1,142 research outputs found

    Quantum anti-Zeno effect in artificial quantum systems

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    In this paper, we study a quantum anti-Zeno effect (QAZE) purely induced by repetitive measurements for an artificial atom interacting with a structured bath. This bath can be artificially realized with coupled resonators in one dimension and possesses photonic band structure like Bloch electron in a periodic potential. In the presence of repetitive measurements, the pure QAZE is discovered as the observable decay is not negligible even for the atomic energy level spacing outside of the energy band of the artificial bath. If there were no measurements, the decay would not happen outside of the band. In this sense, the enhanced decay is completely induced by measurements through the relaxation channels provided by the bath. Besides, we also discuss the controversial golden rule decay rates originated from the van Hove's singularities and the effects of the counter-rotating terms.Comment: 12 pages, 8 figure

    Aspisol inhibits tumor growth and induces apoptosis in breast cancer

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    Nonsteroidal anti-inflammatory drugs inhibit cell proliferation and induce apoptosis in various cancer cell lines, which is considered to be an important mechanism for their anti-tumor activity and cancer prevention. However, the molecular mechanisms through which these compounds induce apoptosis are not well understood. Aim: to determine the effects of nonselective cyclooxygenase-2 (COX-2) inhibitor, aspisol on breast cancer cells in vitro and in vivo. Methods: The cytotoxic activity of aspisol was evaluated by MTT assay. The apoptosis index of cells was measured by flow cytometry. Immunohistochemical staining was used to detect expressions of COX-2 and caspase-3 in MDA-MB-231 cells. The expression of bcl-2 and bax was analyzed by Western blot analysis. The content of prostaglandin E2 (PGE2) in MDA-MB-231 cells was estimated by ELISA. In vivo apoptosis of the tumor cells was detected by the terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL). Results: Our results showed that aspisol reduced viability of MDA-MB-231 cells in time- and dose- dependent fashions and induced apoptosis by increase of caspase-3 and bax expressions while decrease of COX-2 and bcl-2 expression in vitro. In addition, exposure to aspisol decreased the basal release of PGE2. In vivo, aspisol also inhibited the proliferation of breast cancer cells and induced their apoptosis. Conclusions: Our in vitro and in vivo data indicated that the antitumor effects of aspisol on breast cancer cells was probably mediated by the induction of apoptosis, and it could be linked to the downregulation of the COX-2 or bcl-2 expression and up-regulation of caspase-3 or bax expression.НСстСроидныС ΠΏΡ€ΠΎΡ‚ΠΈΠ²ΠΎΠ²ΠΎΡΠΏΠ°Π»ΠΈΡ‚Π΅Π»ΡŒΠ½Ρ‹Π΅ ΠΏΡ€Π΅ΠΏΠ°Ρ€Π°Ρ‚Ρ‹ ΠΈΠ½Π³ΠΈΠ±ΠΈΡ€ΡƒΡŽΡ‚ ΠΏΡ€ΠΎΠ»ΠΈΡ„Π΅Ρ€Π°Ρ†ΠΈΡŽ ΠΊΠ»Π΅Ρ‚ΠΎΠΊ ΠΈ Π²Ρ‹Π·Ρ‹Π²Π°ΡŽΡ‚ Π°ΠΏΠΎΠΏΡ‚ΠΎΠ· Π²ΠΎ ΠΌΠ½ΠΎΠ³ΠΈΡ… ΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²Ρ‹Ρ… ΠΊΠ»Π΅Ρ‚ΠΎΡ‡Π½Ρ‹Ρ… линиях, Ρ‡Ρ‚ΠΎ считаСтся Π²Π°ΠΆΠ½Ρ‹ΠΌ ΠΌΠ΅Ρ…Π°Π½ΠΈΠ·ΠΌΠΎΠΌ ΠΈΡ… ΠΏΡ€ΠΎΡ‚ΠΈΠ²ΠΎΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²ΠΎΠΉ активности ΠΈ ΠΏΡ€ΠΎΡ„ΠΈΠ»Π°ΠΊΡ‚ΠΈΠΊΠΈ развития Ρ€Π°ΠΊΠ°. Π’Π΅ΠΌ Π½Π΅ ΠΌΠ΅Π½Π΅Π΅ молСкулярныС ΠΌΠ΅Ρ…Π°Π½ΠΈΠ·ΠΌΡ‹ апоптотичСского дСйствия этих ΠΏΡ€Π΅ΠΏΠ°Ρ€Π°Ρ‚ΠΎΠ² ΠΈΠ·ΡƒΡ‡Π΅Π½Ρ‹ нСдостаточно. ЦСль: ΠΈΠ·ΡƒΡ‡ΠΈΡ‚ΡŒ дСйствиС нСспСцифичСского ΠΈΠ½Π³ΠΈΠ±ΠΈΡ‚ΠΎΡ€Π° циклогСксиназы-2 (COX-2) β€” аспизола β€” Π½Π° злокачСствСнныС ΠΊΠ»Π΅Ρ‚ΠΊΠΈ Ρ€Π°ΠΊΠ° ΠΌΠΎΠ»ΠΎΡ‡Π½ΠΎΠΉ ΠΆΠ΅Π»Π΅Π·Ρ‹ in vitro ΠΈ in vivo. ΠœΠ΅Ρ‚ΠΎΠ΄Ρ‹: Π²Ρ‹ΠΆΠΈΠ²Π°Π΅ΠΌΠΎΡ‚ΡŒ ΠΊΠ»Π΅Ρ‚ΠΎΠΊ MDA-MB-231 опрСдСляли с ΠΏΠΎΠΌΠΎΡ‰ΡŒΡŽ MTT-тСста. АпоптотичСский индСкс измСряли с ΠΏΠΎΠΌΠΎΡ‰ΡŒΡŽ ΠΏΡ€ΠΎΡ‚ΠΎΡ‡Π½ΠΎΠΉ Ρ†ΠΈΡ‚ΠΎΠΌΠ΅Ρ‚Ρ€ΠΈΠΈ ΠΈ иммуногистохимичСским ΠΎΠΊΡ€Π°ΡˆΠΈΠ²Π°Π½ΠΈΠ΅ΠΌ с Π°Π½Ρ‚ΠΈΡ‚Π΅Π»Π°ΠΌΠΈ ΠΏΡ€ΠΎΡ‚ΠΈΠ² COX-2 ΠΈ каспазы-3. Π­ΠΊΡΠΏΡ€Π΅ΡΡΠΈΡŽ bcl-2 ΠΈ bax ΠΈΠ·ΡƒΡ‡Π°Π»ΠΈ с ΠΏΠΎΠΌΠΎΡ‰ΡŒΡŽ ВСстСрн-Π±Π»ΠΎΡ‚-Π°Π½Π°Π»ΠΈΠ·Π°. Π‘ΠΎΠ΄Π΅Ρ€ΠΆΠ°Π½ΠΈΠ΅ простагландина E2 (PGE2 ) Π² ΠΊΠ»Π΅Ρ‚ΠΊΠ°Ρ… MDA-MB-231 ΠΎΡ†Π΅Π½ΠΈΠ²Π°Π»ΠΈ ΠΌΠ΅Ρ‚ΠΎΠ΄ΠΎΠΌ ELISA. In vivo Π°ΠΏΠΎΠΏΡ‚ΠΎΠ· ΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²Ρ‹Ρ… ΠΊΠ»Π΅Ρ‚ΠΎΠΊ опрСдСляли ΠΏΡƒΡ‚Π΅ΠΌ выявлСния Ρ€Π°Π·Ρ€Ρ‹Π²ΠΎΠ² Π”ΠΠš с ΠΏΠΎΠΌΠΎΡ‰ΡŒΡŽ ΠΊΠΎΠ½Ρ†Π΅Π²ΠΎΠΉ дСзоксинуклСот-ΠΈΠ΄ΠΈΠ»Ρ‚Ρ€Π°Π½Ρ„Π΅Ρ€Π°Π·Ρ‹ (ΠΌΠ΅Ρ‚ΠΎΠ΄ TUNEL). Π Π΅Π·ΡƒΠ»ΡŒΡ‚Π°Ρ‚Ρ‹: ΠΏΠΎΠΊΠ°Π·Π°Π½ΠΎ, Ρ‡Ρ‚ΠΎ Π² зависимости ΠΎΡ‚ Π²Ρ€Π΅ΠΌΠ΅Π½ΠΈ ΠΈΠ½ΠΊΡƒΠ±Π°Ρ†ΠΈΠΈ ΠΈ Π΄ΠΎΠ·Ρ‹ аспизол ΡƒΠ³Π½Π΅Ρ‚Π°Π» рост ΠΊΠ»Π΅Ρ‚ΠΎΠΊ MDA-MB-231 in vitro ΠΈ Π²Ρ‹Π·Ρ‹Π²Π°Π» ΠΈΡ… Π°ΠΏΠΎΠΏΡ‚ΠΎΠ· Π½Π° Ρ„ΠΎΠ½Π΅ ΠΏΠΎΠ²Ρ‹ΡˆΠ΅Π½ΠΈΡ экспрСссии каспазы-3 ΠΈ bax, Π° Ρ‚Π°ΠΊΠΆΠ΅ сниТСния экспрСссии COX-2 ΠΈ bcl-2. Π’ условиях in vivo аспизол Ρ‚Π°ΠΊΠΆΠ΅ ΠΈΠ½Π³ΠΈΠ±ΠΈΡ€ΠΎΠ²Π°Π» ΠΏΡ€ΠΎΠ»ΠΈΡ„Π΅Ρ€Π°Ρ†ΠΈΡŽ злокачСствСнных ΠΊΠ»Π΅Ρ‚ΠΎΠΊ Ρ€Π°ΠΊΠ° ΠΌΠΎΠ»ΠΎΡ‡Π½ΠΎΠΉ ΠΆΠ΅Π»Π΅Π·Ρ‹ ΠΈ Π²Ρ‹Π·Ρ‹Π²Π°Π» ΠΈΡ… Π°ΠΏΠΎΠΏΡ‚ΠΎΠ·. Π’Ρ‹Π²ΠΎΠ΄Ρ‹: Π΄Π°Π½Π½Ρ‹Π΅, ΠΏΠΎΠ»ΡƒΡ‡Π΅Π½Π½Ρ‹Π΅ in vitro ΠΈ in vivo, ΡΠ²ΠΈΠ΄Π΅Ρ‚Π΅Π»ΡŒΡΡ‚Π²ΡƒΡŽΡ‚ ΠΎ ΠΏΡ€ΠΎΡ‚ΠΈΠ²ΠΎΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²ΠΎΠΌ эффСктС аспизола Π½Π° ΠΊΠ»Π΅Ρ‚ΠΊΠΈ Ρ€Π°ΠΊΠ° ΠΌΠΎΠ»ΠΎΡ‡Π½ΠΎΠΉ ΠΆΠ΅Π»Π΅Π·Ρ‹, Ρ‡Ρ‚ΠΎ скорСС всСго опосрСдовано Π΅Π³ΠΎ проапоптотичСским дСйствиСм ΠΈ ΠΌΠΎΠΆΠ΅Ρ‚ Π±Ρ‹Ρ‚ΡŒ связано со сниТСниСм экспрСссии COX-2 ΠΈ bcl-2, Π° Ρ‚Π°ΠΊΠΆΠ΅ ΠΏΠΎΠ²Ρ‹ΡˆΠ΅Π½ΠΈΠ΅ΠΌ экспрСссии каспазы-3 ΠΈ bax

    Dynamics of quantum entanglement in the reservoir with memory effects

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    The non-Markovian dynamics of quantum entanglement is studied by the Shabani-Lidar master equation when one of entangled quantum systems is coupled to a local reservoir with memory effects. The completely positive reduced dynamical map can be constructed in the Kraus representation. Quantum entanglement decays more slowly in the non-Markovian environment. The decoherence time for quantum entanglement can be markedly increased by the change of the memory kernel. It is found out that the entanglement sudden death between quantum systems and entanglement sudden birth between the system and reservoir occur at different instants.Comment: 14 pages, 3 figure

    Candidates for membrane progestin receptors: past approaches and future challenges

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    Progestins have a broad range of functions in reproductive biology. Many rapid nongenomic actions of progestins have been identified, including induction of oocyte maturation, modulation of reproductive signaling in the brain, rapid activation of breast cancer cell signaling, induction of the acrosomal reaction and hypermotility in mammalian sperm. Currently, there are three receptor candidates for mediating rapid progestin actions: (1) membrane progestin receptors (mPRs); (2) progestin receptor membrane components (PGRMCs); and (3) nuclear progestin receptors (nPRs). The recently-described mPR family of proteins has seven integral transmembrane domains and mediates signaling via G-protein coupled pathways. The PGRMCs have a single transmembrane with putative Src homology domains for potential activation of second messengers. The classical nPRs, in addition to having well defined transcriptional activity, can also mediate rapid activation of intracellular signaling pathways. However, details of the mechanisms by which these three classes of progestin receptors mediate rapid intracellular signaling and their subcellular localization remain unclear. In addition, mPRs, nPRs and PGRMCs exhibit overlapping expression and functions in multiple tissues, implying potential interactions during oocyte maturation, parturition, and breast cancer signaling in individual cells. However, the overwhelming majority of studies to date have focused on the functions of one of these groups of receptors in isolation. This review will summarize recent findings on the three major progestin receptor candidates, emphasizing the different approaches used, some experimental pitfalls, and current controversies. We will also review evidence for the involvement of mPRs and nPRs in one of the most well-characterized nongenomic steroid actions in basal vertebrates, oocyte maturation, and conclude by suggesting some future areas of research. Clarification of the controversies surrounding the identities and localization of membrane progestin receptors may help direct future research that could advance our understanding of rapid actions of steroids.Animal science

    Hadronic Parity Violation and Inelastic Electron-Deuteron Scattering

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    We compute contributions to the parity-violating (PV) inelastic electron-deuteron scattering asymmetry arising from hadronic PV. While hadronic PV effects can be relatively important in PV threshold electro- disintegration, we find that they are highly suppressed at quasielastic kinematics. The interpretation of the PV quasielastic asymmetry is, thus, largely unaffected by hadronic PV.Comment: 27 pages, 13 figures, uses REVTeX and BibTe

    Search for the Rare Decays J/Psi --> Ds- e+ nu_e, J/Psi --> D- e+ nu_e, and J/Psi --> D0bar e+ e-

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    We report on a search for the decays J/Psi --> Ds- e+ nu_e + c.c., J/Psi --> D- e+ nu_e + c.c., and J/Psi --> D0bar e+ e- + c.c. in a sample of 5.8 * 10^7 J/Psi events collected with the BESII detector at the BEPC. No excess of signal above background is observed, and 90% confidence level upper limits on the branching fractions are set: B(J/Psi --> Ds- e+ nu_e + c.c.)<4.8*10^-5, B(J/Psi --> D- e+ nu_e + c.c.) D0bar e+ e- + c.c.)<1.1*10^-5Comment: 10 pages, 4 figure

    Pulsar Timing and its Application for Navigation and Gravitational Wave Detection

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    Pulsars are natural cosmic clocks. On long timescales they rival the precision of terrestrial atomic clocks. Using a technique called pulsar timing, the exact measurement of pulse arrival times allows a number of applications, ranging from testing theories of gravity to detecting gravitational waves. Also an external reference system suitable for autonomous space navigation can be defined by pulsars, using them as natural navigation beacons, not unlike the use of GPS satellites for navigation on Earth. By comparing pulse arrival times measured on-board a spacecraft with predicted pulse arrivals at a reference location (e.g. the solar system barycenter), the spacecraft position can be determined autonomously and with high accuracy everywhere in the solar system and beyond. We describe the unique properties of pulsars that suggest that such a navigation system will certainly have its application in future astronautics. We also describe the on-going experiments to use the clock-like nature of pulsars to "construct" a galactic-sized gravitational wave detector for low-frequency (f_GW ~1E-9 - 1E-7 Hz) gravitational waves. We present the current status and provide an outlook for the future.Comment: 30 pages, 9 figures. To appear in Vol 63: High Performance Clocks, Springer Space Science Review

    Study of J/psi decays to Lambda Lambdabar and Sigma0 Sigma0bar

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    The branching ratios and Angular distributions for J/psi decays to Lambda Lambdabar and Sigma0 Sigma0bar are measured using BESII 58 million J/psi.Comment: 11 pages, 5 figure

    Direct Measurements of the Branching Fractions for D0β†’Kβˆ’e+Ξ½eD^0 \to K^-e^+\nu_e and D0β†’Ο€βˆ’e+Ξ½eD^0 \to \pi^-e^+\nu_e and Determinations of the Form Factors f+K(0)f_{+}^{K}(0) and f+Ο€(0)f^{\pi}_{+}(0)

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    The absolute branching fractions for the decays D0β†’Kβˆ’e+Ξ½eD^0 \to K^-e ^+\nu_e and D0β†’Ο€βˆ’e+Ξ½eD^0 \to \pi^-e^+\nu_e are determined using 7584Β±198Β±3417584\pm 198 \pm 341 singly tagged DΛ‰0\bar D^0 sample from the data collected around 3.773 GeV with the BES-II detector at the BEPC. In the system recoiling against the singly tagged DΛ‰0\bar D^0 meson, 104.0Β±10.9104.0\pm 10.9 events for D0β†’Kβˆ’e+Ξ½eD^0 \to K^-e ^+\nu_e and 9.0Β±3.69.0 \pm 3.6 events for D0β†’Ο€βˆ’e+Ξ½eD^0 \to \pi^-e^+\nu_e decays are observed. Those yield the absolute branching fractions to be BF(D0β†’Kβˆ’e+Ξ½e)=(3.82Β±0.40Β±0.27)BF(D^0 \to K^-e^+\nu_e)=(3.82 \pm 0.40\pm 0.27)% and BF(D0β†’Ο€βˆ’e+Ξ½e)=(0.33Β±0.13Β±0.03)BF(D^0 \to \pi^-e^+\nu_e)=(0.33 \pm 0.13\pm 0.03)%. The vector form factors are determined to be ∣f+K(0)∣=0.78Β±0.04Β±0.03|f^K_+(0)| = 0.78 \pm 0.04 \pm 0.03 and ∣f+Ο€(0)∣=0.73Β±0.14Β±0.06|f^{\pi}_+(0)| = 0.73 \pm 0.14 \pm 0.06. The ratio of the two form factors is measured to be ∣f+Ο€(0)/f+K(0)∣=0.93Β±0.19Β±0.07|f^{\pi}_+(0)/f^K_+(0)|= 0.93 \pm 0.19 \pm 0.07.Comment: 6 pages, 5 figure
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