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Biomedical subjects

T Tsujii

Publications and source records attributed to T Tsujii.

At least 163 records · Page 9Linked to original sources

Macromolecular charge and cellular surface charge in adhesion, ingestion, and blood vessel leakage.

To get reliable information about the role of charged groups of tissue components on the integrity of blood circulation, the staining and perfusion experiments of rat organs with cationic (cacodylate iron colloid) and anionic iron colloid (chondroitin iron colloid) particles were carried out. These cationic and anionic iron colloid particles are stable in a wide range of pH's. Dissociation curves of several tissue components at varied pH levels were observed for the analysis of the results obtained by histochemical observations and perfusion experiments. The results indicated that all the intra- and extracellular spaces of living tissues are surrounded by the ionized anionic groups. No ionized cationic groups were found except on the macrophage surface. The cationic iron colloid particles perfused into organs through vessels adhered to the endothelial cell surface inducing the swelling of the cells. The cationic particles invaded into surrounding tissues passing through the damaged endothelial layer, but plasma protein leakage did not occur being prevented by the newly formed fibrin-fibrinogen lining. The anionic iron colloid particles introduced into vessels did not adhere to blood vessel walls but were taken by reticuloendothelial cells or macrophages. The importance of the ionized anionic groups of proteins on the endothelial cell surface and surrounding tissues for the integrity of blood vessel function was stressed.

Animals↗

A morphological study of ferritin synthesis in macrophages with ingested ferric hydroxide-potassium polyvinyl sulfate complexes.

A ferric hydroxide-polyvinyl sulfate colloidal solution (Fe-PVS), prepared by mixing potassium polyvinyl sulfate (PVSK) and ferric hydroxide colloidal solution was used to study ferritin synthesis in rat peritoneal macrophages. The colloidal particles had spherical electron opaque ferric hydroxide cores with diameters of about 250 nm surrounded by radially arranged fibrous PVS molecules. They also had strong negative electric charges. Fe-PVS particles injected into the peritoneal cavity were taken up by the macrophages then disintegrated rapidly. In the phagolysosomes the electron opaque ferric hydroxide cores of Fe-PVS were denuded of their PVS frames then decomposed into small 5-6 nm granules 24 to 48 h after injection. These small granules were released from the lysosomes into the hyaloplasm and the myelin figures were found in the lysosomal vacuoles. No reaccumulation of granules in lysosomes was found even 3 months later. The intracellular distribution of ferritin in macrophages demonstrated by the immunocytochemical method showed a pattern similar to that of the small granules formed by the disintegration of Fe-PVS. This means that in rat peritoneal macrophages that contain ingested Fe-PVS particles ferritin first is synthesized in phagolysosomes by the ferric hydroxide cores that conjugate with apoferritin or protein subunits then they are dispersed into the cytoplasm. Two possible pathways for the biosynthesis of ferritin are discussed.

Animals↗

The anionic barrier of blood vessel walls and the possible pathologic changes due to the deionization of the barrier and plasma proteins.

For the purpose to observe the possible vessel wall damage by deionization of the related anionic groups the perfusion test of rat kidney and aorta with cationic iron colloid particles and the injection experiments with albumin-poly-L-lysine complex were carried out. By staining the fixed tissue sections with the cationic iron colloid at pH 7.3 the ionized anionic sites on vessel walls have been demonstrated histochemically. The perfusion test of living tissue with the cationic iron colloid induced the desquamation of the endothelial cells. The perfused colloid particles were adsorbed to the whole endothelial cell surfaces facing to luminal and subluminal sides. Albumin-poly-L-lysine complex injected into vein deposited in the subendothelial spaces of glomerular capillaries through the endothelial cell layer having the well-kept anionic barriers. Discussion was made on possible damage of vessels due to the deionization of anionic groups of endothelial cells and serum proteins by general cationic molecules.

Adsorption↗

Clinical significance of serum bile acid measurement in liver diseases.

To determine the clinical significance of serum bile acid measurements, changes in the serum bile acid composition in liver diseases and endogenous bile acid clearance due to test meal loads were investigated. In the case of changes in the serum bile acid composition, a characteristic pattern of a remarkable increase of chenodeoxycholic acid (CDCA) was found in fulminant hepatitis. In patients with acute hepatitis, increases in CDCA were somewhat greater than those of cholic acid (CA) and there was tendency for these changes to precede changes in other liver function tests. In cases of extrahepatic obstructive jaundice, the CA/CDCA ratio was a large value exceeding 1.0. In investigations of endogenous bile acid clearance, serum bile acid concentration two hours after the text meal load clearly reflected the hepatic disorder and it was useful in differentiating between active and inactive form in chronic hepatitis and compensation and decompensation in liver cirrhosis.

Acute Disease↗

Liver protocollagen proline hydroxylase in human liver diseases and experimental liver fibrosis.

Liver protocallagen proline hydroxylase activity (PPH activity) was determined in patients with various liver diseases, CCl4-induced liver fibrosis rats and cholin deficiency (tcd) fatty liver rats. The following results were obtained: Liver PPH activity in patients with chronic hepatitis was higher than that in patients with acute hepatitis, while the activity in patients with liver cirrhosis was much higher than that in patients with chronic hepatitis. The activity was higher in patients with chronic active hepatitis than in those with chronic inactive hepatitis. Patients with active and progressive liver cirrhosis were found to have an especially high PPH activity, in whom the activity reflected well the degree of liver fibrosis. Even though fibrosis in persistent hepatitis was almost negligible or slight, the degree of liver PPH activity in persistent hepatitis was similar to that in liver cirrhosis. Liver PPH activities in CCl4-induced liver fibrosis rats and CD fatty liver rats elevated proportionally to the lapse of time. Whilst liver PPH activity in rats of CD fatty liver without fibrosis in 23 to 31 weeks after the start of the experiment was slightly lower than that in rats of CD fatty liver with fibrosis. But liver PPH activity of the former was considerably higher than that of control rats.

Acute Disease↗