Garver D L, Davis J M, Dekirmenjian H, Jones F D, Casper R, Haraszti J
Arch Gen Psychiatry. 1976 Jul;33(7):862-6. doi: 10.1001/archpsyc.1976.01770070092011.
Pharmacokinetics of the phenothiazine, butaperazine, were studied in relationship to acute dystonic reactions. Dystonias appeared on falling drug concentrations, more than one half-life after plasma and red blood cell (RBC) peak butaperazine concentrations. Red blood cell butaperazine kinetics differentiated better than did plasma butaperazine levels those subjects in whom dystonias would develop from those in whom they did not. We conclude that RBC phenothiazine levels may more clearly reflect drug concentration at critical brain sites than do simple plasma drug levels. Furthermore, dystonic reactions may be the result of differential sensitivity of two or more receptor systems to receptor blockade by antischizophrenic agents.
对吩噻嗪类药物丁酰拉嗪的药代动力学与急性肌张力障碍反应的关系进行了研究。肌张力障碍出现在药物浓度下降时,此时血浆和红细胞(RBC)丁酰拉嗪浓度已超过峰值且超过了一个半衰期。红细胞丁酰拉嗪动力学比血浆丁酰拉嗪水平能更好地区分哪些受试者会出现肌张力障碍,哪些不会。我们得出结论,红细胞吩噻嗪水平可能比单纯的血浆药物水平更能清晰地反映关键脑区的药物浓度。此外,肌张力障碍反应可能是两个或更多受体系统对抗精神分裂症药物受体阻断的敏感性差异所致。