4,175 research outputs found

    Multiple-Punishment and the Double Jeopardy Clause: The United States v. Ursery Decision

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    Campaign Expenditure Limits: A Right Turn at Albuquerque

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    Incidence of soft tissue calcifications of the head and neck region on maxillofacial cone beam computed tomography.

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    The aim of the study was to determine the incidence and imaging characteristics of soft tissue calcifications on cone beam computed tomography (CBCT). 556 CBCT image datasets were reviewed and 308 included. The following conditions were recorded: 1) Carotid artery calcifications (CAC), 2) Triticeous cartilage (TC), 3) Superior cornu of the thyroid cartilage (SCT), 4) Tonsilloliths (T) and, 5) Other including lymph nodes (0). The age and sex of patients who were excluded served as controls. 107 (34.75%) demonstrated at least one calcification. Those with calcifications were approximately 12 years older than controls (t value = 6.32, p \u3c 0.001). The incidence of calcifications in decreasing order are TC (11.4%), CAC (10.4%), T (10.4%) and, SCT (5.2%). Differential location and appearance of calcifications were described. Soft tissue calcifications were a common finding with TC, CAC and T presenting in almost equal frequency. Calcifications exhibit unique characteristics on CBCT images

    Acute Pro-inflammatory Immune Response Following Different Resistance Exercise Protocols in Trained Men

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    The successful regeneration of muscle tissue is dependent upon the infiltration of phagocytic CD14++CD16- monocytes that support the proliferation and differentiation of myogenic precursor cells. Physiologically, the magnitude of the cellular response following resistance exercise is dictated by the level of receptor expression on the plasma membrane of the monocyte, as well as the secretion of their cognate ligands from tissue resident cells. However, it remains unclear whether the innate pro-inflammatory immune response varies with different resistance training protocols, and how it may impact recovery and the muscle remodeling process. Therefore, the purpose of this investigation was to examine temporal changes in the expression of chemotactic and adhesion receptors following an acute bout of high-volume, moderate-intensity (VOL) versus high-intensity, low-volume (HVY) lower-body resistance exercise in experienced, resistance trained men. Changes in receptor expression were assessed in conjunction with plasma concentrations of MCP-1, TNF?, and cortisol. Ten resistance-trained men (90.1 ± 11.3 kg; 176.0 ± 4.9 cm; 24.7 ± 3.4 yrs; 14.1 ± 6.1% body fat) performed each resistance exercise protocol in a random, counterbalanced order. Blood samples were obtained at baseline (BL), immediately (IP), 30 minutes (30P), 1 hour (1H), 2 hours (2H), and 5 hours (5H) post-exercise. Analysis of target receptor expression on CD14++CD16- monocytes was completed at BL, IP, 1H, 2H and 5H time points via flow cytometric analysis. Plasma concentrations of myoglobin, and LDH AUC were significantly greater following HVY compared to VOL (p = 0.003 and p = 0.010 respectively). Changes in plasma TNF?, MCP-1, and expression of CCR2, CD11b, and GCR on CD14++CD16- monocytes were similar following HVY and VOL. When collapsed across groups, TNF? was significantly increased at IP, 30P, 1H and 2H post-exercise (p = 0.001 – 0.004), while MCP-1 was significantly elevated at all post-exercise time points (p = 0.002 – 0.033). CCR2 expression was significantly lower at IP, 1H, 2H and 5H post-exercise (p = 0.020 – 0.040). In contrast, CD11b receptor expression was significantly greater at 1H relative to BL (p = 0.001), while GCR expression was not significantly different from baseline at any time point. As expected, plasma cortisol concentrations were significantly higher following VOL compared to HVY (p = 0.001), although this did not appear to be related to changes in receptor expression. Plasma testosterone concentrations and TNFr1 receptor expression did not appear to be affected by resistance exercise. Our results do not support a role for cortisol in the modulation of CCR2 receptors in vivo, while the degree of muscle damage does not appear to influence plasma concentrations of TNF?, or MCP-1. It is therefore likely that both HVY and VOL protocols constitute an exercise stimulus that is sufficient enough to promote a robust pro-inflammatory response, which is similar in timing and magnitude

    The Effects Of Phosphatidylserine On Reaction Time And Cognitive Function Following An Exercise Stress

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    Phosphatidylserine (PS) is an endogenously occurring phospholipid that has been shown to have cognition and mood enhancing properties in humans, possibly through its role as an enzyme co-factor in cellular signal transduction. Specifically, PS has been identified as activator of classical isoforms of protein kinase C, an enzyme known to be involved in the growth and differentiation of neural cells, and is therefore thought to play a role in the protection of neurons. The purpose of this study was to examine the effects of supplementation with PS and caffeine on measures of cognition, reaction time and mood prior to and following an exercise stress. Twenty, healthy, resistance trained males (17) and females (3) (mean ± SD; age: 22.75 ± 3.27 yrs; height: 177.03 ± 8.44cm; weight: 78.98 ± 11.24kg; body fat%: 14.28 ± 6.6), volunteered to participate in this randomized, double-blind, placebo-controlled study. Participants were assigned to a PS group (400mg/day PS; 100mg/day caffeine, N=9) or PL (16g/day Carbs, N=11) delivered in the form of 4 candy chews identical in size, shape and color. Subjects performed an acute bout of full body resistance exercise, prior to (T1) and following 14 days of supplementation (T2). Measures of reaction time (Dynavision® D2 Visuomotor Training Device), cognition (Serial Subtraction Test, SST), and mood (Profile of Mood States, POMS) were assessed immediately before and following resistance exercise in both T1 and T2. Data was analyzed using two-way ANCOVA and repeated measures ANOVA. Supplementation with 400mg PS and 100mg caffeine did not have a significant impact upon measures of reaction time or cognition between groups at baseline or following acute resistance exercise. However, there was a non-significant trend to the attenuation of fatigue iv between groups, following acute resistance exercise (p = 0.071). Interestingly, our data suggests that acute resistance exercise alone may improve cognitive function. Although more research is necessary regarding optimal dosage and supplementation duration, the current findings suggest that supplementation 400mg/day PS with 100mg/day caffeine may attenuate fatigue following acute resistance exercise. It is possible that the lack of significance may be the result of both an inhibition of the PS activated pathway and a withdrawal effect from caffeine

    Interface morphology and Dzyaloshinskii-Moriya interaction in Pt/Co thin films

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    The interfacial morphology and the Dzyaloshinskii-Moriya interaction (DMI) have been investigated in thin films of perpendicularly-magnetised epitaxial Pt(30 A)/Co(7 A)/Pt(10 A) and Pt(30 A)/Co(7, 9, 11 A)/Ir20Mn80(20, 50 A). In Pt/Co/Pt, altering the substrate temperature during deposition of the top Co/Pt bilayer in the range of 100 C to 300 C formed a peak in total interfacial disorder with deposition temperature of 3.3 A at around 250 C. The coercivity increased from 230 +/- 60 Oe to 400 +/- 60 Oe whilst the anisotropy and saturation magnetisation stayed constant at 15.0 +/- 0.3 kOe and 90 +/- 10 microemu, respectively, when the substrate temperature at deposition was reduced in value. In contrast, the anisotropy increased with deposition temperature if either the substrate temperature was increased, or the deposition temperature of only the top Pt layer was varied, though not both simultaneously. The bubble domain expansion technique was used to measure domain wall velocity with applied magnetic fields in various in-plane (IP) and out-of-plane (OOP) configurations. Of the three prominent creep models used, it was found that the most basic model fitted best. A moderate linear correlation was seen between DMI and the difference in disorder between the top and bottom Co interfaces, indicating that as the disorder in one interface increases, its contribution to DMI decreases, allowing the relative interface disorders to dictate the strength, and even sign, of the net DMI. The net DMI increased with increasing deposition temperature, also, showing that such a growth parameter can be used to fine-tune the DMI. Using Pt/Co/Ir20Mn80 samples, the growth temperature and working pressure were optimised for DMI measurements. Samples with 50 A of IrMn, with exchange bias strengths up to 1000 Oe, showed a high density of small, rough domains forming during magnetisation reversal. Samples with 20 A of IrMn, so without exchange bias, produced well-formed bubble domains for Co thicknesses below 9 A, with a Voronoi-like network seen in an 11 A sample. Bubble domain expansion showed severely skewed velocity against IP field graphs, with behaviour at higher fields not predicted by current models, giving DMI constant values between -0.6 and -1.0 mJ/m^2

    Mediators of Monocyte Migration in Response to Recovery Modalities following Resistance Exercise

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    Mediators of monocyte migration, complement receptor-3 (CR3), and chemokine ligand-4 (CCL4) were measured in response to recovery modalities following resistance exercise. Thirty resistance-trained men (23.1 +/- 2.9 y; 175.2 +/- 7.1 cm; 82.1 +/- 8.4 kg) were given neuromuscular electric stimulation (NMES), cold water immersion (CWI), or control (CON) treatments immediately following resistance exercise. Blood samples were obtained preexercise (PRE), immediately (IP), 30 minutes (30 P), 24 hours (24 H), and 48 hours (48 H) after exercise for measurement of circulating CCL4 and CR3 expression on CD14+ monocytes, by assay and flow cytometry. Circulating CCL4 showed no consistent changes. Inferential analysis indicated that CR3 expression was likely greater in CON at 30 P than NMES (90.0%) or CWI (86.8%). NMES was likely lower than CON at 24H (92.9%) and very likely lower at 48H (98.7%). Expression of CR3 following CWI was very likely greater than CON (96.5%) at 24H. The proportion of CR3+ monocytes was likely greater following CWI than NMES (85.8%) or CON (85.2%) at 24 H. The change in proportion of CR3+ monocytes was likely (86.4%) greater following NMES than CON from IP to 30 P. The increased expression of CR3 and increased proportion of CR3+ monocytes following CWI at 24 H indicate a potentially improved ability for monocyte adhesion to the endothelium, possibly improving phagocytosis of damaged tissues
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