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合成大麻素与选择性去甲肾上腺素再摄取抑制剂联合应用对神经损伤诱导的神经性小鼠抗痛觉过敏作用的分析。

Analysis of the anti-allodynic effects of combination of a synthetic cannabinoid and a selective noradrenaline re-uptake inhibitor in nerve injury-induced neuropathic mice.

作者信息

Gunduz O, Topuz R D, Karadag C H, Ulugol A

机构信息

Department of Medical Pharmacology, Faculty of Medicine, Trakya University, 22030-Edirne, Turkey.

出版信息

Eur J Pain. 2016 Mar;20(3):465-71. doi: 10.1002/ejp.752. Epub 2015 Jul 24.

Abstract

BACKGROUND

Combining drugs not only reduces specific adverse effects of each of the drug at a higher dose but also may lead to enhanced efficacy. Tapentadol is a recently discovered analgesic possessing μ-opioid receptor agonism and noradrenaline re-uptake inhibition in a single molecule. Taking into consideration, the pharmacological similarities between opioids and cannabinoids, we assumed that combination of cannabinoids with noradrenaline re-uptake inhibitors might also be effective. We therefore aimed to determine whether combining 1:1, 1:3 and 3:1 fixed ratios of the synthetic cannabinoid WIN 55,212-2 and the selective noradrenaline re-uptake inhibitor maprotiline exert anti-allodynic synergy on nerve-injured neuropathic mice.

METHODS

Partial tight ligation of the sciatic nerve was made in mice; on pre-operative and post-operative 15 days basal mechanical allodynia, cold allodynia and motor function were assessed using von Frey filaments, hot/cold plate and rota rod apparatus.

RESULTS

Mechanical and cold allodynia developed in all groups on post-operative 15 days. Development of cold allodynia was statistically significant in all groups (p < 0.05); therefore, cold allodynia was used in combination studies. As shown by isobolographic analysis, interactions of 1:1 and 3:1 ratios of WIN 55,212-2:maprotiline combinations were supra-additive, whereas 1:3 ratio was sub-additive.

CONCLUSIONS

Overall, our data suggest that combination of a cannabinoid with a selective noradrenaline re-uptake inhibitor may offer a beneficial treatment option for neuropathic pain.

摘要

背景

联合用药不仅能在更高剂量下降低每种药物的特定不良反应,还可能提高疗效。他喷他多是一种最近发现的镇痛药,在单个分子中具有μ-阿片受体激动作用和去甲肾上腺素再摄取抑制作用。考虑到阿片类药物和大麻素之间的药理学相似性,我们推测大麻素与去甲肾上腺素再摄取抑制剂联合使用可能也有效。因此,我们旨在确定合成大麻素WIN 55,212-2与选择性去甲肾上腺素再摄取抑制剂马普替林按1:1、1:3和3:1固定比例联合使用是否对神经损伤的神经性疼痛小鼠发挥抗痛觉过敏协同作用。

方法

对小鼠坐骨神经进行部分紧密结扎;在术前和术后15天,使用von Frey细丝、热/冷板和转棒装置评估基础机械性痛觉过敏、冷痛觉过敏和运动功能。

结果

术后15天所有组均出现机械性和冷痛觉过敏。所有组冷痛觉过敏的发展具有统计学意义(p < 0.05);因此,在联合研究中使用冷痛觉过敏。如等效线图分析所示,WIN 55,212-2与马普替林组合的1:1和3:1比例的相互作用是超相加的,而1:3比例是次相加的。

结论

总体而言,我们的数据表明,大麻素与选择性去甲肾上腺素再摄取抑制剂联合使用可能为神经性疼痛提供一种有益的治疗选择。

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