93 research outputs found

    Ultrastable CO2 Laser Trapping of Lithium Fermions

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    We demonstrate an ultrastable CO2 laser trap that provides tight confinement of neutral atoms with negligible optical scattering and minimal laser-noise- induced heating. Using this method, fermionic 6Li atoms are stored in a 0.4 mK deep well with a 1/e trap lifetime of 300 sec, consistent with a background pressure of 10^(-11) Torr. To our knowledge, this is the longest storage time ever achieved with an all-optical trap, comparable to the best reported magnetic traps.Comment: 4 pages using REVTeX, 1 eps figur

    All-Optical Production of a Degenerate Fermi Gas

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    We achieve degeneracy in a mixture of the two lowest hyperfine states of 6^6Li by direct evaporation in a CO2_2 laser trap, yielding the first all-optically produced degenerate Fermi gas. More than 10510^5 atoms are confined at temperatures below 4μ4 \muK at full trap depth, where the Fermi temperature for each state is 8μ8 \muK. This degenerate two-component mixture is ideal for exploring mechanisms of superconductivity ranging from Cooper pairing to Bose condensation of strongly bound pairs.Comment: 4 pgs RevTeX with 2 eps figs, to be published in Phys. Rev. Let

    Dilute neutron matter on the lattice at next-to-leading order in chiral effective field theory

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    We discuss lattice simulations of the ground state of dilute neutron matter at next-to-leading order in chiral effective field theory. In a previous paper the coefficients of the next-to-leading-order lattice action were determined by matching nucleon-nucleon scattering data for momenta up to the pion mass. Here the same lattice action is used to simulate the ground state of up to 12 neutrons in a periodic cube using Monte Carlo. We explore the density range from 2% to 8% of normal nuclear density and analyze the ground state energy as an expansion about the unitarity limit with corrections due to finite scattering length, effective range, and P-wave interactions.Comment: 25 pages, 7 figures, published versio

    Proliferative and anti-proliferative effects of dietary levels of phytoestrogens in rat pituitary GH3/B6/F10 cells - the involvement of rapidly activated kinases and caspases

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    <p>Abstract</p> <p>Background</p> <p>Phytoestogens are a group of lipophillic plant compounds that can have estrogenic effects in animals; both tumorigenic and anti-tumorigenic effects have been reported. Prolactin-secreting adenomas are the most prevalent form of pituitary tumors in humans and have been linked to estrogen exposures. We examined the proliferative effects of phytoestrogens on a rat pituitary tumor cell line, GH<sub>3</sub>/B<sub>6</sub>/F<sub>10</sub>, originally subcloned from GH<sub>3 </sub>cells based on its ability to express high levels of the membrane estrogen receptor-α.</p> <p>Methods</p> <p>We measured the proliferative effects of these phytoestrogens using crystal violet staining, the activation of several mitogen-activated protein kinases (MAPKs) and their downstream targets via a quantitative plate immunoassay, and caspase enzymatic activities.</p> <p>Results</p> <p>Four phytoestrogens (coumestrol, daidzein, genistein, and <it>trans</it>-resveratrol) were studied over wide concentration ranges. Except <it>trans</it>-resveratrol, all phytoestrogens increased GH<sub>3</sub>/B<sub>6</sub>/F<sub>10 </sub>cell proliferation at some concentration relevant to dietary levels. All four phytoestrogens attenuated the proliferative effects of estradiol when administered simultaneously. All phytoestrogens elicited MAPK and downstream target activations, but with time course patterns that often differed from that of estradiol and each other. Using selective antagonists, we determined that MAPKs play a role in the ability of these phytoestrogens to elicit these responses. In addition, except for <it>trans</it>-resveratrol, a serum removal-induced extrinsic apoptotic pathway was blocked by these phytoestrogens.</p> <p>Conclusion</p> <p>Phytoestrogens can block physiological estrogen-induced tumor cell growth <it>in vitro </it>and can also stimulate growth at high dietary concentrations in the absence of endogenous estrogens; these actions are correlated with slightly different signaling response patterns. Consumption of these compounds should be considered in strategies to control endocrine tumor cell growth, such as in the pituitary.</p

    Multifactorial approach and superior treatment efficacy in renal patients with the aid of nurse practitioners. Design of The MASTERPLAN Study [ISRCTN73187232]

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    BACKGROUND: Patients with chronic kidney disease (CKD) are at a greatly increased risk of developing cardiovascular disease. Recently developed guidelines address multiple risk factors and life-style interventions. However, in current practice few patients reach their targets. A multifactorial approach with the aid of nurse practitioners was effective in achieving treatment goals and reducing vascular events in patients with diabetes mellitus and in patients with heart failure. We propose that this also holds for the CKD population. DESIGN: MASTERPLAN is a multicenter randomized controlled clinical trial designed to evaluate whether a multifactorial approach with the aid of nurse-practicioners reduces cardiovascular risk in patients with CKD. Approximately 800 patients with a creatinine clearance (estimated by Cockcroft-Gault) between 20 to 70 ml/min, will be included. To all patients the same set of guidelines will be applied and specific cardioprotective medication will be prescribed. In the intervention group the nurse practitioner will provide lifestyle advice and actively address treatment goals. Follow-up will be five years. Primary endpoint is the composite of myocardial infarction, stroke and cardiovascular mortality. Secondary endpoints are cardiovascular morbidity, overall mortality, decline of renal function, change in markers of vascular damage and change in quality of life. Enrollment has started in April 2004 and the study is on track with 700 patients included on October 15th, 2005. This article describes the design of the MASTERPLAN study
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