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Biomedical subjects

H Arita

Publications and source records attributed to H Arita.

At least 181 records · Page 10Linked to original sources

Nature of albumin exported from the frog oocyte following microinjection of mouse liver mRNA.

Microinjections of mouse liver mRNA into Xenopus laevis oocytes induced efficient export of a polypeptide with an apparent Mr or 68,000 which was immunoprecipitable with anti-mouse albumin antibody. Analysis of the anti-albumin precipitate of the exported protein by two-dimensional gel electrophoresis showed that the electrophoretic behavior precisely coincided with that of authentic mouse serum albumin. This result indicates that the Xenopus oocyte may perform secretory processes similar or identical to those occurring in liver cells with respect to the processing of albumin.

Albumins↗

Studies on antiviral glycosides. II. Chemical modifications of the envelope of Sendai virus.

Treatment of Sendai virus with p-azidophenyl-6-chloro-6-deoxy-beta-D-glucopyranoside (APG) caused chemical modification of the viral envelope under UV irradiation, which did not affect the hemagglutinin activity of the virus but inhibited the hemolytic activity. Also, the transfer of phospholipid from the viral envelope to chicken erythrocytes was measured using a spinlabel technique by electron spin resonance (ESR). In this experiment, the phospholipid transfer was depressed by the treatment with APG under the conditions which inhibited the hemolytic activity of the virus. These results suggest that APG bound covalently to lipid may disturb the specific interaction between the protein and the lipid of the viral envelope, resulting in the inhibition of the hemolytic activity. The effects of APG on the hemolysis and phospholipid transfer were compared with the results for the concanavalin A- and amphotericin B-treated viruses.

Animals↗

Studies on phenyl glycosides as inhibitors of D-glucose uptake by Rhesus monkey kidney cells.

Some analogs of phenyl 6-halogeno-6-deoxy-beta-D-glucopyranosides have been found to be inhibitors of glucose uptake by Rhesus monkey kidney cells (LLCMK2 cells). The structures of the glycone and aglycone parts were both found to contribute to the inhibitory activity. Introduction of alkyl groups into the phenyl residue caused appreciable enhancement of the inhibition. p-(sec-Butyl)phenyl-6-chloro-6-deoxy-beta-D-glucopyranoside, which is the most potent inhibitor in this series, showed competitive and reversible inhibition. As a result of this study, we prepared p-azidophenyl-6-chloro-6-deoxy-beta-D-glucopyranoside as a possible compound for photoaffinity labeling of the glucose uptake site in animal cells.

Affinity Labels↗

Purification and properties of Haemophilus paragallinarum hemagglutinin.

Hemagglutinin (HA) of Haemophilus paragallinarum was purified, and its immunologic, chemical, and morphologic properties were studied. The HA was purified by gel filtration on Sepharose 6B and by subsequent ultracentrifugation of trypsinized cells after pretreatment with neuraminidase. After gel filtration, the HA component (fractioned HA) gave 1 precipitin line by gel diffusion, and after inoculation in chickens, hemagglutinination-inhibition antibody to trypsin-sensitive HA antigen was found. Chickens inoculated with the fractionated HA were protected from challenge exposure with H paragallinarum. In a sample further purified by ultracentrifugation (purified HA), a single protein band was detected by sodium dodecyl sulfate-polyacrylamide gel electrophoresis; it had a molecular weight of approximately 39,000. A molecular weight of several hundred thousand to several million was observed by gel filtration. Seemingly, HA of H paragallinarum is an aggregate of more than 20 HA sub-units. The purified HA included protein and some sugars, and according to electron microscopic observation, had a filamentous structure.

Animals↗

Computer simulation of exercise hyperpnea.

An analog model which describes the behavior of gas exchange in the lung and of the respiratory control system has been developed to study the physiological mechanisms of exercise hyperpnea. The model consists of three major compartments (lung, brain and tissue) which are connected by circulation. The time delay to reach to the chemoreceptor site and the time constant of the chemoreceptor in response to changes in blood gases are included. Respiration is assumed to be controlled by both neurogenic and humoral factors which act independently and additively. The results showed that the model behavior in terms of steady-state and transient response to exercise and recovery from it was consistent with the experimental observations and suggested that the combination of humoral and neurogenic theory may explain the physiological mechanism of exercise hyperpnea.

Computers, Analog↗

Studies on antiviral glycosides. II. Mode of action for virucidal effects on Sendai virus.

Treatment of Sendai virus with p-(sec-butyl)-phenyl-6-chloro-6-deoxy-beta-D-glucopyranoside, followed by freezing and thawing resulted in a loss of hemolytic and cell fusion activities as well as infectivity without affecting hemagglutinating and neuraminidase activities. The anti-hemolytic activity of this compound was reversed by the addition of phosphatidyl choline to the virus samples. p-Azidophenyl-6-chloro-6-deoxy-beta-D[3H]glucopyranoside was successfully used for photoaffinity labeling of a specific virion site, and we confirmed the affected site of the glucoside to be the lipid components in the viral envelopes.

Antiviral Agents↗

Studies on antiviral glycosides, 4. Inhibition of the multiplication of paramyxoviruses by phenyl-6-chloro-6-deoxy-beta-D-glucopyranoside.

The antiviral activity of phenyl-6-chloro-6-deoxy-beta-D-glucopyranoside (PCG) was studied. PCG specifically inhibited the growth of paramyxoviruses including Sendai, measles and Newcastle disease viruses in LLCMK2 cells at a concentration of 0.5 to 1.0 mM, but did not restrict the multiplication of other RNA viruses (influenza, vesicular stomatitis and polio viruses) at these concentrations. PCG might act in the late stage during virus replication of Sendai virus as it did not inhibit virus RNA and protein synthesis in the infected cells. Comparative studies on the biological properties of virus particles grown in the presence and absence of PCG demonstrated that treatment with it caused the formation of non-haemagglutinating particles.

Antiviral Agents↗

Studies on antiviral glycosides. Synthesis and biological evaluation of various phenyl glycosides.

A variety of analogues and derivatives of phenyl glycosides were synthesized for examination of their biological activities and of the relationship between structure and antiviral activity. For antiviral activity, a 6-deoxy-6-halogeno-D-glucose residue was most suitable for the carbohydrate moiety and p-alkylphenyl groups for the aglycone moiety. Based on these results, p-(sec-butyl)phenyl 6-chloro-6-deoxy-beta-D-glucopyranoside and p-(sec-butyl)phenyl 6-deoxy-6-iodo-beta-D-glucopyranoside were prepared, and the former compound was found to be the most potent antiviral substance, in this series, against influenza and Herpes simplex virus. The anomeric configuration of phenyl glycosides did not contribute to the antiviral activity.

Antiviral Agents↗

Physiological responses to head-out immersion in water at 11 ATA.

Cardiorespiratory, thermal, and renal responses to a 30-min head-out immersion in 15 degree C water were studied at 1-ATA air and 11-ATA helium-oxygne environments in four male subjects wearing dry suits. Cardiorespiratory responses to immersion (reductions in heart rate, expiratory reserve volume, vital capacity, and thoracic impedance; and increases in stroke volume, cardiac output, and inspiratory capacity) were comparable at both pressures. However, thermal responses to immersion (a reduction in mean skin temperature and increases in skin heat flux and suit conductance) were significantly greater at 11 ATA compared to those at 1 ATA. The rate of urinary excretion of norepinephrine increased significantly during and after immersion at 11 ATA but not at 1 ATA. In contrast, the urinary excretion of epinephrine was not altered by pressure or immersion. The immersion diuresis was greater and lasted longer at 11 ATA than at 1 ATA although there was no difference in the endogenous creatinine excretion . This diuresis was accompanied by a significant natriuresis which was more marked at 1 ATA than at 11 ATA. At 1 ATA, the urinary excretion of both aldosterone and antidiuretic hormone (ADH) decreased during immersion. At 11 ATA, the rate of excretion of these hormones before immersion was lower compared to that at 1 ATA and did not change significantly during immersion. These results indicate that immersion in a hyperbaric helium-oxygen environment presents a greater cold stress than at 1-ATA air, and also that immersion diuresis and natriuresis at high pressure may be induced by a factor other than inhibition of aldosterone and ADH.

Adult↗

Cytolipin R from rat spleen.

Normal rat spleen contained a large amount of cytolipin R, N-acetylgalactosaminyl(beta1 leads to 3)-galactosyl(alpha1 leads to 3)galactosyl(beta1 leads to 4)glucosyl ceramide, together with a lesser amount of cytolipin K, N-acetylgalactosaminyl(beta1 leads to 3)galactosyl(alpha1 leads to 4)galactosyl(beta1 leads to 4)glucosyl ceramide, as in the case of rat kidney. Cytolipin R was confirmed to be not a rat tumor-dependent, but a species-specific glycolipid.

Acetylgalactosamine↗