6,937 research outputs found

    Nonlinear Mapping of Gaussian Statistics: Theory and Applications to Spacecraft Trajectory Design

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/76930/1/AIAA-20177-363.pd

    Nonlinear Semi-Analytic Method for Spacecraft Navigation

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/77318/1/AIAA-2006-6399-190.pd

    Nonlinear Semi-Analytic Methods for Trajectory Estimation

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/76298/1/AIAA-29106-621.pd

    Near-infrared spectroscopy detects age-related differences in skeletal muscle oxidative function: promising implications for geroscience

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    Age is the greatest risk factor for chronic disease and is associated with a marked decline in functional capacity and quality of life. A key factor contributing to loss of function in older adults is the decline in skeletal muscle function. While the exact mechanism(s) remains incompletely understood, age-related mitochondrial dysfunction is thought to play a major role. To explore this question further, we studied 15 independently living seniors (age: 72 ± 5 years; m/f: 4/11; BMI: 27.6 ± 5.9) and 17 young volunteers (age: 25 ± 4 years; m/f: 8/9; BMI: 24.0 ± 3.3). Skeletal muscle oxidative function was measured in forearm muscle from the recovery kinetics of muscle oxygen consumption using near-infrared spectroscopy (NIRS). Muscle oxygen consumption was calculated as the slope of change in hemoglobin saturation during a series of rapid, supra-systolic arterial cuff occlusions following a brief bout of exercise. Aging was associated with a significant prolongation of the time constant of oxidative recovery following exercise (51.8 ± 5.4 sec vs. 37.1 ± 2.1 sec, P = 0.04, old vs. young, respectively). This finding suggests an overall reduction in mitochondrial function with age in nonlocomotor skeletal muscle. That these data were obtained using NIRS holds great promise in gerontology for quantitative assessment of skeletal muscle oxidative function at the bed side or clinic

    Candida albicans biofilm heterogeneity does not influence denture stomatitis but strongly influences denture cleansing capacity

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    Approximately 20  % of the UK population wear some form of denture prosthesis, resulting in denture stomatitis in half of these individuals. Candida albicans is primarily attributed as the causative agent, due to its biofilm -forming ability. Recently, there has been increasing evidence of C. albicans biofilm heterogeneity and the negative impact it can have clinically; however, this phenomenon has yet to be studied in relation to denture isolates. The aims of this study were to evaluate C. albicans biofilm formation of clinical denture isolates in a denture environment and to assess antimicrobial activity of common denture cleansers against these tenacious communities. C. albicans isolated from dentures of healthy and diseased individuals was quantified using real-time PCR and biofilm biomass assessed using crystal violet. Biofilm development on the denture substratum poly(methyl methacrylate), Molloplast B and Ufi-gel was determined. Biofilm formation was assessed using metabolic and biomass stains, following treatment with denture hygiene products. Although C. albicans was detected in greater quantities in diseased individuals, it was not associated with increased biofilm biomass. Denture substrata were shown to influence biofilm biomass, with poly(methyl methacrylate) providing the most suitable environment for C. albicans to reside. Of all denture hygiene products tested, Milton had the most effective antimicrobial activity, reducing biofilm biomass and viability the greatest. Overall, our results highlight the complex nature of denture- related disease, and disease development cannot always be attributed to a sole cause. It is the distinct combination of various factors that ultimately determines the pathogenic outcome

    Strong resemblance between surface and deep zonal winds inside Jupiter revealed by high-degree gravity moments

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    Jupiter's atmosphere-interior is a coupled fluid dynamical system strongly influenced by the rapid background rotation. While the visible atmosphere features east-west zonal winds on the order of 100 m/s (Tollefson et al. 2017), zonal flows in the dynamo region are significantly slower, on the order of 1 cm/s or less, according to the latest magnetic secular variation analysis (Bloxham et al. 2022). The vertical profile of the zonal flows and the underlying mechanism remain elusive. The latest Juno radio tracking measurements afforded the derivation of Jupiter's gravity field to spherical harmonic degree 40. Here, we use the latest gravity solution to reconstruct Jupiter's deep zonal winds without a priori assumptions about their latitudinal profile. The pattern of our reconstructed deep zonal winds strongly resembles that of the surface wind within ±\pm 35 degrees latitude from the equator, in particular the northern off-equatorial jet (NOEJ) and the southern off-equatorial jet (SOEJ) (Kulowski et al. 2021). The reconstruction features larger uncertainties in the southern hemisphere due to the north south asymmetric nature of Juno's trajectory. Amplitude of the reconstructed deep NOEJ matches that of the surface wind when the wind is truncated at a depth around 2500 km, and becomes twice that of the surface wind if the truncation depth is reduced to about 1500 km. Our analysis supports the physical picture in which prominent part of the surface zonal winds extends into Jupiter's interior significantly deeper than the water cloud layer.Comment: Accepted for publication in ApJ, 11 pages, 6 figure

    Activation of Flucloxacillin-Specific CD8+ T-Cells With the Potential to Promote Hepatocyte Cytotoxicity in a Mouse Model

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    There are currently no animal models of drug-induced liver injury (DILI) where the adaptive immune system has been shown to damage the liver. Thus, it is difficult to explore the mechanistic basis of the tissue injury. The aim of this study was to use C57BL/6 CD4+-deficient mice with a mutation in the αβ gene encoding for Major histocompatibilty complex (MHC) class II molecules to (1) develop a mouse model of flucloxacillin sensitization, (2) explore whether drug-specific CD8+ kill primary hepatocytes, and (3) analyze perturbations in liver integrity following oral exposure to flucloxacillin. CD8+ T-cells from lymph nodes of flucloxacillin-sensitized mice were stimulated to proliferate, secrete interferon (IFN-γ) and granzyme B, and induce hepatocyte apoptosis in a concentration-dependent manner following ex vivo stimulation. The T-cell response was antigen-specific; T-cells were not activated with other β-lactam antibiotics. Furthermore, T-cell responses only occurred in the presence of flucloxacillin-pulsed antigen presenting cells. In separate experiments, flucloxacillin-specific T-cells were induced to migrate to the mesenteric lymph nodes using retinoic acid, prior to administration of oral flucloxacillin, and analysis of plasma biomarkers of liver injury. Oral exposure to flucloxacillin resulted in mild elevations in alanine aminotransferase, liver, and gall bladder leukocyte infiltration and a marked swelling of the gall bladder. Thus, CD4+-deficient mice represent a promising model to study the role of the adaptive immune system in DIL
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