The aim of this study was to validate continuous arterial spin labeling (CASL) as a quantitative imaging modality for pharmacological MRI (phMRI) based on local cerebral blood perfusion. Specifically, the capability of CASL to assess brain-activity signatures of pharmacological interventions in animal models was evaluated with respect to drug discovery in diseases of the central nervous system (CNS). Perfusion as a surrogate for neuronal activity was measured in various brain areas of the rat. The validation approach was threefold. First, perfusion was shown to reliably reflect differential effects of anesthesia on striatal activation. Different baseline levels and different temporal response profiles after amphetamine challenges under isoflurane, propofol, ketamine, and alpha-chloralose anesthesia were consistent with known properties of these anesthetic. Second, remarkable consistency of multi-area baseline perfusion patterns between independent groups of animals con firmed the notion that CASL is highly reproducible and thus particularly suitable for long-term longitudinal studies. Third administration of the well-characterized psychotomimetic compounds amphetamine and phencyclidine (PCP) elicited dose-dependent activation patterns that were related to the drugs' particular interactions with the dopaminergic and glutamatergic systems, respectively. In conclusion, perfusion-base phMRI is a robust, reliable and valid quantitative technique suitable for evaluating brain-activation patterns in animal mod els of IONS diseases. Magn Reson Med 61:1451-1458, 2009 (C) 2009 Wiley-Liss, Inc.