Onodera K, Sakurai E, Niwa H
Agents Actions. 1987 Apr;20(3-4):229-32. doi: 10.1007/BF02074677.
Chlorpheniramine (5-10 mg/kg) showed a dose-dependent suppressive effect on muricide induced by thiamine deficiency at 1 hr after oral administration. The ED50 value for muricidal suppression was about 7.1 mg/kg (95% confidence limits, 5.4-9.3 mg/kg). The maximum effect of muricidal suppression lasted for 1-2 hr after oral dosage (10 mg/kg). Chlorpheniramine was detectable at 10 min in the blood and brain of thiamine deficient killer-rats by using a high-performance liquid chromatographic method. Maximum brain and blood levels of chlorpheniramine appeared at 45 and 60 min, respectively. In terms of regional distribution, the highest levels were measured in the limbic system, especially in the hippocampus. Although neither blood nor brain levels of chlorpheniramine reflect its pharmacological activity, it can easily enter the brain and suppress muricide more potently than imipramine.
口服给药1小时后,氯苯那敏(5 - 10毫克/千克)对硫胺素缺乏诱导的杀鼠行为表现出剂量依赖性抑制作用。杀鼠抑制的半数有效剂量(ED50)值约为7.1毫克/千克(95%置信区间,5.4 - 9.3毫克/千克)。口服剂量为10毫克/千克后,杀鼠抑制的最大效应持续1 - 2小时。采用高效液相色谱法在硫胺素缺乏的杀鼠大鼠的血液和大脑中,给药10分钟后可检测到氯苯那敏。氯苯那敏在大脑和血液中的最高浓度分别出现在45分钟和60分钟。就区域分布而言,在边缘系统,尤其是海马体中检测到的浓度最高。虽然氯苯那敏的血液和大脑浓度均不能反映其药理活性,但它能轻易进入大脑,且比丙咪嗪更有效地抑制杀鼠行为。