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Diabetes mellitus is a metabolic disease spreading worldwide that has been reported to worsen the development and progression of other diseases (cancer, vascular diseases and dementia). To establish functional rice lines with anti-postprandial hyperglycaemic effects, we developed mutant rice lines, which lack one or two gene(s) related to starch synthesis, and evaluated their effects. Powder of mutant rice lines or other grains was loaded to rats fasted overnight (oral grain powder loading test). Incremental area under time-concentration curves (iAUC) were calculated with monitored blood glucose levels. Rice lines with anti-postprandial hyperglycaemic effects were separated by cluster analysis with calculated iAUC. A double mutant rice #4019 (starch synthase IIIa (ss3a)/branching enzyme IIb (be2b)), one of the screened mutant rice lines, was fed to Goto-Kakizaki (GK) rats, an animal model for type 2 diabetes, for 5 weeks. Plasma levels of C-peptide, a marker of pancreatic insulin secretion, were measured with ELISA. Forin vitrostudy, a rat pancreatic cell line was cultured with a medium containing rat serum which was sampled from rats fed #4019 diet for 2 d. After 24-h of incubation, an insulin secretion test was performed. Through the oral rice powder loading test, seven rice lines were identified as antidiabetic rice lines. The intake of #4019 diet increased plasma C-peptide levels of GK rats. This result was also observedin vitro.In rat serum added to cell medium, ornithine was significantly increased by the intake of #4019. In conclusion, the mutant rice #4019 promoted pancreatic insulin secretion via elevation of serum ornithine levels.

In order to identify potential unanticipated side reactions and immune responses, the evaluation of candidate vaccines should include immunization of the murine model of the disease in question and mutant animals, as well as normal laboratory animals. We employed WBB6F(1)-W/W(v) and WBB6F(1)-Sl/Sl(d) mutant mice, which are genetically mast cell deficient and lack intestinal pacemaker activity due to a severe deficiency in interstitial cells of Cajal. Antigen-specific mucosal and systemic immune responses in the mutant and congenic normal mice were induced by intranasal or intragastric immunization with ovalbumin (OVA) plus cholera toxin as an adjuvant. It was found that the levels of the OVA-specific humoral immune response in the mucosal and systemic tissues of the mutant mice immunized intranasally were roughly equivalent to those of the congenic normal mice. In contrast, the specific humoral immune response in the intragastrically immunized mutant mice was greater than that observed in the congenic normal mice. Unexpectedly, the titers of OVA-specific IgA antibodies and total IgA antibodies in the fecal extracts of both intranasally and intragastrically immunized mutant mice were significantly lower than in those of the congenic normal mice. Although the detailed mechanisms leading to these differences remain unclear, the unexpected immune responses observed in the gastrointestinal tracts of the mice in this study may be related to an abnormality of gastrointestinal motility. Our data therefore suggest that studies using mutant mice and physiological assessments should be carried out during mucosal vaccine development.

We developed an image-shifting subtraction program and carried out embossed radiography (ER) utilizing single- and dual-energy subtractions. In particular, dual-energy subtraction was carried out to decrease the absorption contrast of unnecessary regions. The contrast resolution of a target region was increased using the subtraction program and a linear-contrast system in a flat panel detector (FPD). The X-ray generator had a 100 μm-focus tube, and the subtractions were performed at tube voltages of 40 and 70 kV, a tube current of 0.50 mA, and an X-ray exposure time of 5.0 s. ER was achieved with cohesion imaging using the FPD with pixel sizes of 48×48 μm 2 , and the shifting dimension of an object in the horizontal and vertical directions ranged from 48 to 96 μm. At a shifting distance of 96 μm, the spatial resolutions in the horizontal and vertical directions measured with a lead test chart were both 83 μm. In ER of animal phantoms, we obtained high-contrast embossed images of fine bones, gadolinium oxide particles in blood vessels, iodine-based microspheres in coronary arteries approximately 100 μm in diameter.

An energy-discrimination K-edge X-ray computed tomography (CT) system is useful for increasing the contrast resolution of a target region by utilizing contrast media. The CT system has a cadmium telluride (CdTe) detector, and a projection curve is obtained by linear scanning with use of the CdTe detector in conjunction with an X-stage. An object is rotated by a rotation step angle with use of a turntable between the linear scans. Thus, CT is carried out by repetition of the linear scanning and the rotation of an object. Penetrating X-ray photons from the object are detected by the CdTe detector, and event signals of X-ray photons are produced with use of charge-sensitive and shaping amplifiers. Both the photon energy and the energy width are selected by use of a multi-channel analyzer, and the number of photons is counted by a counter card. For performing energy discrimination, a low-dose-rate X-ray generator for photon counting was developed; the maximum tube voltage and the minimum tube current were 110 kV and 1.0 microA, respectively. In energy-discrimination CT, the tube voltage and the current were 60 kV and 20.0 microA, respectively, and the X-ray intensity was 0.735 microGy/s at 1.0 m from the source and with a tube voltage of 60 kV. Demonstration of enhanced iodine K-edge X-ray CT was carried out by selection of photons with energies just beyond the iodine K-edge energy of 33.2 keV.

HIV infection is a major problem in Indonesia. The number of people living with HIV has been increasing from year to year, especially among injecting drug users (IDUs). Since there were only limited data about molecular epidemiology profiles of HIV/AIDS in Indonesia, a cross-sectional study involving 208 HIV-1-seropositive individuals was conducted in 2007 in Jakarta. The majority of participants were 16–30 years of age (64.9%) and 74.5% were male. The most frequent risk factor was injecting drug use (IDU) (45.7%) followed by heterosexual transmission (34.1%). Phylogenetic analysis of gag (p17 and p6) and env C2V3 regions showed 200 (96.2%) of 208 DNA samples were CRF01_AE and only 3 (1.4%) were subtype B. Five samples (2.4%) indicated discordant subtypes between the three aforementioned regions: three of them showed unique CRF01_AE/B recombination patterns in 2.3-kbp nucleotide sequences (from p17 to part of RT), including one sample showing similarity to CRF33_01B, reported previously in Malaysia. This study shows the current predominant subtype is CRF01_AE in every risk group, with a decreasing number of pure subtype B, and the first identification of CRF01_AE/B recombinant forms among HIV-1-seropositive Indonesians.

人間の体は器官・部位ごとに独立して機能しているわけではなく, 顔面皮膚以外の器官が顔面皮膚に影響を及ぼす例は, 多くの女性が経験し認知している。その影響は, 美容上無視できないほどのものである。昨今, 首から肩にかけた部位の苦痛・不快感 (いわゆる, こり感) を抱く人たちが増加していることに着目し, それが顔面美容に影響を及ぼすのか, 及ぼすとすれば, その状態を緩和することで顔面美容の改善を得ることができるのかを検討した。その結果, 首から肩にかけた部位に抱く苦痛・不快感は, その部位の筋緊張の昂進, 筋硬度の増加と関係しており, 額の表情筋である前頭筋の緊張, ひいては額のシワ程度にも関係していることがわかった。そして, 頸部や背面上部の筋肉の緊張を緩和することを目的としたボディマッサージ施術により, 前頭筋の緊張緩和や額のシワ程度の改善が認められた。顔面以外の要因が顔面美容に悪影響を及ぼしている例はほかにもあると考えられ, われわれの結果は, 今後, 顔面皮膚を美しく健やかにするための方策について, 個体全体で考える必要性があることを示唆するものである。

Rice bran oil is a byproduct of the milling of rice (Oryza sativa L.). It offers various health benefits and has a beneficial fatty acid composition. To increase the amount of rice bran as a sink for triacylglycerol (TAG), we developed and characterized new breeding materials with giant embryos. To induce mutants, we treated fertilized egg cells of the high-yielding cultivar ‘Mizuhochikara’ with N-methyl-N-nitrosourea (MNU). By screening M2 seeds, we isolated four giant embryo mutant lines. Genetic analysis revealed that the causative loci in lines MGE12 and MGE13 were allelic to giant embryo (ge) on chromosome 7, and had base changes in the causal gene Os07g0603700. On the other hand, the causative loci in lines MGE8 and MGE14 were not allelic to ge, and both were newly mapped on chromosome 3. The TAG contents of all four mutant lines increased relative to their wild type, ‘Mizuhochikara’. MGE13 was agronomically similar to ‘Mizuhochikara’ and would be useful for breeding for improved oil content.

The x-ray generator consists of the following components : a constant high-voltage power supply, a filament power supply, a turbomolecular pump, and an x-ray tube. The x-ray tube is a demountable diode which is connected to the turbomolecular pump and consists of the following major devices : a tungsten hairpin cathode (filament), a focusing electrode, a polyethylene terephthalate x-ray window 0.25mm in thickness, a stainless-steel tube body, and a rod target. In the x-ray tube, the positive high voltage is applied to the anode (target) electrode, and the cathode is connected to the tube body (ground potential). In this experiment, the tube voltage applied was from 12 to 18kV, and the tube current was regulated to within 0.10mA by the filament temperature. The electron beams from the cathode are converged to the target by the focusing electrode, and x-rays are produced from the target plane. The x-ray spectra were measured from two directions with angles between the electron trajectory and the x-ray beam axis of 180° and 90°. As compared with the x-ray spectra with an angle of 90°, the bremsstrahlung x-ray intensity decreased slightly with an angle of 180° (opposite direction to that of electron trajectory).

The 100-μm-focus x-ray generator consists of a main controller for regulating the tube voltage and current and a tube unit with a high-voltage circuit and a fixed anode x-ray tube. The maximum tube voltage, current, and electric power were 105kV, 0.5mA, and 50W, respectively. Using a 3-mm-thick aluminum filter, the x-ray intensity was 26.0μGy/s at 1.0m from the source with a tube voltage of 60kV and a current of 0.50 mA. Because the peak photon energy was approximately 35keV using the filter with a tube voltage of 60kV, the bremsstrahlung x-rays were absorbed effectively by iodine-based contrast media with an iodine K-edge of 33.2keV. Enhanced angiography was achieved with a flat panel detector with a pixel size of 50μm using iodine-based microspheres 15μm in diameter. In angiography of non-living animals, we observed fine blood vessels of approximately 100gm with high contrasts.

The cerium-target x-ray tube is useful in order to perform cone-beam K-edge angiography because K-series characteristic x-rays from the cerium target are absorbed effectively by iodine-based contrast media. The x-ray generator consists of a main controller and a unit with a high-voltage circuit and a fixed anode x-ray tube. The tube is a glass-enclosed diode with a cerium target and a 0.5-mm-thick beryllium window. The maximum tube voltage and current were 70kV and 0.40mA, respectively, and the focal-spot sizes were approximately 1×1mm. Cerium K-series characteristic x-rays were left using a cerium oxide powder filter, and the x-ray intensity was 14.3μGy/s at 1.0m from the source with a tube voltage of 60kV, a current of 0.40mA, and an exposure time of 1.0s. Angiography was performed with a computed radiography system using iodine-based microspheres 15μm in diameter. In angiography of non-living animals, we observed fine blood vessels of approximately 100μm with high contrasts.

This generator consists of the following components: a constant high-voltage power supply, a filament power supply, a turbomolecular pump, and an x-ray tube. The x-ray tube is a demountable diode which is connected to the turbomolecular pump and consists of the following major devices: a molybdenum rod target, a tungsten hairpin cathode (filament), a focusing electrode, a polyethylene terephthalate x-ray window 0.25mm in thickness, and a stainless-steel tube body. In the x-ray tube, the positive high voltage is applied to the anode (target) electrode, and the cathode is connected to the tube body (ground potential). In this experiment, the tube voltage applied was from 22 to 36kV, and the tube current was regulated to within 100μA by the filament temperature. The exposure time is controlled in order to obtain optimum x-ray intensity. The electron beams from the cathode are converged to the target by the focusing electrode, and x-rays are produced through the focusing electrode. Using a lithium fluoride curved crystal, clean K-series characteristic x-rays were observed without using a filter. However, bremsstrahlung x-rays were observed using a cadmium telluride detector.

The development of an extremely soft x-ray generator with a tungsten-target tube and its applications including radiography are described. This generator consists of a high-voltage transformer, a filament power supply, and an x-ray tube. Negative high voltages are applied to the cathode electrode in the x-ray tube, and the tube voltage and current are regulated by the input voltage of the transformer and the filament voltage, respectively. The x-ray tube is a glass-enclosed double-focus diode with a tungsten target and a 0.2 mm-thick beryllium window. The maximum tube voltage and the electric power were 60 kV and 400 W, respectively. The focal-spot sizes were 4×4 (large) and 1×1 mm (small), respectively. Radiography was performed with a computed radiography system. In angiography using iodine-based microspheres, we observed fine blood vessels of about 50 μm or less with high contrasts. Using this generator, we designed an experimental setup for disinfection achieved with extremely soft x rays.

In the plasma flash x-ray generator, a high-voltage main condenser of approximately 200 nF is charged up to 50 kV by a power supply, and electric charges in the condenser are discharged to an x-ray tube after triggering the cathode electrode. Flash x rays are then produced. The x-ray tube is a demountable triode connected to a turbo molecular pump with a pressure of approximately 1 mPa. As electrons from the cathode electrode are roughly focused onto a rod nickel target of 3.0 mm in diameter by the electric field in the x-ray tube, a weakly ionized linear plasma consisting of nickel ions and electrons forms by target evaporation. At a charging voltage of 50 kV, the maximum tube voltage was almost equal to the charging voltage of the main condenser, and the peak current was about 17 kA. When the charging voltage was increased, the linear plasma formed, and the intensities of K-series characteristic x rays increased. The K-series lines were quite sharp and intense, and hardly any bremsstrahlung rays were detected. The x-ray pulse widths were approximately 700 ns, and the time-integrated x-ray intensity had a value of approximately 30 μC/kg at 1.0 m from the x-ray source at a charging voltage of 50 kV.

The silkworm larvae plasma (SLP) test has been established based on a cascade reaction triggered by either peptidoglycan or (1, 3)-beta-D-glucan to produce melanin. We applied this test to the diagnosis of bacterial meningitis. Cerebrospinal fluid (CSF) obtained from patients with bacterial meningitis due to gram-positive bacteria, gram-negative bacteria, or fungi, showed positive reactions to the test. In contrast, CSF from patients with viral meningitis or noninfectious illnesses gave negative reactions. Therefore, this test seems to be useful for diagnosis of bacterial and fungal meningitis. When this test was used together with two types of limulus tests, an endotoxin-specific test, and a conventional test, meningitis was further characterized as gram-positive, gram-negative or fungal meningitis. The SLP test requires a computerized instrument for quantitative colorimetric measurement. A qualitative alternative of this test also can be accomplished by visually observing the darkening color. Thus, this method can be applied for simple and rapid diagnosis of meningitis.

It has been reported that subtypes A throughout H of HIV-1 are circulating in the former Soviet Union. In this sequence note, we analyzed the genetic prevalence of HIV-1 among injecting drug users (IDUs) in Ukraine. The subjects studied included two individuals from Kiev and six individuals from Simferopol', the latter located in the Crimean Peninsula. We found that one of eight IDUs was infected with a CRF03 gagA/envB recombinant HIV-1 and was from Simferopol', whereas the others were infected with HIV-1 subtype A. The recombinant was closely related to other A/B recombinants reported previously, and had silent mutations in the V3 region, the same as other envB strains of HIV-1 circulating among IDUs in the former Soviet Union. The data supported reports that the Russian A/B recombinant HIV-1 was probably from Ukraine. This is the first report of a CRF03 gagA/envB recombinant HIV-1 found in Ukraine.

従来から顔面で皮脂の多い部分は, 額, 鼻, 顎とされTゾーンと呼ばれているが, これらと現実の化粧くずれは必ずしも一致していない。そこでわれわれはこの検証を行うため, 美容スタップを対象とした意識調査や顔面各部位の皮脂測定および皮脂分泌状態の観察を行った。その結果, 顔面を19部位に分割することで, 個人の皮脂ランクパターンが表現できることを確認した。次に化粧仕上がりおよび化粧くずれに対する乳液の影響を顔面各部位で評価したところ, その部位の皮脂ランクによりプァンデーションの付着量に差があり化粧くずれ印象も異なることを確認した。これらの結果よりわれわれは, 皮脂量の多い鼻, 眉間, 頬上内側および顎の部位を一括してIゾーンと呼ぶことがふさわしいと考えた。また, ベースメイクを行う際には, 各自の各部位の肌性に合ったモイスチャー品のタイプの選択および使用量の調整を考慮すべきであると考えた。

Neurologic diseases are important complications of measles. The role of virus infection of the central nervous system as well as the route of virus entry has been unclear. Five autopsied cases of individuals who died with severe acute measles 3-10 d after the onset of the rash were studied for evidence of viral involvement of the central nervous system. In all cases, in situ hybridization and RT-PCR in situ hybridization techniques showed endothelial cell infection. Immunoperoxidase staining with an anti-ferritin antibody revealed a reactive microgliosis. These data suggest that endothelial cells in the brain are frequently infected during acute fatal measles. This site of infection may provide a portal of entry for virus in individuals who subsequently develop subacute sclerosing panencephalitis or measles inclusion body encephalitis and a target for immunologic reactions in post-measles encephalomyelitis.

The purpose of this study was to investigate intention to leave in relation to organizational factors and work environments among newly graduated nurses (NGN).A questionnaire was delivered to NGN (n = 762) from baccalaureate programs as well as diploma schools from 19 R-hospitals (R-hospitals were designated as "public medical institutions" by the 1951 Medical Law) in 2010. Spearman's rank correlation coefficients and Mann-Whitney U-test were used to test statistical significance.Only 148 questionnaires were returned for a return rate of 19.4%. The authors found that 8.1% of respondents had a highly to extremely likely desire to leave nursing. Intention to leave was significantly associated with Nursing Work Index total (P 0.01), social support (P 0.001), work barriers (P 0.001), commitment to workplace (P 0.001), job satisfaction (P 0.001), and burnout (P 0.001). Those who graduated from R-schools run by the R-organization had significantly positive impressions of their organizations and significantly lower intentions to leave compared to other graduates.The study results suggest that NGN intention to leave the workplace and nursing predict actual early intention to leave. In order to reduce burnout and turnover, support from colleagues and supervisors appears to be essential in organizational and psychosocial work environments for NGN to experience job satisfaction and be committed to their workplace. The results of this study also suggest that a longitudinal study is needed to reveal the long-term effects of organizational factors and work environments on NGN and how they impact role transition and adaptation of the NGN to professional practice roles.

In order to identify potential unanticipated side reactions and immune responses, the evaluation of candidate vaccines should include immunization of the murine model of the disease in question and mutant animals, as well as normal laboratory animals. We employed WBB6F(1)-W/W(v) and WBB6F(1)-Sl/Sl(d) mutant mice, which are genetically mast cell deficient and lack intestinal pacemaker activity due to a severe deficiency in interstitial cells of Cajal. Antigen-specific mucosal and systemic immune responses in the mutant and congenic normal mice were induced by intranasal or intragastric immunization with ovalbumin (OVA) plus cholera toxin as an adjuvant. It was found that the levels of the OVA-specific humoral immune response in the mucosal and systemic tissues of the mutant mice immunized intranasally were roughly equivalent to those of the congenic normal mice. In contrast, the specific humoral immune response in the intragastrically immunized mutant mice was greater than that observed in the congenic normal mice. Unexpectedly, the titers of OVA-specific IgA antibodies and total IgA antibodies in the fecal extracts of both intranasally and intragastrically immunized mutant mice were significantly lower than in those of the congenic normal mice. Although the detailed mechanisms leading to these differences remain unclear, the unexpected immune responses observed in the gastrointestinal tracts of the mice in this study may be related to an abnormality of gastrointestinal motility. Our data therefore suggest that studies using mutant mice and physiological assessments should be carried out during mucosal vaccine development.

Cocirculation of subtype B and CRF01_AE in Southeast Asia has led to the establishment of new recombinant forms. In our previous study, we found five samples suspected of being recombinants between subtype B and CRF01_AE, and here, we analyzed near full-length sequences of two samples and compared them to known CRFs_01B, subtype B, and CRF01_AE. Five overlapped segments were amplified with nested PCR from PBMC DNA, sequenced, and analyzed for genome mosaicism. The two Indonesian samples, 07IDJKT189 and 07IDJKT194, showed genome-mosaic patterns similar to CRF33_01B references from Malaysia, with one short segment in the 3' end of the p31 integrase-coding region, which was rather more similar to subtype B than CRF01_AE, consisting of unclassified sequences. These results suggest gene-specific continuous diversification and spread of the CRF33_01B genomes in Southeast Asia.

Herpes simplex virus type 1 (HSV1) and type 2 (HSV2) were differentiated on the basis of different plaque appearance on semicontinuous rabbit lens epithelial (RLE) cells. Plaques produced by HSV1 strains were small; the mean diameter was 1.29 +/- 0.37 mm 3 days after inoculation. HSV2 strains produced large and small plaques, with the ratio of large to small about 20:1. The mean diameters of the large and the small plaques of HSV2 were 3.34 +/- 0.56 mm and 0.97 +/- 0.31 mm respectively 3 days after inoculation. The clones from the large plaques consistently produced large and small plaques and the small-plaque clones produced only small plaques. Round cells plus heterokaryotes were characteristic of the CPE of HSV1. Large plaques of HSV2 were produced by a large membranous syncytium that was liable to lyse. Small round cells were characteristic of the CPE of the small-plaque clones of HSV2. Glycoprotein C-negative (gC-) strains produced intermediate-sized plaques and a few pin point ones that consisted of membranous syncytia and round cells, respectively. Except for the HF strain (a reference strain of HSV1 producing a membranous syncytium on RLE cells), the result of the differentiation of HSV1 (179 strains) and HSV2 (40 strains) with the RLE plaque assay system was consistent with that of Syva's monoclonal antibody assay system and the restriction endonuclease digestion method.

An energy-discrimination K-edge x-ray computed tomography (CT) system is useful for controlling the image contrast of a target region by selecting both the photon energy and the energy width. The CT system has an oscillation-type linear cadmium telluride (CdTe) detectror. CT is performed by repeated linear scans and rotations of an object. Penetrating x-ray photons from the object are detected by a CdTe detector, and event signals of x-ray photons are produced using charge-sensitive and shaping amplifiers. Both photon energy and energy width are selected out using a multichannel analyzer, and the number of photons is counted by a counter card. In energy-discrimination CT, the tube voltage and tube current were 80 kV and 20 μA, respectively, and the x-ray intensity was 1.92 μGy/s at a distance of 1.0 m from the source and a tube voltage of 80 kV. The energy-discrimination CT was carried out by selecting x-ray photon energies.

We developed an embossed radiography system utilizing single- and dual-energy subtractions for decreasing the absorption contrast of unnecessary regions, and contrast resolution of a target region was increased using image-shifting subtraction and a linear-contrast system in a flat panel detector (FPD). To carry out embossed radiography, we developed a computer program for two-dimensional subtraction, and a conventional x-ray generator with a 0.5-mm-focus tube was used. Energy subtraction was performed at tube voltages of 42.5 and 70.0 kV, a tube current of 1.0 mA, and an x-ray exposure time of 5.0 s. Embossed radiography was achieved with cohesion imaging by use of the FPD with pixel sizes of 48 ×48 μm, and the shifting dimension of an object in the horizontal and vertical directions ranged from 48 to 144 μm. We obtained high-contrast embossed images of fine bones and coronary arteries approximately 100 μm in diameter.

High-speed photon counting is useful for discriminating photon energy and for decreasing absorbed dose for patients in medical radiography, and the counting is usable for constructing an x-ray computed tomography (CT) system. A photon-counting x-ray CT system is of the first generation type and consists of an x-ray generator, a turn table, a translation stage, a two-stage controller, a multipixel photon counter (MPPC) module, a 1.0-mm-thick LSO crystal (scintillator), a counter card (CC), and a personal computer (PC). Tomography is accomplished by repeating the linear scanning and the rotation of an object, and projection curves of the object are obtained by the linear scanning using the detector consisting of a MPPC module and the LSO. The pulses of the event signal from the module are counted by the CC in conjunction with the PC. The lower level of the photon energy is roughly determined by a comparator circuit in the module, and the unit of the level is the photon equivalent (pe). Thus, the average photon energy of the x-ray spectra increases with increasing the lower-level voltage of the comparator. The maximum count rate was approximately 20 Mcps, and energy-discriminated CT was roughly carried out.

Background Shiga toxins (Stxs) are the major agents responsible for hemorrhagic colitis and hemolytic-uremic syndrome (HUS) during infections caused by Stx-producing Escherichia coli (STEC) such as serotype O157:H7. Central nervous system (CNS) involvement is an important determinant of mortality in diarrhea associated-HUS. It has been suggested that vascular endothelial injuries caused by Stxs play a crucial role in the development of the disease. The current study investigates the relationship between the cytotoxic effects of Stxs and inflammatory responses in a rabbit brain treated with Stx2. Methods In a rabbit model treated with purified Stx2 or PBS(-), we examined the expression of the Stx receptor globotriaosylceramide (Gb3)/CD77 in the CNS and microglial activation using immunohistochemistry. The relationship between inflammatory responses and neuronal cell death was analyzed by the following methods: real time quantitative reverse transcriptase (RT)-polymerase chain reaction (PCR) to determine the expression levels of pro-inflammatory cytokines, and the terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick-end labeling (TUNEL) method to detect apoptotic changes. Results Gb3/CD77 expression was detected in endothelial cells but not in neurons or glial cells. In the spinal cord gray matter, significant levels of Gb3/CD77 expression were observed. Severe endothelial injury and microvascular thrombosis resulted in extensive necrotic infarction, which led to acute neuronal damage. Conversely, in the brain, Stx receptor expression was much lower. The observed neuropathology was less severe. However, neuronal apoptosis was observed at the onset of neurological symptoms, and the number of apoptotic cells significantly increased in the brain at a later stage, several days after onset. Microglial activation was observed, and tumor necrosis factor (TNF)-α and interleukin (IL)-1β mRNA in the CNS parenchyma was significantly up-regulated. There was significant overexpression of TNF-α transcripts in the brain. Conclusion This study indicates that Stx2 may not directly damage neural cells, but rather inflammatory responses occur in the brain parenchyma in response to primary injury by Stx2 in vascular endothelial cells expressing Gb3/CD77. These findings suggest that neuroinflammation may play a critical role in neurodegenerative processes during STEC infection and that anti-inflammatory intervention may have therapeutic potential.

The purpose of skincare is to make the skin keep and improve to physiologically good condition. So, we hypothesized that it was the most important thing for effective skincare to fit in with individual skin condition, which was applied by the skincare system based on scientific and detailed skin classification.The women of 113 were divided to two groups, “individual skin fitting group” whose skin condition were measured by scientific methods and classified, and “control group” who were treating their skin by oneself. We evaluated effectiveness of the system by means of the corneous cell examinations of each skin of two groups before and after the use test of 6 weeks.As the result, individual skin fitting group showed the tendency of improvement on Thick Abration and regularity of corneous cell arrangment in comparison with control group.Therefore, we think it substantiate the effectiveness of the system to fit in with individual skin condition.

A preliminary experiment for producing narrow-photon-energy cone-beam x-rays using a silicon single crystal is described. In order to produce low-photon-energy x-rays, a 100-µm-focus x-ray generator in conjunction with a (111) plane silicon crystal is employed. The x-ray beams from the source are confined by an x-y diaphragm, and monochromatic cone beams are formed by the crystal and three lead plates. The x-ray generator consists of a main controller and a unit with a high-voltage circuit and a 100-µm-focus x-ray tube. In this experiment, the maximum tube voltage and current were 35 kV and 0.50 mA, respectively, and the x-ray intensity of the microfocus generator was 343 μGy/s at 1.0 m from the source with a tube voltage of 30 kV and a current of 0.50 mA. The effective photon energy is determined by Bragg's angle, and the photon-energy width is regulated by the angle delta. Using this generator in conjunction with a computed radiography system, quasi-monochromatic radiography was performed using a cone beam with an effective energy of approximately 15.5 keV.

A microfocus x-ray tube is useful in order to perform magnification digital radiography including phase-contrast effect. The 100-µm-focus x-ray generator consists of a main controller for regulating the tube voltage and current and a tube unit with a high-voltage circuit and a fixed anode x-ray tube. The maximum tube voltage, current, and electric power were 105 kV, 0.5 mA, and 50 W, respectively. Using a 3.0-mm-thick aluminum filter, the x-ray intensity was 26.0 µGy/s at 1.0 m from the source with a tube voltage of 60 kV and a current of 0.50 mA. Because the peak photon energy was approximately 35 keV using the filter with a tube voltage of 60 kV, the bremsstrahlung x-rays were absorbed effectively by iodine-based contrast media with an iodine K-edge of 33.2 keV. Magnification angiography was performed by two-time magnification imaging with a computed radiography system using iodine-based microspheres 15 µm in diameter. In angiography of non-living animals, we observed fine blood vessels of approximately 100 µm with high contrasts.

The samarium-target x-ray tube is useful in order to perform cone-beam K-edge angiography because K-series characteristic x-rays from the samarium target are absorbed effectively by iodine-based contrast media. This generator consists of the following components: a constant high-voltage power supply, a filament power supply, a turbomolecular pump, and an x-ray tube. The x-ray tube is a demountable diode which is connected to the turbomolecular pump and consists of the following major devices: a samarium target, a tungsten hairpin cathode (filament), a focusing (Wehnelt) electrode, a polyethylene terephthalate x-ray window 0.25 mm in thickness, and a stainless-steel tube body. In the x-ray tube, the positive high voltage is applied to the anode (target) electrode, and the cathode is connected to the tube body (ground potential). In this experiment, the tube voltage applied was from 50 to 70 kV, and the tube current was regulated to within 0.10 mA by the filament temperature. The exposure time is controlled in order to obtain optimum x-ray intensity. The electron beams from the cathode are converged to the target by the focusing electrode, and bremsstrahlung x-rays were absorbed using a 50-µm-thick tungsten filter. The x-ray intensity was 1.04 μGy/s at 1.0 m from the x-ray source with a tube voltage of 60 kV and a tube current of 0.10 mA, and angiography was performed using a computed radiography system and iodine-based microspheres 15 µm in diameter. In angiography of non-living animals, we observed fine blood vessels of approximately 100 µm with high contrasts.

A microfocus x-ray tube is useful in order to perform magnification digital radiography. The 100-µm-focus x-ray generator consists of a main controller for regulating the tube voltage and current and a tube unit with a high-voltage circuit and a fixed anode x-ray tube. The maximum tube voltage, current, and electric power were 105 kV, 0.5 mA, and 50 W, respectively. Using a 50-µm-thick tungsten filter, the x-ray intensity was 34.0 µGy/s at 1.0 m from the source with a tube voltage of 100 kV and a current of 0.50 mA. Since K-series characteristic x-rays from tungsten targets are absorbed effectively by gadolinium-based contrast media, these x-rays are very useful to perform enhanced angiography. Magnification angiography was performed by two-time magnification imaging with a computed radiography system. In angiography of non-living animals, we observed fine blood vessels of approximately 100 µm with high contrasts.

Novel monochromatic x-ray generators and their applications to high-speed radiography are described. The five generators are as follows: a weakly ionized linear plasma x-ray generator, a monochromatic compact flash x-ray generator, a super-fluorescent plasma generator, a cerium x-ray generator using a 3.0-mm-thick aluminum filter, and a 100micron-focus x-ray generator utilizing the filter. Using the linear plasma generator with a copper target, we observed clean K lines and their harmonics, and soft flash radiography was performed with pulse widths of approximately 500 ns. The compact monochromatic flash x-ray generator produced clean molybdenum K lines easily, and high-speed radiography was performed with pulse widths of approximately 100 ns. Using a steady-state cerium x-ray generator, we performed real-time angiography utilizing an image intensifier and a high-sensitive camera (MLX) made by NAC Image Technology Inc. with a capture time of 1 ms. Finally, real-time magnification radiography was performed by twofold magnification imaging using a 100micron-focus x-ray generator and the high-sensitive camera.

A microfocus x-ray tube is useful in order to perform magnification digital radiography including phase-contrast effect. The 100-µm-focus x-ray generator consists of a main controller for regulating the tube voltage and current and a tube unit, with a high-voltage circuit and a fixed anode x-ray tube. The maximum tube voltage, current, and electric power were 105 kV, 0.5 mA, and 50 W, respectively. Using a 3.0-mm-thick aluminum filter, the x-ray intensity was 26.0 µGy/s at 1.0 m from the source with a tube voltage of 60 kV and a current of 0.50 mA. Because the peak photon energy was approximately 35 keV using the filter with a tube voltage of 60 kV, the bremsstrahlung x-rays were absorbed effectively by iodine-based contrast media with an iodine K-edge of 33.2 keV. Real-time magnification radiography was performed by twofold magnification imaging with an image intensifier camera, and angiography was achieved with iodine-based microspheres 15 µm in diameter. In angiography of non-living animals, we observed fine blood vessels of approximately 100 µm with high contrasts.

This generator consists of the following components: a constant high-voltage power supply, a filament power supply, a turbomolecular pump, and an x-ray tube. The x-ray tube is a demountable diode which is connected to the turbomolecular pump and consists of the following major devices: a tungsten hairpin cathode (filament), a focusing (Wehnelt) electrode, a polyethylene terephthalate x-ray window 0.25 mm in thickness, a stainless-steel tube body, a pipe target, and a rod target. The pipe and rod targets are useful for forming linear and cone beams, respectively. In the x-ray tube, the positive high voltage is applied to the anode (target) electrode, and the cathode is connected to the tube body (ground potential). In this experiment, the tube voltage applied was from12 to 20 kV, and the tube current was regulated to within 0.10 mA by the filament temperature. The exposure time is controlled in order to obtain optimum x-ray intensity. The electron beams from the cathode are converged to the target by the focusing electrode, and clean K-series characteristic x-rays are produced through the focusing electrode without using a filter. The x-ray intensities of the pipe and rod targets were 1.29 and 4.28 μGy/s at 1.0 m from the x-ray source with a tube voltage of 15 kV and a tube current of 0.10 mA, and quasi-monochromatic radiography was performed using a computed radiography system.

Although there have been many reports of the usefulness of serodiagnosis of enterohemorrhagic Escherichia coli (EHEC) O157, the serotype of the bacteria detected and the increase in anti-LPS antibody have not always been consistent. In this study we investigated the diagnostic significance of measurements of anti-LPS antibody by ELISA in an outbreak of O157 infection among schoolchildren in whom the bacteriological test findings were clarified and the age groups were uniform. The anti-LPS antibody titer was measured in 31 patients (77 serum samples) in an outbreak of EHEC O157 : H7 infection (220 children infected) that occurred in a primary school in Morioka in 1996. The anti-O157 LPS antibody positivity rates of IgM, IgG, and IgA were 98.7%, 85.7%, and 98.7%, respectively. Between the time the meal that caused the outbreak and 19 days later, anti-O157 LPS IgM antibody and IgA antibody were detected in all patients. The specificity was investigated using control serum, and the specificity of IgM, IgG, and IgA was 93.5%, 93.5%, and 97.2%, respectively. Some samples contained antibodies against O111 and O26 LPS, but the titers were lower than the anti-O157 antibody titer. The anti-O111 antibody titer and anti-O26 antibody titer were highly correlated, suggesting that they were crossreactive antibodies for O157 LPS. No significant correlation was found between differences in clinical manifestations and the anti-O157 LPS antibody titer in this O157 outbreak in schoolchildren. It was clarified that an increase in anti-LPS antibody was found to support the diagnosis of mild cases of 0157 infection infection as well as severe cases.

The development of an extremely soft x-ray generator with a tungsten-target tube and its applications to radiography and disinfection are described. This generator consists of a high-voltage power supply, a filament power supply, and an x-ray tube. Negative high voltages are applied to the cathode electrode in the x-ray tube, and the tube voltage and current are regulated by the input of a transformer and the filament voltage, respectively. The x-ray tube is a glass-enclosed double-focus diode with a tungsten target and a 0.2 mm-thick beryllium window. The maximum tube voltage and electric power were 60 kV and 400 W, respectively. The focal-spot sizes were 4×4 (large) and 1×1 mm (small), respectively. Extremely soft radiography was performed with a computed radiography system, and we observed fine blood vessels of about 100 μm with high contrasts. Using this generator, we performed the disinfection achieved with extremely soft x rays.

In the plasma flash x-ray generator, high-voltage main condenser of about 200 nF is charged up to 55 kV by a power supply, and electric charges in the condenser are discharged to an x-ray tube after triggering the cathode electrode. The flash x-rays are then produced. The x-ray tube is of a demountable triode that is connected to a turbo molecular pump with a pressure of approximately 1 mPa. As electron flows from the cathode electrode are roughly converged to a rod cerium target of 3.0 mm in diameter by electric field in the x-ray tube, the weakly ionized linear plasma, which consists of cerium ions and electrons, forms by target evaporating. At a charging voltage of 55 kV, the maximum tube voltage was almost equal to the charging voltage of the main condenser, and the peak current was about 20 kA. When the charging voltage was increased, weakly ionized cerium plasma formed, and the K-series characteristic x-ray intensities increased. The x-ray pulse widths were about 500 ns, and the time-integrated x-ray intensity had a value of about 40 μC/kg at 1.0 m from x-ray source with a charging voltage of 55 kV. In the angiography, we employed a film-less computed radiography (CR) system and iodine-based microspheres. Because K-series characteristic x-rays are absorbed easily by the microspheres, high-contrast angiography has been performed.

A fundamental study on quasi-monochromatic parallel radiography using a polycapillary plate and a copper-target x-ray tube is described. The x-ray generator consists of a negative high-voltage power supply, a filament (hot cathode) power supply, and an x-ray tube. The negative high-voltage is applied to the cathode electrode, and the anode electrode is connected to the ground. In this experiment, the tube voltage was regulated from 12 to 22 kV, and the tube current was regulated within 3.0 mA by the filament temperature. The exposure time was controlled in order to obtain optimum x-ray intensity, and the maximum focal spot dimensions were approximately 2.0 x 1.5 mm. The polycapillary plate was J5022-16 (Hamamatsu Photonics Inc.), and the plate thickness was 1.0 mm. The outer, effective, and hole diameters were 33 mm, 27 mm, and 10 μm, respectively. Quasi-monochromatic x-rays were produced using a 10 μm-thick copper filter with a tube voltage of 17 kV, and these rays were formed into parallel beams by the polycapillary. The radiogram was taken using a computed radiography system utilizing imaging plates. In the measurement of image resolution, the resolution hadly varied according to increases in the distance between the chart and imaging plate using a polycapillary. We could observe a 50 μm tungsten wire clearly, and fine blood vessels of approximately 100 μm were visible in angiography.

In the plasma flash x-ray generator, a high-voltage main condenser of approximately 200 nF is charged up to 50 kV by a power supply, and electric charges in the condenser are discharged to an x-ray tube after triggering the cathode electrode. The flash x-rays are then produced. The x-ray tube is a demountable triode that is connected to a turbo molecular pump with a pressure of approximately 1 mPa. As electron flows from the cathode electrode are roughly converged to a rod copper target of 3.0 mm in diameter by the electric field in the x-ray tube, weakly ionized linear plasma, which consists of copper ions and electrons, forms by target evaporation. At a charging voltage of 50 kV, the maximum tube voltage was almost equal to the charging voltage of the main condenser, and the peak current was about 15 kA. When the charging voltage was increased, the linear plasma formed, and the K-series characteristic x-ray intensities increased. The K-series lines were quite sharp and intense, and hardly any bremsstrahlung rays were detected. The x-ray pulse widths were approximately 700 ns, and the time-integrated x-ray intensity had a value of approximately 30 μC/kg at 1.0 m from the x-ray source with a charging voltage of 50 kV.

HIV-induced neurological disease is postulated to be caused by indirect mechanisms. Tumor necrosis factor (TNF)alpha is increased in the brains in human immunodeficiency virus (HIV)-associated dementia and in the spinal cord in vacuolar myelopathy and may play a pathogenetic role in these diseases. Microglia, astrocytes and infiltrating macrophages can be induced to produce TNF alpha and each has been identified as a source of TNF alpha in neurological disease. Reverse transcriptase synthesis of cDNA and polymerase chain reaction amplification of the cDNA was combined with immunocytochemistry to identify the cellular source of TNF alpha in HIV-induced neurological disease. Cells positive for TNF alpha mRNA were more abundant in white matter than gray matter of the brain from demented individuals. TNF alpha mRNA-positive cells in brains and spinal cords were almost exclusively macrophage-lineage cells. Only rare TNF alpha mRNA-positive cells were astrocytes. We conclude that macrophage-lineage cells are the primary source of elevated central nervous system TNF alpha mRNA in providing further evidence that macrophage activation is an important element in the pathogenesis of HIV-associated neurological disease.

Human immunodeficiency virus type 1 (HIV-1) infects the brains of a majority of patients with the acquired immunodeficiency syndrome (AIDS), and has been linked to the development of a progressive dementia termed “HIV-associated dementia.” This disorder results in severe cognitive, behavioral, and motor deficits. Despite this neurological dysfunction, HIV-1 infection of brain cells does not occur significantly in neurons, astrocytes, or oligodendrocytes, but is restricted to brain macrophages and microglia. To identify possible low-level or latent infection of other brain cells, we combined the techniques of the polymerase chain reaction with in situ hybridization for the detection of HIV DNA, and used immunocytochemistry to identify the HIV-expressing cells. In the 21 adult brains studied (15 AIDS and 6 seronegative control brains), we found that polymerase chain reaction/in situ hybridization was both sensitive and specific for identifying HIV-infected cells. In all brains, the majority of infected cells were macrophages and microglia. In several brains, however, a substantial minority of cells harboring HIV DNA were identified as astrocytes. Neurons, oligodendrocytes, and endothelial cells were not infected with HIV, even in cases with HIV-associated dementia. These findings confirm previous data regarding the importance of macrophage/microglial infection, and essentially exclude neuronal infection in pathogenetic models of HIV-associated neurological disease. These data also demonstrate that latent or low-level infection of astrocytes occurs in AIDS, a finding that may be of importance in understanding HIV neuropathogenesis.

We developed an image-shifting subtraction program and carried out magnification embossed radiography (MER) utilizing single- and dual-energy subtractions. In particular, dual-energy subtraction was carried out to decrease the absorption contrast of unnecessary regions. The contrast resolution of the target region was increased by the use of subtraction software and a linear-contrast system in a flat-panel detector (FPD). The X-ray generator had a 100-µm-focus tube, and the subtractions were performed at tube voltages of 40 and 70 kV, a tube current of 0.50 mA, and an X-ray exposure time of 5.0 s. MER images with threefold magnification were obtained using the FPD with a pixel size of 48×48 µm2, and the shifting dimensions of the imaged object in the horizontal and vertical directions ranged from 48 to 192 µm. At a shifting distance ranging from 48 to 144 µm, the spatial resolutions in the horizontal and vertical directions measured with a lead test chart were both 50 µm. In the MER of nonliving animals, we obtained high-contrast embossed images of fine bones, gadolinium oxide particles in blood vessels, and iodine-based microspheres in coronary arteries of approximately 100 µm diameter.

An energy-discriminating K-edge X-ray computed tomography (CT) system is useful for increasing the contrast resolution of a target region utilizing contrast media and for reducing the absorbed dose for patients. The CT system is of the first-generation type of detector using cadmium telluride (CdTe). CT is performed by repeated translations and rotations of an object. Penetrating X-ray photons from the object are detected by a CdTe detector, and event signals of X-ray photons are produced using charge-sensitive and shaping amplifiers. Both photon energy and energy width are selected out using a multichannel analyzer, and the number of photons is counted by a countercard. To perform energy discrimination, a low-dose-rate X-ray generator for photon counting was developed. Its maximum tube voltage and minimum tube current were 110 kV and 1 µA, respectively. In energy-discriminating CT, the tube voltage and tube current were 100 kV and 20 µA, respectively, and the X-ray intensity was 2.98 µGy/s at a distance of 1.0 m from the source and a tube voltage of 100 kV. The demonstration of enhanced gadolinium K-edge X-ray CT was carried out by selecting photons with energies just beyond the gadolinium K-edge energy of 50.3 keV.

A microfocus x-ray tube is useful to perform magnification digital radiography, including phase-contrast effects. The 100-m-focus x-ray generator consists of a main controller for regulating the tube voltage and current, and a tube unit with a high-voltage circuit and a fixed anode x-ray tube. The maximum tube voltage, current, and electric power are 105 kV, 0.5 mA, and 50 W, respectively. Using a 3-mm-thick aluminum filter, the x-ray intensity is 26.0 Gy/s at 1.0 m from the source, with a tube voltage of 60 kV and a current of 0.50 mA. Because the peak photon energy is approximately 35 keV using the filter with a tube voltage of 60 kV, the bremsstrahlung x-rays are absorbed effectively by iodine-based contrast media with an iodine K-edge of 33.2 keV. Magnification angiography is performed by three-fold magnification imaging with a computed radiography sys-tem using iodine-based microspheres 15 m in diameter. In angiography of nonliving animals, we observe fine blood vessels approximately 100 m with high contrasts.

There have been several reports that lymphocytes of human cord blood have poor functional properties because of their immaturity and/or the presence of suppressor cells. We studied here the in vitro effects of thymopoietin pentapeptide (TP-5) and interleukin 2 (IL-2) on cord blood T cells. Lymphocyte subsets were analyzed by flow cytometry through the use of monoclonal antibodies after a 48 h culture period in TP-5 (optimal dose; 1μg/ml) and/or IL-2 (non-mitogenic dose used; 1% vol/vol). OKT 8-positive cells were significantly decreased after treatment in combination with TP-5 and IL-2. But there were no changes in the propotion of OKT 3-, T4-, T11- and Ial-positive cells. Poor helper activity of cord blood T cells, which was examined by enhancing activity of immunoglobulin-production of normal adult non-T cells stimulated by pokeweed mitogen, was enhanced to a significant level of IgG production after treatment in combination with two agents. Crude IL-2 activity was reevaluated through the use of recombinant IL-2.

It was studied whether the microcytotoxicity test of simple manual method was useful or not to examine the reactivity of monoclonal antibodies (OKT3, T4, T8, T11, M1, Ia1) on human mononuclear cells (MNC). The test materials were MNC of 39 healthy donors and those of 16 patients, and their T and B cells isolated by the column method. Record results of % cell lysis were judged by the 10 grades scale.The results of normal MNC were coincident with those of the other manual methods and the flow cytometry. Our test method was confirmed to be useful also to T and B cells isolated by the column method. In case of abnormal MNC, the results of chronic renal failure and adult T cell leukemia were coincident with those of previous reports. As the result, this method could be put to practical use.