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单核细胞趋化蛋白-1、基质细胞衍生因子-1和视黄酸在大鼠神经性疼痛病理生理学中的作用

Role of monocyte chemoattractant protein-1, stromal derived factor-1 and retinoic acid in pathophysiology of neuropathic pain in rats.

作者信息

Hamed Enas Ahmed, Mohamed Farghaly Hanan Sayed, Abdel Mola Asmaa Fathey, Fahmi Minerva Kamal, Makhlouf Madiha Mohammed, Balfas Mohamed Abdullah

出版信息

J Basic Clin Physiol Pharmacol. 2016 Jun 1;27(4):411-24. doi: 10.1515/jbcpp-2015-0105.

Abstract

BACKGROUND

Chemokines have been recently recognized to play a role in chronic pain syndromes' pathophysiology. This study investigated the role of monocyte chemoattractant protein-1 (MCP-1), stromal cell derived factor-1 (SDF-1), and retinoic acid (RA) as targets for the therapeutic approach of neuropathic pain.

METHODS

A chronic constriction injury (CCI) model of neuropathic pain by unilateral ligation of left sciatic nerve was performed in adult female Wistar rats. The effects of doxycycline (Dox, 50 mg/kg/day i.p. for 7 days), single dose of bicyclam (5 mg/kg i.p.), RA (15 mg/kg/day i.p. for 7 days), and their combination(s) on behavioral tests of nociception (Von Frey filaments; paw pressure test) on days 0, 1, 3, 5, and 7 of operation were studied. Serum concentrations of MCP-1 and SDF-1 were measured by ELISA. Histological examination of the sciatic nerve was investigated.

RESULTS

CCI of sciatic nerve significantly induced mechanical allodynia and hyperalgesia and an increase of MCP-1 and SDF-1 serum levels. Dox-treated groups (Dox, Dox+bicyclam, Dox+RA, Dox+bicyclam+RA) and bicyclam-treated groups (bicyclam, Dox+bicyclam, bicyclam+RA, Dox+bicyclam+RA) attenuated CCI-induced behavioral and biochemical changes. RA inhibited CCI-induced mechanical hyperalgesia but produced a time-dependent reversal of allodynia. Histological findings showed degenerative changes of sciatic nerve after CCI that were partially recovered in Dox-treated groups.

CONCLUSIONS

These findings demonstrate an association between serum MCP-1 and SDF-1 concentrations and behavioral manifestations of neuropathic pain. RA administration decreased neuropathic pain (antihyperalgesic effect) but did not cause any improvement in sciatic nerve tissues, either alone or in combination with chemokine antagonists. Thus, chemokines may serve as potential targets for drug development in neuropathic pain treatment.

摘要

背景

趋化因子最近被认为在慢性疼痛综合征的病理生理学中发挥作用。本研究调查了单核细胞趋化蛋白-1(MCP-1)、基质细胞衍生因子-1(SDF-1)和视黄酸(RA)作为神经性疼痛治疗靶点的作用。

方法

在成年雌性Wistar大鼠中通过单侧结扎左坐骨神经建立神经性疼痛的慢性压迫损伤(CCI)模型。研究了强力霉素(Dox,50mg/kg/天腹腔注射,共7天)、单剂量双环胺(5mg/kg腹腔注射)、RA(15mg/kg/天腹腔注射,共7天)及其组合在手术第0、1、3、5和7天对伤害感受行为测试(von Frey细丝;爪压力测试)的影响。通过酶联免疫吸附测定法测量血清中MCP-1和SDF-1的浓度。对坐骨神经进行组织学检查。

结果

坐骨神经CCI显著诱导机械性异常性疼痛和痛觉过敏,并使MCP-1和SDF-1血清水平升高。Dox治疗组(Dox、Dox+双环胺、Dox+RA、Dox+双环胺+RA)和双环胺治疗组(双环胺、Dox+双环胺、双环胺+RA、Dox+双环胺+RA)减轻了CCI诱导的行为和生化变化。RA抑制了CCI诱导的机械性痛觉过敏,但使异常性疼痛出现时间依赖性逆转。组织学结果显示CCI后坐骨神经出现退行性变化,在Dox治疗组中部分恢复。

结论

这些发现表明血清MCP-1和SDF-1浓度与神经性疼痛的行为表现之间存在关联。单独或与趋化因子拮抗剂联合使用时,RA给药可减轻神经性疼痛(抗痛觉过敏作用),但未使坐骨神经组织有任何改善。因此,趋化因子可能是神经性疼痛治疗药物开发的潜在靶点。

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