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反复鞘内注射吗啡的大鼠脊髓蛋白表达的蛋白质组学分析

Proteomic analysis of spinal protein expression in rats exposed to repeated intrathecal morphine injection.

作者信息

Shui Hao-Ai, Ho Shung-Tai, Wang Jhi-Joung, Wu Chin-Chen, Lin Chih-Huan, Tao Yuan-Xiang, Liaw Wen-Jinn

机构信息

Graduate Institute of Medical Sciences, National Defense Medical Center, Taipei, Taiwan.

出版信息

Proteomics. 2007 Mar;7(5):796-803. doi: 10.1002/pmic.200600699.

Abstract

Repeated administration of morphine for treating severe chronic pain may lead to neuroadaptive changes in the spinal cord that are thought to underlie molecular mechanisms of the development of morphine tolerance and physical dependence. Here, we employed a 2-D gel-based proteomic technique to detect the global changes of the spinal cord protein expression in rats that had developed morphine tolerance. Morphine tolerance at the spinal cord level was induced by repeated intrathecal injections of morphine (20 microg/10 microL) twice daily for 5 days and evaluated by measurements of paw withdrawal latencies and maximal possible analgesic effect at day 5. After behavioral tests, the lumbar enlargement segments of spinal cord were harvested and proteins resolved by 2-DE. We found that eight proteins were significantly up-regulated or down-regulated in spinal cord after morphine tolerance development, including proteins involved in targeting and trafficking of the glutamate receptors and opioid receptors, proteins involved in oxidative stress, and cytoskeletal proteins, some of which were confirmed by Western blot analysis. Morphine-induced expressional changes of these proteins in the spinal cord might be involved in the central mechanisms that underlie the development of morphine tolerance. It is very likely that these identified proteins may serve as potential molecular targets for prevention of the development of morphine tolerance and physical dependence.

摘要

反复给予吗啡治疗严重慢性疼痛可能会导致脊髓发生神经适应性变化,这些变化被认为是吗啡耐受性和身体依赖性形成的分子机制基础。在此,我们采用基于二维凝胶的蛋白质组学技术来检测已产生吗啡耐受性的大鼠脊髓蛋白质表达的整体变化。通过每天两次鞘内注射吗啡(20微克/10微升),持续5天来诱导脊髓水平的吗啡耐受性,并在第5天通过测量爪部缩腿潜伏期和最大可能镇痛效果进行评估。行为测试后,采集脊髓腰膨大节段,通过二维电泳分离蛋白质。我们发现,在产生吗啡耐受性后,脊髓中有8种蛋白质显著上调或下调,包括参与谷氨酸受体和阿片受体靶向与转运的蛋白质、参与氧化应激的蛋白质以及细胞骨架蛋白,其中一些通过蛋白质印迹分析得到了证实。吗啡诱导的这些蛋白质在脊髓中的表达变化可能参与了吗啡耐受性形成的中枢机制。很有可能这些已鉴定的蛋白质可作为预防吗啡耐受性和身体依赖性形成的潜在分子靶点。

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