17 research outputs found

    Runoff forecasting benefit evaluation for long-term power generation scheduling

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    Long-term runoff forecasting important reference significance for the long-term planning of cascade hydropower stations. The traditional forecast accuracy evaluation is based on the deviation between the predicted runoff and the measured hydrological sequence, but fails to consider the effect on long-term scheduling. In this paper, a runoff forecasting evaluation method for long-term scheduling is presented. First, a monthly distribution method based on the forecast value of annual runoff is proposed to describe the uncertainty of the forecast. Then, a power generation plan model with the maximum generation objective and an actual generation benefit evaluation model are established to study the effect of runoff forecasting in scheduling. At last two indexes of ā€œIncremental generationā€ and ā€œIncremental benefitā€ based on the comparison of actual benefit with and without a forecast plan are given to evaluate the performance of forecasting. The case study shows that the proposed evaluation method can reflect the actual benefit brought by the forecast information, which provide more practical guidance for the hydropower station

    Runoff forecasting benefit evaluation for long-term power generation scheduling

    No full text
    Long-term runoff forecasting important reference significance for the long-term planning of cascade hydropower stations. The traditional forecast accuracy evaluation is based on the deviation between the predicted runoff and the measured hydrological sequence, but fails to consider the effect on long-term scheduling. In this paper, a runoff forecasting evaluation method for long-term scheduling is presented. First, a monthly distribution method based on the forecast value of annual runoff is proposed to describe the uncertainty of the forecast. Then, a power generation plan model with the maximum generation objective and an actual generation benefit evaluation model are established to study the effect of runoff forecasting in scheduling. At last two indexes of ā€œIncremental generationā€ and ā€œIncremental benefitā€ based on the comparison of actual benefit with and without a forecast plan are given to evaluate the performance of forecasting. The case study shows that the proposed evaluation method can reflect the actual benefit brought by the forecast information, which provide more practical guidance for the hydropower station

    Manganese-Mediated Electrochemical Dearomatization of Indoles To Access 2ā€‘Azido Spirocyclic Indolines

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    An efficient and environmentally friendly electrochemical protocol for dearomatization of indoles was developed, delivering a series of azido-containing spirocyclic indolines with good functional group tolerance. This dearomatization process is proposed to result from the oxidation of MnIIā€“N3 species, supported by cyclic voltammetry experiments. Moreover, synthetic transformations can provide an alternative approach to a range of functionalized indolines

    Tetrandrine citrate suppresses lung adenocarcinoma growth via SLC7A11/GPX4-mediated ferroptosis

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    Abstract Ferroptosis is a mode of programmed cell death that plays a crucial role in tumor biology processes. Although tetrandrine citrate (TetC) has been demonstrated to exert anti-tumor effects, it is still unclear whether TetC inhibits lung adenocarcinoma (LUAD) progression by inducing ferroptosis. The study showcased the inhibitory effect of TetC on the viability and progression of tumor cells, including intracellular iron overload, accumulation of reactive oxygen species (ROS), over-expression of malondial-dehyde (MDA), and depletion of glutathione (GSH). Notably, TetC-induced cell death was clearly reversed by three different ferroptosis-related inhibitors. TetC also induced changes in the mitochondrial morphology of LUAD cells, similar to those observed in typical ferroptosis. Further analysis through Western blot (WB) and Immunofluorescence (IF) assays identified that TetC inhibited the expression and fluorescence intensity of both solute carrier family 7 (SLC7A11) and glutathione peroxidase-4 (GPX4). More importantly, over-expression of SLC7A11 could rescue the TetC-induced ferroptosis. Finally, in our vivo experiment, we discovered that TetC significantly slowed the growth rate of subcutaneous transplanted A549 cells, ultimately proving to be biosafe. In conclusion, our study first identified the mechanism by which TetC-induced ferroptosis in LUAD via SLC7A11/GPX4 signaling

    The challenges and opportunities of Ī±vĪ²3-based therapeutics in cancer: From bench to clinical trials

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    Integrins are main cell adhesion receptors serving as linker attaching cells to extracellular matrix (ECM) and bidirectional hubs transmitting biochemical and mechanical signals between cells and their environment. Integrin Ī±vĪ²3 is a critical family member of integrins and interacts with ECM proteins containing RGD tripeptide sequence. Accumulating evidence indicated that the abnormal expression of integrin Ī±vĪ²3 was associated with various tumor progressions, including tumor initiation, sustained tumor growth, distant metastasis, drug resistance development, maintenance of stemness in cancer cells. Therefore, Ī±vĪ²3 has been explored as a therapeutic target in various types of cancers, but there is no Ī±vĪ²3 antagonist approved for human therapy. Targeting-integrin Ī±vĪ²3 therapeutics has been a challenge, but lessons from the past are valuable to the development of innovative targeting approaches. This review systematically summarized the structure, signal transduction, regulatory role in cancer, and drug development history of integrin Ī±vĪ²3, and also provided new insights into Ī±vĪ²3-based therapeutics in cancer from bench to clinical trials, which would contribute to developing effective targeting Ī±vĪ²3 agents for cancer treatment

    Tibial cortex transverse transport promotes ischemic diabetic foot ulcer healing via enhanced angiogenesis and inflammation modulation in a novel rat model

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    Abstract Background Tibial Cortex Transverse Transport (TTT) represents an innovative surgical method for treating lower extremity diabetic foot ulcers (DFUs), yet its underlying mechanisms remain elusive. Establishing an animal model that closely mirrors clinical scenarios is both critical and novel for elucidating the mechanisms of TTT. Methods We established a diabetic rat model with induced hindlimb ischemia to mimic the clinical manifestation of DFUs. TTT was applied using an external fixator for regulated bone movement. Treatment efficacy was evaluated through wound healing assessments, histological analyses, and immunohistochemical techniques to elucidate biological processes. Results The TTT group demonstrated expedited wound healing, improved skin tissue regeneration, and diminished inflammation relative to controls. Marked neovascularization and upregulation of angiogenic factors were observed, with the HIF-1Ī±/SDF-1/CXCR4 pathway and an increase in EPCs being pivotal in these processes. A transition toward anti-inflammatory M2 macrophages indicated TTT's immunomodulatory capacity. Conclusion Our innovative rat model effectively demonstrates the therapeutic potential of TTT in treating DFUs. We identified TTT's roles in promoting angiogenesis and modulating the immune system. This paves the way for further in-depth research and potential clinical applications to improve DFU management strategies

    Determination of the number of Ļˆ(3686)\psi(3686) events at BESIII

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    The numbers of Ļˆ(3686) events accumulated by the BESIII detector for the data taken during 2009 and 2012 are determined to be and , respectively, by counting inclusive hadronic events, where the uncertainties are systematic and the statistical uncertainties are negligible. The number of events for the sample taken in 2009 is consistent with that of the previous measurement. The total number of Ļˆ(3686) events for the two data taking periods is
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