A study paradigm allowing comparison of multiple high‐resolution rCBV‐maps for the examination of drug effects

Owing to the neuro‐vascular coupling, measurement of changes in regional cerebral blood flow and blood volume (rCBV) can be used as surrogates reflecting the effects of central nervous system active drugs on neural transmission. As most such drugs are administered orally or intramuscularly and, in many cases, beneficial effects due to drug treatment can be observed only after chronic administration for days or weeks, the evaluation of drug efficacy requires the development of acquisition and analysis tools that allow for comparison of imaging data sets obtained in multiple sessions and for multiple subjects. In the present study, high‐resolution susceptibility contrast MR perfusion imaging using a super‐paramagnetic contrast agent (CA) was applied to study the effect of a single oral administration of the acetylcholine‐esterase inhibitor rivastigmine (Exelon®) on rCBV in rats. rCBV maps were calculated from two T2‐weighted three‐dimensional fast‐spin‐echo scans recorded before and after the injection of the CA, respectively. All MRI data sets were mapped to a reference data set obtained from a normal male Sprague–Dawley rat using an automated co‐registration procedure prior to the analysis for drug effects. Rivastigmine was orally administered at doses of 2, 4 or 8 mg/kg 1 h prior to the rCBV measurement. Rivastigmine increased rCBV in several brain areas including cortex, caudate putamen and hippocampus. The observed effects were dose‐dependent and the changes reached the order of 5–12% as compared with baseline levels. Vehicle‐treated animals showed no significant alterations of blood volume, demonstrating the reproducibility and stability of rCBV measurements. Copyright © 2005 John Wiley & Sons, Ltd.

[1]  T. Reese,et al.  Regional brain activation by bicuculline visualized by functional magnetic resonance imaging. Time‐resolved assessment of bicuculline‐induced changes in local cerebral blood volume using an intravascular contrast agent , 1995, NMR in biomedicine.

[2]  J. Mazziotta,et al.  MRI‐PET Registration with Automated Algorithm , 1993, Journal of computer assisted tomography.

[3]  Karl J. Friston,et al.  The Relationship between Global and Local Changes in PET Scans , 1990, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[4]  J. Detre,et al.  Assessment of cerebral blood flow in Alzheimer's disease by spin‐labeled magnetic resonance imaging , 2000, Annals of neurology.

[5]  R. Buxton,et al.  A Model for the Coupling between Cerebral Blood Flow and Oxygen Metabolism during Neural Stimulation , 1997, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[6]  R. Dykes,et al.  Mechanisms controlling neuronal plasticity in somatosensory cortex. , 1997, Canadian journal of physiology and pharmacology.

[7]  Mark Preece,et al.  Detection of pharmacologically mediated changes in cerebral activity by functional magnetic resonance imaging: the effects of sulpiride in the brain of the anaesthetised rat , 2001, Brain Research.

[8]  Markus Rudin,et al.  Compromised Hemodynamic Response in Amyloid Precursor Protein Transgenic Mice , 2002, The Journal of Neuroscience.

[9]  Klaus Scheffler,et al.  Titration of the BOLD effect: Separation and quantitation of blood volume and oxygenation changes in the human cerebral cortex during neuronal activation and ferumoxide infusion , 1999, Magnetic resonance in medicine.

[10]  A. Enz,et al.  Pharmacologic and Clinicopharmacologic Properties of SDZ ENA 713, a Centrally Selective Acetylcholinesterase Inhibitor , 1991, Annals of the New York Academy of Sciences.

[11]  Karl J. Friston,et al.  Statistical parametric maps in functional imaging: A general linear approach , 1994 .

[12]  B R Rosen,et al.  Detection of dopaminergic neurotransmitter activity using pharmacologic MRI: Correlation with PET, microdialysis, and behavioral data , 1997, Magnetic resonance in medicine.

[13]  B. Rosen,et al.  Regional sensitivity and coupling of BOLD and CBV changes during stimulation of rat brain , 2001, Magnetic resonance in medicine.

[14]  J C Gore,et al.  Physiological basis for BOLD MR signal changes due to neuronal stimulation: Separation of blood volume and magnetic susceptibility effects , 1998, Magnetic resonance in medicine.

[15]  M. Rausch,et al.  Bicuculline‐induced brain activation in mice detected by functional magnetic resonance imaging , 2001, Magnetic resonance in medicine.

[16]  P. Luiten,et al.  Cerebral microvascular pathology in aging and Alzheimer's disease , 2001, Progress in Neurobiology.

[17]  M. D’Esposito,et al.  The Inferential Impact of Global Signal Covariates in Functional Neuroimaging Analyses , 1998, NeuroImage.

[18]  J. A. Dani,et al.  Overview of nicotinic receptors and their roles in the central nervous system , 2001, Biological Psychiatry.

[19]  B. Rosen,et al.  Dynamic functional imaging of relative cerebral blood volume during rat forepaw stimulation , 1998, Magnetic resonance in medicine.

[20]  F. Aspestrand Demonstration of thoracic and abdominal fistulas by computed tomography. , 1980, Journal of computer assisted tomography.