1 maps. Patlak plots were constructed using time course of blood and tissue T 1 changes induced by Gd for estimating K i . Among the nine rats, 14 sizable regions of AIB uptake were found; 13 were also identified by ISODATA segmentation. Although the 13 MRI-ROIs spatially approximated those of AIB uptake, the segmentation sometimes missed small areas of lesser AIB uptake that did not extend through more than 60% of the 2.0-mm-thick slice. Mean K i 's of AIB were highly correlated with those of Gd-DTPA across the 13 regions; the group means (؎SD) were similar for the two tracers (7.1 ؎ 3.3 ؋ 10 ؊3 and 6.8 ؎ 3.5 ؋ 10 ؊3 ml.g ؊1 ⅐ min ؊1 , respectively). The capillary endothelium plus the basal lamina, the pericytes enclosed within the basal lamina, and the surrounding cuff of astrocytic foot processes form the blood-brain barrier (BBB) complex. This barrier greatly restricts the passive movement of water and most water-soluble materials across the BBB and protects brain cells from exposure to neurotoxic or adversely neuroactive blood-borne agents. It is likely that its failure to do so contributes to or drives tissue damage in central nervous system disorders such as cerebral edema and intraparenchymal hemorrhage.The barrier function has often been evaluated in animal models of brain injury or disease. Such assessments are usually made with indicators that very slowly penetrate the normal BBB (e.g., radiolabeled sucrose) or are essentially impermeable (e.g., Evans blue-tagged albumin). When done quantitatively, the blood and tissue data yield a blood-to-brain influx rate constant (K i ) that is a function of local cerebral blood flow (CBF) and the permeabilitysurface area (PS) product of the local capillary network to the indicator.In a recent MRI study (1), a method of quantitating gadolinium-diethylenetriaminepentaacetic acid (Gd-DTPA) distribution in a rat model of transient focal ischemia and calculating local K i numbers via Patlak plots (2) was presented. As an initial check on the accuracy and reliability of these results, the K i of Gd-DTPA in each area of BBB opening was compared to that of 14 C-sucrose assayed by QAR at the same locus about 30 min later. In support of this approach of determining Gd-DTPA influx, a good correlation was found between the K i 's of Gd-DTPA and sucrose, two extracellular markers of comparable size and blood-brain distribution properties.The current study extends that of Ewing et al. (1) and, in the main, examines the power of the Gd-DTPA-MRI technique to spatially resolve BBB opening. As in the work by Ewing et al., the K i of i.v. administered Gd-DTPA (MW 551 Da) was assessed in a group of transiently ischemic rats by MRI. In contrast, 14 C-␣-aminoisobutyric acid (AIB; MW 102 Da) was i.v. injected approximately 45 min after administration of Gd-DTPA, and its K i was assessed by QAR. The QAR parts of the present study and that of Ewing et al., therefore, differ with respect to the radiotracer used, their mode of administration (bolus injection of AIB vs. continuous infusion ...