737 research outputs found
Syntheses of Technetium β-Diketone and 8-Quinolinol Complexes
開始ページ、終了ページ: 冊子体のページ付
Comparison of the Effects of Two Types of Stretching Warm Ups for Rehabilitation
This pilot study compares the effects of static therapeutic trunk stretching using an unstable flex chair, a stretching bench and a stretching stick on physical fitness with those of a general Japanese style of static stretching. The participants underwent physical fitness tests. Before and after warming up using a general Japanese style of stretching and trunk treatment stretching. Twenty-three healthy college students (age, 20.7 ± 1.2 years; height, 165.3 ± 7.6 cm; weight, 59.0 ± 9.7 kg; BMI 21.4 ± 2.3) were enrolled in this study. The physical fitness test assesses grip strength, sit-ups, eyes-closed single-leg stance, sit-and-reach flexibility, six-minute walk, and ten-meter obstacle course. The participants performed vertical jump, forward standing flexion measured using the analog flexion meter, thoracolumbar extension, horizontal flexure, deep forward bow. These results suggest that trunk stretching improves flexibility, walking ability, endurance and explosive power more effectively than the general Japanese style of stretching. Three static trunk stretches can improve flexibility, walking ability, endurance and explosive power. Trunk treatment stretching before physical activity might reduce the incidence of injury and improve the physical performance of individuals who participate in exercise, athletes and injured persons undergoing rehabilitation.ArticleBAOJ Medical and nursing.1(1):003(2015)journal articl
Degradation of human kininogens with the release of kinin peptides by extracellular proteinases of Candida spp.
The secretion of proteolytic enzymes by pathogenic microorganisms is one of the most successful strategies used by pathogens to colonize and infect the host organism. The extracellular microbial proteinases can seriously deregulate the homeostatic proteolytic cascades of the host, including the kinin-forming system, repeatedly reported to he activated during bacterial infection. The current study assigns a kinin-releasing activity to secreted proteinases of Candida spp. yeasts, the major fungal pathogens of humans. Of several Candida species studied, C. parapsilosis and C. albicans in their invasive filamentous forms are shown to produce proteinases which most effectively degrade proteinaceous kinin precursors, the kininogens. These enzymes, classified as aspartyl proteinases, have the highest kininogen-degrading activity at low pH (approx. 3.5), but the associated production of bradykinin-related peptides from a small fraction of kininogen molecules is optimal at neutral pH (6.5). The peptides effectively interact with cellular B2-type kinin receptors. Moreover, kinin-related peptides capable of interacting with inflammation-induced B1-type receptors are also formed, but with a reversed pH dependence. The presented variability of the potential extracellular kinin production by secreted aspartyl proteinases of Candida spp. is consistent with the known adaptability of these opportunistic pathogens to different niches in the host organism
Moderate exercise improves cognitive performance and decreases cortical activation in the go/no-go task
Background: A lot of studies have reported that physical activity has a beneficial influence not only on physical and mental disorders but also on cognitive and brain function. Performance of a go/no-go task improves after exercise. However, few studies have compared neural activity in a go/no-go task performed before and after exercise to identify brain regions that may respond to exercise and underlie this result. Therefore, the purpose of this study was to examine the brain blood flow and compare the cortical activation pattern during a go/no-go task performed before and after exercise.Method: Fifteen healthy subjects performed a go/no-go task before and after exercise. Functional near-infrared spectroscopy (fNIRS) was used to measure oxygenated hemoglobin concentration at 44 locations over both hemispheres. The exercise was of moderate intensity, defined as 50% of peak oxygen uptake.Result: The reaction time on the go/no-go task was significantly faster after exercise than before. The oxygenated hemoglobin concentration quantified across the whole brain was lower after exercise, and this was the case for go trials and no-go trials. In go trials, the oxygenated hemoglobin concentration in dorsolateral prefrontal cortex and supplementary motor area were significantly lower after exercise.Conclusion: These results suggest that the dorsolateral prefrontal cortex and supplementary motor area had lower activity in go trials in the go/no-go task performed after exercise than in go trials in the go/no-go task performed before exercise.ArticleBAOJ Medical and nursing.1(1):002(2015)journal articl
Three-dimensional femtosecond laser nanolithography of crystals
Nanostructuring hard optical crystals has so far been exclusively feasible at
their surface, as stress induced crack formation and propagation has rendered
high precision volume processes ineffective. We show that the inner chemical
etching reactivity of a crystal can be enhanced at the nanoscale by more than
five orders of magnitude by means of direct laser writing. The process allows
to produce cm-scale arbitrary three-dimensional nanostructures with 100 nm
feature sizes inside large crystals in absence of brittle fracture. To showcase
the unique potential of the technique, we fabricate photonic structures such as
sub-wavelength diffraction gratings and nanostructured optical waveguides
capable of sustaining sub-wavelength propagating modes inside yttrium aluminum
garnet crystals. This technique could enable the transfer of concepts from
nanophotonics to the fields of solid state lasers and crystal optics.Comment: Submitted Manuscript and Supplementary Informatio
UGT1A1 sequence variants and bilirubin levels in early postnatal life: a quantitative approach
<p>Abstract</p> <p>Background</p> <p>Fundamental to definitively identifying neonates at risk of developing significant hyperbilirubinemia is a better understanding of the genetic factors associated with early bilirubin rise. Previous genetic studies have focused on the UGT1A1 gene, associating common variation in the coding or promoter regions with qualitative assessments of bilirubin (i.e. significantly elevated or not). These studies have had conflicting results and limited success. We chose to approach the problem by focusing on the quantitative (absolute) change in bilirubin levels early in post-natal life. We apply this approach to the UGT1A1 gene - exploring the contribution of both rare and common variants to early bilirubin changes.</p> <p>Methods</p> <p>We sequenced the exons, PBREM, 5'-, and 3'- regions of the UGT1A1 gene in 80 otherwise healthy term neonates who had repeat bilirubin levels measured within the first five days of life.</p> <p>Results</p> <p>Three novel coding variants were observed, but there was no clear relationship between rare coding variants and bilirubin rise. Adjusted linear regression models fit to evaluate the relationship between changing bilirubin levels and common UGT1A1variants found that among 39 neonates whose bilirubin was resampled within 33 hours, individuals homozygous for the mutant allele of a 3'UTR SNP had significantly smaller changes in bilirubin (P = 0.003) than individuals carrying the wild-type allele.</p> <p>Conclusions</p> <p>Collectively, rare UGT1A1 coding variants do not appear to play a prominent role in determining early bilirubin levels; however common variants in the 3' UTR of UGT1A1 may modulate the early bilirubin rise. A quantitative approach to evaluating early bilirubin kinetics provides a more robust framework in which to better understand the genetics of neonatal hyperbilirubinemia.</p
The Effect of Epstein-Barr Virus Latent Membrane Protein 2 Expression on the Kinetics of Early B Cell Infection
Infection of human B cells with wild-type Epstein-Barr virus (EBV) in vitro leads to activation and proliferation that result in efficient production of lymphoblastoid cell lines (LCLs). Latent Membrane Protein 2 (LMP2) is expressed early after infection and previous research has suggested a possible role in this process. Therefore, we generated recombinant EBV with knockouts of either or both protein isoforms, LMP2A and LMP2B (Δ2A, Δ2B, Δ2A/Δ2B) to study the effect of LMP2 in early B cell infection. Infection of B cells with Δ2A and Δ2A/Δ2B viruses led to a marked decrease in activation and proliferation relative to wild-type (wt) viruses, and resulted in higher percentages of apoptotic B cells. Δ2B virus infection showed activation levels comparable to wt, but fewer numbers of proliferating B cells. Early B cell infection with wt, Δ2A and Δ2B viruses did not result in changes in latent gene expression, with the exception of elevated LMP2B transcript in Δ2A virus infection. Infection with Δ2A and Δ2B viruses did not affect viral latency, determined by changes in LMP1/Zebra expression following BCR stimulation. However, BCR stimulation of Δ2A/Δ2B cells resulted in decreased LMP1 expression, which suggests loss of stability in viral latency. Long-term outgrowth assays revealed that LMP2A, but not LMP2B, is critical for efficient long-term growth of B cells in vitro. The lowest levels of activation, proliferation, and LCL formation were observed when both isoforms were deleted. These results suggest that LMP2A appears to be critical for efficient activation, proliferation and survival of EBV-infected B cells at early times after infection, which impacts the efficient long-term growth of B cells in culture. In contrast, LMP2B did not appear to play a significant role in these processes, and long-term growth of infected B cells was not affected by the absence of this protein. © 2013 Wasil et al
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