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慢性抗精神病药物治疗对大鼠抗精神病药物结合试验的残留效应。

The residual effect of chronic neuroleptic treatment on the neuroleptic binding assay in rats.

作者信息

Wan C W, Peck E J, Ho B T, Schoolar J C

出版信息

Life Sci. 1983 Mar 14;32(11):1255-62. doi: 10.1016/0024-3205(83)90195-9.

Abstract

Chronic chlorpromazine administration to rats (25 mg/Kg/day) for 30 days followed by a washout period of 10 days resulted in an increase in both the measured maximum number of binding sites, Bmax, and the apparent dissociation constant, Kd, for the binding of 3H-spiroperidol to neural membranes of the brain. When membrane suspensions were progressively diluted before the binding assay, it was found that the apparent Bmax did not change with dilution, remaining higher in membranes of chlorpromazine-treated rats than in controls. The apparent increase in Kd, on the other hand, was found to be an artifact of the assay. Thus extrapolation of the measured or apparent Kd value to infinite dilution resulted in identical value for Kd regardless of the treatment.

摘要

给大鼠连续30天每日注射氯丙嗪(25毫克/千克),随后经过10天的洗脱期,结果显示,对于3H-螺哌啶醇与大鼠脑神经元膜的结合,所测得的最大结合位点数(Bmax)和表观解离常数(Kd)均增加。在结合试验前逐步稀释膜悬液时,发现表观Bmax并不随稀释而变化,氯丙嗪处理组大鼠膜中的表观Bmax仍高于对照组。另一方面,表观Kd的增加被发现是该试验的假象。因此,无论处理如何,将测得的或表观的Kd值外推至无限稀释时,Kd值均相同。

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