2.4 Gbit/s repeaterless transmission over 306 kmnon-dispersion-shifted fibre using directly modulated DFB-LD anddispersion-compensating fibre

Based on system optimisation through theoretical model simulations, 2.4 Gbit/s repeaterless transmission over 306 km nondispersion-shifted fibre has been demonstrated with no power penalty, using a directly modulated DFB laser with a bulk active layer and dispersion-compensating fibres     

Macrophage recognition of saccharide chains on the erythrocytes damaged by iron-catalyzed oxidation

Mouse erythrocytes oxidized with an iron catalyst ADP/Fe3+ chelate attached to the monolayers of mouse resident and thioglycollate-induced peritoneal macrophages in the absence of serum, indicating that the macrophages recognized the oxidized erythrocytes. The recognition was partially prevented when the oxidized cells were treated with dithiothreitol, suggesting that disulfide formation is involved, in part, in the generation of the membrane sites recognized by macrophages. Phosphatidylserine is unlikely to be the determinant on the oxidized cells because it was not detected on the outer surface of the oxidized cells. The recognition by resident macrophages was effectively inhibited by N-acetylneuramin lactose, N-acetylneuraminic acid, glycophorin A, and disialoganglioside GD1a, but poorly by lactose, asialoglycophorin A, and monosialoganglioside GM1. In addition, the recognition was partially inhibited by L-fucose and human lactoferrin. The recognition by thioglycollate-induced macrophages was not inhibited by glycophorin A but was partially inhibited by L-fucose, lactoferrin, and oligosaccharides from band 3 glycoprotein. Enzymatic cleavage of the poly-N-acetyllactosaminyl saccharide chains of band 3 and lactoferrin resulted in a loss of the inhibitory activity. These results suggest that sialosaccharide chains of ADP/Fe(3+)-oxidized erythrocytes, possibly those on glycophorin A, are mainly involved in the recognition by resident macrophages, and poly-N-acetyllactosaminyl saccharide chains, possibly those on band 3, are partly involved in the recognition both by resident and thioglycollate-induced macrophages. Oxidation of erythrocytes may induce change in these membrane glycoproteins, like aggregation, which renders their saccharide chains susceptible to the macrophage recognition.     

Expression of cellular adhesion regulatory molecule in hepatocellular carcinoma

OBJECTIVE: Studying gender differences in fat mass and distribution in a homogeneous group of children. DESIGN: Cross-sectional study. SUBJECTS: 610 children aged 5-7 y in Kiel, Germany. METHODS: Anthropometric measures, bioelectrical impedance analysis (BIA). RESULTS: Although boys had increased body weights (P<0.05), body mass indexes (BMI's) (P<0.001) and waist/hip ratios (WHRs) (P<0.001), the %fat mass as assessed by BIA (P<0.05) was increased in girls. Although the increased BMI in boys was independent of the percentile used, gender differences (that is, lower values for boys than for girls at the same age) in WHR, the sum of four skinfolds and %fat were seen up to the 90th percentile. By contrast, above the 90th percentile there were no differences in skinfold thickness and %fat between boys and girls. Studying 42 BMI-matched pairs (boys and girls) also showed that the %fat estimated by BIA (P<0.001) was increased in girls. Plotting the average of %fat as obtained from skinfold- and BAI-measurements against the difference between data obtained by the use of the two methods shows that BIA %fat overestimates skinfold %fat at low or normal percent fat mass (that is, up to 20%) in both genders. By contrast, at increased fat mass, BIA %fat seems to underestimate skinfold %fat in both genders. CONCLUSIONS: Gender differences in fat mass and fat distribution are obvious in children aged 5-7 y. These differences are independent of gender differences in body weight. However, the nutritional state has an influence and gender differences cannot be detected in overweight and obese children. Our data also suggest that a children-specific formula used to calculate %fat from skinfold measurements is inappropriate.     

Ecological Risks Due to Immunotoxicological Effects on Aquatic Organisms

The immunotoxic effects of some anthropogenic pollutants on aquatic organisms are among the causes of concern over the presence of these pollutants in the marine environment. The immune system is part of an organism’s biological defense necessarily for homeostasis. Thus, the immunotoxicological impacts on aquatic organisms are important to understand the effects of pollutant chemicals in the aquatic ecosystem. When aquatic organisms are exposed to pollutant chemicals with immunotoxicity, it results in poor health. In addition, aquatic organisms are exposed to pathogenic bacteria, viruses, parasites, and fungi. Exposure to pollutant chemicals has reportedly caused aquatic organisms to show various immunotoxic symptoms such as histological changes of lymphoid tissue, changes of immune functionality and the distribution of immune cells, and changes in the resistance of organisms to infection by pathogens. Alterations of immune systems by contaminants can therefore lead to the deaths of individual organisms, increase the general risk of infections by pathogens, and probably decrease the populations of some species. This review introduced the immunotoxicological impact of pollutant chemicals in aquatic organisms, including invertebrates, fish, amphibians, and marine mammals; described typical biomarkers used in aquatic immunotoxicological studies; and then, discussed the current issues on ecological risk assessment and how to address ecological risk assessment through immunotoxicology. Moreover, the usefulness of the population growth rate to estimate the immunotoxicological impact of pollution chemicals was proposed.     

Antitumor agents. 180. Chemical Studies and cytotoxic evaluation of cumingianosides and cumindysoside A, antileukemic triterpene glucosides with a 14,18-cycloapotirucallane skeleton

Treatment of cumingianosides and cumindysoside A, which possess a 14,18-cycloapotirucallane skeleton, with p-toluenesulfonic acid in CH2Cl2 yielded new triterpene glucosides. Cumingianoside A (1) gave 10 and 11, along with cumingianoside Q (5). The structures of 10 and 11 were determined on the basis of spectral examination and contained a dammar-13(17)-ene and a 17(R),23(R)-epoxydammarane skeleton, respectively. Cumingianoside C (2) afforded, together with cumingianoside P (6), products 12 and 13, which were similar to 10 and 11, respectively. With a short reaction time at room temperature, cumingianoside E (3) yielded cumingianoside D (4). In contrast, when 3 was treated with p-toluenesulfonic acid in CH2Cl2 overnight at 5 degrees C, it gave two products, 9 and 14. Extensive spectroscopic examination revealed that 9 possessed a dammar-12-ene skeleton, while 14 was a pentacyclic tetranortriterpene glucoside with a novel skeleton. Cumindysoside A (8) gave a product (15) similar to 14. The cytotoxicities of 9-15 were evaluated against a panel of 58 human tumor cell lines. Compounds 11-15 exhibited potent cytotoxicity with log GI50 values ranging from -7.11 to -4.94, especially against leukemia and colon-tumor cell lines.     

The congruent melting composition of strontium barium niobate

The congruent melting composition of strontium barium niobate has been investigated over the ternary composition region by DTA, X-ray fluorescence, Curie temperature and lattice parameter measurements. The composition of congruent melt was found to be close tox=0.61,y=0.4993 for the formula (Sr _x Ba_1–x O)_1–y . (Nb₂O₅) _y . Striation-free single crystals are grown from the melt with this composition. The conceivable reasons for the discrepancy between the results of this work and the previous data are briefly discussed.     

Fish test for endocrine-disruption and estimation of water quality of Japanese rivers

The LC50 values (72 h) of 17beta-estradiol (E2), p-nonylphenol (NP) and bis-phenol-A (BPA) to adult male and female medaka were 3.5 and 3.5, 0.85 and 0.87, and 6.8 and 8.3 mg L(-1), respectively; the LC50 values to embryos were 0.46, 0.13 and 5.1 mg L(-1), respectively. The IC50 values for inhibition to egg hatching were 0.47, 0.85 and 9.0 mg L(-1), respectively. These values were much higher than concentrations detected in river water in Japan and the chemicals were considered to have no lethal effect on the fish in an aquatic environment. Mature male medaka was continuously exposed to 0.005, 0.05 or 1.0 microg L(-1) of E2, or to 0.1, 10 or 100 microg L(-1) of NP or BPA. Female specific proteins (FSP) were induced in the blood of male medaka that were exposed for 5 weeks to E2 higher than 0.005 microg L(-1), NP higher than 0.1 microg L(-1), or BPA higher than 10 microg L(-1). Based on these FSP inducible concentrations and reported concentrations of E2, NP and BPA in Japanese river water, some river water contaminated by E2 or NP could be estimated as the FSP inducible in male medaka.     

Silver nanocolloids disrupt medaka embryogenesis through vital gene expressions

Silver nanomaterials are the major components of healthcare products largely because of their antimicrobial effects. However, their unintended toxicity to biological organisms and its mechanism are not well understood. Using medaka fish embryo model, the toxic effects and corresponding mechanisms of silver nanocolloids (SNC, particle size 3.8 ± 1.0-diameter nm) were investigated. SNC caused morphological changes in embryos including cardiovascular malformations, ischemia, underdeveloped central nervous system and eyes, and kyphosis at exposures of 0.5 mg/L. Interestingly, SNC were observed inside the eggs at a level of 786.1 ± 32.5 pg/mg egg weight, and TEM analysis showed that SNC adhered to the surface and inside of the chorion. Meanwhile, medaka oligo DNA microarray and qRT-PCR were used for gene expression analysis in the embryos exposed to 0.05 mg/L SNC for 48 h. As a result, expressions of six of the oxidative stress-, embryogenesis- and morphogenesis-related genes, ctsL, tpm1, rbp, mt, atp2a1, and hox6b6, were affected by the SNC exposure, and these genes' involvement in those malformations was implied. Thus, SNC could potentially cause malformations in the cardiovascular and central nervous systems in developing medaka embryo through SNC-induced differential expression of the genes related to oxidative stress, embryonic cellular proliferation, and morphological development.     

Use of chitosan for removal of bisphenol A and bisphenol derivatives through tyrosinase‐catalyzed quinone oxidation

In this study, the availability of chitosan was systematically investigated for removal of bisphenol A (BPA, 2,2‐bis(hydroxyphenyl)propane) through the tyrosinase‐catalyzed quinone oxidation and subsequent quinone adsorption on chitosan beads. In particular, the process parameters, such as the hydrogen peroxide (H₂O₂)‐to‐BPA ratio, pH value, temperature, and tyrosinase dose, were discussed in detail for the enzymatic quinone oxidation. Tyrosinase‐catalyzed quinone oxidation of BPA was effectively enhanced by adding H₂O₂ and the optimum conditions for BPA at 0.3 mM were determined to be pH 7.0 and 40°C in the presence of H₂O₂ at 0.3 mM ([H₂O₂]/[BPA] = 1.0). Removal of BPA from aqueous solutions was accomplished by adsorption of enzymatically generated quinone derivatives on chitosan beads. The use of chitosan in the form of beads was found to be more effective because heterogeneous removal of BPA with chitosan beads was much faster than homogeneous removal of BPA with chitosan solutions, and the removal efficiency was enhanced by increasing the amount of chitosan beads dispersed in the BPA solutions and BPA was completely removed by quinone adsorption in the presence of chitosan beads more than 0.10 cm³/cm³. In addition, a variety of bisphenol derivatives were completely or effectively removed by the procedure constructed in this study, although the enzyme dose or the amount of chitosan beads was further increased as necessary for some of the bisphenol derivatives used. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

γ-ray irradiation durability of erbium-doped fibres

The long-term behaviour of erbium-doped fibres under γ-ray irradiation at a low dose rate of 0.5R/year was predicted for the purpose of applying the fibres to transoceanic transmission systems, based on the experimental result that permanent defects in fibres were dominantly generated at low dose rates. The estimated degradation of transmission loss and amplification gain after 25 years in undersea were 0.04 dB/km and 0.3 dB, respectively