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Biomedical subjects

A Sakoda

Publications and source records attributed to A Sakoda.

13 recordsLinked to original sources
PubMed2005

Elution and adsorptive concentration of Japanese cedar (Cryptomeria japonica) pollen allergen in environmental water.

Elution of Japanese cedar pollen allergens (Cry j I and others) from pollen grains and its adsorptive concentration onto hydrophobic and hydrophilic surfaces were investigated using the surface plasmon resonance technique. Results showed that the allergen elution was obviously enhanced when the ion concentration was higher than that within the human body, indicating that the pollen tend to release its allergen in environmental water having a high ion concentration. However, higher adsorption capacity was observed on hydrophobic surface than hydrophilic surface. These results indicate that water puddles on roadsides beside heavy traffic including large amounts of ion compounds and hydrophobic diesel exhaust particles (DEPs) are a pollen allergen-DEP complex generator. DEPs are easily absorbed into the living body; therefore these mechanisms may be responsible for causing the highest incidence of pollinosis among residents living alongside roads with heavy automobile traffic.

Adsorption↗
PubMed2003

Enhanced in vitro maturation of subcultivated fetal human hepatocytes in three dimensional culture using poly-L-lactic acid scaffolds in the presence of oncostatin M.

Fetal human liver cell fractions, which contain large numbers of hepatocyte progenitors, have high proliferation potential in vitro. To create an engineered liver tissue equivalent of a clinically significant size, however, repeated subcultivation and functional maturation are necessary in vitro. A commercially available human fetal liver cell fraction that was cultivated for some time in vitro has been reported to lose liver specific functions almost completely. We therefore investigated the effects of oncostatin M (OSM) and hepatocyte growth factor (HGF) in long-term three-dimensional (3D) culture using macroporous poly-L-lactic acid (PLLA) scaffolds on the restoration of such liver-specific functions of the fraction. 3D culture using PLLA scaffolds with OSM remarkably enhanced the albumin production and cytochrome P450 1A1/2 capacity with the culture time. HGF alone had no preferable effect on these functions even in 3D culture. Alpha-fetoprotein production was consistently suppressed in the 3D culture compared with that in monolayers. This suppression was not observed in the same types of culture of hepatocarcinoma Hep G2 cells. Despite these favorable observations on the 3D culture with OSM, the final attained functional levels at the 5th week were still over ten-times lower than those of Hep G2 cells when standardized with a cellular DNA amount. Although further improvement is needed for the complete functional restoration and maturation in vitro, these results demonstrate that a combination of 3D culture using PLLA scaffolds and OSM offers promising culture conditions for in vitro maturation of human hepatocyte progenitors.

Albumins↗
PubMed2002

Catalytic ozonation of an organophosphorus pesticide using microporous silicate and its effect on total toxicity reduction.

Catalytic ozonation is promising as one of the advanced oxidation processes because of its effective use of ozone and its improved treatability of organic compounds through radical reactions. In this article, we investigated the feasibility of microporous silicates as a potential catalyst for a catalytic ozonation process. Organophosphorus insecticide, dichlorvos (DDVP), was employed as a model chemical for assessing conventional ozonation and catalytic ozonation, because its oxidative intermediate is toxic and is not degraded by direct ozonation. It was found that ozone was well adsorbed and simultaneously decomposed in microporous silicates, resulting in the production of possible radical species. In the presence of microporous silicates, radical reactions by decomposed ozone were evidenced by phosphate ion release that shows a degradation of a toxic intermediate of DDVP. Accordingly, cytotoxicity was successfully decreased. In a continuous treatment process combining a conventional ozonation vessel and a microporous silicate column for an effective use of residual ozone, enhanced degradation of DDVP was demonstrated by a decrease of DOC, an increase of the PO4(3-) concentration and reduction in the cytotoxicity. This new treatment mechanism is likely to be promising as an advanced water treatment process particularly when we think about better toxicity reduction of wastewaters.

Adsorption↗
PubMed2002

Preservation of human cell bioassay device for the on-site evaluation of environmental waters.

We have already developed a novel disposable bioassay device based on the low-density lipoprotein (LDL) uptaking activity of human hepatoblastoma Hep G2 cells in our previous work. However, this device is not readily applicable to evaluate river water toxicity on-site because it cannot be preserved for more than one week. In this work, we developed the method for preservation of the device to enable it to be preserved for at least one month. The device can be supplied to individual environmental sites without any facilities for cell culture. We can evaluate river water toxicity by 2 hours of exposure after thawing. Therefore, this kind of device could be a promising tool for daily water quality management.

Biological Assay↗
PubMed2001

A mathematical model of a shallow and eutrophic lake (the Keszthely Basin, Lake Balaton) and simulation of restorative manipulations.

Concern about the overall management of lakes has been growing, and a lake ecological model provides the guidelines necessary for such management. In this study, an ecological model describing the ecosystem of the Keszthely Basin, Lake Balaton, Hungary, one of the typical shallow and eutrophic lakes, was proposed. This model includes three types of zooplankton and two types of fish as well as two types of algae and nutrients. Parameters concerning the algae and fish were estimated based on observations in the basin between 1991 and 1995. The other parameters and the structure of the model were determined by our previous study. The parameters of the model were calibrated with the Monte Carlo technique, and its predictability was confirmed. The effects on the basin's ecosystem of three restorative manipulations, namely a biomanipulation, reduction of loading phosphorus, and dredging the sediment, were assessed by simulation studies using the proposed model. The simulation results indicated that a biomanipulation that removed 90% of the bream should suppress the growth of algae temporarily through bottom-up regulation; however, this effect seemed to not be perpetuated in this basin. The reduction of loading phosphorus seemed to be the most effective means to suppress algal growth, while dredging of sediment seemed to be the most desirable restoration method from the standpoint of the overall management of the lake, because it was expected to accelerate the growth of fish population as well as to suppress algal growth. Furthermore, the algal growth suppression mechanism of the dredging was discussed on the basis of the model calculations.

Animals↗
PubMed2001

A modelling approach to global nitrate leaching caused by anthropogenic fertilisation.

Water quality associated with nitrate (NO3-) leaching from agricultural soils is an important environmental issue. This paper describes a new modelling approach to quantitatively evaluate the effect of the use of fertilisers on global nitrate leaching. A global process-based simulation model was previously developed for the nitrogen cycle in terrestrial ecosystems, in which soil inorganic nitrogen in the form of ammonium (NH4+) and NO3- was considered. After introducing data on world fertiliser consumption (FAO, 1995) into the steady-state model, the extent of disturbance to the nitrogen cycle caused by fertilisation was calculated. Although fertilisation resulted in an annual increase in net primary production (NPP, represented as carbon) of 18 Gt year-1, NO3- leaching and gaseous losses of nitrogen oxides and ammonia were also accelerated. Most regions with heavy fertiliser application (over 100 kg ha-1 year-1) showed a high annual leaching load equal to or more than 20 kg ha-1 year-1. About 2.5% of the land area occupied by terrestrial ecosystems suffered a serious leaching load of more than 30 kg ha-1 year-1. Of the total amount of applied fertilisers (138 Tg year-1) 19% was lost to NO3- leaching, 8% to gaseous ammonia, and 3% to gaseous nitrogen oxides. The rest was assumed to be fixed in the ecosystems through vegetation uptake.

Ammonia↗
PubMed2001

Biological efficiency and nutritional value of Pleurotus ostreatus cultivated on spent beer grain.

Unpretreated spent beer grains were successfully used as a basic substrate material for the cultivation of Pleurotus ostreatus. The effects of spent grain types, additives, substrate moisture content, and substrate packing density on the yield and nutrition of fruit bodies were investigated. The cultivation results showed that few fruit bodies were formed on spent grain alone; however, a significantly high biological efficiency (19.1%) was obtained with the addition of wheat bran to (45%). The chemical analysis of fruit bodies indicated that P. ostreatus cultivated on spent grain substrate had a higher nutritional value than those grown on other reported types of substrates. The total amino acid content in the fruit bodies was 347.5 mg/g dry matter, and the crude protein content was as high as 53.3% on a dry weight basis. It was also found that the cultivation of P. ostreatus increased the crude protein content, while it decreased the ratio of lignin to cellulose, of the spent grain substrate.

Animal Feed↗
PubMed2001

Cultured human-cell-based bioassay for environmental risk management.

Among bioassays for evaluating various impacts of chemicals on humans and ecosystems, those based on cultured mammalian-cells can best predict acute lethal toxicity to humans. We expect them to be employed in the future in environmental risk management alongside mutagenicity tests and endocrine-disrupting activity tests. We recently developed a disposable bioassay device that immobilizes human hepatocarcinoma cells in a small micropipette tip. This enables very quick (within 2 h) evaluation of acute lethal toxicity to humans. For bioassay-based environmental management, 2 promising approaches have been demonstrated by the US-EPA: toxicity identification evaluation (TIE) and toxicity reduction evaluation (TRE). The Japanese Ministry of Environment has been supporting a multi-center validation project, aimed at assembling a bioassay database. To make full use of these resources, we present a numerical model that describes contribution of individual chemical to observed toxicity. This will allow the selection of the most effective countermeasure to reduce the toxicity. Bioassay-based environmental risk management works retrospectively, whereas impact assessment using substance flow models and toxicity databases works prospective. We expect that these 2 approaches will exchange information, act complementarily, and work effectively in keeping our environment healthy in the 21 st century.

Biological Assay↗
PubMed2000

Development of a rapid and sensitive bioassay device using human cells immobilized in macroporous microcarriers for the on-site evaluation of environmental waters.

We developed a novel disposable bioassay device based on the fluorescein isothiocyanate-labelled low-density lipoprotein-uptake activity of human hepatoblastoma Hep G2 cells. The cells were cultured in porous microcarriers at a high cell density and packed in a filter tip that has a hydrophobic membrane. Upon evaluation of water samples, the culture medium was decanted by pipetting it down with a micropipet, and the samples were then introduced to the cell-immobilizing part of the tip only by pipetting them up after mixing them with x10 concentrated culture medium. The new device enabled us to detect almost the same toxicity levels of river water within 2 h of exposure as those detected by a conventional 48-h cell-survival assay. This is the first bioassay device for the rapid on-site evaluation of environmental waters using cultured human cells, and therefore promising for water-quality management based on risk to humans.

Biological Assay↗
PubMed2000

Rapid and sensitive neurotoxicity test based on the morphological changes of PC12 cells with simple computer-assisted image analysis.

In order to develop a rapid and sensitive bioassay for the screening of chemicals with possible neurotoxicity, a computer-assisted simple image-analysis system was developed to quantify small changes in the specific morphology of the cultured pheochromocytoma cell line, PC12. This cell forms a neuron-like microfibril network (neurites) in response to a nerve growth factor (NGF) stimulation in vitro. Dichrolvos (DDVP) and methylmercury chloride (MMC) were employed as model neurotoxicants. In DDVP treatment, there was no large difference in the ED50s (effective dose that reduces the morphological index by 50%) among the toxicities determined from various morphological indices, but they were significantly lower than those observed by whole-cell-area-based toxicity assay using the hepatoblastoma cell line, Hep G2. In contrast, in MMC treatment, neurite-length-based toxicity was observed as early as 2 h, and at 48 h this was lower by over three orders of magnitude compared with whole-cell-area-based one (2.06 x 10(-7) mM vs. 6.42 x 10(-4) mM). These results demonstrate that the developed bioassay using image analysis of nerve-tissue-derived cell morphology allows us to screen possible neurotoxic chemicals very rapidly with highly enhanced sensitivity, particularly for some chemicals that preferentially act on nerve fibers.

Journal Article↗
PubMed1993

Long-term culture of primary rat hepatocytes with high albumin secretion using membrane-supported collagen sandwich.

Primary cultured rat hepatocytes in a membrane-supported collagen sandwich maintained their normal cell morphology and high level of albumin secretion for over 56 days. It was found that the existence of an upper layer of collagen gel is crucial for long-term culture and that the transference of cellular nutrients between the culture media and hepatocytes from both the upper and the lower sides of gel layers promotes albumin secretion. These facts suggest that the membrane-supported collagen sandwich mimics well the in vivo environment of hepatocytes. This method has great potential for the long-term culture of primary cells.

Albumins↗
PubMed1990

Protein separation using membrane-encapsulated soluble ligand conjugates.

A new approach for isolating and recovering biological macromolecules using membrane-encapsulated soluble ligand conjugates was investigated. Membrane-encapsulated solid adsorbents have been successfully developed and employed in our laboratory to isolate and purify proteins and enzymes directly from culture broths. This new concept also makes it possible to use soluble ligand conjugates instead of solid adsorbents inside membrane capsules. In this work, model membrane-encapsulated soluble and insoluble ligands comprising Blue Dextran and Blue Sepharose entrapped within calcium alginate membranes were studied to compare adsorption characteristics such as capacities and rates. Experimental results suggest that membrane-encapsulated soluble ligands may be expected to result in higher overall adsorption capacity compared to membrane-encapsulated solid adsorbents with comparable adsorption rates.

Adsorption↗