization was readily induced by mustard oil application to the tooth pulp. However, this mustard-oil-induced central sensitization could be completely blocked by continuous intrathecal superfusion of the wide-spectrum P2X receptor antagonist pyridoxal-phosphate-6-azophenyl-2, 4-disulphonic acid tetra-sodium (33-100 microM) and by apyrase (an ectonucleotidase enzyme, 30 units/ml). Superfusion of the selective P2X1, P2X3 and P2X(2/3) receptor antagonist 2',3'-O-(2,4,6-trinitrophenyl) adenosine 5'-triphosphate (6-638 microM) partially blocked the Vc central sensitization. The two P2X receptor antagonists did not significantly affect the baseline nociceptive properties of the Vc neurons. These findings implicate endogenous ATP as an important mediator contributing to the development of central sensitization in nociceptive neurons of the deep laminae of the dorsal horn.

摘要

中枢敏化表现为背角伤害性神经元的一种持续的超敏状态,可由外周炎症或神经及组织损伤诱发。它反映了神经可塑性变化,如神经元自发活动增加、感受野大小增加、对阈上刺激的反应增加以及激活阈值降低。我们最近证明,三叉神经尾侧亚核(Vc;延髓背角)中的嘌呤能受体机制也参与了三叉神经口侧亚核脑干伤害性神经元中枢敏化的起始和维持。本研究的目的是调查内源性ATP是否参与Vc自身中枢敏化的发展。实验在乌拉坦/α-氯醛糖麻醉并固定的大鼠身上进行。在Vc深层记录单个神经元并鉴定为伤害性特异性(NS)神经元。在尾侧延髓持续灌注生理盐水(0.6 ml/h)期间,通过向牙髓施加芥子油可轻易诱导Vc神经元中枢敏化。然而,这种芥子油诱导的中枢敏化可被鞘内持续灌注广谱P2X受体拮抗剂磷酸吡哆醛-6-偶氮苯-2,4-二磺酸四钠(33 - 100 μM)和腺苷三磷酸双磷酸酶(一种外切核苷酸酶,30单位/ml)完全阻断。选择性P2X1、P2X3和P2X(2/3)受体拮抗剂2',3'-O-(2,4,6-三硝基苯基)腺苷5'-三磷酸(6 - 638 μM)的灌注部分阻断了Vc中枢敏化。这两种P2X受体拮抗剂对Vc神经元的基线伤害性特性没有显著影响。这些发现表明内源性ATP是背角深层伤害性神经元中枢敏化发展的重要介质。

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