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作 者:夏星[1] 潘颖[1] 欧阳臻[2] 王琚[1] 潘璐琳[1] 朱钦[1] 黄君健[3] 孔令东[1]
机构地区:[1]南京大学生命科学学院医药生物技术国家重点实验室,南京210093 [2]江苏大学药学院,镇江212013 [3]军事医学科学院生物工程研究所,北京100850
出 处:《中国天然药物》2011年第4期293-304,共12页
基 金:supported by the National Nat-ural Science Foundation of China (Nos. 81025025, 81001671 and J0730641);Specialized Research Fund for the Doctoral Program of Higher Education (No. 20070284024);Natural Science Founda-tion of Jiangsu Province (No. BK2010365)~~
摘 要:目的:在抑郁症动物模型上分析姜黄素药代动力学、药效动力学及其效应特征。方法:在强迫游泳 (FST)小鼠上分别单次和重复灌胃给予 2.5, 5 和 10 mg?kg-1姜黄素。分别测定脑区单胺氧化酶 A(MAO-A)活性及动物行为。采用 HPLC方法测定血浆中姜黄素水平。利用兼有滞后时间的二房室模型分析姜黄素药代动力学。结果:口服给予姜黄素,血药浓度峰值分别出现给药 0.75 h (单次)和 2.75-3 h (重复)后,其检测限大约在 6 h (单次)和 14 h (重复)内。毫微克级姜黄素血药浓度状态下,可呈现出 FST 小鼠 MAO-A 的抑制活性及行为的改善作用。姜黄素对 FST 小鼠攀爬、游泳、不动等异常行为的逆转作用分别在口服给药 1-2 h (单次)和 3-4 h (重复) 后达到最大效应,这与其抑制前额叶皮层和海马 MAO-A 活性的时效一致。结论:这些研究结果表明姜黄素可能不直接产生改善抑郁行为作用,其效应也可能不依赖于其血药浓度。AIM:To characterize the pharmacokinetic,pharmacodynamic and efficacy profiles of curcumin in animal model of depression.METHODS:The forced swimming test(FST) in mice was used in this study.The single and repeated(hourly for three times) oral administration of 2.5,5 and 10 mg·kg^-1 curcumin was performed in the FST.Brain monoamine oxidase A(MAO-A) in vitro and in vivo as well as behaviors were determined.The plasma curcumin concentration was analyzed using high performance liquid chromatography(HPLC) method.The pharmacokinetics of curcumin was described by a two-compartment pharmacokinetic model with a lag time in the mouse FST.RESULTS:The peak plasma concentration was observed at 0.75 h(single) and 2.75-3 h(repeated) after oral curcumin administration,and the plasma concentration was around detection limit at 6 h(single) and 14 h(repeated),respectively.Curcumin at nanogram concentrations showed monoamine oxidase A(MAO-A) inhibitory activity and behavioral improvement in the mouse FST.The maximum behavioral effects of climbing,swimming and immobility were achieved at 1-2 h(single) and 3-4 h(repeated),which paralleled that of the maximum MAO-A inhibitory effects in frontal cortex and hippocampus after oral curcumin administration in the mouse FST,respectively.CONCLUSION:These results suggest that curcumin may indirectly produce behavioral improvement,and its antidepressant potency may not be dependent on its plasma concentration.
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