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Biomedical subjects

K Shida

Publications and source records attributed to K Shida.

At least 37 records · Page 2Linked to original sources

Electron microscopic observations on pulmonary connective tissue stained by Ruthenium Red.

Ultrastructural studies on human lung were performed with special attention to the interstitial acid mucopolysaccharides by Ruthenium Red staining and several enzyme digestion tests with Streptomyces hyaluronidase, chondroitinase ABC, chondroitinase AC, heparinase, trypsin and collagenase. Periodic lateral granules on the major cross bands of collagen fibrils and amorphous coats on them became visible by Ruthenium Red staining. The surface of elastic fibres, associated microfibrils, and some fine fibrils 10-20 nm in diameter were stained. Ruthenium Red also stained the surface of fibroblast and smooth muscle cells, basement membrane and filamentous long segments. In the interstructural space, granular substances 10-80 nm in diameter and fine filaments 3--4 nm thick, which formed a fine reticular network, were clearly observed. They were not visible on the usual thin section. The granular substances were located on the cross points of the fine filaments. They spread continuously and connected with each of the cells and extracellular structures in the pulmonary interstitium. The results of the enzyme digestion tests on the Ruthenium Red-positive material are discussed.

Basement Membrane

In vivo release of testosterone from protein--vinyl polymer composites.

Hydrophilic vinyl polymer-protein composites containing testosterone were made by means of thermal denaturation of albumin after radiation-induced polymerization of 2-hydroxyethylmethacrylate (HEMA) at--78 degrees C. The albumin-HEMA mixed polymer can be considerably digested with trypsin. The degree of digestion was smaller than that expected from calculation. It was deduced that the digestion of the albumin component was retarded in the presence of HEMA. The same tendency was observed in in vivo experiments. At the same time, in vivo release of testosterone was depressed in albumin-HEMA mixed polymer composite in accordance with the weight decrease of polymer composite resulting from digestion. The effect of testosterone on the weight of ventral prostate was investigated using composites in castrated Wistar rats. The effect was larger in the controlled slow release from implanted composites rather than that of dosage by injection. The microscopic observation showed that the inflammation and foreign body reaction in rat tissue were retarded in albumin-HEMA mixture polymer composite compared with 100% albumin composite.

Animals

Ultrastructure of the Lewis lung carcinoma.

ELectron microscopic observations were made on the Lewis lung carcinoma, which has frequently been used in various experiments. Although the tumor cells had desmosomes, interdigitation, microvilli and basement membranes which were of epithelial nature, they did not show either squamous or adenomatous differentiation. On the basis of microscopic and ultrastructural findings, this tumor falls into the category of large cell carcinomas. At the periphery of the tumor, sinusoidal clefts between the strands of tumor cells contained many red blood cells without fibrin. While perfect blood vessels were observed towards the center of the tumor, large necrotic areas were observed. Dilated large vessels possessed some endothelial fenestrations. Light endothelial cells were also observed, which were penetrated by red blood cells. Interstitial components were very scant and collagen fibres were frequently observed to be dissolved.

Animals

Analysis of Estramustine binding protein (EBP) in rat dorsal prostate by means of high pressure liquid chromatography.

High pressure liquid chromatography (HPLC, Toyo Soda TSK-GEL G3000 SW column) was used to analyse the properties of Estramustine binding protein (EBP) in the cytosol of rat dorsal prostate. There exist in the cytosol of rat dorsal prostate two binding components having a high affinity for Estramastine. When estimated by HPLC, the molecular weights of these Estramustine binding components are 45,000-50,000 and 25,000-30,000 daltons, respectively. The binding of 3H-Estramustine to a macromolecule with a molecular weight of 25,000-30,000 is more heat labile than binding of 3H-Estramustine to a macromolecule with a molecular weight of 45,000-50,000. The present study also demonstrates that the HPLC method offers higher resolution, smaller sample size and faster analysis than other methods used in binding studies.

Animals

Antiandrogenic therapy for the treatment of early stage prostatic cancer.

The goal of this study was to achieve clinical application of antiandrogens for the treatment of carcinoma of the prostate. Based on the results obtained from animal experiments and from a pilot clinical trial on prostatic cancer patients using various antiandrogenic compounds, chlormadinone acetate (CMA) was selected for a clinical trial in patients with carcinoma of the prostate. With nine universities and their affiliated hospitals participating, the therapeutic effect of CMA for carcinoma of the prostate was investigated nationwide. Highly satisfactory antitumor effects with CMA were observed in stage A and B patients of the primary treatment group. For stage C patients in the primary treatment group, good antitumor effects were obtained with CMA treatment. For stage D patients, however, results were poor. No serious side effects were observed in spite of the long period (as long as 6.3 years) and relatively large doses (100 mg daily) of CMA. Therefore, it was concluded that CMA can be recommended as a first choice drug for patients with carcinoma of the prostate.

Androgen Antagonists

Comparative examination of three radioimmunoassay kits for human prostatic acid phosphatase.

Three commercial radioimmunoassay kits for prostatic acid phosphatase (PAP) were compared on the basis of their ability to measure the enzyme in normal male sera. These kits, issued by Eiken ICL (EIK), Clinical Assays (CLA), and Mallinckrodt (MKT), could measure the serum samples containing PAP above normal levels with precision and reproducibility, and showed excellent linearity on the dilution tests and good correlation with the enzymatic activity. PAP in the serum did not lose immunoreactivity for two weeks if stored below 4 degrees C. However, the sensitivity of CLA and MKT kits should be improved to give reliable values for normal sera with lower PAP contents (less than 1 ng/ml). The upper mean + 2 SD normal limits in ng/ml obtained with these kits were 2.2 (MKT), 2.5 (EIK), and 2.8 (CLA). Some differences in the purity of the standard preparations among these kits were also found. These kits gave different assays values for PAP control sera from CLA and multipurpose QC-RIA sera from Eiken ICL.

Acid Phosphatase

Mechanism of retention of estramustine in the rat prostate and results of a clinical trial of Estracyt in Japan.

To clarify the mechanism of action of Estracyt, we performed experiments using 3H-estramustine of high specific activity. 3H-Radioactivity accumulated selectively in the ventral prostate of castrated male rats after the administration of 3H-estramustine. Estramustine and its metabolites were retained in the ventral prostate for long time periods. The uptake of 3H-radioactivity was almost totally localized in the cytosol fraction, but not in a purified receptor fraction. The apparent equilibrium dissociation constant of the estramustine binding protein was 18.9 nM, and the apparent equilibrium Bmax value was 0.76 nmoles/mg of cytosol protein. In addition, we wish to report in this paper the results of clinical trials of Estracyt studied by a cooperative research group in Japan from 1977 to 1979. It was concluded that Estracyt was effective in 89% of previously untreated prostatic cancer patients and in 38% of reactivated cancer patients.

Animals

Neurogenic muscular atrophy and low density of large myelinated fibres of sural nerve in chorea-acanthocytosis.

In three cases of chorea-acanthocytosis (acanthocytosis and neurological disease, or familial degeneration of the basal ganglia with acanthocytosis), biopsies of short peroneal muscles and sural nerves were studied histologically. The muscles showed groups of atrophic fibres with clumping of sarcolemmal nuclei in all cases. It was concluded that neurogenic muscular atrophy should be included as one of the main pathological findings in chorea-acanthocytosis. The sural nerves showed a small number of large myelinated fibres in two cases. This finding remains to be confirmed in other cases.

Acanthocytes

Cytoplasmic microtubules of rat ascites hepatoma cells.

Cytoplasmic microtubules of 4 strains of rat ascites hepatoma cells including YS, AH 66F, AH 130 and AH 100B were investigated electron microscopically. Microtubules were clearly demonstrated when the cells were fixed at 20 degrees C or 37 degrees C and stained by tannic acid. Morphology, localization and volume density (AH 130 greater than AH 66F greater than YS greater than AH 100B) of microtubules were examined comparatively in these 4 strains and correlation between microtubules and cell deformability was discussed.

Animals

Action of a novel nonsteroidal antiandrogen, AA560.

The antiandrogenic properties of a new nonsteroidal antiandrogens, AA560 (N-2-chloromethyl-2-hydroxypropionyl)-3, 4, 5-trichloroaniline) were investigated. The ventral prostate, dorselateral prostate and coagulating gland weights in rats given AA560 at 1-9 mg/head were significantly less than those in the intact rats. The seminal vesicle weights in rats given 3-9 mg/head were significantly less than those of the intact group. In intact animals given daily 3 or 9 mg of AA560 there were significantly increases of serum FSH, LH and testosterone concentrations. In the in vivo experiment, the pretreatment with AA560 decreased the uptake of 3H-androgens in the nuclear fraction of the ventral prostate. On the other hand, a significant increase in the uptake of 3H-radioactivity in the cytosol fraction was observed. It was proved by the in vitro displacement study that AA560 inhibited the binding of 5 alpha-dihydrotestosterone with a receptor protein in the prostatic cytosol.

Androgen Antagonists