Perlstein I, Stepensky D, Sapoznikov D, Hoffman A
Department of Pharmaceutics, School of Pharmacy, The Hebrew University of Jerusalem, Israel.
Pharm Res. 2001 Aug;18(8):1220-5. doi: 10.1023/a:1010995414541.
To utilize power spectral analysis (PSA) of heart rate variability (HRV) as a pharmacodynamic (PD) measure of atropine parasympathetic effect, and to model the kinetics of action.
Heart rate data was collected following atropine administration to rats and was analyzed off-line for high frequency peaks by PSA of HRV as a measure of parasympathetic tone. A temporal cumulative approach (TCA) detected transient changes in parasympathetic activity. The pharmacokinetics (PK) was analyzed and linked to both direct and indirect PK-PD models.
TCA enabled a quantitative measure of atropine parasympathetic activity. A simultaneous fit of the indirect PK-PD model to the experimental data of all three atropine doses successfully captured the experimental data.
TCA can be used as a quantitative measure of parasympathetic tone. Our work has established a preclinical model to investigate the kinetics of drug action on the autonomic nervous system.
利用心率变异性(HRV)的功率谱分析(PSA)作为阿托品副交感神经效应的药效学(PD)指标,并对作用动力学进行建模。
给大鼠注射阿托品后收集心率数据,并离线通过HRV的PSA分析高频峰值,作为副交感神经张力的指标。采用时间累积法(TCA)检测副交感神经活动的瞬时变化。分析药代动力学(PK)并将其与直接和间接的PK-PD模型相联系。
TCA能够定量测定阿托品的副交感神经活动。间接PK-PD模型对所有三种阿托品剂量的实验数据进行同时拟合,成功地捕捉到了实验数据。
TCA可作为副交感神经张力的定量指标。我们的工作建立了一个临床前模型,用于研究药物对自主神经系统的作用动力学。