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作 者:朱冠秀[1] 王宇光[1] 马增春[1] 梁乾德[1] 肖成荣[1] 谭洪玲[1] 汤响林[1] 高月[1]
机构地区:[1]军事医学科学院放射与辐射医学研究所,北京100850
出 处:《中药药理与临床》2013年第3期107-111,共5页Pharmacology and Clinics of Chinese Materia Medica
基 金:国家重点基础研究发展计划(No.2011CB505304;No.2012CB518402)资助项目
摘 要:目的:研究中药十八反:北沙参与藜芦配伍对P450同工酶的影响,以阐明二者配伍基于药物代谢酶的层面产生相反作用的机制。方法:采用Cocktail底物探针法结合HPLC同时测定大鼠体内CYP1A2、CYP3A4、CYP2C9及CYP2C19的酶活性。结果:与空白组相比,黎芦组(0.81g生药/kg)、北沙参组(10.8g生药/kg)对大鼠CYP2C9酶具有诱导作用,合用组(11.61g生药/kg)对大鼠CYP1A2、CYP2C9酶具有显著诱导作用;与藜芦组相比,合用组对大鼠CYP3A4酶具有抑制作用,对CYP1A2、CYP2C9酶具有诱导作用;与北沙参组相比,合用组对大鼠CYP3A4酶具有抑制作用,对CYP1A2酶具有诱导作用,对CYP2C9、CYP2C19无明显影响。结论:北沙参与藜芦配伍前后对部分CYP亚型的酶活性影响具有差异,可能会使藜芦中的毒性成分在体内的代谢特征发生改变,使配伍前后毒性具有差异,产生中药间相互作用,但需进一步通过代谢研究并综合分析,以进一步阐明相反作用的机制。Objective:To study the compatible effects of Radix Glehniae and Veratrum nigrum on cytochromeP450 isoenzymes activities in rat livers and elucidate the imcompatible mechanism of traditional Chinese Medicine.Methods: The influence of Radix Glehniae coadministrated with Veratrum nigrum on cytochromeP450 isoforms CYP1A2,CYP3A4,CYP2C9 and CYP2C19 were simultaneous determined by cocktail probe drugs in rats.Results: Compared with the blank control group,Radix Glehniae(0.81g crude drug/kg) and Veratrum nigrum(10.8g crude drug/kg) can induce CYP2C9 activities,combined groups(11.61g crude drug/kg) acan induce CYP1A2 and CYP2C9 activities significantly;Compared with the Veratrum nigrum group,combined can inhibit CYP3A4 activity and induce CYP1A2 and CYP2C9 activity significantly;Compared with the Radix Glehniae group,CYP3A4 activities was significantly inhibited and CYP1A2 activities was significantly induced in combined groups,and had no effects on the activities of CYP2C9 and CYP2C19.Conclusion: These results indicated that compatibilit y of Radix Glehniae and Veratrum nigrum in a prescription have effect on the activity of cytochrome and its subtype enzymes,which may influence the toxic component's metabolism,phamacological effect and the toxicity,resultedin herb-herb interactions based on P450.The possible mechanisms of its incompatible effects need to be further analysised via integrating with metabolic studies.
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