Onodera K
Department of Pharmacology, Tohoku University School of Dentistry, Sendai, Japan.
Physiol Behav. 1987;41(1):71-8. doi: 10.1016/0031-9384(87)90132-6.
The effects of thiamine deficiency on pharmacological and pharmacokinetic activities of chlorpheniramine were investigated in rats. Chlorpheniramine (5-10 mg/kg) showed a dose-dependent suppressive effect on muricide induced by thiamine deficiency. The ED50 value for muricidal suppression at 1 hr was approximately 7.1 mg/kg (95% confidence limits, 5.4-9.3 mg/kg) after oral administration. Using a high-performance liquid chromatographic (HPLC) method, chlorpheniramine was detectable at 10 min in the blood and brain of rats. The present pharmacokinetic data suggest that chlorpheniramine can easily pass through the blood-brain barrier (B.B.B.) and enter the brain. It is stored therein and is later slowly released and excreted. In thiamine deficient rats, chlorpheniramine entered the brain in much higher concentrations than in normal and pair-fed rats, and significantly higher levels were maintained for a period of 1.5 hr. These results suggest that thiamine deficiency affects pharmacological and pharmacokinetic activities in rats, and support the view that there is a malfunction of the B.B.B. in thiamine deficient rats. These factors should be taken into consideration in clinical usage and dosage.
研究了硫胺素缺乏对大鼠氯苯那敏药理和药代动力学活性的影响。氯苯那敏(5 - 10毫克/千克)对硫胺素缺乏诱导的杀鼠行为呈现剂量依赖性抑制作用。口服给药后1小时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)。采用高效液相色谱(HPLC)法,在大鼠血液和脑中10分钟时可检测到氯苯那敏。目前的药代动力学数据表明,氯苯那敏能够轻易穿过血脑屏障(BBB)并进入脑内。它在脑内储存,随后缓慢释放并排泄。在硫胺素缺乏的大鼠中,氯苯那敏进入脑内的浓度远高于正常和配对喂养的大鼠,并且在1.5小时内维持显著更高的水平。这些结果表明硫胺素缺乏会影响大鼠的药理和药代动力学活性,并支持硫胺素缺乏的大鼠血脑屏障存在功能障碍的观点。在临床使用和剂量设定时应考虑这些因素。