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硝苯地平对大鼠巴比妥或地西泮身体依赖性的影响。

Effects of nifedipine on physical dependence on barbital or diazepam in rats.

作者信息

Suzuki T, Mizoguchi H, Motegi H, Awano H, Misawa M

机构信息

Department of Pharmacology, School of Pharmacy, Hoshi University, Tokyo, Japan.

出版信息

J Toxicol Sci. 1995 Sep;20(4):415-25. doi: 10.2131/jts.20.4_415.

Abstract

The effects of nifedipine on the development of physical dependence on barbital and diazepam in rats were examined using the drug-admixed food method. Rats were chronically treated with either barbital- or barbital in combination with nifedipine-admixed food for 28 days, and with either diazepam- or diazepam in combination with nifedipine-admixed food for 26 days, on schedules of gradually increasing doses of barbital or diazepam. Withdrawal was conducted by substituting normal food for drug-admixed food on the last day of the treatment. Co-administration of nifedipine with barbital potentiated weight loss and withdrawal scores after the termination of barbital treatment. However, the withdrawal signs after the termination of diazepam treatment were not affected by co-administration of nifedipine with diazepam. These results suggest that nifedipine potentiates the development of physical dependence on barbital but not diazepam. It is known that co-administration of dihydropyridine derivative nitrendipine suppresses the development of physical dependence on ethanol. Basing on the differences in sensitivity of central depressants, barbiturates, benzodiazepines and ethanol, to three types of voltage-dependent Ca2+ channels, such as L-, N- and T-types studied so far, the development of physical dependence on central depressants may be modified differently by L-type Ca2+ channel blockers, corresponding to respective depressants.

摘要

采用药物混合食物法研究了硝苯地平对大鼠巴比妥和地西泮身体依赖性发展的影响。大鼠分别用含巴比妥或含巴比妥与硝苯地平混合的食物进行慢性处理28天,用含地西泮或含地西泮与硝苯地平混合的食物进行慢性处理26天,巴比妥或地西泮的剂量逐渐增加。在处理的最后一天,用正常食物替代含药物的食物进行撤药。在巴比妥处理终止后,硝苯地平与巴比妥共同给药增强了体重减轻和撤药评分。然而,地西泮处理终止后的撤药症状不受硝苯地平与地西泮共同给药的影响。这些结果表明,硝苯地平增强了对巴比妥的身体依赖性发展,但对苯二氮卓没有影响。已知二氢吡啶衍生物尼群地平共同给药可抑制对乙醇的身体依赖性发展。基于中枢抑制剂、巴比妥类、苯二氮卓类和乙醇对三种类型电压依赖性Ca2+通道(如迄今为止研究的L型、N型和T型)的敏感性差异,L型Ca2+通道阻滞剂可能会根据各自的抑制剂对中枢抑制剂身体依赖性的发展产生不同的影响。

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