首页> 外文期刊>Journal of Pharmacological and Toxicological Methods >Establishment of a novel objective and quantitative method to assess pain-related behavior in monosodium iodoacetate-induced osteoarthritis in rat knee
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Establishment of a novel objective and quantitative method to assess pain-related behavior in monosodium iodoacetate-induced osteoarthritis in rat knee

机译:建立一种新颖的客观定量方法来评估碘乙酸单钠诱导的大鼠膝关节骨关节炎的疼痛相关行为

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Introduction: Pain in osteoarthritis (OA) patients can be present at rest but typically worsens with movement of the affected joint. However, useful assessment methods of movement-induced pain in animal models are limited. Here, we describe the reduction of spontaneous activity in a rat model of OA as an objective and quantifiable behavioral pain that can predict the analgesic activity of a variety of agents following single-dose administration. Methods: OA was induced in male Sprague-Dawley (SD) rats by intra-articular injection of monoiodoacetate (MIA), and the joint degeneration was assessed with histologic and radiographic analyses. Spontaneous activities were measured in nonhabituated rats using standard, photocell-based monitor systems in the dark. To investigate the potential of the OA model to predict analgesic activity, a number of nonsteroidal anti-inflammatory drugs (NSAIDs) and atypical analgesic drugs were used. Results: Biphasic reduction of total distance and number of rears was observed during the course of experiment after administering 1. mg and 0.3. mg of MIA, respectively. We found that number of rears was the most sensitive to MIA-induce OA and displayed the greatest percentage decrease in activity. Joint degeneration was observed with decreased bone mineral density and loss of articular cartilage 28. days post-MIA injection. Appropriate dosage of opioids reversed MIA-induced decrease of number of rears indicating that reduction of this vertical spontaneous activity reflects pain-associated behavior. As high-doses of opioids reduced spontaneous activity, the sedative effect can be distinguished from the analgesic effect. Analgesic treatment indicates the coexistence of an inflammatory pain state (early phase) sensitive to NSAIDs and a non-inflammatory pain state (late phase) resistant to NSAID treatment. Discussion: This study indicates that unlike standard measures of analgesia such as alteration in thermal or mechanical sensitivity, measurement of spontaneous activity is a validated method for measuring the effects of analgesics in rats with OA knee joints. Moreover, the animals require no habituation, and thus behavioral observation subjectivity is eliminated.
机译:简介:骨关节炎(OA)患者的疼痛可以出现在休息时,但通常随着受影响关节的运动而加重。但是,在动物模型中有用的运动诱发疼痛评估方法受到限制。在这里,我们描述了OA大鼠模型中的自发活动减少,这是一种客观且可量化的行为痛,可以预测单剂给药后多种药物的镇痛作用。方法:通过关节腔内注射单碘乙酸盐(MIA)诱导雄性Sprague-Dawley(SD)大鼠OA,并通过组织学和放射学分析评估关节变性。使用标准的基于光电管的监测系统在黑暗中测量非习惯性大鼠的自发活动。为了研究OA模型预测镇痛活性的潜力,使用了许多非甾体抗炎药(NSAIDs)和非典型镇痛药。结果:在实验过程中,分别服用1. mg和0.3 mg后,两相的总距离和后方数量均减少。每毫克MIA。我们发现,后方的数量对MIA诱导的OA最敏感,并且活动性下降的百分比最大。 MIA注射后28天,观察到关节变性,骨矿物质密度降低,关节软骨丢失。适当剂量的阿片类药物逆转了MIA引起的后背数量减少,表明这种垂直自发活动的减少反映了疼痛相关行为。由于大剂量的阿片类药物会降低自发活性,因此镇静作用与镇痛作用可以区分开。镇痛药表明对NSAID敏感的炎性疼痛状态(早期)和对NSAID治疗有抵抗力的非炎性疼痛状态(晚期)并存。讨论:这项研究表明,与标准镇痛措施(例如热或机械敏感性改变)不同,自发活动的测量是一种有效的方法,可以测量OA膝关节大鼠的镇痛效果。此外,动物不需要习惯,因此消除了行为观察的主观性。

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