212 research outputs found

    Antiproliferative activity of neem leaf extracts obtained by a sequential pressurized liquid extraction

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    Azadirachta indica A. Juss (neem) extracts have been used in pharmaceutical applications as antitumor agents, due to their terpenes and phenolic compounds. To obtain extracts from neem leaves with potential antiproliferative effect, a sequential process of pressurized liquid extraction was carried out in a fixed bed extractor at 25◦C and 100 bar, using hexane (SH), ethyl acetate (SEA), and ethanol (SE)assolvents. Extractions using only ethanol(EE) was also conducted to compare the characteristics of the fractionated extracts. The results obtained by liquid chromatography-electrospray ionization mass spectrometry suggested a higher concentration of terpenes in the SEA extract in comparison to SH, SE, and EE extracts. Therefore, antiproliferative activity showed that SEA extracts were the most efficient inhibitor to human tumor cells MCF-7, NCI-H460, HeLa, and HepG2. Hepatocellular cells were more resistant to SH, SEA, SE, and EE compared to breast, lung, hepatocellular, and cervical malignant cells. Neem fractioned extracts obtained in the present study seem to be more selective for malignant cells compared to the non-tumor cells.Klebson Silva Santos thanks CAPES (Process: PDSE 99999.003409/15-5) for the financial support during his Ph.D. studies in Portugal. Authors are grateful to CAPES, and FAPITEC (EDITAL CAPES/FAPITEC Nº 11/2016–PROEF/Processo de AUXPE 88881.157437/2017-01) for the financial support. The study was also carried out with financial support from FEDER, under the Partnership Agreement PT2020.info:eu-repo/semantics/publishedVersio

    Pair production of the heavy leptons in future high energy linear e^{+}e^{-} colliders

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    The littlest Higgs model with T-parity predicts the existence of the T-odd particles, which can only be produced in pair. We consider pair production of the T-odd leptons in future high energy linear e+ee^{+}e^{-} collider (ILCILC). Our numerical results show that, as long as the T-odd leptons are not too heavy, they can be copiously produced and their possible signals might be detected via the processes e+eLˉiLje^{+}e^{-}\to \bar{L}_{i}L_{j} in future ILCILC experiments.Comment: Discussions added, typos and references correcte

    Lepton flavor violation decays τμP1P2\tau^-\to \mu^- P_1 P_2 in the topcolor-assisted technicolor model and the littlest Higgs model with TT parity

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    The new particles predicted by the topcolor-assisted technicolor (TC2TC2) model and the littlest Higgs model with T-parity (called LHTLHT model) can induce the lepton flavor violation (LFVLFV) couplings at tree level or one loop level, which might generate large contributions to some LFVLFV processes. Taking into account the constraints of the experimental data on the relevant free parameters, we calculate the branching ratios of the LFVLFV decay processes τμP1P2\tau^-\to\mu^- P_1 P_2 with P1P2P_1 P_2 = π+π\pi^+\pi^-, K+KK^+K^- and K0K0ˉK^0\bar{K^0} in the context of these two kinds of new physics models. We find that the TC2TC2 model and the LHTLHT model can indeed produce significant contributions to some of these LFVLFV decay processes.Comment: 24 pages, 7 figure

    Computer Simulations of Hippocampal Mossy Fiber Cleft Zinc Movements

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    Zinc ions have key regulatory, structural, and catalytic functions and mediate a variety of intra- and intercellular processes. The hippocampal mossy fiber boutons contain large amounts of free or loosely bound vesicular zinc, which can be co-released with glutamate. Zinc can interact with a variety of ionic channels (N-VDCCs, L-VDCCs, KATP), glutamate receptors (AMPA, KA, NMDA 2A, 2B), glutamate transporters (GLAST, EAAT4), and molecules (ATP). The dynamic properties of cleft free, complexed, and total zinc were addressed, considering the known concentration and affinity of various cleft zinc sensitive sites, mainly in the postsynaptic area and in glial cells. The computer model included three different zinc release processes, with short, medium, and long duration, described, like the uptake ones, by alpha functions. The results suggest that, depending on the amount of release, zinc clearance is largely due, either, to zinc binding to NMDA 2A receptor sites or to glial GLAST transporters

    Non-bee insects are important contributors to global crop pollination

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    Wild andmanaged bees arewell documented as effective pollinators of global crops of economic importance. However, the contributions by pollinators other than bees have been little explored despite their potential to contribute to crop production and stability in the face of environmental change. Non-bee pollinators include flies, beetles, moths, butterflies, wasps, ants, birds, and bats, among others. Here we focus on non-bee insects and synthesize 39 field studies from five continents that directly measured the crop pollination services provided by non-bees, honey bees, and other bees to compare the relative contributions of these taxa. Non-bees performed 25-50% of the total number of flower visits. Although non-bees were less effective pollinators than bees per flower visit, they made more visits; thus these two factors compensated for each other, resulting in pollination services rendered by non-bees that were similar to those provided by bees. In the subset of studies that measured fruit set, fruit set increased with non-bee insect visits independently of bee visitation rates, indicating that non-bee insects provide a unique benefit that is not provided by bees. We also show that non-bee insects are not as reliant as bees on the presence of remnant natural or seminatural habitat in the surrounding landscape. These results strongly suggest that non-bee insect pollinators play a significant role in global crop production and respond differently than bees to landscape structure, probably making their crop pollination services more robust to changes in land use. Non-bee insects provide a valuable service and provide potential insurance against bee population declines.Peer Reviewe

    Rivaroxaban or Aspirin for Extended Treatment of Venous Thromboembolism.

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    Although many patients with venous thromboembolism require extended treatment, it is uncertain whether it is better to use full- or lower-intensity anticoagulation therapy or aspirin. In this randomized, double-blind, phase 3 study, we assigned 3396 patients with venous thromboembolism to receive either once-daily rivaroxaban (at doses of 20 mg or 10 mg) or 100 mg of aspirin. All the study patients had completed 6 to 12 months of anticoagulation therapy and were in equipoise regarding the need for continued anticoagulation. Study drugs were administered for up to 12 months. The primary efficacy outcome was symptomatic recurrent fatal or nonfatal venous thromboembolism, and the principal safety outcome was major bleeding. A total of 3365 patients were included in the intention-to-treat analyses (median treatment duration, 351 days). The primary efficacy outcome occurred in 17 of 1107 patients (1.5%) receiving 20 mg of rivaroxaban and in 13 of 1127 patients (1.2%) receiving 10 mg of rivaroxaban, as compared with 50 of 1131 patients (4.4%) receiving aspirin (hazard ratio for 20 mg of rivaroxaban vs. aspirin, 0.34; 95% confidence interval [CI], 0.20 to 0.59; hazard ratio for 10 mg of rivaroxaban vs. aspirin, 0.26; 95% CI, 0.14 to 0.47; P<0.001 for both comparisons). Rates of major bleeding were 0.5% in the group receiving 20 mg of rivaroxaban, 0.4% in the group receiving 10 mg of rivaroxaban, and 0.3% in the aspirin group; the rates of clinically relevant nonmajor bleeding were 2.7%, 2.0%, and 1.8%, respectively. The incidence of adverse events was similar in all three groups. Among patients with venous thromboembolism in equipoise for continued anticoagulation, the risk of a recurrent event was significantly lower with rivaroxaban at either a treatment dose (20 mg) or a prophylactic dose (10 mg) than with aspirin, without a significant increase in bleeding rates. (Funded by Bayer Pharmaceuticals; EINSTEIN CHOICE ClinicalTrials.gov number, NCT02064439 .)
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