摘要
目的:观察复康片、肌苷和吗丁啉对大鼠卡马西平(CBZ)血药浓度的影响。方法:SD大鼠随机分为6组,每组16只。正常对照组每d灌胃蒸馏水,其余不做任何处理;余5组以分步逐渐增加灌胃剂量法灌服CBZ90d。复康片低剂量组、高剂量组、肌苷组和吗丁啉组灌服CBZ同时分别灌胃复康片750mg/(kg·d)、1500mg/(kg·d)、肌苷600mg/(kg·d)和吗丁啉15mg/(kg·d),每d1次。各组于灌服CBZ第60d、90d、120d及CBZ停药30d后(150d)眼眶静脉丛采血,用高效液相色谱法检测CBZ血药浓度。结果:正常对照组血清中未检出CBZ。不同时间点复康片组、肌苷组、吗丁啉组及模型组大鼠CBZ血药浓度组间比较,差异均无统计学意义。结论:复康片、肌苷和吗丁啉灌胃对大鼠CBZ血药浓度无明显影响。
Aim: To observe the effect of Fukang tablets, inosine, and motilium on blood carbamazepine(CBZ) concentration in rats. Methods: A total of 96 rats were randomly allocated into 6 groups:normal control group was given distilled water, and the other 5 groups were given CBZ for 90 d,among which,model group was only given CBZ,and low-dose Fukang tablet group,high-dose Fukang tablet group,inosine group,and motilium group were given 750 mg/kg Fukang tablet, 1 500 mg/kg Fukang tablet,60 mg/kg inosine,and 15 mg/kg motilium per day by gavage. On the 60th d,90th d, 120th d,and 150th d,blood samples were prepared for determining the blood CBZ concentration using HPLC. Results: CBZ could not be detected in the normal control group. There were no significant differences in the blood CBZ concentration among other 5 groups at each time point. Conclusion: Fukang tablet,inosine,and motilium have no effects on the blood CBZ concentration in rats.
出处
《郑州大学学报(医学版)》
CAS
北大核心
2005年第6期1016-1018,共3页
Journal of Zhengzhou University(Medical Sciences)
基金
河南省科技攻关基金资助项目991170620
河南省教育科研基金资助项目1999360018
关键词
卡马西平
复康片
肌苷
吗丁啉
血药浓度
大鼠
carbamazepine
Fukang tablet
inosine
motilium
blood drug concentration
rat