8,869 research outputs found

    Effective Field Theory of Dipolar Braiding Statistics in Two Dimensions

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    A rank-2 toric code (R2TC) Hamiltonian in two dimensions can be constructed as a Higgsed descendant of rank-2 U(1) lattice gauge theory. As noted by the authors recently, [Y.-T. Oh, J. Kim, E.-G. Moon, and J. H. Han, Phys. Rev. B {\bf 105}, 045128] the quasiparticles in that model showed braiding statistics that depends on the initial locations of the particles which participate in the braiding. We argue that this new kind of statistical phase captures the total dipole moment of quasiparticles encompassed in the braiding, whereas conventional anyonic braiding sees the total charge. An Aharonov-Bohm interpretation of such {\it dipolar braiding statistics} can be made in terms of emergent, rank-1 vector potentials built from the underlying rank-2 gauge fields. Pertinent field theories of the quasiparticle dynamics in the R2TC are developed, which turn out to be highly interacting theories predicting their constrained dynamics. The accompanying conservation laws are also of unusual types. A {\it dipolar BF theory} of the rank-2 gauge fields is constructed and shown to correctly capture the dipolar braiding statistics, in contrast to the conventional BF theory capturing the {\it monopolar braiding statistics} of anyons in the rank-1 toric code. A tight-binding model for the quasiparticle dynamics in the R2TC involves two-particle as well as the one-particle hopping, both of which are coupled to the tensor gauge fields.Comment: 6 pages, supplementary materials, 3 figure

    Time Dependent Gene Expression Changes in the Liver of Mice Treated with Benzene

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    Benzene is used as a general purpose solvent. Benzene metabolism starts from phenol and ends with p-benzoquinone and o-benzoquinone. Liver injury inducted by benzene still remains a toxicologic problem. Tumor related genes and immune responsive genes have been studied in patients suffering from benzene exposure. However, gene expression profiles and pathways related to its hepatotoxicity are not known. This study reports the results obtained in the liver of BALB/C mice (SLC, Inc., Japan) administered 0.05 ml/100 g body weight of 2% benzene for six days. Serum, ALT, AST and ALP were determined using automated analyzer (Fuji., Japan). Histopathological observations were made to support gene expression data. c-DNA microarray analyses were performed using Affymetrix Gene-chip system. After six days of benzene exposure, twenty five genes were down regulated whereas nineteen genes were up-regulated. These gene expression changes were found to be related to pathways of biotransformation, detoxification, apoptosis, oxidative stress and cell cycle. It has been shown for the first time that genes corresponding to circadian rhythms are affected by benzene. Results suggest that gene expression profile might serve as potential biomarkers of hepatotoxicity during benzene exposure

    Pharmacological and Nonpharmacological Treatments for Painful Diabetic Peripheral Neuropathy

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    Diabetic peripheral neuropathy (DPN) is one of the most prevalent chronic complications of diabetes. The lifetime prevalence of DPN is thought to be >50%, and 15%–25% of patients with diabetes experience neuropathic pain, referred to as “painful DPN.” Appropriate treatment of painful DPN is important because this pain contributes to a poor quality of life by causing sleep disturbance, anxiety, and depression. The basic principle for the management of painful DPN is to control hyperglycemia and other modifiable risk factors, but these may be insufficient for preventing or improving DPN. Because there is no promising diseasemodifying medication for DPN, the pain itself needs to be managed when treating painful DPN. Drugs for neuropathic pain, such as gabapentinoids, serotonin–norepinephrine reuptake inhibitors, tricyclic antidepressants, alpha-lipoic acid, sodium channel blockers, and topical capsaicin, are used for the management of painful DPN. The U.S. Food and Drug Administration (FDA) has approved pregabalin, duloxetine, tapentadol, and the 8% capsaicin patch as drugs for the treatment of painful DPN. Recently, spinal cord stimulation using electrical stimulation is approved by the FDA for the treatment for painful DPN. This review describes the currently available pharmacological and nonpharmacological treatments for painful DPN

    Analysis of Building Energy Savings Potential for Metal Panel Curtain Wall Building by Reducing Thermal Bridges at Joints Between Panels

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    AbstractTo achieve national greenhouse gas reduction in the building sector, heating and cooling energy in buildings should be reduced. The government has strengthened regulations on insulation performance for building energy savings. However, the building envelope has various thermal bridges. In particular, a metal panel curtain wall comprises a number of thermal bridges at joints between the panels and the fixing units, thus degrading the overall thermal performance. To reduce building energy, it is necessary to reduce thermal bridges in building envelopes. This study aims to analyze the energy saving potential achieved by reducing thermal bridges. For this, the insulation performance and building energy needs of the existing and alternative metal panel curtain wall were evaluated. The alternative metal panel curtain wall that uses plastic molds at joints between panels and the thermally-broken brackets was suggested to reduce heat loss through thermal bridges. As results, the effective U-value of the alternative metal panel curtain wall was reduced by 72% compared with the existing metal panel curtain wall. In addition, annual heating energy needs of the alternative metal panel curtain wall building was reduced by 26%, and annual total energy needs was reduced by 6% because annual cooling energy needs of it slightly increased compared with the existing metal panel curtain wall. In conclusion, the alternative metal panel curtain wall considerably influenced the savings in building energy needs by reducing thermal bridges
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