Original Article

Journal of Cerebral Blood Flow & Metabolism (2006) 26, 274–282. doi:10.1038/sj.jcbfm.9600185; published online 20 July 2005

Regional variation of cerebral blood flow and arterial transit time in the normal and hypoperfused rat brain measured using continuous arterial spin labeling MRI

This work was supported by the Wellcome Trust.

David L Thomas1,2, Mark F Lythgoe1, Louise van der Weerd1, Roger J Ordidge2 and David G Gadian1

  1. 1RCS Unit of Biophysics, Institute of Child Health, University College London, London, UK
  2. 2Wellcome Trust High Field MR Research Laboratory, Department of Medical Physics and Bioengineering, University College London, London, UK

Correspondence: Dr D Thomas, Wellcome Trust High Field MR Research Laboratory, Department of Medical Physics and Bioengineering, University College London, 12 Queen Square, London WC1N 3AR, UK. E-mail: thomas@medphys.ucl.ac.uk

Received 15 April 2005; Revised 24 May 2005; Accepted 16 June 2005; Published online 20 July 2005.

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Abstract

Continuous arterial spin labeling (CASL) is a noninvasive magnetic resonance (MR) method for measuring cerebral perfusion. In its most widely used form, CASL incorporates a postlabeling delay to minimize the sensitivity of the technique to transit time effects, which otherwise corrupt cerebral blood flow (CBF) quantification. For this delay to work effectively, it must be longer than the longest transit time present in the system. In this work, CASL measurements were made in four coronal slices in the rat brain using a range of postlabeling delays. By doing this, direct estimation of both CBF and arterial transit time (deltaa) was possible. These measurements were performed in the normal brain and during hypoperfusion induced by occlusion of the common carotid arteries. It was found that, in the normal rat brain, significant regional variation exists for both CBF and deltaa. Mean values of CBF and deltaa in the selected gray matter regions of interest were 233 mL/100 g min and 266 ms, respectively, with the latter ranging from 100 to 500 ms. Therefore, use of a 500-ms postlabeling delay is suitable for any location in the normal rat brain. After common carotid artery occlusion, CBF decreased and deltaa increased by regionally dependent amounts. In the sensory cortex, deltaa increased to a mean value of 740 ms, significantly greater than 500 ms. These results highlight the importance of either (a) determining deltaa as part of the CASL measurement or (b) knowing the approximate range of values deltaa is likely to take for a given application, so that the parameters of the CASL sequence can be chosen appropriately.

Keywords:

arterial spin labeling, arterial transit time, cerebral hypoperfusion, magnetic resonance imaging, perfusion quantification, rat brain

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