Pharmacokinetic-pharmacodynamic modeling of the electroencephalogram effects of scopolamine in healthy volunteers

Research output: Contribution to journalResearch articleContributedpeer-review


  • Ulrike Ebert - , TUD Dresden University of Technology (Author)
  • Matthias Grossmann - , TUD Dresden University of Technology (Author)
  • Reinhard Oertel - , Institute of Clinical Pharmacology, TUD Dresden University of Technology (Author)
  • Thomas Gramatté - , TUD Dresden University of Technology, Apogepha Arzneimittel GmbH (Author)
  • Wilhelm Kirch - , TUD Dresden University of Technology (Author)


Scopolamine is a muscarinic receptor antagonist commonly used as a pharmacological model substance based on the 'cholinergic hypothesis' of memory loss in senile dementia of the Alzheimer type. The objective of the study was to relate pharmacodynamic electroencephalogram (EEG) changes and scopolamine serum concentration using pharmacokinetic-pharmacodynamic (PK-PD) modeling techniques. This was a randomized, three-way crossover, open-label study involving 10 healthy non-smoking young male volunteers who received either scopolamine 0.5 mg as an intravenous (IV) infusion over 15 minutes or an intramuscular (IM) injection or a placebo. The pharmacodynamic EEG measure consists of the total power in delta, theta, alpha, and beta bands over frontal, central and occipital brain areas. The values of the pharmacokinetic parameters of scopolamine after IV infusion were clearance (CL) 205 ± 36.6 L/h, volume of distribution (Vd) 363±66.7 L, distribution half-life (t(1/2α)) 2.9 ± 0.67 min, and terminal half-life (t(1/2β)) 105.4±9.94 rain (mean ± SEM). Mean peak serum concentrations (C(max)) were 4.66 and 0.96 ng/ml after IV and IM administration, respectively (p < 0.05). The area under the serum concentration versus time curve (AUC) after IM administration (81.27±11.21 ng/ml/min) was significantly lower compared to the value after IV infusion (157.28±30.86 ng/ml/min) (mean±SEM, p <0.05). Absolute bioavailability of scopolamine after IM injection was 57%±0.08% (mean±SEM). After both IV and IM administration, scopolamine induced a decrease in EEG alpha power (7.50-11.25 Hz) over frontal, central, and occipital brain areas compared to placebo (p < 0.05). The individual concentration-EEG effect relationships determined after IV infusion of scopolamine were successfully characterized by a sigmoidal E(max) model. The averaged values of the pharmacodynamic parameters were E0 = 0.58 μV2, E(max) =0.29 μV2, EC50 = 0.60 ng/ml, and y = 1.17. No time delay between serum concentrations and changes in alpha power was observed, indicating a rapid equilibration between serum and effect site. The results provide the first demonstration of a direct correlation between serum concentrations of scopolamine and changes in total power in alpha frequency band in healthy volunteers using PK-PD modeling techniques. As regards the effect on the EEG, 0.5 mg of scopolamine administered IV appears to be a suitable dose. (C) 2001 the American College of Clinical Pharmacology.


Original languageEnglish
Pages (from-to)51-60
Number of pages10
JournalJournal of clinical pharmacology
Issue number1
Publication statusPublished - 2001

External IDs

PubMed 11144994
ORCID /0000-0003-1526-997X/work/142247260


ASJC Scopus subject areas