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N Hasimoto

Publications and source records attributed to N Hasimoto.

2 recordsLinked to original sources

[Imaging of myocardial perfusion and metabolism with positron emission tomography].

Positron emission tomography (PET) has been providing new information in the diagnosis and the pathophysiological assessment of heart diseases. The PET tracers commonly used in Japan are 13N-ammonia, 18F-fluorodeoxyglucose (FDG) for imaging of myocardial perfusion and metabolism, respectively. Measurement of regional myocardial blood flow by 13N-ammonia dynamic PET scan and a compartment model analysis is applied to the functional estimation of coronary stenotic lesions and the detection of perfusion abnormalities in hypertrophic heart diseases, familial hyperchlesterolemia and other diseases with possible microvascular lesions. 18F-FDG is commonly used to differentiate ischemic but viable tissue from myocardial scar in coronary artery disease and also used to detect cardiac tumor and the cardiac involvement in sarcoidosis. In addition to these two tracers, 11C-acetate is now expected to provide the clinical analysis of pathophysiology of heart failure by estimating the efficiency of energy conversion of the heart into external work.

Acetates↗

Experimentally induced cerebral aneurysms in rats: VII. Scanning electron microscope study.

The luminal surfaces of experimentally induced cerebral aneurysms and the branching sites in the circle of Willis in rats were investigated by scanning electron microscopy. Gap formation at the junctions of the endothelial cells was one of the most obvious changes on the endothelial surface of the aneurysms. Many leukocytes were observed adhering to these gaps. Regressive changes of endothelial cells, such as balloonlike protrusions and craterlike depressions, were also found in the aneurysms. At the branching site, where cerebral aneurysms often develop, endothelial cells were disarranged, rounded, and varied in size. A deep groove was also found adjacent to the apex. The role of endothelial cells and leukocytes in the development of cerebral aneurysms is discussed.

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