144 research outputs found

    Internationalization of Jerusalem as a basis for peace in the Middle East re-appreciating the 1947 United Nations general assembly resolution 181(II)

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    The dawn of the twenty-first century was met with feeling of apprehension and disillusionment among those hoping for lasting peace in the Middle East. With armed clashes between Israelis and Palestinians intensifying since 2001, escalating into what the mass media described as a state of “mini-war," the future can no longer be regarded with optimism. In a last-ditch effort as a peace broker before his eight-year term expired, United States President Bill Clinton welcomed Prime Minister Ehud Barak of Israel and Ra'ees (President ) Yasser Arafat of the Palestinian Authority (PA) on July 11, 2000 to Camp David, the presidential mountain retreat in Mainland, where the first Israeli-Arab rapprochement had been achieved 22 years before. This time, however, no historical milestone could be reached. The parties to the triumvirate summit conference discussed the “permanent status" of Jerusalem and other important issues in a charged atmosphere of high anticipation, but the conference ended inconclusively. Clinton admitted that peace talks were in a stalemate “at this time." However, he was unable to sponsor new summit talks during the reminder of his term, and the target date of September 13, 2000 for finalizing a permanent status agreement on the West Bank (including Jerusalem) and the Gaza Strip between the Israeli government and the autonomous Palestinian Authority passed without a deal being struck. Arafat repeatedly insisted prior to this date that he would declare the establishment of a Palestinian state on September 13 whether the Camp David meeting succeeded or not. But he refrained from making a proclamation of independence on that date, allegedly due to strong pressure from Clinton. Many Palestinians voiced disappointment and frustration, which soon erupted into violence. The issue of Jerusalem, as many had predicted, proved to be an insurmountable obstacle in the Barak-Arafat negotiations. It may now take many years before Israel and Palestine can restore mutual credibility. Restarting negotiat

    Distributed Cooperative Relaying Based on Space-Time Block Code: System Description and Measurement Campaign

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    In cooperative relaying, intermediate stations are required to enhance the end-to-end transmission performance. The performance of the cooperative relaying scheme has been investigated theoretically and via computer simulations. However, cooperative relaying using transmit diversity techniques in actual environments has not been investigated thus far. This paper presents an experimental system for distributed cooperative relaying using space-time block code and evaluations of its transmission performances in real propagation channels. To this end, four wireless stations-specifically, one source, two relays, and one destination-were developed using analog transceivers and field-programmable gate arrays for real-time digital signal processing. Sample timing and frequency synchronizations among the four wireless stations were established by using the received signals as a reference. The end-to-end error performance of distributed cooperative relaying was compared to those of noncooperative relaying schemes, and the performances of three relaying schemes were evaluated quasisimultaneously in terms of their cumulative distribution functions of the bit-error ratios (BERs). The experimental results indicated that the BER performance of the two-hop distributed cooperative relaying scheme was substantially superior to those of noncooperative two-hop relaying schemes, including a route diversity scheme

    Goblet Cell Hyperplasia and Muscular Layer Thickening in the Small Intestine of a Cynomolgus Monkey

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    We report here the interesting case of a 5-year-old male cynomolgus monkey with goblet cell hyperplasia and thickening of the muscular layer throughout the small intestine without exhibiting any clinical symptoms. Necropsy examination showed diffuse thickening of the intestinal wall from the jejunum to the ileum, with an appearance likened to a rubber tube. Histopathologically, marked thickening was observed in both the mucosal and muscular layers in the jejunum and ileum, and slight thickening was observed in the duodenum. Goblet cell hyperplasia with extension of the circular folds and villi was prominently observed. The mucosal surface was covered with a thick mucus layer containing desquamated mucosal epithelial cells, and both the inner and outer muscular layers were markedly thickened due to smooth muscle hypertrophy. Neither macroscopic nor histopathological examination identified any causative factors, such as infection, enteritis and intestinal stenosis, or obstruction that may have caused development of this lesion. Given these observations, this case may simply be considered of spontaneous goblet cell hyperplasia and muscular layer thickening in the small intestine of a cynomolgus monkey

    Bubble fragmentation dynamics in a subsonic Venturi tube for the design of a compact microbubble generator

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    Microbubble generators are in wide demand in industry following the discovery of a number of new functions of microbubble mixtures. This paper deals with a Venturi tube microbubble generator in which air bubbles at the inlet are fragmented in the diverging part of the tube. In contrast with past studies, we here regulated the flow subsonic so that fragmentation occurred without the help of pressure shock waves. Counting the microbubbles in image processing, we found that a single bubble fragmented into 20–400 microbubbles depending on the Weber number. The power efficiency is found to range from 30 to 50 percent and insensitive to the liquid viscosity. The mechanism of subsonic fragmentation is elucidated adopting particle tracking velocimetry, in association with a theoretical description of the translational motion and the shape oscillation of the bubble. The key event was found to be the bubble’s rapid slipback in the diverging part of the Venturi tube due to a positive pressure gradient. This provides a function that prevents large bubbles from being released from the subsonic Venturi tube

    L type Ca2+ channel blockers prevent oxaliplatin-induced cold hyperalgesia and TRPM8 overexpression in rats

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    <p>Abstract</p> <p>Background</p> <p>Oxaliplatin is an important drug used in the treatment of colorectal cancer. However, it frequently causes severe acute and chronic peripheral neuropathies. We recently reported that repeated administration of oxaliplatin induced cold hyperalgesia in the early phase and mechanical allodynia in the late phase in rats, and that oxalate derived from oxaliplatin is involved in the cold hyperalgesia. In the present study, we examined the effects of Ca<sup>2+ </sup>channel blockers on oxaliplatin-induced cold hyperalgesia in rats.</p> <p>Methods</p> <p>Cold hyperalgesia was assessed by the acetone test. Oxaliplatin (4 mg/kg), sodium oxalate (1.3 mg/kg) or vehicle was injected i.p. on days 1 and 2. Ca<sup>2+ </sup>(diltiazem, nifedipine and ethosuximide) and Na<sup>+ </sup>(mexiletine) channel blockers were administered p.o. simultaneously with oxaliplatin or oxalate on days 1 and 2.</p> <p>Results</p> <p>Oxaliplatin (4 mg/kg) induced cold hyperalgesia and increased in the transient receptor potential melastatin 8 (TRPM8) mRNA levels in the dorsal root ganglia (DRG). Furthermore, oxalate (1.3 mg/kg) significantly induced the increase in TRPM8 protein in the DRG. Treatment with oxaliplatin and oxalate (500 μM for each) also increased the TRPM8 mRNA levels and induced Ca<sup>2+ </sup>influx and nuclear factor of activated T-cell (NFAT) nuclear translocation in cultured DRG cells. These changes induced by oxalate were inhibited by nifedipine, diltiazem and mexiletine. Interestingly, co-administration with nifedipine, diltiazem or mexiletine prevented the oxaliplatin-induced cold hyperalgesia and increase in the TRPM8 mRNA levels in the DRG.</p> <p>Conclusions</p> <p>These data suggest that the L type Ca<sup>2+ </sup>channels/NFAT/TRPM8 pathway is a downstream mediator for oxaliplatin-induced cold hyperalgesia, and that Ca<sup>2+ </sup>channel blockers have prophylactic potential for acute neuropathy.</p

    Evaluation of the Electronic and Local Structure of Mn in Proton-Conducting Oxide, Ca(Zr,Mn)O3-δ, To Elucidate a Direct Hydrogen-Dissolution Reaction

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    The protonation mechanism in Mn-doped CaZrO3 (CZM), which involves a direct hydrogen dissolution from the surrounding H2 gas, was investigated by thermogravimetry (TG) and X-ray absorption spectroscopy (XAS). The TG results implied the formation of oxygen vacancies in a H2 atmosphere. The Mn K-edge XAS spectra indicated a reduction of the Mn ions and local structure variations around the Mn ion, but the Zr K-edge spectra were independent of the surrounding atmosphere. The amount of oxygen vacancies was smaller with respect to the reduction of the Mn ions, suggesting direct dissolution of hydrogen. Unlike many typical perovskite-type proton conductors, protonation by direct dissolution of hydrogen and not hydration was the predominant reaction in Mn-doped CaZrO3. Our experimental results demonstrated that the hydration reaction was suppressed because the oxygen vacancy was stable in the distorted ZrO6 symmetry in the CaZrO3 crystal host, whereas protonation proceeded by the direct dissolution of hydrogen stabilizing near the Mn ions in the interstitial sites at the distorted MnO6 octahedron symmetry. The experimental results showed that the structural configurations around dopants play important roles in the stabilization of protons in perovskite-type CZM materials. We demonstrated a new group of proton conductors that can overcome issues with conventional proton conductors by utilizing the direct hydrogen dissolution reaction

    Association between periodontal condition and kidney dysfunction in Japanese adults : A cross‐sectional study

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    Recent studies have demonstrated that chronic kidney disease (CKD) may be associated with the progression of periodontal disease. Diabetes mellitus (DM) is a major risk factor for CKD. The objective of this study was to clarify the relationship between periodontal condition and kidney dysfunction in patients who had kidney failure with or without DM. One hundred sixty‐four patients with kidney dysfunction were enrolled (male: N = 105; female: N = 59), and the relationship between periodontal condition and kidney dysfunction was analyzed in a cross‐sectional study. The subjects were divided into three groups: (a) patients with DM, (b) dialysis patients with nephropathy due to various kidney diseases, and (c) dialysis patient with nephropathy due to DM (diabetic nephropathy). Then, the effect of DM on the periodontal condition was analyzed. The patients were also stratified by CKD stage (into G1–G5) using the estimated glomerular filtration rate (eGFR), and the G5 group was divided in patients with or without DM. Correlations between eGFR and parameters of periodontal condition were calculated in patients from G1 to G4. The number of missing teeth was significantly higher in dialysis patients with diabetic nephropathy than in patients with DM, whereas alveolar bone loss did not show a significant difference among the three groups. In addition, the G5 patients with DM had a significantly higher number of missing teeth than the other CKD groups, whereas alveolar bone loss did not show a significant difference. In G5 patients with DM, Community Periodontal Index and Oral Hygiene Index scores were significantly higher than in G1‐4 patients with DM. There was a significant negative correlation between eGFR and the number of missing teeth. Patients with diabetic nephropathy have a higher rate of periodontal problems such as missing teeth in Japanese adults

    Feasibility of Dedicated Breast Positron Emission Tomography Image Denoising Using a Residual Neural Network

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    Objective(s): This study aimed to create a deep learning (DL)-based denoising model using a residual neural network (Res-Net) trained to reduce noise in ring-type dedicated breast positron emission tomography (dbPET) images acquired in about half the emission time, and to evaluate the feasibility and the effectiveness of the model in terms of its noise reduction performance and preservation of quantitative values compared to conventional post-image filtering techniques.Methods: Low-count (LC) and full-count (FC) PET images with acquisition durations of 3 and 7 minutes, respectively, were reconstructed. A Res-Net was trained to create a noise reduction model using fifteen patients’ data. The inputs to the network were LC images and its outputs were denoised PET (LC + DL) images, which should resemble FC images. To evaluate the LC + DL images, Gaussian and non-local mean (NLM) filters were applied to the LC images (LC + Gaussian and LC + NLM, respectively). To create reference images, a Gaussian filter was applied to the FC images (FC + Gaussian). The usefulness of our denoising model was objectively and visually evaluated using test data set of thirteen patients. The coefficient of variation (CV) of background fibroglandular tissue or fat tissue were measured to evaluate the performance of the noise reduction. The SUVmax and SUVpeak of lesions were also measured. The agreement of the SUV measurements was evaluated by Bland–Altman plots.Results: The CV of background fibroglandular tissue in the LC + DL images was significantly lower (9.10 2.76) than the CVs in the LC (13.60  3.66) and LC + Gaussian images (11.51  3.56). No significant difference was observed in both SUVmax and SUVpeak of lesions between LC + DL and reference images. For the visual assessment, the smoothness rating for the LC + DL images was significantly better than that for the other images except for the reference images.Conclusion: Our model reduced the noise in dbPET images acquired in about half the emission time while preserving quantitative values of lesions. This study demonstrates that machine learning is feasible and potentially performs better than conventional post-image filtering in dbPET denoising

    Resveratrol promotes expression of SIRT1 and StAR in rat ovarian granulosa cells: an implicative role of SIRT1 in the ovary

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    <p>Abstract</p> <p>Background</p> <p>Resveratrol is a natural polyphenolic compound known for its beneficial effects on energy homeostasis, and it also has multiple properties, including anti-oxidant, anti-inflammatory, and anti-tumor activities. Recently, silent information regulator genes (Sirtuins) have been identified as targets of resveratrol. Sirtuin 1 (SIRT1), originally found as an NAD<sup>+</sup>-dependent histone deacetylase, is a principal modulator of pathways downstream of calorie restriction, and the activation of SIRT1 ameliorates glucose homeostasis and insulin sensitivity. To date, the presence and physiological role of SIRT1 in the ovary are not known. Here we found that SIRT1 was localized in granulosa cells of the human ovary.</p> <p>Methods</p> <p>The physiological roles of resveratrol and SIRT1 in the ovary were analyzed. Immunohistochemistry was performed to localize the SIRT1 expression. SIRT1 protein expression of cultured cells and luteinized human granulosa cells was investigated by Western blot. Rat granulosa cells were obtained from diethylstilbestrol treated rats. The cells were treated with increasing doses of resveratrol, and subsequently harvested to determine mRNA levels and protein levels. Cell viability was tested by MTS assay. Cellular apoptosis was analyzed by caspase 3/7 activity test and Hoechst 33342 staining.</p> <p>Results</p> <p>SIRT1 protein was expressed in the human ovarian tissues and human luteinized granulosa cells. We demonstrated that resveratrol exhibited a potent concentration-dependent inhibition of rat granulosa cells viability. However, resveratrol-induced inhibition of rat granulosa cells viability is independent of apoptosis signal. Resveratrol increased mRNA levels of SIRT1, LH receptor, StAR, and P450 aromatase, while mRNA levels of FSH receptor remained unchanged. Western blot analysis was consistent with the results of quantitative real-time RT-PCR assay. In addition, progesterone secretion was induced by the treatment of resveratrol.</p> <p>Conclusions</p> <p>These results suggest a novel mechanism that resveratrol could enhance progesterone secretion and expression of luteinization-related genes in the ovary, and thus provide important implications to understand the mechanism of luteal phase deficiency.</p

    Neuroimaging at 7 Tesla: a pictorial narrative review

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    Neuroimaging using the 7-Tesla (7T) human magnetic resonance (MR) system is rapidly gaining popularity after being approved for clinical use in the European Union and the USA. This trend is the same for functional MR imaging (MRI). The primary advantages of 7T over lower magnetic fields are its higher signal-to-noise and contrast-to-noise ratios, which provide high-resolution acquisitions and better contrast, making it easier to detect lesions and structural changes in brain disorders. Another advantage is the capability to measure a greater number of neurochemicals by virtue of the increased spectral resolution. Many structural and functional studies using 7T have been conducted to visualize details in the white matter and layers of the cortex and hippocampus, the subnucleus or regions of the putamen, the globus pallidus, thalamus and substantia nigra, and in small structures, such as the subthalamic nucleus, habenula, perforating arteries, and the perivascular space, that are difficult to observe at lower magnetic field strengths. The target disorders for 7T neuroimaging range from tumoral diseases to vascular, neurodegenerative, and psychiatric disorders, including Alzheimer’s disease, Parkinson’s disease, multiple sclerosis, epilepsy, major depressive disorder, and schizophrenia. MR spectroscopy has also been used for research because of its increased chemical shift that separates overlapping peaks and resolves neurochemicals more effectively at 7T than a lower magnetic field. This paper presents a narrative review of these topics and an illustrative presentation of images obtained at 7T. We expect 7T neuroimaging to provide a new imaging biomarker of various brain disorders
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