Spin 3/2 Pentaquarks

We investigate the possible existence of the spin 3/2 pentaquark states using interpolating currents with K-N color-octet structure in the framework of QCD finite energy sum rule (FESR). We pay special attention to the convergence of the operator product expansion

Controversies in the Facial Inversion Effect: Face Specificity and Expertise

This paper reviews studies on the face inversion effect and expertise. It is suggested that the inversion effect be considered as evidence of specific processing in face recognition or expertise of the objects, which meet three prerequisites. Some disputes are also pointed out in the review. It is proposed that further studies should be addressed to the visual differences, physiological basis of cognitive modules, and anatomical and functional location of the respective networks.Надано огляд робіт, у котрих обговорюються ефект інверсії зображення обличчя та експертний підхід у процесі його аналізу. Вважається, що ефект інверсії має розглядатись як свідоцтво специфічної обробки інформації при розпізнанні обличчя або базуватися на експертній оцінці об’єктів з наявністю трьох передумов. В огляді виділені декілька аспектів, що викликають дискусії. Пропонується, щоб наступні дослідження були спрямовані на з’ясування візуальних відмінностей, фізіологічного базису когнітивних модулів та анатомічної та функціональної локалізації відповідних нейронних мере

Roles of insulin-like growth factor II in cardiomyoblast apoptosis and in hypertensive rat heart with abdominal aorta ligation

Although IGF-II activating the IGF-II receptor signaling pathway has been found to stimulate cardiomyocyte hypertrophy, the role of IGF-II in cardiac cell apoptosis remains unclear. This study aimed to identify the roles of IGF-II and/or IGF-II receptors (IGF-II/IIR) in cardiomyoblast apoptosis and in hypertensive rat hearts with abdominal aorta ligation. Cultured rat heart-derived H9c2 cardiomyoblasts and excised hearts from Sprague-Dawley rats with 0- to 20-day complete abdominal aorta ligation, a model of ANG II elevation and hypertension, were used. IGF-II/IIR expression, caspase activity, DNA fragmentation, and apoptotic cells were measured by RT-PCR, Western blot, agarose gel electrophoresis, and TUNEL assay following various combinations of ANG II, IGF-II/IIR antibody, CsA (calcineurin inhibitor), SP-600125 (JNK inhibitor), SB-203580 (p38 inhibitor), U-0126 (MEK inhibitor), or Staurosporine (PKC inhibitor) in H9c2 cells. ANG II-induced DNA fragmentation and TUNEL-positive cells were blocked by IGF-II/IIR antibodies and antisense IGF-II, but not by IGF-II sense. IGF-II-induced apoptosis was blocked by IGF-IIR antibody and CsA. The increased gene expressions of IGF-II and -IIR induced by ANG II were reversed by U-0126 and Sp600125, respectively. Caspase 8 activities induced by ANG II were attenuated by U-0126, SP-600125, and CsA. DNA fragmentation induced by ANG II was totally blocked by SP-600125, and CsA and was attenuated by U-0126. In rats with 0- to 20-day complete abdominal aorta ligation, the increases in IGF-II/IIR levels in the left ventricle were accompanied by hypertension as well as increases in caspase 9 activities and TUNEL-positive cardiac myocytes. ANG II-induced apoptosis was reversed by IGF-II/IIR blockade and coexisted with increased transactivation of IGF-II and -IIR, which are mediated by ERK and JNK pathways, respectively, both of which further contributed to cardiomyoblast apoptosis via calcineurin signaling. The increased cardiac IGF-II, IGF-IIR, caspase 9, and cellular apoptosis were also found in hypertensive rats with abdominal aorta ligation

Effects of Mn and Ti doping on superconductivity and charge ordering in NaxCoO2 system

The superconductivity in Na0.3Co1-xMxO2.1.3H2O and the charge ordering in Na0.5Co1-xMxO2 have been investigated for M = Mn and Ti substituting for Co. We have first successfully synthesized the single-phase Na0.7Co1-xMxO2(M= Mn and Ti) materials with 0 < = x < = 0.1, then we obtained Na0.5Co1-xMxO2 (0 < = x < = 0.1, M = Mn and Ti) by Na deintercalation and Na0.3Co1-xMxO2.1.3H2O (0 < = x < = 0.1, M = Mn and Ti) by an additional water intercalations. X-ray diffraction measurements revealed that all samples are single-phase materials, their lattice parameters depend systematically on the Ti and Mn contents. Measurements of physical properties indicate that the superconductivity in Na0.3Co1-xMxO2.1.3H2O is suppressed evidently by Co-site doping and killed at x = 0.02 for Mn doping and x = 0.01 for Ti doping. Charge ordering and magnetic properties in Na0.5Co1-xMxO2 were also influenced by M-atom doping.Comment: 22 pages, 3 tables, and 6 figure

Role of calcineurin in Porphyromonas gingivalis-induced myocardial cell hypertrophy and apoptosis

Background and objective: Periodontal pathogen Porphyromonas gingivalis (P. gingivalis) increased cardiomyocyte hypertrophy and apoptosis whereas Actinobaeillus actinomycetemcomitans and Prevotella intermedia had no effects. The purpose of this study is to clarify the role of calcineurin signaling pathway in P. gingivalis-induced H9c2 myocardial cell hypertrophy and apoptosis. Methods: DNA fragmentation, nuclear condensation, cellular morphology, calcineurin protein, Bcl2- associated death promoter (Bad) and nuclear factor of activated T cell (NFAT)-3 protein products in cultured H9c2 myocardial cell were measured by agarose gel electrophoresis, DAPI, immunofluorescence, and Western blotting following P. gingivalis and/or pre-administration of CsA (calcineurin inhibitors cyclosporin A). Results: P. gingivalis not only increased calcineurin protein, NFAT-3 protein products and cellular hypertrophy, but also increased DNA fragmentation, nuclear condensation and Bad protein products in H9c2 cells. The increased cellular sizes, DNA fragmentation, nuclear condensation, and Bad of H9c2 cells treated with P. gingivalis were all significantly reduced after pre-administration of CsA. Conclusion: Our findings suggest that the activity of calcineurin signal pathway may be initiated by P. gingivalis and further lead to cell hypertrophy and death in culture H9c2 myocardial cells

Cardiomyoblast apoptosis induced by insulin-like growth factor (IGF)-I resistance is IGF-II dependent and synergistically enhanced by angiotensin II

Objective: This study explores the synergistic effect of cardiomyoblast apoptosis induced by angiotensin II (Ang II) and Insulin-like growth factor (IGF)-I resistance, and elucidates the role of IGF-II via IGF-II receptor (R) and calcineurin pathways in apoptosis induced by Ang II and IGF-I resistance. Methods: Apoptosis of cultured cardiomyoblast H9c2 cells was assessed by DNA fragmentation on agarose gel electrophoresis, nuclear condensation stained with DAPI, and Western blot analysis of pro-apoptotic Bad and cytochrome c in various combinations of control, Ang II, antisense IGF (I or II), IGF (I or II) antibody, IGF (I or II) receptor (R) antibody, or calcineurin inhibitor (Cyclosporine A, (CsA)). Results: We found the following: (I) The combination of Ang II and IGF-I deficiencies had a synergistic effect on apoptosis, confirmed by DNA fragmentation, nuclei condensation, and increases in such proapoptotic proteins as Bad, cytochrome c, caspase 9, and caspase 3 in H9c2 cells. (2) IGF-II and IGF-IIR protein products were increased by antisense IGF-I and IGF-I resistance, but these IGF-II protein products were not affected by sense IGF-I and non-specific antibody IgG in H9c2 cells. (3) The alteration of Bad protein level and the release of cytochrome c, both induced by treatments containing combinations of Ang II and antisense IGF-I, IGF-I antibody or IGF-IR antibody, were inhibited by IGF-II antibody. (4) DNA fragmentation, Bad, and cytochrome c which was induced by treatments combining IGF-IR antibody with Ang II or combining IGF-IR antibody with IGF-II were remarkably attenuated by CsA. Conclusion: IGF-I deficiency and/or IGF-IR resistance induced apoptosis in cardiomyoblast cells. The apoptosis, which might have been caused by the upregulation of IGF-II and IGF-IIR genes possibly activated the downstream calcineurin pathway, was synergistically augmented by Ang II

In situ synchrotron radiography and spectrum analysis of transient cavitation bubbles in molten aluminium alloy

The melt processing of conventional and advanced metallic materials with high-intensity ultrasonic vibrations significantly improves the quality and properties of molten metals during their solidification. These improvements are primarily attributed to ultrasonic cavitation: the creation, growth, pulsation, and collapse of bubbles in the liquid. However, the development of practical applications is limited by the lack of fundamental knowledge on the dynamics of the cavitation bubbles; it is very difficult to directly observe ultrasonic cavitation using conventional techniques in molten metals due their high temperature and opaqueness. In this study, an in situ synchrotron radiography experiment was performed to investigate bubble dynamics in an Al-10 wt.% Cu alloy under an external ultrasound field at 30 kHz. Radiographs with an exposure time of 78 ms were collected continuously during the sonication of molten alloys at temperatures of 660±10 °C. To the best of our knowledge, this is the first time that transient cavitation bubbles have been observed in liquid aluminium. Quantification of bubble parameters such as average size and time of collapse were evaluated from radiographs using advanced image analysis. Additionally, broadband noise associated with the acoustic emissions from shock waves of transient cavitation bubbles and estimation of the real-time acoustic pressure at the driving frequency were assessed using an advanced high-temperature cavitometer in separate bulk experiments.The ExoMet Project (FP7-NMP3-LA-2012-280421), the UK Engineering and Physical Sciences Research Council (EPSRC) (EP/K005804/1 and EP/I02249X/1), and provision of beamtime on the Diamond Manchester Branchline at Diamond Light Source (expt. MT9082-1)

The profile of cardiac cytochrome c oxidase (COX) expression in an accelerated cardiac-hypertrophy model

The contribution of the mitochondrial components, the main source of energy for the cardiac hypertrophic growth induced by pressure overload, is not well understood. In the present study, complete coarctation of abdominal aorta was used to induce the rapid development of cardiac hypertrophy in rats. One to two days after surgery, we observed significantly higher blood pressure and cardiac hypertrophy, which remained constantly high afterwards. We found an early increased level of cytochrome c oxidase ( COX) mRNA determined by in-situ hybridization and dot blotting assays in the hypertrophied hearts, and a drop to the baseline 20 days after surgery. Similarly, mitochondrial COX protein level and enzyme activity increased and, however, dropped even lower than baseline 20 days following surgery. In addition, in natural hypertension- induced hypertrophic hearts in genetically hypertensive rats, the COX protein was significantly lower than in normotensive rats. Taken together, the lower efficiency of mitochondrial activity in the enlarged hearts of long-term complete coarcted rats or genetically hypertensive rats could be, at least partially, the cause of hypertensive cardiac disease. Additionally, the rapid complete coarctation-induced cardiac hypertrophy was accompanied by a disproportionate COX activity increase, which was suggested to maintain the cardiac energy-producing capacity in overloaded hearts

Single Spin Asymmetry ANA_N in Polarized Proton-Proton Elastic Scattering at s=200\sqrt{s}=200 GeV

We report a high precision measurement of the transverse single spin asymmetry $A_N$ at the center of mass energy $\sqrt{s}=200$ GeV in elastic proton-proton scattering by the STAR experiment at RHIC. The $A_N$ was measured in the four-momentum transfer squared $t$ range $0.003 \leqslant |t| \leqslant 0.035$ \GeVcSq, the region of a significant interference between the electromagnetic and hadronic scattering amplitudes. The measured values of $A_N$ and its $t$-dependence are consistent with a vanishing hadronic spin-flip amplitude, thus providing strong constraints on the ratio of the single spin-flip to the non-flip amplitudes. Since the hadronic amplitude is dominated by the Pomeron amplitude at this $\sqrt{s}$, we conclude that this measurement addresses the question about the presence of a hadronic spin flip due to the Pomeron exchange in polarized proton-proton elastic scattering.Comment: 12 pages, 6 figure