A noninvasive technique for measuring local cerebral blood flow (LCBF) by xenon-enhanced x-ray transmission computed tomography (Xe/Ct) has been developed and a broad range of clinical applications reported. The Xe/Ct CBF method has been integrated into current CT technology and it has the potential to become widely available at a relatively low cost compared to other tomographic CBF techniques. Xe/Ct CBF also provides direct anatomic reference of CBF information to the baseline CT, relatively high resolution, and the unique ability to record low flow values that predict the nonviability of tissue. Although preliminary reports suggest that Xe/Ct CBF information could be of clinical utility in the early diagnosis and management of emergent clinical problems, especially stroke or head trauma, the observation that the inhalation of xenon can elevate CBF precludes its use in these areas. The concern has been expressed that a xenon-induced rise of CBF could elevate the intracranial pressure in a patient with a mass lesion or cause a reduction of needed blood flow in an ischemic area. An unpredictable elevation of CBF due to xenon would also disqualify it as a useful tracer of CBF. A series of studies is proposed to systematically examine the extent and time course of CBF activation that accompanies xenon inhalation. Dynamic flow changes, as well as global and local flow alterations, will be examined, as will the intracranial pressure, electroencephalogram, and the metabolic rates of oxygen and glucose. The interaction of the changes in these physiological measurements to variations in the pCO2 and/or the pO2 will also be detafled, as will the dose response to a range of xenon concentrations. Models of an intracranial mass lesion and a focal ischemic injury will be created, and the physiological effect of xenon inhalation examined. Until the proposed questions are fully answered, the potential application of Xe/CT CBF in clinical medicine will remain limited.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
2R01HL027208-07A1
Application #
3338997
Study Section
(SSS)
Project Start
1984-09-01
Project End
1992-03-31
Budget Start
1989-04-01
Budget End
1990-03-31
Support Year
7
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Pittsburgh
Department
Type
Schools of Medicine
DUNS #
053785812
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Nemoto, E M; Klementavicius, R; Melick, J A et al. (1996) Suppression of cerebral metabolic rate for oxygen (CMRO2) by mild hypothermia compared with thiopental. J Neurosurg Anesthesiol 8:52-9
Nemoto, E M; Klementavicius, R; Melick, J A et al. (1996) Norepinephrine activation of basal cerebral metabolic rate for oxygen (CMRO2) during hypothermia in rats. Anesth Analg 83:1262-7
Webster, M W; Makaroun, M S; Steed, D L et al. (1995) Compromised cerebral blood flow reactivity is a predictor of stroke in patients with symptomatic carotid artery occlusive disease. J Vasc Surg 21:338-44;discussion 344-5
Whitehurst, S L; Nemoto, E M; Yao, L et al. (1994) MAC of xenon and halothane in rhesus monkeys. J Neurosurg Anesthesiol 6:275-9
Chavko, M; Nemoto, E M; Melick, J A (1993) Regional lipid composition in the rat brain. Mol Chem Neuropathol 18:123-31
Yonas, H; Smith, H A; Durham, S R et al. (1993) Increased stroke risk predicted by compromised cerebral blood flow reactivity. J Neurosurg 79:483-9
Darby, J M; Nemoto, E M; Yonas, H et al. (1993) Local cerebral blood flow measured by xenon-enhanced CT during cryogenic brain edema and intracranial hypertension in monkeys. J Cereb Blood Flow Metab 13:763-72
Yao, L P; Bandres, J; Nemoto, E M et al. (1992) Effect of 33% xenon inhalation on whole-brain blood flow and metabolism in awake and fentanyl-anesthetized monkeys. Stroke 23:69-74
Nemoto, E M; Yao, L; Yonas, H et al. (1992) Active and basal whole brain blood flow, oxygen and glucose metabolism in monkeys. Adv Exp Med Biol 317:695-9
Marks, E C; Yonas, H; Sanders, M H et al. (1992) Physiologic implications of adding small amounts of carbon dioxide to the gas mixture during inhalation of xenon. Neuroradiology 34:297-300

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