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美洛昔康可预防小鼠剖腹术后COX-2介导的炎症,但不能预防疼痛。

Meloxicam prevents COX-2-mediated post-surgical inflammation but not pain following laparotomy in mice.

作者信息

Roughan J V, Bertrand H G M J, Isles H M

机构信息

Comparative Biology Centre, The Medical School, University of Newcastle, Newcastle upon Tyne, UK.

出版信息

Eur J Pain. 2016 Feb;20(2):231-40. doi: 10.1002/ejp.712. Epub 2015 Apr 23.

DOI:10.1002/ejp.712
PMID:25908253
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4728739/
Abstract

BACKGROUND

Inflammation is thought to be a major contributor to post-surgical pain, so non-steroidal anti-inflammatory drugs (NSAIDs) are commonly used analgesics. However, compared to rats, considerably less is known as to how successfully these prevent pain in mice.

METHODS

A fluorescent COX-2 selective probe was used for the first time to evaluate the post-surgical anti-inflammatory effects of meloxicam, and automated behaviour analyses (HomeCageScan; HCS), the Mouse Grimace Scale (MGS) and body weight changes to assess its pain-preventative properties. Groups of 8-9 BALB/c mice were subcutaneously injected with saline (0.3 mL) or meloxicam at (1, 5 or 20 mg/kg) 1 h before a 1.5-cm midline laparotomy. The probe or a control dye (2 mg/kg) was injected intravenously 3 h later. Imaging was used to quantify inflammation at 7, 24 and 48 h following surgery. HCS data and MGS scores were respectively obtained from video recordings and photographs before surgery and 24 h later.

RESULTS

Post-surgical inflammation was dose dependently reduced by meloxicam; with 5 or 20 mg/kg being most effective compared to saline. However, all mice lost weight, MGS scores increased and behavioural activity was reduced by surgery for at least 24 h with no perceivable beneficial effect of meloxicam on any of these potentially pain-associated changes.

CONCLUSIONS

Although meloxicam prevented inflammation, even large doses did not prevent post-laparotomy pain possibly arising due to a range of factors, including, but not limited to inflammation. MGS scoring can be applied by very naïve assessors and so should be effective for cage-side use.

摘要

背景

炎症被认为是术后疼痛的主要促成因素,因此非甾体抗炎药(NSAIDs)是常用的镇痛药。然而,与大鼠相比,对于这些药物在小鼠中预防疼痛的效果了解甚少。

方法

首次使用荧光COX-2选择性探针评估美洛昔康的术后抗炎作用,并采用自动行为分析(HomeCageScan;HCS)、小鼠 grimace 量表(MGS)和体重变化来评估其预防疼痛的特性。将8-9只BALB/c小鼠分为几组,在进行1.5厘米中线剖腹手术前1小时皮下注射生理盐水(0.3毫升)或美洛昔康(1、5或20毫克/千克)。3小时后静脉注射探针或对照染料(2毫克/千克)。在手术后7、24和48小时利用成像技术量化炎症。HCS数据和MGS评分分别从手术前和术后24小时的视频记录和照片中获取。

结果

美洛昔康能剂量依赖性地减轻术后炎症;与生理盐水相比,5或20毫克/千克的剂量效果最佳。然而,所有小鼠体重均下降,MGS评分增加,并且手术使行为活动减少至少24小时,美洛昔康对这些任何潜在的疼痛相关变化均无明显有益作用。

结论

尽管美洛昔康可预防炎症,但即使大剂量也无法预防剖腹手术后可能因一系列因素(包括但不限于炎症)引起的疼痛。MGS评分可由经验极少的评估者应用,因此应适用于笼旁使用。

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