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同型半胱氨酸诱导大鼠血管内皮依赖性痛觉过敏减弱

Homocysteine-induced attenuation of vascular endothelium-dependent hyperalgesia in the rat.

作者信息

Joseph E K, Green P G, Ferrari L F, Levine J D

机构信息

Department of Medicine, Division of Neuroscience, University of California at San Francisco, San Francisco, CA 94143-0440, United States; Department of Oral & Maxillofacial Surgery, University of California at San Francisco, San Francisco, CA 94143-0440, United States.

Department of Medicine, Division of Neuroscience, University of California at San Francisco, San Francisco, CA 94143-0440, United States; Department of Oral & Maxillofacial Surgery, University of California at San Francisco, San Francisco, CA 94143-0440, United States.

出版信息

Neuroscience. 2015 Jan 22;284:678-684. doi: 10.1016/j.neuroscience.2014.10.056. Epub 2014 Nov 4.

Abstract

We have recently demonstrated a role of the vascular endothelium in peripheral pain mechanism by disrupting endothelial cell function using intravascular administration of octoxynol-9, a non-selective membrane active agent. As an independent test of the role of endothelial cells in pain mechanisms, we evaluated the effect of homocysteine, an agent that damages endothelial cell function. Mechanical stimulus-induced enhancement of endothelin-1 hyperalgesia in the gastrocnemius muscle of the rat was first prevented then enhanced by intravenous administration of homocysteine, but was only inhibited by its precursor, methionine. Both homocysteine and methionine significantly attenuated mechanical hyperalgesia in two models of ergonomic muscle pain, induced by exposure to vibration, and by eccentric exercise, and cutaneous mechanical hyperalgesia in an ischemia-reperfusion injury model of Complex Regional Pain Syndrome type I, all previously shown responsive to octoxynol-9. This study provides independent support for a role of the endothelial cell in pain syndromes thought to have a vascular basis, and suggests that substances that are endothelial cell toxins can enhance vascular pain.

摘要

我们最近通过血管内给予辛苯昔醇-9(一种非选择性膜活性剂)破坏内皮细胞功能,证明了血管内皮在外周疼痛机制中的作用。作为对内皮细胞在疼痛机制中作用的独立测试,我们评估了同型半胱氨酸(一种损害内皮细胞功能的物质)的作用。静脉注射同型半胱氨酸首先阻止然后增强了机械刺激诱导的大鼠腓肠肌内皮素-1痛觉过敏,但仅被其前体蛋氨酸抑制。同型半胱氨酸和蛋氨酸均显著减轻了两种由接触振动和离心运动引起的人体工程学肌肉疼痛模型中的机械性痛觉过敏,以及I型复杂性区域疼痛综合征缺血再灌注损伤模型中的皮肤机械性痛觉过敏,所有这些模型先前均显示对辛苯昔醇-9有反应。这项研究为内皮细胞在被认为具有血管基础的疼痛综合征中的作用提供了独立支持,并表明作为内皮细胞毒素的物质可增强血管性疼痛。

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本文引用的文献

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