Resonant plasma excitation by single-cycle THz pulses

In this paper, an alternative perspective for the generation of millimetric high-gradient resonant plasma waves is discussed. This method is based on the plasma-wave excitation by energetic single-cycle THz pulses whose temporal length is comparable to the plasma wavelength. The excitation regime discussed in this paper is the quasi-nonlinear regime that can be achieved when the normalized vector potential of the driving THz pulse is on the order of unity. To investigate this regime and determine the strength of the excited electric elds, a Particle-In-Cell (PIC) code has been used. It has been found that by exploiting THz pulses with characteristics currently available in laboratory, longitudinal electron plasma waves with electric gradients up to hundreds MV/m can be obtained. The mm-size nature of the resonant plasma wave can be of great utility for an acceleration scheme in which high-brightness electron bunches are injected into the wave to undergo a strong acceleration. The long-size nature of the acceleration bucket with respect to the short length of the electron bunches can be handled in a more robust manner in comparison with the case when micrometric waves are employed

New Ultra Small Iron-Oxide Nanoparticles with Titanium-Carbamate Coating: Preparation and Magnetic Properties

This work deals with the preparation and chemical characterization of new Ultra-Small Iron-Oxide Superparamagnetic Nanoparticles (USPIONs) functionalized with Titanium-carbamate. The synthesis was performed starting from oleate-coated and 2-pyrrolidone-coated USPIONs having a maghemite ( -Fe2O3) and magnetite (Fe3O4) crystalline core, respectively. Zero-field-cooled (ZFC) and field-cooled (FC) magnetic susceptibility curves as well as the magnetization behavior as a function of temperature are reported and discussed in view of the superparamagnetic properties and coating effect of these new magnetic nanoparticles. When you are citing the document, use the following link http://essuir.sumdu.edu.ua/handle/123456789/3545

The Potential of Omega-3 Supplementation to Reduce Muscle-Inflammation after Muscle-Damaging Exercise

Muscle Damaging exercise (EIMD) induces inflammation and relates to strength loss, muscle-soreness and impaired recovery. Overall, this means a performance impairment which might be relevant for those who engages in competitions or strenuous physical activities. It remains unclear whether Omega-3 fatty acids (O-3) supplementation blunts the exercise-induced inflammation associated with EIMD and therefore prevents performance impairment. PURPOSE: Following a three-week supplementation with O-3, indirect markers of muscle damage were examined after a bout of EIMD to determine if supplementation had any beneficial effect in maintaining leg-strength levels. METHODS: Eight healthy, recreationally active caucasian males (28.13 ± 3.4 yr) were randomly allocated to a supplementation group (SUP, n = 4) to receive 2.85g/day O-3 supplementation or a control group (CON, n = 4) for three weeks. Following supplementation, participants performed a bout of EIMD, which consisted of performing 10 sets of 15 repetitions of leg extension at a self-assessed intensity of 7/10 on the Rate of Perceived Exertion scale. Creatine Kinase (CK) from venous blood samples, isometric right-leg strength, squat-jump test and perceived soreness were determined, as indirect markers of muscle-damage at Baseline, immediately after EIMD (POST) and 48 hours after EIMD to coincide with the delayed muscle inflammatory response. RESULTS: No statistically significant differences were found between Baseline and POST. There was a trend for smaller increase of CK levels (pre vs 48-h post EIMD) on the SUP group (38.8% increase) compared with the CON group (105.6% increase; P = 0.051). There was no significant effect (baseline vs. 48-h post EIMD) on muscle strength between SUP and CON group (P > 0.05), however, CON showed a larger decrease in strength compared to SUP (> 6.3% vs SUP). No differences in jump height were found between SUP and CON (P > 0.05). There was no significant difference in muscle soreness at 48-h post EIMD between SUP and CON group (P = 0.171). CONCLUSION: Three weeks of O-3 supplementation might decrease exercise-induced muscle inflammation after eccentric exercise. The lack of statistical significance may be adduced to the limitations of the study design and sample size. Supplementation with O-3 can be beneficial in athletes undergoing heavy exercise regimes and in sedentary individuals restarting physical activity, decreasing the exercise related muscle inflammation. The encouraging results from this pilot study have led to designing further work related to this topic

A Crystallographic and Spectroscopic Study of the Reactions of WCl6 with Carbonyl Compounds

WCl6, 1, reacted with two equivalents of HC(O)NR2 (R = Me, Et) in CH2Cl2 to afford the W(VI) oxo-derivatives WOCl4(OCHNR2) (R = Me, 2a; R = Et, 2b) as main products. The hexachlorotungstate(V) salts [{ }2(-H)][WCl6], 3, and [PhNHC(Me)N(Ph)C(O)Me][WCl6], 4, were isolated in moderate yields from the 1:2 molar reactions of 1 with N-methyl-2-pyrrolidone (in CH2Cl2) and acetanilide (in CDCl3), respectively. The additions of two equivalents of ketones/aldehydes to 1/CH2Cl2 yielded the complexes WOCl4[OC(R)(R’)] (R = Me, R′ = Ph, 5a; R = R’ = Ph, 5b; R = R’ = Me, 5c; R = R’ = Et, 5d; R = H, R’ = 2-Me-C6H4, 5e) and equimolar amounts of C(R)(R’)Cl2. Analogously, WOCl3[2-{1,2-C6H4(O)(CHO)}], 5f, and 1,2-C6H4(OH)(CHCl2) were obtained from 1 and salicylaldehyde. The 1:1 reaction of 1 with acetone in CH2Cl2 resulted in the clean formation of WOCl4 and 2,2-dichloropropane. Compounds 5a,b,f were isolated as crystalline solids, whereas 5c,d,e could be detected by solution NMR only. The interaction of 1/CH2Cl2 with isatin, in 1:1 molar ratio, revealed to be a new, convenient route for the synthesis of 3,3-dichloro-2,3-dihydro-1H-indol-2-one, 6. The 1:1 reactions of 1 with R’OCH(R)CO2Me (R = H, R’ = Me; R = Me, R’ = H) in chlorinated solvent afforded the tungsten(V) adducts WCl4[2-OCH(R)CO2Me] (R = H, 7a; R = Me, 7b). 1/CH2Cl2 reacted sluggishly with equimolar quantities of trans-(CO2Et)CH=CH(CO2Et) and CH2(CO2Me)2 to give, respectively, the W(IV) derivatives WCl4[2-CH2(CO2Me)2], 8a, and [WCl4-2-{trans-(CO2Et)CH=CH (CO2Et)}]n, 8b, in about 70% yields. The molecular structures of 2a, 3, 4, 5a, 5f, 7a and 7b were ascertained by X-ray diffraction studies

Role of c-kit in mammalian spermatogenesis

The tyrosine-kinase receptor c-kit and its ligand, stem cell factor (SCF), are essential for the maintenance of primordial germ cells (PGCs) in both sexes. However, c-kit and a post-meiotic-specific alternative c-kit gene product play important roles also during post-natal stages of spermatogenesis. In the adult testis, the c-kit receptor is re-expressed in differentiating spermatogonia, but not in spermatogonial stem cells, whereas SCF is expressed by Sertoli cells under FSH stimulation. SCF stimulates DNA synthesis in type A spermatogonia cultured in vitro, and injection of anti-c-kit antibodies blocks their proliferation in vivo. A point mutation in the c-kit gene, which impairs SCF-mediated activation of phosphatidylinositol 3-kinase, does not cause any significant reduction in PGCs number during embryonic development, nor in spermatogonial stem cell populations. However males are completely sterile due to a block in the initial stages of spermatogenesis, associated to abolishment of DNA-synthesis in differentiating A1-A4 spermatogonia. With the onset of meiosis c-kit expression ceases, but a truncated c-kit product, tr-kit, is specifically expressed in post-meiotic stages of spermatogenesis, and is accumulated in mature spermatozoa. Microinjection of tr-kit into mouse eggs causes their parthenogenetic activation, suggesting that it might play a role in the final function of the gametes, fertilization

Impact of total automation consolidating first-line laboratory tests on diagnostic blood loss

Background: Blood loss for laboratory testing may contribute to hospital-acquired anemia. When implementing the core laboratory (core-lab) section, we consolidated first-line tests decreasing the number of tubes previously dispatched to different sites. Here, hypothesized benefits of the amount of blood volume drawn were explored. Methods: We retrieved, using a laboratory information system (LIS), the number of tubes received by laboratories interested in the change from all clinical wards in a year-based period, i.e. 2013 for pre-core-lab and 2015 for core-lab system, respectively. Data were expressed as the overall number of tubes sent to laboratories, the corresponding blood volume, and the number of laboratory tests performed, normalized for the number of inpatients. Results: After consolidation, the average number of blood tubes per inpatient significantly decreased (12.6 vs. 10.7, p\u2009<\u20090.001). However, intensive care units (ICUs) did not reduce the number of tubes per patient, according to the needs of daily monitoring of their clinical status. The average blood volume sent to laboratories did not vary significantly because serum tubes for core-lab required higher volumes for testing up to 55 analytes in the same transaction. Finally, the number of requested tests per patient during the new osystem slightly decreased ( 122.6%). Conclusions: Total laboratory automation does not automatically mean reducing iatrogenic blood loss. The new system affected the procedure of blood drawing in clinical wards by significantly reducing the number of handled tubes, producing a benefit in terms of costs, labor and time consumption. Except in ICUs, this also slightly promoted some blood saving. ICUs which engage in phlebotomizing patients daily, did not take advantage from the test consolidation

Developmental expression of BMP4/ALK3/SMAD5 signaling pathway in the mouse testis: a potential role of BMP4 in spermatogonia differentiation

It is well established that the c-kit gene plays an essential role in the proliferation of differentiating spermatogonia in prepuberal mice. However, the mechanisms that regulate the onset of spermatogenesis, i.e. differentiation of spermatogonial stem cells and c-kit expression, are poorly understood. Here we identify a novel signal transduction system in mouse prepuberal testis regulating this developmental event, involving bone morphogenetic protein 4 (BMP4) and its transduction machinery. BMP4 is produced by Sertoli cells very early in the postnatal life and is successively down regulated in peri-puberal Sertoli cells. Its receptor Alk3 and the R-Smad Smad5 are specifically expressed both in proliferating primordial germ cells and in postnatal spermatogonia. BMP4 stimulation of cultured spermatogonia induces Smad4/5 nuclear translocation and the formation of a DNA-binding complex with the transcriptional coactivator p300/CBP. In vitro exposure of undifferentiated spermatogonia to BMP4 exerts both mitogenic and differentiative effects, inducing [3H]thymidine incorporation and Kit expression. As a result of the latter event, Kit-negative spermatogonia acquire sensitivity to Stem Cell Factor

UV and genotoxic stress induce ATR relocalization in mouse spermatocytes

During meiosis, phosphorylation of H2AX is one of the earliest cellular responses to the generation of DNA double-strand breaks (DSBs) by the SPO11 topoisomerase. ATM is the kinase which mediates the formation of phosphorylated H2AX (H2AX) meiotic foci, while ATR is the kinase which signals chromosome asynapsis at the level of the XY bivalent. To investigate the possible role of ATR also in DNA damage signalling in meiotic cells, we studied the effect of UV radiation and chemotherapy drugs on H2AX phosphorylation and ATR relocalization in mouse pachytene spermatocytes. Here, we report that UV, a single strand break DNA-damaging agent, induces ATR relocalization from the XY sex body to nuclear foci and intense H2AX phosphorylation. Other DNA damage proteins such as MDC1, NBS1 and 53BP1 showed a similar relocalization following UVA microirradiation of spermatocytes. We found that DNA damage induced by UV increased the intensity and the number of H2AX foci also in Atm null spermatocytes. Inhibition of RNA synthesis was found to induce the formation of H2AX foci, but it did not influence the DNA damage response to UV irradiation. Finally, exposure of spermatocytes to double strand break DNA-damaging agents such as cisplatin, bleomycin or etoposide also induced ATR relocalization and intense H2AX phosphorylation and led to anomalies in synaptonemal assembly. Our results demonstrate that DNA damage induced by genotoxic stress can activate ATR and influence meiotic chromatin remodelling through H2AX phosphorylation, likely as part of a response which normally ensures germ cell genomic integrity