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Antinociceptive effects of buprenorphine in zebrafish larvae: An alternative for rodent models to study pain and nociception?

机译:丁丙诺啡对斑马鱼幼虫的镇痛作用:啮齿动物模型研究疼痛和伤害感受的替代方法吗?

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The underlying processes of nociception and pain are, despite the rodent models available, still not fully understood. One of the drawbacks of rodent model systems is the difficulty to screen compound libraries for their influence on nociception, thus slowing down the discovery of novel analgesics for clinical use. Rodent behavioural tasks have been previously adapted for larval zebrafish in our group and in the current manuscript we investigated the possibilities of zebrafish larvae as an additional model system to study nociception and pain and their underlying mechanisms. Zebrafish larvae were exposed to different concentrations of diluted acetic acid, a chemical noxious stimulus, and we measured nociceptive-specific behaviours. Cyclooxygenase-2 (cox-2), a gene known to be involved in nociception, was used as a marker for the activation of nociceptive pathways. Upon exposure to diluted acetic acid, five-day old larval zebrafish showed a concentration dependent increase in locomotor activity. This increase in locomotor activity was accompanied by a stimulus dependent increase in cox-2 mRNA expression, demonstrating that nociceptive pathways were indeed activated. Pre-treatment of the larvae with 0.1 mu g/ml buprenorphine before exposure to the noxious stimulus, prevented the behavioural changes induced by the diluted acid. Further, the antinociceptive properties of buprenorphine could be reversed by co-treatment with the p-receptor antagonist naloxone. In conclusion, our results demonstrate that larval zebrafish as young as five days, show behavioural responses upon exposure to a noxious stimulus. The magnitude of the responses is dependent on the intensity of the stimulus applied and activation of nociceptive pathways was confirmed by altered cox-2 mRNA expression. The analgesic buprenorphine has similar antinociceptive properties in this model as in higher vertebrates and mammals and is able to prevent the behavioural responses induced by the noxious stimulus. We therefore propose zebrafish larvae as a novel model system in nociception and pain related research
机译:尽管有可用的啮齿动物模型,但伤害和疼痛的潜在过程仍未完全了解。啮齿动物模型系统的缺点之一是难以筛选化合物库对伤害感受的影响,从而减慢了用于临床的新型镇痛药的发现。啮齿类动物的行为任务以前已经适应了我们小组中的幼虫斑马鱼,在本手稿中,我们调查了斑马鱼幼虫作为研究伤害感受和疼痛及其潜在机制的附加模型系统的可能性。斑马鱼的幼虫暴露于不同浓度的稀乙酸中,这是一种化学有害刺激物,我们测量了伤害特异性行为。环氧合酶2(cox-2),一种已知与伤害感受有关的基因,被用作伤害感受途径激活的标记。暴露于稀乙酸中后,五天大的幼体斑马鱼表现出运动活动的浓度依赖性增加。运动活性的这种增加伴随着cox-2 mRNA表达的刺激依赖性增加,表明伤害性途径确实被激活。在暴露于有害刺激物之前,先用0.1μg / ml丁丙诺啡对幼虫进行预处理,以防止稀释酸引起的行为变化。此外,丁丙诺啡的抗伤害感受特性可以通过与p受体拮抗剂纳洛酮共同治疗而逆转。总之,我们的结果表明,幼小的斑马鱼只有五天幼龄,在暴露于有害刺激下会表现出行为反应。响应的大小取决于所施加刺激的强度,并且通过改变cox-2 mRNA的表达证实了伤害感受途径的激活。在该模型中,止痛丁丙诺啡具有与高级脊椎动物和哺乳动物类似的镇痛特性,并且能够防止有害刺激引起的行为反应。因此,我们提出斑马鱼幼虫作为一种新的模型系统,用于伤害感受和疼痛相关研究

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