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Gallium nitride (GaN)-based power conversion systems exhibit striking competitivity in realizing compact and high-efficiency power management modules. Recently emerging GaN-based p-channel field-effect transistors (FETs) and monolithic integration techniques enable the implementation of GaN-based complementary logic (CL) circuits and thereby offer an additional pathway to improving the system-level energy efficiency and functionality. In this article, holistic analyses are conducted to evaluate the potential benefits of introducing GaN CL circuits into the integrated power systems, based on the material limit of GaN and state-of-the-art experimental results. It is revealed that the propagation delay of a single-stage CL gate based on the commercial p-GaN gate power HEMT (high-electron-mobility transistor) platform could be as short as sub-nanosecond, which sufficiently satisfies the requirement of power conversion systems with operating frequencies less than 10 MHz. By replacing the currently adopted n-FET-based logic gates (e.g., directly coupled FET logic) with CL gates, the power consumption of peripheral logic circuits could be substantially suppressed by more than 103 times, mainly due to the elimination of the pronounced static power loss. Consequently, the energy efficiency of the entire system could be substantially improved.

Herein, a ternary blend from poly(butylene succinate) (PBS), poly(propylene carbonate) (PPC), and poly(vinyl acetate) (PVAc) with improved crystallization rate, stiffness, and toughness was initially prepared via melt compounded. The influence of PVAc content on morphology, miscibility, thermal behavior, and rheological and mechanical properties was investigated. Scanning electron microscopy observation showed phase morphology of PBS/PPC/PVAc ternary blends evolved from sea-island dispersion to co-continuous structure. Dynamic mechanical analysis revealed that PBS and PPC were immiscible. The presence of PPC inhibited the crystallization of PBS, while simultaneous incorporation of PVAc and PPC promoted the crystallization. Furthermore, the introduction of PPC and PVAc enhanced the rheological properties of PBS. Unexpectedly, prominent improvement in tensile modulus, yield strength, and elongation was obtained for the PBS/PPC/PVAc ternary blend with 10 wt% PVAc due to the morphological evolution from sea-island to co-continuous structure, which was respectively increased by 93%, 52%, and 26% compared with neat PBS.

Natural product bufotenine (5) which could be isolated from Venenum Bufonis, has been widely used as a tool in central nervous system (CNS) studies. We present here its quaternary ammonium salt (6) which was synthesized with high yields using 5-benzyloxyindole as raw materials, and we firstly discover its analgesic effects in vivo. The analgesic evaluation showed that compounds 5 and 6 had stronger effects on the behavior of formalin induced pain in mice. Moreover, the combination of compound 6 and morphine has a synergistic effect. We intended to explain the molecular mechanism of this effect. Therefore, 36 analgesic-related targets (including 15 G protein-coupled receptors, 6 enzymes, 13 ion channels, and 2 others) were systemically evaluated using reverse docking. The results indicate that bufotenine and its derivatives are closely related to acetyl cholinesterase (AChE) or α4β2 nicotinic acetylcholine receptor (nAChR). This study provides practitioners a new insight of analgesic effects.

The threshold voltage ( V TH) of an enhancement-mode Schottky-type p -GaN gate high-electron-mobility transistor (HEMT) is found to have a special dependence on the drain bias. The device commonly requires higher gate voltage to switch on the transistor from a high-drain-voltage off -state than what is expected from the static device characteristics. The reason behind the dynamic V TH has been proved to be the floating p -GaN layer, where charges could be stored and further influence V TH under different drain bias. In this article, a SPICE-compatible equivalent circuit model is presented according to the structure of Schottky-type p -GaN gate HEMTs. It features a floating node to imitate the charge storage process within the gate stack. Compared to conventional models, the proposed model could accurately predict the dynamic V TH characteristics and switching behaviors of power electronics circuits, where Schottky-type p -GaN gate HEMTs are deployed as power transistors. The phenomena related to the dynamic V TH, including the disappearance of Miller plateau, the overestimated false-turn- on problem, and the higher reverse conduction loss are evaluated with a half-bridge circuit and the merits of the proposed model are verified.

Summary The limitation of commercial single-crystal substrates and the lack of continuous strain tunability preclude the ability to take full advantage of strain engineering for further exploring novel properties and exhaustively studying fundamental physics in complex oxides. Here, we report an approach for imposing continuously tunable epitaxial strain in oxide heterostructures beyond substrate limitations by inserting an interface layer through tailoring of its gradual strain relaxation. Taking BiFeO3 as a model system, we demonstrate the introduction of an ultrathin interface layer that allows the creation of desired strain states that can induce phase transition and stabilize a super-tetragonal phase as well as morphotropic phase boundaries, overcoming substrate limitations. Continuously tunable strain from tension to compression can be generated by precisely adjusting the interface layer thickness, enabling the achievement of continuous orthorhombic–rhombohedral-like–tetragonal-like phase transition. This proposed route could be extended to other oxide heterostructures, providing a platform for creating exotic phases and emergent phenomena.

Protoporphyrinogen oxidase (PPO, EC 1.3.3.4) is an effective target for green herbicide discovery. In this work, we reported the unexpected discovery of a novel series of N-phenylaminomethylthioacetylpyrimidine-2,4-diones (2-6) as promising PPO inhibitors based on investigating the reaction intermediates of our initially designed N-phenyluracil thiazolidinone (1). An efficient one-pot procedure that gave 41 target compounds in good to high yields was developed. Systematic Nicotiana tabacum PPO (NtPPO) inhibitory and herbicidal activity evaluations led to identifying some compounds with improved NtPPO inhibition potency than saflufenacil and good post-emergence herbicidal activity at 37.5-150 g of ai/ha. Among these analogues, ethyl 2-((((2-chloro-4-fluoro-5-(3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl)phenyl)amino)methyl)thio)acetate (2c) (Ki = 11 nM), exhibited excellent weed control at 37.5-150 g of ai/ha and was safe for rice at 150 g of ai/ha, indicating that compound 2c has the potential to be developed as a new herbicide for weed management in paddy fields. Additionally, our molecular simulation and metabolism studies showed that the side chains of compound 2c could form a hydrogen-bond-mediated seven-membered ring system; substituting a methyl group at R1 could reinforce the hydrogen bond of the ring system and reduce the metabolic rate of target compounds in planta.

Design and fabrication of high-efficiency electrocatalysts are important to generate hydrogen via urea electrocatalysis with the minimum required energy. In this study, in situ growth of a branch-like Mo-doped Ni3S2 nanoforest on Ni foam was achieved through a facile one-pot hydrothermal process. The as-obtained catalyst exhibited excellent activity and robust durability because of its unique hierarchical nanostructures and doping-optimized electronic structural configuration, and required merely 1.33 V (vs. RHE) and 90 mV (overpotential) to attain a current density of 10 mA cm−2 for the urea oxidation reaction (UOR) and hydrogen evolution reaction (HER), without any noticeable loss in activity even after 120 h of operation. On the basis of the experimental results and theoretical calculations, it was confirmed that the incorporation of Mo in Ni3S2 altered the morphology and electronic structure of the catalyst; hence, more active sites were exposed and the Gibbs adsorption energy of the intermediates in the UOR was optimized. Notably, the overall urea electrolysis cell could afford a low voltage of 1.45 V (vs. RHE) to attain a current density of 10 mA cm−2 and showed excellent durability over 120 h. The findings from this study provide new insights into efficient electrocatalysts for urea electrolyzers, which hold great potential in electrochemical energy conversion and sewage treatment applications.

Due to increasing concentrations in the atmosphere, carbon dioxide has, in recent times, been targeted for utilisation (Carbon Capture Utilisation and Storage, CCUS). In particular, the production of CO from CO2 has been an area of intense interest, particularly since the CO can be utilized in Fischer–Tropsch synthesis. Herein we report that CO2 can also be used as a source of atomic oxygen that is efficiently harvested and used as a waste-free terminal oxidant for the oxidation of alkenes to epoxides. Simultaneously, the process yields CO. Utilization of the atomic oxygen does not only generate a valuable product, but also prevents the recombination of O and CO, thus increasing the yield of CO for possible application in the synthesis of higher-order hydrocarbons., Selective formation of atomic oxygen to form epoxides in a waste free process is reported. Simultaneously generating carbon monoxide from carbon dioxide for further use.

Incorporating metal clusters within the skeleton of the organic polymers through click reaction can not only effectively prepare cluster-polymer composites, but also effectively avoid the cluster aggregation. Herein, an azide-contatining Lanthanide-Titanium oxo cluster of Eu 8 Ti 10 -N 3 ( Eu 8 Ti 10 -N 3 = [Eu 8 Ti 10 ( µ 3 -O) 14 (H 2 O) 4 (OAc) 2 (tbba) 30 (paza) 4 (THF) 2 ]•4THF•8H 2 O ( 1 ), Htbba = 4-tert-butylbenzoic acid, Hpaza = 4-azidobenzoate, HOAc = acetic acid, THF = Tetrahydrofuran) through in situ solvothermal reaction of 4-Azidobenzoic acid and 4-tert-butylbenzoic acid. Reaction of 1 with PEG ( PEG = Methoxypoly(ethyleneglycol)alkyne, 2000 g/mol) through Cu(I)-catalyzed click chemistry generates a lanthanide-polymer composite of Eu 8 Ti 10 -N 3 @PEG ( 2 ). Investigation on IR, 1 H NMR ICP-OES of 2 indicates that the structural integrity of 1 is maintained in 2 . Study on luminescent properties of 1 and 2 reveals that the quantum yield of 1 itself basically keeps unchanged in 2 . Significantly, the formation of 2 can not only effectively prevent the cluster 1 from aggregation, but also greatly enhance its solubility and adhesion to the substrate. Owing to the solubility and adhesion of luminescent materials being the key to their practical application, present work is thus of great significance for the development of metal cluster-polymer composite luminescent materials.

Diabetic nephropathy (DN) is a common microvascular complication of diabetes and the main cause of end-stage nephropathy (ESRD). Inflammation and fibrosis play key roles in the development and progression of diabetic nephropathy. By using in vivo and in vitro DN models, our laboratory has identified the protective role of carnosine (CAR) on renal tubules. Our results showed that carnosine restored the onset and clinical symptoms as well as renal tubular injury in DN. Furthermore, carnosine decreased kidney inflammation and fibrosis in DN mice. These results were consistent with high glucose (HG)-treated mice tubular epithelial cells (MTECs). Using web-prediction algorithms, cellular thermal shift assay (CETSA) and molecular docking, we identified glycine N-methyltransferase (GNMT) as a carnosine target. Importantly, we found that GNMT, a multiple functional protein that regulates the cellular pool of methyl groups by controlling the ratio of S-adenosylmethionine (SAM) to S-adenosylhomocysteine (SAH), was down-regulated significantly in the serum of Type 1 DM patients and renal tissues of DN mice. Moreover, using cultured TECs, we confirmed that the increased GNMT expression by transient transfection mimicked the protective role of carnosine in reducing inflammation and fibrosis. Conversely, the inhibition of GNMT expression abolished the protective effects of carnosine. In conclusion, carnosine might serve as a promising therapeutic agent for DN and GNMT might be a potential therapeutic target for DN.

Extracting uranium from seawater with a chemically stable adsorbent is one of the most promising strategies for challenges originating from sustainable nuclear energy industries. Covalent organic f...

Protoporphyrinogen oxidase (PPO, EC 1.3.3.4) is an important target for green agrochemical discovery. Herein, a novel N-phenylisoxazoline-thiadiazolo[3,4-a]pyridazine herbicidal active scaffold was designed by the scaffold hybridization strategy. Systematic structural optimization enabled the discovery of a series of derivatives with excellent weed control at 9.375-150 g ai/ha by the post-emergent application. Some derivatives exhibited improved Nicotiana tabacum PPO (NtPPO)-inhibitory activity than fluthiacet-methyl. Of these, 2b, with Ki = 21.8 nM, displayed higher weed control than fluthiacet-methyl at the rate of 12-75 g ai/ha, and selective to maize at 75 g ai/ha. In planta, 2b was converted into a bioactive metabolite 5 (Ki = 4.6 nM), which exhibited 4.6-fold more potency than 2b in inhibiting the activity of NtPPO. Molecular dynamics simulation explained that 5 formed stronger π-π interaction with Phe392 than that of 2b. This work not only provides a promising lead compound for weed control in maize fields but is also helpful to understand the molecular mechanism and basis of the designed hybrids.

Herein, lignin derived hierarchical porous carbon (LHPC) supported Pd nanoparticles (Pd/LHPC) were synthesized and developed as advanced electrocatalysts for ethanol oxidation. In the Pd/LHPC, the special hierarchical porous carbon with the interconnected micropores and mesopores uniformly distribute on the surface and walls of macropores can provide facile transport for electroactive species and more reaction available surface. The Pd/LHPC exhibits larger specific electrochemically active surface area, higher electrocatalytic activity and better stability toward the oxidation of ethanol than the black carbon (Vulcan XC-72) supported Pd (Pd/XC-72) and commercial Pd/C electrocatalysts. The strategy reported will open a new road to effectively use industrial waste to synthesize advanced carbon material for efficient electrocatalysts and other electrochemical energy-conversion devices.

Flavonoids possess diverse bioactivity and potential medicinal values. Glycosylation of flavonoids, coupling flavonoid aglycones and glycosyl groups in conjugated form, can change the biological activity of flavonoids, increase water solubility, reduce toxic and side effects, and improve specific targeting. Therefore, it is desirable to synthesize various flavonoid glycosides for further investigation on their medicinal values. Compared with chemical glycosylations, biotransformations catalyzed by uridine diphospho-glycosyltransferases provide an environmentally friendly way to construct glycosidic bonds without repetitive chemical synthetic steps of protection, activation, coupling, and deprotection. In this review, we will summarize the existing knowledge on the biotechnological glycosylation reactions either in vitro or in vivo for the synthesis of flavonoid O- and C-glycosides and other rare analogs.Key points• Flavonoid glycosides usually show improved properties compared with their flavonoid aglycones.• Chemical glycosylation requires repetitive synthetic steps and purifications.• Biotechnological glycosylation reactions either in vitro or in vivo were discussed.• Provides representative synthetic examples in detail.

Kaempferol (kaem) is a dietary flavonoid found in a variety of fruits and vegetables. The inhibitory effects of kaem on primary tumour growth have been extensively investigated; however, its effects on tumour metastasis are largely unknown. In the present study, we found that kaem significantly suppresses both primary tumour growth and lung metastasis in mouse breast tumour model. Furthermore, decreased expression of citrullinated histone H3 (H3‐cit), a biomarker of neutrophil extracellular traps (NETs), had been founded in metastatic lung upon treated with kaem. The reduction of H3‐cit is not, however, due to the cytotoxicity of kaem on neutrophils since the frequency of CD11b+Ly6G+ neutrophils did not change in lung, tumour or blood in the presence of kaem. We then confirm the anti‐NETs effects of kaem in vitro by co‐culturing mouse neutrophils and kaem. Supplementing the neutrophils with GSK484, a potent NET inhibitor, totally abrogated the inhibitory effects of kaem on tumour metastasis while having little or no impact on primary tumour growth, indicating the specificity of kaem acting on NET formation and tumour metastasis. We also found that kaem suppressed ROS production in mouse bone‐marrow derived neutrophils. Supplementing with the ROS scavenger DPI abrogated kaem's effects on NET formation, suggesting the involvement of kaempferol in NADPH/ROS‐NETs signalling. Finally, we applied the kaem on NET‐deficient PAD4‐/‐ mice and found decreased primary tumour volume and weight but similar lung metastatic tumour with kaempferol treatment. Therefore, our findings reveal a novel mechanism of kaem in breast cancer development by targeting NETs induced tumour metastasis.

Development of multifunctional theranostics is of great significance for cancer management. Herein, we develop polyethylene glycol (PEG) modified cobalt carbide nanoparticles (Co2C-PEG NPs) as cancer photothermal theranostic agents for multimodal imaging and photothermal therapy (PTT). Co2C NPs are synthesized by a high-temperature thermal decomposition method. Afterwards, the morphology, photothermal effect, multimodal imaging capacities, biocompatibility, and PTT efficacy of Co2C-PEG NPs are carefully investigated. The as-prepared Co2C-PEG NPs exhibit high photothermal conversion efficiency (PCE, η = 35.7%) and good photostability. Through photoacoustic (PA), magnetic resonance (MR), and photothermal (PT) tri-modal imaging, in vivo pharmacokinetics and tumor temperature elevation could be monitored during the PTT process. Meanwhile, the Co2C-PEG NPs also show good PTT efficacy both in vitro and in vivo. Our findings suggest that Co2C-PEG NPs are effective for cancer photothermal theranostics.

A simple and mild protocol for copper-catalyzed bromination of quinoline at the C5 site of quinoline by anodic oxidation was developed, affording the desired remote C–H activation products with iso...

Tryptophan regulates and participates in various physiological systems in the human body, and its excessive intake has harmful effects. Therefore, detecting and monitoring tryptophan in water and distinguishing it from other amino acids are necessary. In addition to their excellent luminescence, coordination polymer-based sensors have good stability and high sensitivity and selectivity for sensing applications. In this work, two luminescent coordination polymers (CPs), [Zn(ttb)Cl]n (1) and [Zn2(ttb)2(OH)(NO3)]n (2), were obtained through the solvothermal reaction of different Zn(II) salts with a rarely studied multidentate N-donor ligand, 1-(tetrazo-5-yl)-3-(triazo-1-yl) benzene (Httb). Crystallographic investigations revealed that the structure of 1 exhibits a 2D fes net with Cl- anions acting as terminal charge balancers, and that of 2 features a 3D ant net with NO3- anions in a rare monodentate bridging (μ2-O-η1:η1) mode. In terms of stability tests, 2 has better thermal and water stability than 1. Although both show good fluorescence performance, specific tryptophan detection, and excellent anti-interference ability, 2 has higher KSV (111 852.6 M-1), a lower limit of detection (LOD = 23.6 nM), and a better recovery rate than 1. Cytotoxicity experiments proved that 2 has extremely low toxicity and thus has great potential for in vivo detection. Therefore, CP 2 is a suitable candidate for advanced practical applications for the efficient sensing of tryptophan in water. The luminescence of the ligands was also calculated using DFT theory and further discussed through experiments. The quenching mechanism that occurs after tryptophan addition was explored through Hirshfeld surface analysis.

Carnation (Dianthus caryophyllus L.) is one of the most important and typical ethylene sensitive cut flowers worldwide, although how ethylene influences the petal senescence process in carnation remains largely unknown. Here, we screened out one of the key transcription factors, DcWRKY75, using a constructed ethylene induced petal senescence transcriptome in carnation and found that it shows quick induction by ethylene treatment. Silencing of DcWRKY75 delays ethylene induced petal senescence in carnation. Molecular evidence confirms that DcWRKY75 can bind to the promoter regions of two main ethylene biosynthetic genes (DcACS1 and DcACO1) and a couple of senescence associated genes (DcSAG12 and DcSAG29) to activate their expression. Furthermore, we show that DcWRKY75 is a direct target gene of DcEIL3-1, which is a homolog of the ethylene signaling core transcription factor EIN3 in Arabidopsis. DcEIL3-1 can physically interact with DcWRKY75 and silencing of DcEIL3-1 also delays ethylene induced petal senescence in carnation and inhibits the ethylene induced expression of DcWRKY75 and its target genes. The present study demonstrates that the transcriptional regulation network is vitally important for ethylene induced petal senescence process in carnation and potentially in other ethylene sensitive cut flowers.

The specificity of CRISPR/Cas9 genome editing is largely determined by the sequences of guide RNA (gRNA) and the targeted DNA, yet the sequence-dependent rules underlying off-target effects are not fully understood. Here we systematically investigated the sequence determinants governing CRISPR/Cas9 specificity by measuring the off-on ratios of 1,902 gRNAs on 13,314 target sequences using an improved synthetic system with dual-target design. Our study revealed a comprehensive set of rules including 3 factors in CRISPR/Cas9 off-targeting: 1) the nucleotide context and position of a single mismatch; 2) an “epistasis-like” combinatorial effect of multiple mismatches; and 3) a guide-intrinsic mismatch tolerance (GMT) independent of the mismatch context. Notably, the combinatorial effect and GMT are associated with the free-energy landscape in R-loop formation and are explainable by a multi-state kinetic model. Based on these rules, we developed a model-based off-target prediction tool (MOFF), which showed superior performance compared to the existing methods.

Near-infrared (NIR) phosphorescent iridium(III) complexes have been demonstrated to possess photophysical properties superior to those of traditional NIR dyes. However, the NIR emission wavelength is restricted in the range of 700–800 nm. For realizing deeper NIR emission, a novel type of iridium(III) complex was designed and synthesized in this work. The main ligand of the iridium(III) complex was constructed using a donor-acceptor structure containing benzothiophene as the donor and quinoxaline as the acceptor. The β-diketone derivative was chosen as the auxiliary ligand owing to its symmetrical structure and p-donating character. The complex exhibits deep NIR-I phosphorescence (764 nm in CH2Cl2, 811 nm in aqueous solution) and broad full width at half maximum (108 nm in CH2Cl2, 154 nm in aqueous solution). Theoretical calculations based on the density function and time-dependent density function were carried out to support the experimental data. Moreover, in vitro biological performance of the complex was determined as well. This work supports the possibility that via a systematic transformation between the D and A units, the photophysical performance of NIR emissive iridium(III) complexes can be greatly improved.

The present paper aimed to investigate the roles of quinones contained in wastewater and the enhanced effects on microbial fuel cells (MFCs) under different redox conditions. The feasibility of using wastewater rich in quinones to act as co-substrate and redox mediators (RMs) library to strengthen the synergistic removal of azo dye in MFCs was evaluated. The results demonstrated that quinones achieved enhanced effects on electricity generation and COD removal of MFC better at higher current intensity. The addition of pure quinone decreased electron transfer resistance (Rct) of MFCs from 4.76 Ω to 2.13 Ω under 1000 Ω resistance and 1.16 Ω–0.75 Ω under 50 Ω resistance. Meanwhile, higher coulombic efficiency was achieved. Compared with sodium acetate, using quinone-rich traditional Chinese medicine (TCM) wastewater as the co-substrate enhanced the synergistic removal of reactive red 2 (RR2) in MFCs from 79.58% to 92.45% during 24 h. RR2 was also degraded more thoroughly due to the accelerated electron transfer process mediated by RMs. Microbial community analysis demonstrated that the presence of quinone in TCM wastewater can enrich different exoelectrogens under varied redox conditions and thus influenced the enhanced effects on MFC. Metagenomic functional prediction results further indicated that the abundance of functional genes involved in carbohydrate metabolism, membrane transport metabolism, biofilm formation, and stress tolerance increased significantly in presence of RMs. Redundancy analyses revealed that RMs addition was the more important factor driving the variation of the microorganism community. This study revealed the potential effect of quinones as redox mediators on the bioelectrochemical system for pollutants removal.

The ability of mammalian taste cells to respond to fatty acids (FAs) has garnered significant attention of late and has been proposed to represent a sixth primary taste. With few exceptions, studies on FA taste have centered exclusively on polyunsaturated FAs, most notably on linoleic acid. In the current study, we have identified an additional FA receptor, GPR84, in the gustatory system that responds to the medium chains saturated FAs (MCFAs) in male mice. GPR84 ligands activate both Type II and Type III taste cells in calcium imaging and patch clamp recording assays. MCFAs depolarize and lead to a rise in intracellular free [Ca2+] in mouse taste cells in a concentration-dependent fashion and the relative ligand specificity in taste cells is consistent with the response profile of GPR84 expressed in a heterologous system. A systemic Gpr84-/- mouse model reveals a specific deficit in both the neural (via chorda tympani recording) and behavioral responses to administration of oral MCFAs compared to wild type mice. Together, we show that the peripheral taste system can respond to an additional class of FAs, the saturated FAs, and that the cognate receptor necessary for this ability is GPR84. Significance Statement Recognition of fatty acids by taste receptor cells in the oral cavity has been suggested to underlie the taste cue for dietary fat. In vitro and in vivo studies in both animal models and humans supports the notion fat may represent an additional taste primer. However, virtually all these studies have focused on the ability of polyunsaturated fatty acids, like linoleic acid, to activate taste pathways. We have identified GPR84 in the taste system that underlies the ability of mice to recognize and respond to medium chain saturated fatty acids. The ability to sense the taste of saturated fats may be important for controlling the intake of this class of fats whose intake is a greater concern for human health.

Purpose Long-chain noncoding RNAs (lncRNAs) are involved in regulating the sensitivity of cancer cells to chemotherapeutic drugs, but the specific mechanism of action is not well understood. The aim of this study was to investigate the effect of lncRNA growth-stasis specific transcript 5 (GAS5) on triple-negative breast cancer (TNBC). Methods Quantitative real-time polymerase chain reaction and flow cytometry were used to screen lncRNA associated with tumor resistance. Double luciferase reporter gene assay, flow cytometry, and Western blot assay were used to determine whether miRNA 378a-5p and SUFU were involved in tumor cell apoptosis induced by lncRNA GAS5. A mouse model of subcutaneous xenografts was established to investigate the relationship between lncRNA GAS5 and tumor resistance in vivo. Results In this study, the expression of lncRNA GAS5 was significantly downregulated in cells treated with paclitaxel (PTX) or cisplatin (CIS). Furthermore, TNBC cells with low expression of lncRNA GAS5 had a lower percentage of apoptosis under stress conditions, especially in serum-free medium. More interestingly, the expression level of lncRNA GAS5 in TNBC patients was associated with tumor resistance to PTX and CIS. In addition, RNA immunoprecipitation experiments confirmed that lncRNA GAS5 and miR-378 could directly bind to each other. Moreover, the miR-378a-5p target of SUFU could promote lncRNA GAS5-induced apoptosis of TNBC cells. Finally, lncRNA GAS5 overexpressed MDA-231R could enhance the sensitivity of TNBC to PTX. Conclusion The above results confirmed that lncRNA GAS5 could induce apoptosis in TNBC cells by targeting miR-378a-5p/SUFU signaling.

A fundamental understanding of the electrochemical reactions and the associated transport processes in electrodes of solid oxide fuel cells (SOFCs) is critical to the development of new electrode materials. To date, however, our understanding of the electrode processes is still very limited due to the lack of well-designed experiments and carefully-validated predictive models. To facilitate studies in this area, we have developed a numerical model that has taken into consideration of the coupling between the transport of mobile charged species (e.g., ions and electrons) in conducting phases and the electrochemical reactions at the three phase boundaries of an SOFC anode. The validity of this model has been confirmed by the electrochemical performance of test cells with a patterned anode consisting of well-defined electronic and ionic conducting phases. The model is then applied to quantifying the factors that critically influence the performance of a patterned anode, resulting in three key dimensionless parameters governing the coupling of transport and reactions in the anode: the ratio of electronic-to-ionic conductivity (σel/σion), the dimensionless exchange current density (iex/i0), and the dimensionless electric potential (Fϕ0/RT). In particular, it is found that only iex/i0 and Fϕ0/RT play a significant role under typical SOFC operating conditions: anode performance increases with the increase in iex/i0 and Fϕ0/RT. Accordingly, we have constructed a phase map to demonstrate the combined effect of iex/i0 and Fϕ0/RT, which is helpful for rational design and operation of SOFC patterned electrodes of different materials and geometries. More importantly, our present model is also applicable to the study of actual porous SOFC electrodes with known 3D microstructures.

Coal fly ash (CFA) catalyzed Fenton-like process was studied under microwave (MW) irradiation for the decolorization of Rhodamine B (RhB) wastewater. The physical-chemical properties of CFA were characterized, including the specific surface area, micromorphology, chemical and crystal components, and the distribution and chemical valence of metallic elements. The metallic oxidants in the CFA indicate CFA can work as Fenton-like catalyst and MW-absorbent simultaneously. The results reveal OH is more significant in the decolorization of RhB than HO2 and O2 −. The generation of more OH in the MW-Fenton-like process (293–326 K) than that in the conventional heated Fenton-like process (326 K) reflects the function of hot spot effect and possible non-thermal effect of MW. Under the optimum condition ([H2O2] 2 mmol L−1, [CFA] 15 g L−1, pH 3, PMW 0.1 kW), the decolorization rate reaches 91.6% after 20 min. The intrinsic kinetic model of RhB decolorization is - d C R h B dt = 1.76 × 10 - 4 · C R h B · C H 2 O 2 1.89 · C C F A 1.97 - d C R h o d a m i n e B / d t = 1.76 × 10 - 4 · C R h o d a m i n e B · C H 2 O 2 1.89 · C c o a l f l y a s h 1.97 . The loss of catalytic metallic elements causes the decline of catalytic capacity of CFA. The energy consumption (4313.3 kW·h kg−1 RhB) is a limitation for the MW-Fenton-like process, which can be overcame by the safe application of nuclear energy. The intermediates and the path of RhB decolorization were detected and proposed, respectively.

The unsaturated modified linoleate based on linoleic acid (LA) was synthesized by a three-step reaction. The linoleic acid was first reacted with glycidyl methacrylate (GMA), then the resulting pro...

The detection of fluoride ion (F−) in living subjects is of value for healthcare and environmental fields. Here, a near-infrared (NIR) turn-on photoacoustic (PA) probe composed of naphthalimide unit, namely LET-1, was developed for chemoselective photoacoustic detection (PAD) of F−. The response and mechanism of the interaction between F− and LET-1 were evaluated through kinetic optical studies, 1HNMR spectra analysis and docking calculations. The results demonstrated that LET-1 could rapidly recognize F− with good selectivity and high sensitivity. Upon the interaction with F−, this non-photoacoustic LET-1 probe could produce a turn-on PA signal at 680 nm, which was used as an indicator for PAD of F− in living subjects, such as soybean sprout and mouse. The present study provides a new approach for in vivo chemoselective PA detection of anions.

Background Autologous cultivated oral mucosal epithelial transplantation (COMET) is an important treatment for limbal stem cell deficiency. However, peripheral corneal neovascularization after surgery hinders its application. This study aims to employ a culture system using allogenic limbal niche cells (LNCs) instead of mouse-derived 3T3 cells as a feeder layer that could relieve postoperative neovascularization. Methods Rat oral mucosal epithelial cells (OMECs) were co-cultured with rat LNCs or 3T3 cells. Cultivated oral mucosal epithelial cells (COMECs) of different culture systems were identified by hematoxylin and eosin staining and immunocytochemistry. The expression levels of the angiogenesis-related factors were analyzed by RT-qPCR and western blotting/ELISA. Angiogenic potential was reconfirmed by cell viability and tube formation assays with human umbilical vein endothelial cells (HUVECs). Results COMECs were obtained from both culture systems successfully. Immunocytochemistry showed approximately equal percentages of positive staining cells for p63α (p = 0.9177), ABCG2 (p = 0.526), Ki67 (p = 0.0987), and CK3 (p = 0.4000) in COMECs of different groups. RT-qPCR and western blotting/ELISA showed that COMECs of the LNC group expressed a significantly lower amount of basic fibroblast growth factor (bFGF) (p = 0.0038 for RT-qPCR, p = 0.0026 for western blotting) but more pigment epithelium-derived factor (PEDF) (p = 0.0172 for RT-qPCR, p = 0.0253 for western blotting) and soluble fms-like tyrosine kinase-1 (sFlt-1) (p

Carbon nanotubes (CNTs) and poly(3,4-ethylenedioxythiophene):poly (styrene sulfonate) (PEDOT:PSS) were employed to prepare sandwich-structured CNT/PEDOT:PSS/CNT transparent conductive films (TCFs) on flexible polyethylene terephthalate (PET) substrate by a spraying method. Based on the film morphology, we suggest that the CNTs were embedded in PEDOT:PSS. The structured film was more stable and did not peel off during post-processing nitric acid treatment. Ethylene glycol (EG) was used to improve the conductivity of the film, and the best ratio of PEDOT:PSS to EG was 10:5. XPS and Raman spectroscopy studies revealed that the non-conductive sodium dodecylbenzene sulfonate and PSS were removed during the nitric acid treatment. TCF sheet resistance as low as 95.15 Ω/sq at 87.72% transmittance (at a wavelength of 550 nm) was obtained. When the CNT/PEDOT:PSS/CNT-TCF was used as an anode in an organic light emitting diode, the high luminance of the device was 1598 cd/cm2 at 14 V, and the maximum current efficiency was 1.5 cd/A at 13 V.

Highly branched metallic nanostructures, which possess a large amount of catalyst active sites and surface-enhanced Raman scattering (SERS) hot spots owing to their large surface areas, multi-level branches, corners, and edges, have shown potential in various applications including catalysis and SERS. In this study, well-defined dendritic silver (Ag) nanostructures were prepared by a facile and controllable electrochemical deposition strategy. The morphology of Ag nanostructures is controlled by regulating electrodeposition time and concentration of AgNO3 in the electrolyte solution. Compared to conventional Ag nanoparticle films, dendritic Ag nanostructures exhibited larger SERS enhancement ascribed to the numerous hot spots exist in the nanogaps of parallel and vertically stacked multilayer Ag dendrites. In addition, the prepared dendritic Ag nanostructures show 3.2-fold higher catalytic activity towards the reduction of 4-nitrophenol (4-NP) by NaBH4 than the Ag nanoparticle films. The results indicate that the dendritic Ag nanostructures represent a unique bifunctional nanostructure that serves as both efficient catalysts and excellent SERS substrates, which may be further employed as a nanoreactor for in situ investigation and real-time monitoring of catalytic reactions by SERS technique.

Two new coordination compounds {[Cu(L1)]·(ClO4)·2H2O} (1) and [Cu2(L2)2]·(ClO4)2 (2) were synthesized with novel tripodal ligands N1-(2-Amino-ethyl)-N1-(1H-imidazol-2-ylmethyl)-ethane-1,2-diamine (HL1) and N1-(2-Amino-ethyl)-N1-(2H-pyrazol-3-ylmethyl)-ethane-1,2-diamine (HL2), respectively. Interestingly, coordination compound 1 exhibits one-dimensional (1D) zig-zag chain structure, coordination compound 2 displays dinuclear structure. The results showed that nitrogen-position of the ligands have distinct impact on the frameworks of the coordination compounds. In addition, the magnetic studies indicated that 1 and 2 exhibit antiferromagnetic interactions between the Cu(II) atoms.

Next generation sequencing (NGS) technologies play a powerful role in the preparation of large DNA databases such as DNA barcoding since it can produce a large number of sequence reads. Here we demonstrate a primer-induced sample labeling method aiming at sequencing a large number of samples simultaneously on NGS platforms. The strategy is to label samples with a unique oligo attached to the 5′-ends of primers. As a case study, 894 unique pentanucleotide oligoes were attached to the 5′-ends of three pairs of primers (for amplifying ITS, matK and rbcL) to label 894 samples. All PCR products of three barcodes of 894 samples were mixed together and sequenced on a high throughput sequencing platform. The results showed that 87.02%, 89.15% and 95.53% of the samples were successfully sequenced for rbcL, matK and ITS, respectively. The mean ratio of label mismatches for the three barcodes was 5.68%, and a sequencing depth of 30 ×to 40× was enough to obtain reliable sequences. It is flexible to label any number of samples simply by adjusting the length of oligoes. This easy, reliable and cost efficient method is useful in sequencing a large number of samples for construction of reference libraries for DNA barcoding, population biology and community phylogenetics.

A phase-field model for growth of iron whiskers that includes convection around a particle was investigated during the process of fluidized pre-reduction. In the simulations, the phase-field method was coupled with flow field and reduction of iron oxide particles. The results showed that the reduction rate at local place had significant effects on the iron ions diffusion and the iron whiskers were more easily grown on the area containing low mole fraction of oxygen. The growth of iron whiskers in the model was investigated in two important simple situations: a velocity change flow and a CO concentration change flow. Because of high reduction rate and low surface energy, iron whiskers were more easily grown on the windward surface and the length of iron whiskers increased with gas velocity increasing. However, both the length and numbers of iron whiskers increased with CO concentration increasing due to the more nucleation site of iron whiskers created by CO adsorbed. When the gas velocity is higher than 0.3 m/s or CO mole fraction is high than 0.6, the nucleation incubation time would be rapidly decreased, which could give suggestions to control the operational parameters in the fluidized pre-reduction process.

This paper describes the investigation of the correlation between molecular structures and gelation behaviors. First, three types of cholesterol-based compounds as potential gelators were synthesized and their gelation behaviors in various organic solvents were investigated. We found that only molecules with two cholesteryl moieties and a carboxylic group could form organogels in cyclohexane, toluene, o-xylene, m-xylene and p-xylene. The organogels were thoroughly investigated using the vial inversion method, transmission electron microscopy (TEM), atomic force microscopy (AFM), Fourier transform infrared (FT-IR) spectroscopy and X-ray diffraction (XRD). The gel-to-sol transition temperature indicated that the organogels exhibited outstanding thermal stabilities. The TEM and AFM measurements showed that the supramolecular structures of the organogels were composed of fibrous aggregates. On the basis of FT-IR characterization and XRD analysis, a probable molecular packing model of gelators in aggregates has been proposed. The present investigation suggested that the carboxylic group and the number of cholesteryl moieties have an important influence on the gelation behavior. Also, it possibly provided some insights into the design of new types of gelators.

Five transition metals (Ni, Ru, Rh, Ag, and Au) were investigated here using DFT calculations for their catalytic activities in the CsbndO bond coupling to form CH3COOH (CH3CO∗ + OH∗ → CH3COOH∗ + ∗) and the CsbndC bond cleavage (CHCO∗ + ∗ → CH∗ + CO∗) that are key competing reactions towards compete ethanol oxidation reaction (EOR). These results were also compared with the previous studies of Ir, Pt, Pd, and Cu. The DFT results show that Ni, Ru, and Ir exhibit the most desired activities toward the complete EOR and Pt, Au, Ag, and Cu show the activities towards the CsbndO coupling reaction. In addition to the geometric effects of the adsorbed reactants, the intrinsic properties were considered and correlated to the distinct performances of these catalysts for a better understanding of the results. The current theoretical investigations provide a systematic assessment and fundamental guidance for the screening of potential catalysts towards complete EOR in future experimental studies.

Phloretin, a dihydrochalcone structural flavonoid compound, possesses antioxidant activity. In this study, we conducted studies to explore the function of phloretin on high palmitic acid-induced oxidative stress in human umbilical vein endothelial cells and investigated the potential mechanism using ribonucleic acid sequencing (RNA-Seq). Our findings reveal that phloretin significantly decreased the levels of intracellular reactive oxygen species (ROS) and malondialdehyde (MDA), increased superoxide dismutase (SOD) and glutathione peroxidase-1 (Gpx-1) activity, and restored the loss of mitochondrial membrane potential (MMP). Next, whole transcriptome analysis was performed using RNA-Seq The results indicated more than 3000 differentially expressed genes (DEGs). Gene Ontology analysis revealed that the DEGs were categorized functionally, mainly by the biological processes, cell metabolism, and cellular response to chemical stimulus. The Kyoto Encyclopedia of Genes and Genomes indicated that they were mainly enriched in cAMP, apoptosis, and cytoskeletal regulation signaling pathways. Furthermore, on the basis of the results of RNA-Seq and Western blotting, our study verified that phloretin upregulated the expression of p-Nrf2 and HO-1 by promoting the phosphorylation of AMPK at Thr

Chromophoric dissolved organic matter (CDOM) in rivers is mainly affected by natural conditions and human activities and can reflect the watershed pollution status to a certain extent. The Yellow River is one of the largest contributors to the global riverine sediment flux from the land to ocean, and there is a paucity of information on how the optical properties of CDOM have the potential to serve as an indicator of water quality for the sediment-laden Yellow River. In this study, a three-dimensional fluorescence parallel factor (PARAFAC) analysis method was applied to investigate the seasonal and spatial variations in CDOM fluorescence components and spectral characteristics from the source region to the estuary in the mainstream of Yellow River. The relationships of CDOM with water quality indicators and trophic state were also analyzed. Six PARAFAC components (C1–C6) were identified and grouped into two categories: humic-like components (C1–C4), which accounted for 85.8 %, and protein-like components (C5 and C6), which accounted for only 14.2 %. The CDOM components, spectral parameters, and their clear correlations with the main ions (Na+ and Cl−) all indicated that the humic-like components may be primarily derived from nonpoint source erosion, and the protein-like components were mainly derived from point source discharges in the watershed. The combination of the CDOM absorption coefficient at 254 nm (a(254)), spectral slope ratio (SR), specific UV absorbance SUVA254, and fluorescence index (FI) had a good predictive ability for the key water quality indicators (total nitrogen (TN), dissolved total nitrogen (DTN), total phosphorus (TP), dissolved total phosphorus (DTP), and chlorophyll a (Chl a)) and trophic state index (TSI). Therefore, some fluorophores and UV spectral parameters of CDOM in the Yellow River can be used for rapid water quality monitoring and pollution source indication, especially pollutants related to nitrogen and phosphorus nutrients in the basin.

Background: The increased risk of cardiovascular disease (CVD) in postmenopausal women and ovariectomized patients suggests that estrogen has a protective effect on cardiac function. Oxidative stress is the main cause of CVD, and the cellular defensive Nrf2 antioxidant pathway plays a protective role in various pathologies. However, the regulation of Nrf2 by estrogen has received little attention. Objective: The present study aimed to investigate the role of Nrf2 in the effect of estrogen on cardiac function. Methods: In the present study, female SD rats were divided into three groups as follows: sham operation (SHAM), bilateral ovariectomy (OVX) and bilateral ovariectomy with estradiol valerate (EV) supplementation (OVX+EV). Vaginal smears and E2 concentrations were used to confirm the success of the model. We compared cardiac morphology and function by echocardiography and HE staining. The levels of oxidative stress markers and antioxidant enzymes as well as protein expression of antioxidant genes were evaluated by Western blotting and immunohistochemistry. Results: Our results showed that supplementation with estrogen restored the parameters to some extent. Left ventricular end diastolic diameter at diastolic (LVID;d) and left ventricular volume at diastolic (LV vol;d) increased but MV E wave/A wave (E/A) significantly decreased. The oxidative stress indicators (malondialdehyde) increased, and the antioxidant activity indicators, such as superoxide dismutase (SOD) and catalase (CAT), decreased. Further, the expression of most Nrf2 antioxidant pathway-related proteins in the heart decreased after ovariectomy. Conclusion: The present study demonstrated that estrogen may protect cardiac function by regulating antioxidant capacity through the Nrf2 pathway.

Three series of copper hydride clusters [Cu8H6L6]2+ (1), [Cu4HX2L4]+ where X− = Cl− (2a), Br− (2b), I− (2c), N3− (2d) and SCN− (2e), and [Cu4HX3L3] where X− = Br− (3b) and I− (3c) (L = 2-(diphenylphosphino)pyridine, dppy) were synthesized and characterized by single-crystal X-Ray crystallography and standard spectroscopic techniques. The metal core of 1, Cu8, can be described as a bicapped octahedron, while those of 2 and 3 series adopt tetrahedral structures. The hydride positions were deduced from difference electron density maps and corroborated by NMR and DFT calculations. For 1, there are two μ4-H−, one each in the two tetrahedral cavities of the two capping atoms and four μ3-H− on the six triangular faces around the waist of the octahedron. For [Cu4HX2L4]+ and [Cu4HX3L3] series, the single μ4-H− resides in the center of the Cu4 tetrahedron. It was found that these three series of copper clusters are intimately connected and can convert from one to another under specific reaction conditions. Their transformation pathways were investigated in detail. Spontaneous resolution to form optically pure enantiomeric single crystals was observed for [Cu4H(SCN)2L4]+ (2e) and [Cu4HBr3L3] (3b). Photoluminescence was observed for [Cu4HX2L4]+, as well as [Cu4HX3L3] with strong emissions from green to yellow regions.

Strategies to direct the differentiation of endogenous bone marrow derived mesenchymal stem cells (BMSCs) in vivo following recruitment to the injured site are critical to realizing the potential of stem cell-based therapies. But the differentiation efficiency of BMSCs remains limited without direction. Here we demonstrated a novel strategy to promote neuronal differentiation of BMSCs using cross-linked polyethylenimine (PEI) grafted graphene oxide (GO) as the enzyme responsive vector for delivering active genes to BMSCs. In vivo, a core–shell microfiber arrayed hydrogel with a chemokine (SDF-1α) and the cross-linked GO-PEI/pDNAs-bFGF microparticles incorporated into the shell and core, respectively, were constructed. The arrayed hydrogel was shown to recruit and stimulate the neural-like differentiation of BMSCs effectively by delivering the CXCL12 and GO-PEI/pDNAs-bFGF in a self-controlled manner. With this strategy, both in vitro and in vivo neuronal differentiation of BMSCs with function were accelerated significantly. The cross-linked GO-PEI mediated gene transfection together with a multi-functional microfiber arrayed hydrogel provide a translatable approach for endogenous stem cell-based regenerative therapy.

Reactive red 2 (RR2) is a highly recalcitrant and toxic azo dye that can cause the collapse of biological treatment system. Although MFC can decolorize RR2 effectively, its performance is still inevitably affected by toxicity. Anthraquinone can enhance MFCs’ performance through mediating electron transfer. In this study, an anthraquinone-rich natural plants (B.rheum (Rheum offcinale Baill)) was extracted and then added to MFCs. The optimal dosage was selected and the enhanced effects were investigated. The results showed that adding 5%(V/V) extract resulted in the optimal performance elevation of MFC. When 5% extract was added together with RR2, 15.63% and 1.33-fold improvement in RR2 decolorization efficiency and rate were achieved compared with the control group. Meanwhile, higher power density (2.75 W/m3), coulombic efficiency (6.45%), and lower internal resistance (233.69 Ω) were also observed when 5% B.rheum extract and RR2 were added. B.rheum extract in MFCs enhanced microbial activity and enriched the dye-degrading microorganisms, such as Enterobacter, Raoultella, Comamonas and Shinella. B.rheum extract acts as “antidote” in alleviating the biotoxicity of RR2 was firstly illustrated in this study. The results provided a new strategy for using plant-source electron mediators to simultaneously improve biological detoxification, bioelectricity generation and dye decolorization in bioelectrochemical system.

The clustered regularly interspaced short palindromic repeat (CRISPR)-associated endonuclease Cas13a can specifically bind and cleave RNA. After nucleic acid pre-amplification, bacterial Cas13a has been used to detect genetic mutations. In our study, using a transcription-mediated amplification together with Cas13a, we can isothermally amplify and detect mitochondrial point mutations under non-denaturing conditions from human genomic DNA. Unlike previous reports, we prepared CRISPR DNA with T7 promoter sequences and generated CRISPR RNA via transcription-mediated amplification instead of synthesizing and adding CRISPR RNA in a separate step. As a proof-of-concept, we showed that both m.1494C > T and m.1555A > G mutations were detected within 90 min. In addition, we explored various designs of CRISPR DNA to improve assay specificity, including the location and number of nucleotide mismatches, length of protospacer sequence, and different buffering conditions. We also confirmed the possibility of a “one-step single-tube” reaction for mutation detection. This assay can robustly distinguish circular DNA templates that differ by a single nucleotide. It has the potential to be adapted for automated applications, such as the screening of mitochondrial diseases.

GaN power IC’s are expected to help unlock the full potential of GaN power electronics, especially in terms of promoting the high-frequency power switching applications. This paper first discusses a GaN power integration technology platform based on commercially available p-GaN gate HEMT technology. An integrated gate driver is presented as an example of GaN power IC with enhanced performance, in which a bootstrap unit is adopted to realize rail-to-rail output voltage and fast switching speed. To deal with GaN-specific design issues such as the unique dynamic V TH , a SPICE model of p-GaN gate HEMT is developed to improve design accuracy. Future prospects for GaN power integration are discussed by extending the integration’s landscape to multi-functional GaN power devices, GaN CMOS technology, and GaN/SiC hybrid power IC’s.

Using a melt-mixing technique, ethylene–vinyl acetate (EVA) copolymers based composites containing Multi-Wall Carbon nanotubes (MWCNTs), aluminum trihydrate (ATH), zinc borate (ZB), and gadolinium oxide (Gd2O3) were fabricated. Then, the as-prepared samples were irradiated with an electron beam (EB) at the dose range varied from 0 to 275 kGy. Moreover, we investigated the properties of irradiated and unirradiated samples. Morphological observation showed good dispersion of MWCNTs and other additives in EVA. Furthermore, the gel content, mechanical properties, the limit oxygen index (LOI) values of irradiated composites increased to 28.4% after 250 kGy after irradiated. All the conclusions indicated that the comprehensive properties of the WMCNTs/EVA composites were improved by using high energy electron beam irradiation.

In this study, a microbial fuel cell coupled with constructed wetland (CW-MFC) was built to demonstrate that integration of MFC can enhance antibiotics (sulfadiazine (SDZ) and ciprofloxacin (CIP)) removal in CWs and control CH4 emissions. Better COD and antibiotics removal performance was obtained in CW-MFC. Notably, both reactors can remove more than 90.00% of CIP. A decline in methane fluxes (by 15.29%) was also observed in CW-MFC compared with CW. The presence of Acorus tatarinowii had no obvious effect on antibiotics removal but the application of manganese ore substrate reduced methane emissions. Further study showed that Proteobacteria was enriched on the Mn substrate anode and the relative abundance of Methanothrix was declined. The results suggested that suppression of methanogenesis may be contributed to a low methane flux in CW-MFC. This study will facilitate the application of CW-MFC to treat antibiotics wastewater and control the ecological risks of greenhouse gas emissions.

BackgroundAbnormal renal metabolism is closely related to the development of chronic kidney disease. It is well known that renal inflammation plays an important role in the occurrence and development of tubulointerstitial damage in the renal tubules. The purpose of the experiment was to observe the bioactivity ofAlpina oxyphyllaextract (AOE) on renal injury in diabetic nephropathy (DN) rats induced by streptozotocin (STZ).MethodsThirty male Wistar rats were randomly divided into five group (n = 6): (1) intact control (non-diabetic, ND); (2) intact diabetic (STZ), (3) diabetic rats treated with gliclazide 5 mg/kg (STZ-gli), (4) diabetic rats treated with AOE 400 mg/kg (AOE 400), (5) diabetic rats treated with AOE 800 mg/kg (AOE 800). The diabetic nephropathy rat model was established by single intraperitoneal injected 50 mg/kg STZ. Fasting blood glucose (FBG) and body weight was observed at 1、3、6 weeks. After 6 weeks, the renal function parameters of five groups and 24 h urinary protein were detected. Expression of transforming growth factor-beta1 (TGF-β1) and myeloid differentiation factor 88 (MyD88) were assessed by Western Blot.ResultsThe STZ group showed hyperglycemia, proteinuria, renal function damage, and the levels of 24 h urinary protein, fasting blood glucose (FBG), blood urea nitrogen (BUN), serum creatinine (Scr), triglyceride (TG), high-density lipoprotein cholesterol (HDL-C) and interleukin-6 (IL-6) in the STZ group increased significantly compared with the ND group. The expression of TGF-β1 in STZ group was increase (p p ConclusionsAOE can effectively protect kidney tissues of diabetic nephropathy, and probably through regulating level of TGF-β1/MyD88.