The magnetic diagnostic of Mirnov probe arrays has been upgraded on the J-TEXT tokamak to measure the magnetohydrodynamic instabilities with higher spatial resolution and better amplitude-frequency characteristics. The upgraded Mirnov probe array contains one poloidal array with 48 probe modules and two toroidal arrays with 25 probe modules. Each probe module contains two probes which measure both the poloidal and the radial magnetic fields (B and B). To ensure that the Mirnov probe possess better amplitude-frequency characteristics, a novel kind of Mirnov probe made of low temperature co-fired ceramics is utilized. The parameters and frequency response of the probe are measured and can meet the experiment requirement. The new Mirnov arrays have been normally applied for a round of experiments, including the observation of tearing modes and their coupling as well as high frequency magnetic perturbation due to the Alfvén eigenmode. In order to extract useful information from raw signals, visualization processing methods based on singular value decomposition and cross-power spectrum are applied to decompose the coupled modes and to determine the mode number.
The injection of a large amount of impurities is one of the possible ways of mitigating disruption in large-scale tokamaks. The deposition of impurities at the center of the plasma is the key to the radiation of plasma energy and suppression of runaway. The interaction of the gas jet with the rational surfaces has been studied by scanning the plasma current. The experimental results show that the injection of a massive amount of argon can cool the plasma from the edge to the core region, and the cooling process is accompanied by different magnetohydrodynamic (MHD) modes when the gas jet reaches the corresponding rational surfaces. It is observed that with different edge safety factors and electron density, gas injection can induce different poloidal modes at first. Then, the poloidal mode traverses to lower m (where m is the poloidal mode number) MHD activities until a 2/1 mode is initiated and a thermal quench is started. The experimental results show that the penetration of a gas jet across the rational surfaces is faster in the plasmas with pre-existing large 2/1 tearing modes, which indicates that the 2/1 mode plays an important role in the penetration process. Disruptions triggered by supersonic molecular beam injection display a slower cooling process compared with massive gas injection, which can be divided into four stages. The dominant poloidal mode transition from m = 3 to m = 2 is associated with electron temperature recovery.
The operation region and the parameter region of magnetohydrodynamic (MHD) modes are analyzed for J-TEXT Ohmic discharges. The operation region is described by the Hugill diagram, which combines low-q and high density limits. It is found that the operation region has expanded over the years on J-TEXT. In detail, the high density limit has increased from less than 0.5n G to 0.7n G and the low-q limit has lowered from 2.8 to 2.2; this is due to the reduced impurity content that results from coating graphite on the wall. Furthermore, the operation region has further expanded to 0.85n G and q a ~ 2.0, respectively-a result of suppressing the disruptive precursor MHD by using externally-applied resonant magnetic perturbations (RMPs). Here, n G and q a are the Greenwald density limit and edge safety factor, respectively. Corresponding to the results of the operation region, the parameter regions of MHD modes are presented. It is found that a m/n = 2/1 tearing mode (TM) appears for a wide parameters region with 2.4 < q a < 4 and n e < 3 × 10 19 m −3 -here m and n are the poloidal and toroidal mode numbers. Furthermore, other MHD modes such as m/n = 5/2, 3/1, 4/1 and 7/2, appear only when their rational surfaces are close to the plasma edge or m/n ~ q a , and these MHD modes may transit to a 2/1 TM when changing the plasma parameters. In addition, correlation analysis between the amplitude and frequency of the dominant 2/1 TM for different plasma conditions reveals that there is a threshold between normal discharges and density-limit discharges, which would be a reference to predict density-limit disruptions.
Background: Hypoxia-inducible factor-1α (HIF-1α) induces the expression of glycolysis-related genes, which plays a direct and key role in Warburg effect. In a recent study, honokiol (HNK) was identified as one of the potential agents that inhibited the HIF-1α signaling pathway. Because the HIF- 1α pathway is closely associated with glycolysis, we investigated whether HNK inhibited HIF-1α-mediated glycolysis.Methods: The effects of HNK on HIF-1α-mediated glycolysis and other glycolysis-related genes’ expressions, cancer cells apoptosis and tumor growth were studied in various human breast cancer models in vitro and in vivo. We performed the following tests: extracellular acidification and oxygen consumption rate assays, glucose uptake, lactate, and ATP assays for testing glycolysis; WST-1 assay for investigating cell viability; colony formation assay for determining clonogenicity; flow cytometry for assessing cell apoptosis; qPCR and Western blot for determining the expression of HIF-1α, GLUT1, HK2 and PDK1. The mechanisms of which HNK functions as a direct inhibitor of HIF-1α were verified through the ubiquitination assay, the Co-IP assay, and the cycloheximide (CHX) pulse-chase assay.Results: HNK increased the oxygen consumption rate while decreased the extracellular acidification rate in breast cancer cells; it further reduced glucose uptake, lactic acid production and ATP production in cancer cells. The inhibitory effect of HNK on glycolysis is HIF-1α-dependent. HNK also downregulated the expression of HIF-1α and its downstream regulators, including GLUT1, HK2 and PDK1. A mechanistic study demonstrated that HNK enhanced the self-ubiquitination of HIF-1α by recruiting two E3 ubiquitin ligases (UFL1 and BRE1B). In vitro, HNK inhibited cell proliferation and clonogenicity, as well as induced apoptosis of cancer cells. These effects were also HIF1α-dependent. In vivo, HNK inhibited tumor growth and HIF-1α-mediated glycolysis.Conclusion: HNK has an inhibitory effect on HIF-1α-mediated glycolysis in human breast cancer. Our research revealed a new mechanism of HNK as an anti-cancer drug, thus representing a novel strategy to improve the prognosis of cancer.
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