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Depending on the PV power, load power, and battery status, the system may operate in different modes. The control loop may have to switch between operating modes. In practice, it is difficult to implement control loop switching because the transition and dynamic process are difficult to control. As a result, this paper presents a generalized mode control method that avoids loop switching across modes. First, system structure and topology are introduced. The operating conditions for both grid-connected and off-grid modes are then divided into six sub-cases. Furthermore, the control architecture, control loop, and reference transition for various scenarios are described. Finally, an experimental platform is built, and the results are presented to verify the proposed method. [ABSTRACT FROM AUTHOR]

In this study, analysis of the chemical constituents and bioactivities of the unpolar fractions [petroleum ether (PE) and chloroform (C)] of fruits and leaves of Alpinia oxyphylla Miq. were carried out, as well as the bioactivities of the main compounds nootkatone and valencene. From PE and C fractions of the fruits, and PE fraction of the leaves, 95.80%, 59.30%, and 82.11% of the chemical constituents respectively were identified by GC-MS. Among these identified compounds, nootkatone was the main compound in all of three fractions, while valencene was the second main compound in the PE fractions of the fruits and leaves. The bioactivities results showed that all of the fractions and the major compound nootkatone showed tyrosinase inhibitory, as well as inhibitory effect on NO production in LPS-stimulated RAW264.7 cells. While valencene only presented inhibitory activity on NO production in RAW264.7 cells. The critical genes involved in nootkatone biosynthesis in A. oxyphylla were identified from the public transcriptome datasets, and protein sequences were preliminarily analyzed. Our studies develop the usage of the unpolar fractions of A. oxyphylla, especially its leaves as the waste during its production, and meanwhile provide the gene resources for nootkatone biosynthesis. [ABSTRACT FROM AUTHOR]

It is simple to implement conventional current control with a proportional integral (PI) controller. However, system stability and dynamic performance are not perfect, particularly when operating under unfavorable conditions. In this paper, an improved control method is proposed by introducing a compensation unit. The compensation unit can effectively compensate the system's phase around the crossover frequency, greatly enhancing the system's phase margin and stability. It is also capable of handling weak-grid conditions. In this paper, the concept of the proposed compensation unit is explained first. Then, the corresponding mathematical model for the current control loop is built, and system bode diagrams for the conventional and proposed methods are compared. Furthermore, the effect of the parameters for the compensation unit is investigated, and an optimization method is proposed to determine optimal parameters. In addition, to handle weak-grid conditions, the proposed scheme is expanded by including the compensation unit in the grid's feed-forward loop. Finally, an experimental platform is constructed, and the experimental results are presented to validate the proposed method. [ABSTRACT FROM AUTHOR]

In order to achieve efficient utilization of solar energy resources, this study combines the trans-critical organic Rankine cycle (ORC) power cycle (TORC) with the trans-critical CO2 refrigeration cycle (TCO2). Additionally, a comprehensive three-level index decision evaluation system is developed based on system safety and environmental protection, thermodynamics, and techno-economic performance. The evaluation focuses on typical medium- and high-temperature solar energy applications and considers six organic working gases. The evaluation results demonstrate that the R600 + CO2 solution outperformed the others. This solution achieved a maximum net output power (Pnet) of 1531.31 kW and 2306.43 kW, a maximum coefficient of performance (COP) of 3.16, a predicted payback period of 2.651 years and 2.033 years, and a benefit–investment ratio of 4.533 and 5.773. [ABSTRACT FROM AUTHOR]

The use of electric vehicles (EVs) for household uninterruptible power supplies (UPSs), particularly in rural areas, can greatly improve household power reliability. However, because EVs are mobile, the evaluation of backup capacity for EV-UPS systems is completely different when compared to traditional UPSs. As a result, the focus of this paper is on the evaluation and improvement of backup capacity for EV-UPS systems. The architectures for EV-UPS systems are presented first. The methodology for calculating backup capacity for EV-UPS systems is then presented, followed by four detailed cases based on different grid failure times. Furthermore, the impact of system operating parameters on backup capacity, such as different load power, EV mobility pattern parameters, and grid outage durations, is investigated. The results of backup capacity in cases of different operating parameters are detailed using an EV mobility model. An improved strategy for increasing backup capacity is proposed, in which more backup energy can be released during a power outage. Meanwhile, the next trip requirement is unaffected. The backup capacity with the improved strategy is then calculated and compared to the results with the traditional strategy. Finally, a 5 kW EV-UPS experimental platform is constructed, and the experimental results are presented to validate the proposed method. [ABSTRACT FROM AUTHOR]

The commutation torque ripple of a brushless dc motor (BLDCM) in a six-step driving mode generates vibration noise. To minimize the commutation torque ripple of the BLDCM, this article analyzes the cause of torque ripple and establishes the model of torque ripple suppression by using the phase current predictive method based on the trapezoidal back electromotive force (EMF). In addition, based on the prediction model of the non-commutation phase current, the pulsewidth modulation model predictive control (PWM-MPC) algorithm is proposed. By changing the duty cycle with prior evaluation, the predictive control avoids commutation current hopping, thereby reducing torque ripple during commutation. This control approach is more accessible to be implemented, because it does not require changing the topology of the motor driving circuit. Simulation models of the proposed control scheme constructed in the MATLAB/Simulink environment are given, compared with the conventional square-wave driving method. Moreover, experiments are performed to verify the feasibility. The output torque during experiments is transmitted to the computer software through the torque transducer. Compared with the traditional driving methods, the simulation and experimental results show that the proposed novel algorithm in this article could suppress the torque ripple efficiently. [ABSTRACT FROM AUTHOR]

Vascular dementia (VaD) is caused by chronic decreases in brain blood flow and accounts for 15-20% of dementia cases worldwide. In contrast to Alzheimer's disease (AD), no effective drug treatments are currently available for VaD. Previous studies have suggested that oxidative stress and neuroinflammation in the brain play important roles in the pathogenesis of VaD. Honokiol (HKL) is a well-known bioactive and nutraceutical compound that can act as an antioxidant and anti-inflammatory molecule. HKL can protect against memory impairments in AD mouse models. In this study, we explored whether the application of HKL was also protective against the insult of chronic cerebral hypoperfusion (CCH) in rats. We found that HKL supplementation prevented the memory impairments in the inhibitory avoidance step-down and Morris water maze tasks in CCH rats. HKL also suppressed the levels of oxidative stress and inflammation in CCH rats. Moreover, HKL prevented dendritic spines abnormalities in CCH rats. We also found that HKL inhibited the activity of GSK-3β, which may be critical for the neuroprotective activity of HKL. Thus, our study demonstrated the protective role of HKL in VaD. [ABSTRACT FROM AUTHOR]

Introduction: Recently, increasing evidence has shown that long non-coding RNAs (lncRNAs) play critical roles in tumor progression and development. However, the expression pattern and biological function of lncRNA HULC (highly upregulated in liver cancer) in prostate cancer (PCa) remain largely unclear.Material and Methods: The expression of lncRNA HULC in 53 paired PCa tissues and cell lines was detected by quantitative real-time polymerase chain reaction (qRT-PCR). The χ2 test was used to explore the association of lncRNA HULC expression with clinicopathologic features. Kaplan-Meier analysis was used to detect the association between HULC expression and overall survival of PCa patients. Furthermore, the function of HULC in cell growth and metastasis was detected in PCa cells.Results: Our data showed that HULC expression was upregulated in PCa tissues and cell lines compared to adjacent non-tumor tissues and the normal prostate cell line RWPE-1 (p < 0.05). High HULC expression was positively associated with advanced clinicopathologic features and poor overall survival (OS) for PCa patients (p < 0.05). HULC inhibition suppressed PCa cell growth and metastasis both in vitro and in vivo (p < 0.05). Furthermore, HULC knockdown reduced N-cadherin and vimentin expression and increased E-cadherin expression in PCa cells (p < 0.05).Conclusions: Our data suggested that lncRNA HULC might play oncogenic roles in PCa progression, which provided a novel therapeutic strategy for PCa patients. [ABSTRACT FROM AUTHOR]

Purpose: Accumulating evidence indicates that micro (mi)RNAs play a critical role in carcinogenesis and cancer progression; however, their role in the tumorigenesis of gastric adenocarcinoma remains unclear so the present study investigated this in gastric cancer (GC) tissues and cell lines.Methods: Human GC specimens (n = 57) and patient-paired non-cancerous specimens were obtained from patients at the First Affiliated Hospital, Henan University of Science and Technology. The AGS and GC9811 gastric cancer cell lines were also used. Expression levels of miR-216b and HDAC8 were examined by quantitative real-time PCR and the expression of HDAC8 was also examined by Western blotting and immunohistochemistry assay. The cell cycle progression was determined by FACS. MiR-216b inhibitor, mimics, and siRNA-HDAC8 transfections were performed to study the loss and gain of function.Results: We reported a significantly decreased expression of miR-216b in GC clinical specimens compared with paired non-cancerous tissues. We also observed a significant down-regulation of miR-216b expression in GC cell lines AGS and GC9811 (p < 0.0001). The introduction of miR-216b suppressed GC cell proliferation and cell cycle progression by targeting HDAC8, an oncogene shown to promote malignant tumor development with a potential miR-216b binding site in its 3' untranslated region. HDAC8 expression was shown to be significantly increased in AGS and GC9811 cell lines (p < 0.0001) and GC tissues compared with controls. Moreover, HDAC8 inhibition suppressed cell cycle progression compared with control groups (22 % ± 1.6 % vs 34 % ± 2.1), indicating that HDAC8 may function as an oncogene in the development of GC. Furthermore, HDAC8 expression was negatively correlated (p < 0.0001), while miR-216b expression was positively correlated with the clinical outcome of GC patients (p < 0.0001).Discussion: Our data suggest that miR-216b functions as a tumor suppressor in human GC by, at least partially, targeting HDAC8. [ABSTRACT FROM AUTHOR]

The effect of chemotherapy of gastric cancer (GC) remains very poor because of multidrug resistance (MDR). However, the mechanisms underlying MDR of GC remains far from fully understood. The aim of this study is to illustrate the potential mechanisms of the MDR of GC at mainly the long non-coding RNA (lncRNA) level. In this study, GC cell line, SGC7901, and two MDR sublines, SGC7901/VCR and SGC7901/ADR were subjected to an lncRNA microarray analysis. Bioinformatics and verification experiments were performed to investigate the potential lncRNAs involved in the development of MDR. Pathway analysis indicated that 15 pathways corresponded to down-regulated transcripts and that 20 pathways corresponded to up-regulated transcripts (p-value cut-off is 0.05). GO analysis showed that the highest enriched GOs targeted by up-regulated transcripts were “system development” and the highest esenriched GOs targeted by the down-regulated transcripts were “sterol biosynthetic process”. Our study is the first to interrogate differentially expressed lncRNAs in human GC cell line and MDR sublines and indicates that lncRNAs are worthwhile for further study to be the novel candidate biomarkers for the clinical diagnosis of MDR and potential targets for further therapy. [ABSTRACT FROM AUTHOR]

Ferroptosis is a novel form of regulated cell death characterized by accumulated lipid reactive oxygen species (ROS) and inactivation of glutathione peroxidase 4 (GPX4). The present study aimed to investigate the role of microRNA (miRNA/miR)-15a in ferroptosis of prostate cancer cells. Bioinformatics analysis was performed to predict the potential interaction between miR-15a and the 3′-untranslated region (UTR) of GPX4 mRNA. The prostate cancer cell line, LNCAP was transfected with miR-15a mimics or small interfering (si)-GPX4. Reverse transcription-quantitative PCR and western blot analyses were performed to detect the mRNA and protein expression levels of GPX4, respectively. Biotin-RNA pull-down and dual-luciferase reporter assays were performed to verify the interaction between miR-15a and GPX4 mRNA. The Cell Counting Kit-8 assay was performed to assess cell proliferation, while lactate dehydrogenase (LDH) and intracellular ferrous iron levels were detected via ELISA. Lipid ROS and mitochondrial membrane potential (MMP) were assessed via flow cytometry and staining with C11-BIODIPY probes or JC-1. Furthermore, lipid peroxidation was identified by measuring malondialdehyde (MDA) levels. The results demonstrated that transfection with miR-15a mimics decreased GPX4 protein expression. Bioinformatics analysis revealed potential binding sites between miR-15a and the 3′-UTR region of GPX4, and RNA pull-down and the dual-luciferase reporter assays further confirmed the interaction between miR-15a and GPX4 mRNA. Both transfection with miR-15a mimics and si-GPX4 suppressed cell proliferation, elevated LDH release, accumulated intracellular ferrous iron and ROS, disrupted MMP and increased MDA levels. Taken together, the results of the present study suggest miR-15a induces ferroptosis by regulating GPX4 in prostate cancer cells, which provides evidence for investigating the therapeutic strategies of prostate cancer. [ABSTRACT FROM AUTHOR]