203 research outputs found

    Economic and environmental impacts of changes in culling parity of cows and diet composition in Japanese beef cow–calf production systems

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    The effects of changes in culling parity of cows and diet composition on economic and environmental outputs in Japanese beef cow–calf production systems were deterministically analyzed using a herd model simulation. The model simulated the annualized net revenue as an economic indicator and the overall environmental index derived from a life cycle assessment (LCA) as an environmental indicator. Biological factors (survivability, growth, reproduction, and feed requirements) and economic factors (returns from sales of live calves and cows’ carcasses and production costs) were included in the model. The model also included modified feed formulation methods, allowing us to analyze the effect of reductions in environmental loads caused by the change in diet compositions. The results of the present study indicated that later culling was economically and environmentally optimal under the current production system, which suggested that the selection of economically optimal culling parity of cows could result in environmentally optimization of the beef cow–calf production system. The difference in feed composition derived from the difference in feed formulation methods did not affect the determination of optimal culling parity, whereas the use of modified feed formulation methods could reduce environmental loads at a higher rate than that of economic benefits. However, the reduction rate of the environmental impact was much higher in the case of selection of the optimal culling parity than in the case of use of modified feed formulation methods, which stressed the importance of choosing the optimal culling parity of cows both from the economic and environmental points of view

    Antibacterial Effects of Disulfiram in Helicobacter pylori

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    Background: Helicobacter pylori infection poses a risk of the occurrence of gastrointestinal diseases, such as gastric cancer. Its incidence rate is significantly reduced by eradication, and thereby, eradication therapy is generally performed. Disulfiram is an oral prescription drug mainly used for the treatment of alcohol dependence. In recent years, reports have been made on its anticancer and antibacterial effects, and thus, it has recently become an interesting subject. This study aimed to examine the antibacterial activity of disulfiram, investigate the presence or absence of its antibacterial activity on H. pylori, and determine whether it could be a new bactericidal drug against drug-resistant H. pylori. Materials and Methods: Drug-sensitive strains of H. pylori and amoxicillin-resistant, clarithromycin-resistant, and metronidazole-resistant strains were used, and a growth inhibition test of H. pylori using disulfiram was performed. Furthermore, the expression of urease, vacuolating cytotoxin A (VacA), and CagA, the virulence proteins of H. pylori, was quantitatively analyzed using the Western blotting method. In addition, for H. pylori used in this study, the 16SrDNA sequence, a ribosomal gene involved in protein production, was analyzed to examine the presence or absence of gene mutation. Results: Disulfiram suppressed the growth of 7 out of 12 H. pylori strains at 1 mu g/mL, and no correlation was observed between their susceptibility/resistance to current eradication antimicrobial drugs and disulfiram resistance. Disulfiram reduced the expression levels of urease, VacA, and CagA proteins. H. pylori, which showed resistance to disulfiram, tended to have fewer gene deletions/insertions in the 16S rDNA sequence; however, no specific mutation was detected. Conclusion: Disulfiram has a bactericidal effect on H. pylori at low concentrations, suggesting that it can be used as a supplement for current H. pylori eradication drugs

    Carbon footprint assessment of a whole dairy farming system with a biogas plant and the use of solid fraction of digestate as a recycled bedding material

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    Biogas generated from livestock manure is a renewable energy source and the digestate is used as a fertilizer. Moreover, dewatered biogas digestate can be used as a bedding material (recycled bedding material). The aims of the present study were to model a whole dairy system with a biogas plant using recycled bedding material and to assess the life cycle greenhouse gas (GHG) emissions. Emissions from the material flow of dairy cattle production, manure treatment and organic fertilizer application to on-farm crops were evaluated. In the emissions from organic fertilizer storage and recycled bedding material production, CH4 emission was decreased by 43.0%, and consequently the system with a biogas plant reduced total GHG emissions by 6.8% compared with conventional slurry storage and straw bedding. The use of recycled bedding material from a biogas plant has the potential to create a resource cycle and to be beneficial as a GHG mitigation strategy

    Efficient Assay for Total Antioxidant Capacity in Human Plasma Using a 96-Well Microplate

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    In the present study, we tried to establish an efficient assay for total antioxidant capacity (TAC) in human plasma using a 96-well microplate. TAC was assessed using lag time by antioxidants against the myoglobin-induced oxidation of 2,2'-azino-di(3-ethylbenzthiazoline-6-sulfonic acid (ABTS) with hydrogen peroxide, and expressed as Trolox equivalent. The linearity of the calibration curve with Trolox was maintained with the Trolox concentration range from 2.5 µM to 25 µM (R2 = 0.997). The assay was applied to the measurement of TAC in healthy human plasma. Coefficient of variation in intraday assay was 2.4%. Difference was not observed in interday assay. Plasma TAC of men ((569 ± 41) µM Trolox equivalent; n = 6) was higher than that of women ((430 ± 28) µM Trolox equivalent; n = 4). After the vegetable juice was drunk for 1 week, the increase in plasma TAC was observed in almost all the volunteers. In summary, we developed the efficient assay for plasma TAC using a 96-well microplate

    Preparation and Characterization of a Polyclonal Antibody against Brominated Protein

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    (Di)bromotyrosine is formed by the specific reaction of eosinophil peroxidase and can be used as an eosinophil activation marker. In the present study, an antibody for (di)bromotyrosine in proteins was prepared to investigate the pathogenesis of eosinophil-related diseases such as allergic responses. A rabbit polyclonal antibody was raised against brominated keyhole limpet hemocyanin. The specificity of the antiserum was investigated with an enzyme-linked immunosorbent assay (ELISA). The antiserum recognized brominated bovine serum albumin (BSA) and dibromotyrosine-conjugated BSA. The antiserum also reacted with chlorinated BSA and di-iodotyrosine-conjugated BSA. Moreover, the specificity of the antiserum was investigated using competitive ELISA. Dibromotyrosine and di-iodotyrosine inhibited the recognition of brominated BSA by the antiserum. However, the recognition of brominated BSA by the antiserum was not inhibited by bromotyrosine, chlorotyrosine, iodotyrosine, nitrotyrosine, aminotyrosine, phosphotyrosine, or tyrosine. These results suggested that the epitope of the antiserum is dihalogenated tyrosine. Immunohistochemically, the antiserum stained brominated rat eosinophils but not chlorinated or nitrated eosinophils. In conclusion, an antiserum for dihalogenated protein was prepared. It is expected that the antiserum will be useful for the analysis of the pathogenesis of allergic diseases such as asthma and atopic dermatitis

    Synthesis and physical properties of Ca1-xRExFeAs2 with RE = La ~ Gd

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    Synthesis of a series of layered iron arsenides Ca1-xRExFeAs2 (112) was attempted by heating at 1000 C under a high-pressure of 2 GPa. The 112 phase successfully forms with RE = La, Ce, Nd, Sm, Eu and Gd, while Tb, Dy and Ho substituted and RE free samples does not contain the 112 phase. The Ce, Nd, Sm, Eu and Gd doped Ca1-xRExFeAs2 are new compounds. All of them exhibit superconducting transition except for the Ce doped sample. The behaviour of the critical temperature, with the RE ionic radii have been investigated
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