The synergistic mechanism of action of Dajianzhong decoction in conjunction with ketamine in the treatment of depression.

Depression is a multifactorial syndrome with a variety of underlying pathological mechanisms. While ketamine, an N-methyl-D-aspartate receptor (NMDAR) antagonist, exhibits a rapid antidepressant action in the central never system (CNS), the potential addiction and psychotomimetic adverse effects of ketamine limit its chronic use in clinical practice. Therefore, it is necessary to discover an additional agent that shows a synergistic antidepressant activity with ketamine to sustain its therapeutic action so as to reduce its use frequency in depression treatment. The present study indicated that Dajianzhong decoction (DJZT), an empirical herbal formula used for the clinical treatment of several inflammation-related intestinal disorders, sustains behavioral and synaptic action of ketamine in depressive mouse models. Additionally, ketamine was also demonstrated to exert a synergistic action with DJZT to alleviate the chronic unpredictable mild stress (CUMS)-induced abnormalities in gut barrier proteins and colonic histology, and subsequently to normalize the diversity and composition of gut microbiota. Furthermore, DJZT was shown to possess an anti-inflammatory activity to prevent activation of NF-κB from releasing proinflammatory cytokines, specifically through inhibiting Th17 cells/IL-17A pathway. Our results uncovered the mechanism of action of DJZT in conjunction with ketamine in depression treatment by which these agents target different pathological factors across biological systems and exert a synergistic activity through a bidirectional communication in the gut-brain axis, and also provided new insights into the systematic treatment of depression.

Defect-Rich W/Mo-Doped V2O5 Microspheres as a Catalytic Host To Boost Sulfur Redox Kinetics for Lithium-Sulfur Batteries.

It is very important to develop ideal electrocatalysts to accelerate the sulfur redox kinetics in both the discharging and charging processes for high-performance lithium-sulfur batteries. Herein, defect-rich cation-doped V2O5 yolk-shell microspheres are reported as a catalytic host of sulfur. The doping of W or Mo cations induces no impurities, broadens the lattice spacing of V2O5, and enriches the oxygen vacancy defects. Thus, the doped V2O5 host affords sufficient active sites for chemically anchoring polysulfides and promising catalytic effect on the mutual conversion between different sulfur intermediates. As a result, the S/W-V2O5 cathode delivers a discharging capacity of 1143.3 mA g-1 at an initial rate of 0.3 C and 681.8 mA g-1 at 5 C. Even under a sulfur loading of up to 5.5 mg cm-2 and a minimal electrolyte/sulfur ratio of 6 µL mg-1, the S/W-V2O5 cathode could still achieve good sulfur utilization and dependable cycle stability. Thus, this work offers an electrocatalytic host based on the cation doping strategy to greatly enhance the sulfur redox kinetics for high-performance Li-S batteries.

2D MOF with Compact Catalytic Sites for the One-pot Synthesis of 2,5-Dimethylfuran from Saccharides via Tandem Catalysis.

One pot synthesis of 2,5-dimethylfuran (2,5-DMF) from saccharides under mild conditions is of importance for the production of biofuel and fine chemicals. However, the synthesis requires a multitude of active sites and suffers from slow kinetics due to poor diffusion in most composite catalysts. Herein, a metal-acid functionalized 2D metal-organic framework (MOF; Pd/NUS-SO3 H), as an ultrathin nanosheet of 3-4 nm with Lewis acid, Brønsted acid, and metal active sites, was prepared based on the diazo method for acid modification and subsequent metal loading. This new composite catalyst gives substantially higher yields of DMF than all reported catalysts for different saccharides (fructose, glucose, cellobiose, sucrose, and inulins). Characterization suggests that a cascade of reactions including polysaccharide hydrolysis, isomerization, dehydration, and hydrodeoxygenation takes place with rapid molecular interactions.

Facile Synthesis of a "Two-in-One" Sulfur Host Featuring Metallic-Cobalt-Embedded N-Doped Carbon Nanotubes for Efficient Lithium-Sulfur Batteries.

The exploration of efficient host materials of sulfur is significant for the practical lithium-sulfur (Li-S) batteries, and the hosts are expected to be highly conductive for high sulfur utilization and exhibit strong interaction toward polysulfides to suppress the shuttle effect for long-lasting cycle stability. Herein, we propose a simple synthesis of metallic cobalt-embedded N-doping carbon nanotubes (Co@NCNT) as a "two-in-one" host of sulfur for efficient Li-S batteries. In the binary host, the N-doped CNTs, cooperating with metallic Co nanoparticles, can serve as 3D conductive networks for fast electron transportation, while the synergetic effect of metallic Co and doping N heteroatoms helps to chemically confine polysulfides, acting as active sites to accelerate electrochemical kinetics. With these advantages, the S/Co@NCNT composite delivers an excellent cycling stability with a capacity decay of 0.08% per cycle averaged within 500 cycles at a current density of 1 A g-1 and a high rate performance of 530 mA h g-1 at 5 A g-1. Further, the superior electrochemical performance of the S/Co@NCNT electrode can be maintained under a high sulfur loading up to 4 mg cm-2. Our work demonstrates a feasible strategy to design promising host materials simultaneously featuring high conductivity and strong confinement toward polysulfides for high-performance Li-S batteries.

MiR-22-3p Regulates Amyloid ß Deposit in Mice Model of Alzheimer's Disease by Targeting Mitogen-activated Protein Kinase 14.

Propose: To investigate whether miR-22-3p is able to regulate AD development and its molecular mechanism. METHODS: Morris water maze test was performed to test the spatial memory. Quantitative polymerase chain reaction (qPCR) was used to assess the expression level of miR-22-3p. The enzymelinked immunosorbent assay (ELISA) was used to assess the levels of Aß40 and Aß42. Immunoblotting analysis was performed to detect the protein expression levels of amyloid precursor protein (APP), mitogen-activated protein kinase 14 (MAPK14) and beta-site Amyloid precursor protein Cleaving Enzyme 1 (BACE1). Luciferase assay was used to identify the interaction between miR- 22-3p and MAPK14. The tetrazolium dye (MTT) colorimetric assay was used to test the influence of miR-22-3p overexpression on cell viability. Flow cytometry analysis was performed to evaluate the effect of miR-22-3p overexpression on cell apoptosis. RESULTS: Morris water maze test showed that mice model of AD had impaired spatial memory, which was able to be ameliorated by miR-22-3p overexpression. Immunoblotting analysis revealed that the protein expression levels of APP, MAPK14 and BACE1 were enhanced in AD model, which could be prevented by miR-22-3p overexpression. ELISA showed that Aß40 and Aß42 levels were dramatically increased in AD model, which were inhibited by miR-22-3p overexpression. Luciferase assay and immunoblotting analysis indicated that miR-22-3p targeted and regulated MAPK14 expression. CONCLUSION: MiR-22-3p overexpression reduced Aß deposit and alleviated AD symptoms by targeting and regulating MAPK14 expression, which ameliorated AD symptoms.

Cobalt-Tungsten Bimetallic Carbide Nanoparticles as Efficient Catalytic Material for High-Performance Lithium-Sulfur Batteries.

Lithium-sulfur (Li-S) batteries are promising candidates for next-generation energy storage devices owing to their advantages such as high theoretical specific capacity and energy density. However, the shuttle effect of polysulfide intermediates and the slow electrochemical kinetics have a severe passive effect on the cycling stability and rate performance. A Co3 W3 C@C composite was prepared through a simple one-pot pyrolysis method and used as a modifying layer on a commercial separator. The obtained modified separator not only prevented the shuttle effect through both strong chemical interaction and a physical barrier toward polysulfides, but also acted as a catalytic membrane to catalyze the electrochemical redox of active sulfur species. By employing the coated separator, the cathode with 60 wt % sulfur delivered a high initial capacity of 1345 mAh g-1 at 0.1 A g-1 , excellent rate performance with a high capacity of 670 mAh g-1 even at 7 A g-1 , and outstanding cycle performance with a low decay rate of 0.06 % per cycle and an average Coulombic efficiency of 99.3 % within 500 cycles at 1 A g-1 . Even at a sulfur loading of 3 mg cm-1 , a high initial capacity of 869 mAh g-1 and 632 mAh g-1 after 200 cycles at 1 A g-1 were obtained. The results demonstrate the advantages of Co-W bimetallic carbide in preventing the shuttle effect and promoting the redox kinetics for high performance Li-S batteries.

A Chemical Blowing Strategy to Fabricate Biomass-Derived Carbon-Aerogels with Graphene-Like Nanosheet Structures for High-Performance Supercapacitors.

The efficient exploitation and utilization of low-cost and biomass-derived carbon materials will play an active role in developing sustainable energy storage systems. However, the difficult morphology control and incomplete activation limits their pervasive application in electrochemical energy storage. Inspired by the famous Chinese folk handicraft of sugar-figure blowing, biomass-derived carbon aerogels (GCA) with 2 D graphene-like thin nanosheets were fabricated by a simple chemical blowing strategy from a viscous agaric solution obtained through hydrothermal treatment of agaric. A chemical blowing agent (NH4 Cl) was used to effectively exfoliate the bulk biomass-derived carbon flake into 2 D graphene-like nanosheets, which resulted in a highly porous structure and high specific area (2200 m2 g-1 ) after the activation process. As a result, a high specific capacitance of 340 F g-1 at 3 A g-1 and a high specific energy of 25.5 Wh kg-1 at a power density of 2 kW kg-1 was obtained for the GCA electrode, which can be attributed to the abundant electrochemically active surfaces, short ion transport paths, and effective electrolyte infiltration.. This work demonstrates an effective and low-cost strategy to prepare hierarchical and well-organized porous biomass carbon materials with graphene-like nanosheets for high-performance supercapacitors.

Molten-Salt-Assisted Synthesis of Hierarchical Porous MnO@Biocarbon Composites as Promising Electrode Materials for Supercapacitors and Lithium-Ion Batteries.

Biomass-derived carbon composites (e.g., metal oxide/biocarbon) have been used as promising electrode materials for energy storage devices owing to their natural abundance and simple preparation process. However, low loading content/inhomogeneous distribution of metal oxides and inefficient cracking of biocarbon (BC) are intractable obstacles that impede the efficient utilization of biomass. In this work, hierarchical porous MnO/BC composites were prepared by a facile molten-salt-assisted strategy based on the superior salt-water absorption ability of agaric. The addition of NaCl induces a liquid reaction medium by formation of a molten salt mixture at high temperature to effectively realize the activation and cracking of the bulk carbon, and it also acts as a recyclable sacrificial template to form mesopores and macropores in the as-prepared hierarchical porous MnO/BC composites. The highly porous and uniform BC framework effectively enhances ion diffusion and electron-transfer ability, serves as a protective layer to prevent fracturing and agglomeration of MnO, and thus enables superior rate performance and cycling stability of the MnO/BC composite for both supercapacitor electrodes (94 % capacity retention at 20 mA cm-2 after 5000 cycles) and lithium-ion battery anodes (783 mA h g-1 after 1000 cycles). Notably, considering the simple and low-cost preparation process, this work opens a promising avenue for the large-scale production of advanced metal oxide/BC hybrid electrode materials for electrochemical energy storage.

Photochromism of Amphiphilic Dithienylethenes as Langmuir-Schaefer Films.

Surface pressure-area isotherms were recorded under different irradiation conditions for single-component Langmuir films of three photochromic amphiphilic dithienylethenes. Nonirradiated films of these photochromic amphiphiles were mechanically stable. In addition, a shift of the isotherms to larger mean molecular areas was observed for films prepared from UV-light-irradiated dithienylethenes. Unexpectedly, a significant expansion was observed for a film prepared from visible-light-irradiated dithienylethene incorporating large branched alkyl chains. Upon further study, atomic force microscopy and transmission electron microscopy images of Langmuir-Schaefer films revealed that this pronged dialkyl derivative undergoes a photoinduced change in morphology, as circular aggregates coalesce into larger continuous aggregated structures. Nevertheless, its photoisomerization was completely reversible as single-component multilayer thin films upon direct UV or visible light irradiation.

Molybdenum-doped ZnS sheets with dominant {111} facets for enhanced visible light photocatalytic activities.

ZnS is widely used as a semiconductor photocatalyst in photo-electrochemical water splitting and photodegradation under ultraviolet (UV)-light irradiation. In this work, Molybdenum (Mo)-doped ZnS sheets with dominant {111} facets are developed using a hydrothermal method with Mo ions as precursors to realize non-visible-light photocatalytic activity and reduce the recombination rate of photoexcited carriers in ZnS. Mo ions are found to play a key role in the growth process of the sheet-like structure. Mo-dopants in the ZnS sheets introduce the acceptor energy levels among the bandgaps. The light absorption range of Mo-doped ZnS sheets covers the entire visible light and even extends to the near-infrared light region. The p-type Mo-doped ZnS sheets exhibit enhanced photocatalytic activities under visible light irradiation, which is promising for the photo-electrochemistry and photo-oxidation applications.

Contralesional Cortical Structural Reorganization Contributes to Motor Recovery after Sub-Cortical Stroke: A Longitudinal Voxel-Based Morphometry Study.

Although changes in brain gray matter after stroke have been identified in some neuroimaging studies, lesion heterogeneity and individual variability make the detection of potential neuronal reorganization difficult. This study attempted to investigate the potential structural cortical reorganization after sub-cortical stroke using a longitudinal voxel-based gray matter volume (GMV) analysis. Eleven right-handed patients with first-onset, subcortical, ischemic infarctions involving the basal ganglia regions underwent structural magnetic resonance imaging in addition to National Institutes of Health Stroke Scale (NIHSS) and Motricity Index (MI) assessments in the acute (<5 days) and chronic stages (1 year later). The GMVs were calculated and compared between the two stages using nonparametric permutation paired t-tests. Moreover, the Spearman correlations between the GMV changes and clinical recoveries were analyzed. Compared with the acute stage, significant decreases in GMV were observed in the ipsilesional (IL) precentral gyrus (PreCG), paracentral gyrus (ParaCG), and contralesional (CL) cerebellar lobule VII in the chronic stage. Additionally, significant increases in GMV were found in the CL orbitofrontal cortex (OFC) and middle (MFG) and inferior frontal gyri (IFG). Furthermore, severe GMV atrophy in the IL PreCG predicted poorer clinical recovery, and greater GMV increases in the CL OFG and MFG predicted better clinical recovery. Our findings suggest that structural reorganization of the CL "cognitive" cortices might contribute to motor recovery after sub-cortical stroke.

Laser-Limited Signatures of Quantum Coherence.

Quantum coherence is proclaimed to promote efficient energy collection by light-harvesting complexes and prototype organic photovoltaics. However, supporting spectroscopic studies are hindered by the problem of distinguishing between the excited state and ground state origin of coherent spectral transients. Coherence amplitude maps, which systematically represent quantum beats observable in two-dimensional (2D) spectroscopy, are currently the prevalent tool for making this distinction. In this article, we present coherence amplitude maps of a molecular dimer, which have become significantly distorted as a result of the finite laser bandwidth used to record the 2D spectra. We argue that under standard spectroscopic conditions similar distortions are to be expected for compounds absorbing over a spectral range similar to, or exceeding, that of the dimer. These include virtually all photovoltaic polymers and certain photosynthetic complexes. With the distortion of coherence amplitude maps, alternative ways to identify quantum coherence are called for. Here, we use numerical simulations that reproduce the essential photophysics of the dimer to unambiguously determine the excited state origin of prominent quantum beats observed in the 2D spectral measurements. This approach is proposed as a dependable method for coherence identification.

Photocontrol of ion permeation in lipid vesicles with (bola)amphiphilic spirooxazines.

Three (bola)amphiphilic spirooxazines have been synthesized and their photochromism has been characterized. The large biphotochromic structure of 2 significantly affects its conformational flexibility and the rate constants for thermal ring closure are particularly dependent on the lipid phase state. Two comprehensive ion permeation studies were performed to examine the effect of spirooxazine inclusion and isomerization on membrane permeability. In all cases, the open-ring isomers of these spirooxazines are more disruptive in bilayer membranes than their closed-ring isomers. Further, the rate of ion permeation and net release are highly dependent on the lipid bilayer phase state and the relative position of the photochromic moiety in the bilayer membrane. Moreover, the difference in potassium ion permeability under UV and visible irradiation is more pronounced than previously reported photoresponsive membrane disruptors with reversible photocontrols.

Photocontrol of ion permeation in lipid vesicles with amphiphilic dithienylethenes.

The integration of photochromic dithienylethenes (DTEs) with lipid vesicles as photoresponsive membrane disruptors for ion transport applications has been examined. We have synthesized three amphiphilic DTEs 1-3 that incorporate a terminally charged alkyl chain, and contain methyl or phenylethynyl substituents at the reactive carbons. Our photochromic reactivity studies suggest that the inclusion of a single alkyl chain favors the photoactive antiparallel conformation of DTEs, given the significant improvement in the cyclization quantum yield over previous phenylethynyl derivatives. Our ion permeation studies show that the open-ring isomers of these DTEs are more disruptive than the closed-ring isomers in the four lipid vesicle systems studied, regardless of their lamellar phase at room temperature. In addition, a steric effect was clearly observed as DTEs incorporating the comparatively smaller methyl group exhibited lower rates of ion permeation than the bulkier phenylethynyl group. In all cases, UV irradiation led to a reduction in ion permeability. In fact, the methyl analog exhibited a significant reduction in ion permeability in gel-phase lipid vesicles upon UV exposure. Also, the hexyl chain derivatives had a greater effect on membrane permeability than the dodecyl derivative owing to their relative position in the bilayer membrane of lipid vesicles.

Assessing the decontamination efficiency of a three-component flocculating system in the treatment of oilfield-produced water.

Produced water is a complex mixture of oil, water, dissolved solids, and suspended solids. It represents the largest volume of waste associated with the oil and gas industry, and its management is a costly aspect of oil recovery. Therefore, the development of effective treatment technologies for produced water is essential from both ecological and economic standpoints. We have developed a sensitive, fluorescence-based method to demonstrate the decontamination efficiency of a three-component polymeric flocculating system, the microencapsulating flocculating dispersion (MFD) technology. We have shown that the MFD technology can remove 90 ± 2% of the pyrene, a model wastewater contaminant, in a 0.4 ppm aqueous stock solution. The optimal flocculant concentrations used to remove pyrene was determined by fluorescence spectroscopy and zeta potential measurements. Under these conditions, flocculation and settling times were fast (i.e., <1 min). We have also demonstrated rapid removal of crude oil from an oilfield-produced water sample with a remarkable decontamination efficiency of ≥98 ± 1%. Using this fluorescence-based method, we will be better able to formulate the components of this technology and other polymeric flocculants in the treatment of oilfield-produced water, which will benefit wastewater treatment technologies.

[Field evaluation of a novel plant molluscicide "Luo-Wei" against Oncomelania hupensis I molluscicidal effect by the spraying method in lake and marshland regions].

OBJECTIVE: To evaluate the field effect of a novel plant molluscicide "Luo-wei" (Tea-seed distilled saponins, TDS) against Oncomelania hupensis in the lake and marshland regions. METHODS: A spraying experiment was carried out in the grassland of two schistosomiasis endemic counties, including Xingzi in Jiangxi Province and the Huarong in Hunan Province, to assess the molluscicidal effect of 4% TDS comparing with 50% wettable powder of niclosamide ethanolamine salt (WPN). The chi2 test was used to examine the differences between regions, molluscicides, or days after spraying. RESULTS: Following 1, 3, 7, and 15 days of test, the snail mortality showed a simultaneous increase both in TDS group (70.43%-86.88%) and WPN group (70.21%-85.35%). There is no significant difference between TDS and WPN of day 1, 7 and 15 (all P values > 0.05), but except for day 3 (chi2 = 3.910, P = 0.048). By the end of day 15, the snail mortality for TDS was 86.53% in Xingzi and 88.28% in Huarong, while for WPN was 83.04% in Xingzi and 93.69% in Huarong respectively; the decline rate of snail density for TDS was 85.29% in Xingzi and 93.53% in Huarong, while for WPN was 85.29% in Xingzi and 93.53% in Huarong respectively. The adjusted mortality of different days ranged from 69.63% to 86.54% in the the TDS group, and 69.41% to 86.54% in the WPN group. CONCLUSION: The molluscicidal effect of TDS by spraying is similar to that of WPN. It is time to popularize this new plant molluscicide (TDS) in a wider field.

[Endemic situation of schistosomiasis in Donggou Village, a surveillance site, in Huarong County from 2005 to 2010].

From 2005 to 2010, the infection rates of schistosomiasis among residents (above 6 years old) were 13.34%, 9.59%, 4.81%, 3.03%, 2.35% and 2.19%, respectively. The positive rates of schistosomiasis among domestic animals fluctuated from 2.50% to 25.92%. Oncomelania snails were not found inside embankment since 1980, yet a high density of infected snails was found at low and uneven areas outside embankment. The cattle were the main infectious source and we should strengthen the administration and control of cattle.

Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss.

Mutations in mitochondrial DNA is one of the important causes of hearing loss. Here, we performed a mutational screening of tRNA(Ser(UCN)) gene in 1542 Chinese subjects with hearing loss. One subject and five subjects carried tRNA(Ser(UCN)) A7445C and G7444A mutations, respectively, while two subjects harbored both G7444A and 12S rRNA A1555G mutations. Clinical evaluation revealed the variable phenotype of bilateral hearing impairment including severity and audiometric configuration in these subjects. Six pedigrees carrying only G7444A or A7445C mutation exhibited extremely low penetrance of hearing loss, while two families carrying both G7444A and A1555G mutations displayed high penetrance of hearing loss. Of 94 matrilineal relatives in these families, eight subjects suffered from aminoglycoside-induced hearing loss, while seven hearing-impaired subjects did not have a history of exposure to aminoglycosides. Those suggest that G7444A and A7445C mutations themselves are insufficient to produce a clinical phenotype and aminoglycosides are the major modifier factors for the development of deafness in these Chinese families. The combination of A1555G and G7444A mutations increased deafness expression. These observations provide an additional evidence for the early diction and prevention of deafness at the high risk populations carrying these mitochondrial DNA mutations.