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首页> 外文期刊>Pain. >Anti-hyperalgesic activity of the cox-2 inhibitor lumiracoxib in a model of bone cancer pain in the rat.
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Anti-hyperalgesic activity of the cox-2 inhibitor lumiracoxib in a model of bone cancer pain in the rat.

机译:Cox-2抑制剂lumiracoxib在大鼠骨癌疼痛模型中的抗痛觉过敏活性。

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摘要

Chronic pain resulting from metastatic bone cancer remains poorly understood and resistant to treatment. Here we have examined the effect of the novel COX-2 enzyme inhibitor lumiracoxib in a model of bone cancer pain in the rat. Lumiracoxib was administered orally twice daily from day 10 to day 20 after injection of MRMT-1 tumour cells into one tibia. Mechanical hyperalgesia, measured as the reduction in weight-bearing of the ipsilateral limb, and the development of static and dynamic allodynia were significantly inhibited by repeated lumaricoxib administration. A similar reduction in hyperalgesia and allodynia was noted after twice daily administration of another COX-2 inhibitor, valdecoxib, whilst a single acute administration of either drug on day 20, produced no anti-nociceptive activity. Bone mineral density measurements, radiological scores and histological analysis showed that chronic lumaricoxib treatment also significantly attenuated bone destruction induced by tumour cell injection. These data indicate that lumiracoxib and other COX-2 inhibitors have potential therapeutic benefit in the treatment of bone cancer pain.
机译:由转移性骨癌引起的慢性疼痛仍知之甚少,并且对治疗没有抵抗力。在这里,我们检查了新型COX-2酶抑制剂lumiracoxib在大鼠骨癌疼痛模型中的作用。在将MRMT-1肿瘤细胞注入一个胫骨后,从第10天到第20天,每天口服两次Lumiracoxib。机械性痛觉过敏(以同侧肢体负重的减少来衡量)以及静态和动态异常性疼痛的发生,可以通过反复使用lumaricoxib来明显抑制。每天两次服用另一种COX-2抑制剂valdecoxib后,注意到痛觉过敏和异常性疼痛有类似的减轻,而在第20天一次急性给药两种药物均未产生抗伤害感受活性。骨矿物质密度测量,放射学评分和组织学分析表明,慢性路莫昔布治疗也显着减轻了肿瘤细胞注射引起的骨破坏。这些数据表明,lumiracoxib和其他COX-2抑制剂在骨癌疼痛的治疗中具有潜在的治疗益处。

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