Abstract #4755
            Cerebral Vascular Reactivity Assessment Using the SR-T 1 Method in Normal and MCAO Rat Brain
                      Xiao Wang                     1                    , Xiao-Hong Zhu                     1                    , Afshin 						A Divani                     2                    , and Wei Chen                     1          
            
            1
           
           Center for Magnetic Resonance Research, 
						Department of Radiology, University of Minnesota Medical 
						School, Minneapolis, Minnesota, United States,
           
            2
           
           Neurology, 
						University of Minnesota, Minnesota, United States
          
            
          Cerebral vascular reactivity (CVR) is an important 
						physiologic property of assessing brain arteries 
						response to vasoactive challenge and it is of great 
						value of studying many cerebrovascular diseases, such as 
						arterial stenosis, ischemic stroke and hypertension. CVR 
						could be evaluated by positron emission tomography 
						(PET), single-photon emission computed tomography 
						(SPECT), transcranail Doppler (TCD) ultrasonography as 
						well as magnetic resonance imaging (MRI) approaches, 
						such as blood-oxygen-level dependent (BOLD) response, 
						arterial spin labeling (ASL) based cerebral blood flow 
						(CBF) calculation. In the present study, we demonstrate 
						that the saturation-recover T1 (SR-T1) imaging method is 
						sensitive and reliable to evaluate CVR by comparing it 
						with the CASL based CBF method. Data show that the 
						spatial pattern of CVR images generated with these two 
						techniques is very similar in both normal and MCAO rat 
						brain. Moreover, there is an excellent agreement of 
						percentage CVR change imaged with these two techniques 
						although their absolute scales are different. Therefore, 
						the SR-T1 method provides a simple and reliable way of 
						evaluating CVR in addition to measure parametric tissue 
						property of T1/R1, CBF change and BOLD simultaneously.
         
				
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