吗啡对小鼠纹状体细胞外尿嘧啶释放的影响及机制初探 |
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引用本文: | 王天琳,吴春福.吗啡对小鼠纹状体细胞外尿嘧啶释放的影响及机制初探[J].中国药物应用与监测,2011,8(1):17-21. |
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作者姓名: | 王天琳 吴春福 |
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作者单位: | 1. 解放军总医院药品保障中心,北京,100853 2. 沈阳药科大学神经药理实验室,辽宁,沈阳,110016 |
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基金项目: | 辽宁省教育厅高等学校优秀人才项目计划(2006R50) |
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摘 要: | 目的:研究吗啡对小鼠纹状体细胞外尿嘧啶释放的影响并探讨相关机制。方法:采用脑内微透析技术结合高效液相紫外检测器检测尿嘧啶含量,紫外分光光度法检测纹状体总RNA含量。结果:与空白对照组相比,吗啡(10,20mg.kg-1,ip)可显著降低小鼠纹状体尿嘧啶含量且呈现剂量依赖性;盐酸纳洛酮(4mg.kg-1,ip)自身对小鼠纹状体尿嘧啶的释放无影响,却可以显著回升尿嘧啶含量至基础水平。吗啡(10,20mg.kg-1,ip)对小鼠纹状体细胞内RNA含量呈下调作用,与对尿嘧啶含量的下调结果一致,呈现剂量依赖性;盐酸纳洛酮(4mg.kg-1,ip)对小鼠纹状体总RNA含量无明显影响但能拮抗吗啡对总RNA含量的下调作用。结论:吗啡引起小鼠纹状体尿嘧啶释放降低的作用可能与μ受体相关且与细胞内总RNA的含量变化存在相关性。
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关 键 词: | 尿嘧啶 吗啡 纳洛酮 总RNA 纹状体 微透析 |
Effect of morphine on brain uracil release in mice striatum and its preliminary mechanisms |
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Authors: | WANG Tian-lin WU Chun-fu |
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Institution: | WANG Tian-lin1,WU Chun-fu2(1.Department of Pharmaceutical Care,PLA General Hospital,Beijing 100853,China,2.Department of Pharmacology,Shenyang Pharmaceutical University,Shenyang 110016,China) |
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Abstract: | Objective:To investigate the effects of morphine on extracellular uracil release in mice striatum and its preliminary mechanisms.Methods:In vivo microdialysis coupled to high performance liquid chromatography(HPLC) was employed to detect the extracellular contents of uracil in mice striatum,and total RNA level was determined by ultraviolet spectrophotometry.Results:Morphine(10,20 mg·kg-1,ip) could decrease uracil level significantly and it was in a dose-dependent manner.Meanwhile,naloxone(4 mg·kg-1,ip),antagonists of μ-opioid receptor,had no effect on uracil release in mice striatum.However,it could increase uracil to the normal level.Morphine(10,20 mg·kg-1,ip) decreased the total RNA level in mice striatum and it was in a dose-dependent manner.Naloxone(4 mg·kg-1,ip) had no effect on total RNA level in mice striatum,but it could antagonise the down-regulation of morphine on RNA level.Conclusion:The decrease of uracil induced by morphine may be related to μ-opioid receptors and total RNA level. |
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Keywords: | Uracil Morphine Naloxone Total RNA Striatum Microdialysis |
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