3-Allyl-1-(3-cyano­phenyl­methyl­ene)-2-methyl-1H-benzoimidazol-3-ium bromide monohydrate

In the title compound, C19H18N3 +·Br−·H2O, the dihedral angle between the allyl group and the imidazole ring is 89.59 (14)°, while the dihedral angle between the cyanophenyl ring and the imidazole ring is 78.72 (7)°. O—H⋯Br hydrogen bonds form an infinite chain in the c-axis direction and C—H⋯Br and C—H⋯O inter­actions expand this chain into an infinite three-dimensional network

Effects of Influent Organic Loading Rates and Electrode Locations on the Electrogenesis Capacity of Constructed Wetland-Microbial Fuel Cell Systems

Three novel constructed wetland-microbial fuel cells (CW-MFCs), based on electrode location, were developed for wastewater treatment and sustainable electricity production by embedding a MFC into a CW system. In the three CW-MFCs, electrodes were placed in different locations, including bottom anode-rhizosphere cathode CW-MFC (BA-RC-CW-MFC), rhizosphere anode-air cathode CW-MFC (RA-AC-CW-MFC), and bottom anode-air cathode CW-MFC (BA-AC-CW-MFC), to investigate the combined effects of organic loading rates (OLRs) and reactor configurations on the electrogenesis capacity of the hybrid system. All the systems operated continuously to treat five types of synthetic wastewater with increasing OLRs: 9.2, 18.4, 27.6, 55.2, and 92.0 g chemical oxygen demand (COD) m(-2) d(-1). The BA-RC-CW-MFC failed to produce electricity at any OLR, whereas the maximum power densities of 0.79 +/- 0.01 and 10.77 +/- 0.52 mW m(-2) were achieved in the RA-AC-CW-MFC with 18.4 g COD m(-2) d(-1) influent OLR and in the BA-AC-CW-MFC with 27.6 g COD m(-2) d(-1) influent OLR, respectively. The coulombic efficiencies of the RA-AC-CW-MFC and BA-AC-CW-MFC decreased gradually with the increase in influent OLRs. (C) 2016 American Institute of Chemical Engineers Environ Prog, 36: 435-441, 2017</p

Astragaloside IV Downregulates β-Catenin in Rat Keratinocytes to Counter LiCl-Induced Inhibition of Proliferation and Migration

Re-epithelialization is a crucial step towards wound healing. The traditional Chinese medicine, Astragalus membranaceus (Fisch) Bge, has been used for hundreds of years for many kinds of ulcerated wounds. Recent research has identified the active compound in this drug as astragaloside IV (AS-IV), but the underlying molecular mechanisms of its therapeutic action on keratinocytes remain poorly understood. In this study, we used an in vitro model of ulcer-like wound processes, lithium chloride (LiCl)-induced cultured mouse keratinocytes, to investigate the effects of AS-IV treatment. The effects on cell proliferation were evaluated by the MTS/PMS colorimetric assay, effects on cell migration were determined by a wound-healing scratch experiment, effects on the cell cycle were analyzed by flow cytometry, and effects on protein expression were analyzed by immunoblotting and immunofluorescence. LiCl strongly inhibited cell proliferation and migration, up-regulated β-catenin expression, and down-regulated proliferating cell nuclear antigen (PCNA) expression. AS-IV treatment attenuat the inhibition of proliferation and migration, significantly reducing the enhanced β-catenin expression, and recovering PCNA and β-tubulin expression. Thus, AS-IV mediates mouse keratinocyte proliferation and migration via regulation of the Wnt signaling pathway. Down-regulating β-catenin to increase keratinocyte migration and proliferation is one mechanism by which AS-IV can promote ulcerated wound healing

Tetra­aqua­tetra­kis{μ3-3,3′-[(E,E)-ethane-1,2-diylbis(nitrilo­methyl­idyne)]benzene-1,2-diolato}octa­zinc(II) N,N-dimethyl­formamide hexa­solvate

The asymmetric unit of the title compound [Zn8(C16H12N2O4)4(H2O)4]·6C3H7NO, consists of eight ZnII cations, four tetra­valent anionic ligands, L 4− (L 4− = 3,3′-(1E,1′E)-(ethane-1,2-diylbis(azan-1-yl-1-yl­idene))bis­(methan-1-yl-1-yl­idene)dibenzene-1,2-bis­(olate), four coordinated water mol­ecules and six N,N-dimethyl­formamide solvate mol­ecules. The coordination complex comprises an octa­nuclear ZnII unit with its ZnII centers coordinated in two discrete distorted square-pyramidal geometries. Four ZnII atoms each coordinate to two nitro­gen atoms and two phenolate oxygen atoms from an individual L 4− ligand and one coordinated water mol­ecule. The other four ZnII atoms each bind to five phenolate oxygen atoms from three different L 4− ligands. In the crystal structure, the ZnII complex unit, coordinated water mol­ecules and dimethyl­formamide solvate mol­ecules are linked via O—H⋯O and C—H⋯O hydrogen bonds. Mol­ecules are connected by additional inter­molecular O—H⋯O and C—H⋯O hydrogen bonds, forming an extensive three dimensional framework

Tanshinone IIA Inhibits Growth of Keratinocytes through Cell Cycle Arrest and Apoptosis: Underlying Treatment Mechanism of Psoriasis

The aim of the present investigation was to elucidate the cellular mechanisms whereby Tanshinone IIA (Tan IIA) leads to cell cycle arrest and apoptosis in vitro in keratinocytes, the target cells in psoriasis. Tan IIA inhibited proliferation of mouse keratinocytes in a dose- and time-dependent manner and induced apoptosis, resulting in S phase arrest accompanied by down-regulation of pCdk2 and cyclin A protein expression. Furthermore, Tan IIA-induced apoptosis and mitochondrial membrane potential changes were also further demonstrated by DNA fragmentation, single-cell gel electrophoresis assay (SCGE), and flow cytometry methods. Apoptosis was partially blocked by the caspase-3 inhibitor Ac-DEVD-CHO. Mitochondrial regulation of apoptosis further downstream was investigated, showing changes in the mitochondrial membrane potential, cytochrome c release into the cytoplasm, and enhanced activation of cleaved caspase-3 and Poly ADP-ribose polymerase (PARP). There was also no translocation of apoptosis-inducing factor (AIF) from mitochondria to the nucleus in apoptotic keratinocytes, indicating Tan IIA-induced apoptosis occurs mainly through the caspase pathway. Our findings provide the molecular mechanisms by which Tan IIA can be used to treat psoriasis and support the traditional use of Salvia miltiorrhiza Bungee (Labiatae) for psoriasis and related skin diseases

An Update on the Evolution of Glucosyltransferase (Gtf) Genes in Streptococcus

In many caries-promoting Streptococcus species, glucosyltransferases (Gtfs) are recognized as key enzymes contributing to the modification of biofilm structures, disruption of homeostasis of healthy microbiota community and induction of caries development. It is therefore of great interest to investigate how Gtf genes have evolved in Streptococcus. In this study, we conducted a comprehensive survey of Gtf genes among 872 streptococci genomes of 37 species and identified Gtf genes from 364 genomes of 18 species. To clarify the relationships of these Gtf genes, 45 representative sequences were used for phylogenic analysis, which revealed two clear clades. Clade I included 12 Gtf genes from nine caries-promoting species of the Mutans and Downei groups, which produce enzymes known to synthesize sticky, water-insoluble glucans (WIG) that are critical for modifying biofilm structures. Clade II primarily contained Gtf genes responsible for synthesizing water-soluble glucans (WSG) from all 18 species, and this clade further diverged into three subclades (IIA, IIB, and IIC). An analysis of 16 pairs of duplicated Gtf genes revealed high divergence levels at the C-terminal repeat regions, with ratios of the non-synonymous substitution rate (dN) to synonymous substitution rate (dS) ranging from 0.60 to 1.03, indicating an overall relaxed constraint in this region. However, among the clade I Gtf genes, some individual repeat units possessed strong functional constraints by the same criterion. Structural variations in the repeat regions were also observed, with detection of deletions or recent duplications of individual repeat units. Overall, by establishing an updated phylogeny and further elucidating their evolutionary patterns, this work enabled us to gain a greater understanding of the origination and divergence of Gtf genes in Streptococcus

From Indeterminacy to Determinacy: Augmenting Logical Reasoning Capabilities with Large Language Models

Recent advances in LLMs have revolutionized the landscape of reasoning tasks. To enhance the capabilities of LLMs to emulate human reasoning, prior works focus on modeling reasoning steps using specific thought structures like chains, trees, or graphs. However, LLM-based reasoning continues to encounter three challenges: 1) Selecting appropriate reasoning structures for various tasks; 2) Exploiting known conditions sufficiently and efficiently to deduce new insights; 3) Considering the impact of historical reasoning experience. To address these challenges, we propose DetermLR, a novel reasoning framework that formulates the reasoning process as a transformational journey from indeterminate premises to determinate ones. This process is marked by the incremental accumulation of determinate premises, making the conclusion progressively closer to clarity. DetermLR includes three essential components: 1) Premise identification: We categorize premises into two distinct types: determinate and indeterminate. This empowers LLMs to customize reasoning structures to match the specific task complexities. 2) Premise prioritization and exploration: We leverage quantitative measurements to assess the relevance of each premise to the target, prioritizing more relevant premises for exploring new insights. 3) Iterative process with reasoning memory: We introduce a reasoning memory module to automate storage and extraction of available premises and reasoning paths, preserving historical reasoning details for more accurate premise prioritization. Comprehensive experimental results show that DetermLR outperforms all baselines on four challenging logical reasoning tasks: LogiQA, ProofWriter, FOLIO, and LogicalDeduction. DetermLR can achieve better reasoning performance while requiring fewer visited states, highlighting its superior efficiency and effectiveness in tackling logical reasoning tasks.Comment: Code repo: https://github.com/XiaoMi/DetermL

Absorption, Distribution and Excretion of 14C-Probimane in Mice Bearing Lewis Lung Carcinoma

Spontaneous neoplasm metastasis, a fatalist pathological feature of cancer, is a long-evolving, multi-steps process that can now only be treated or controlled by drugs or immuno-modulators. Probimane (Pro), as a representative of the well-known class of antimetastatic agents ‘Bisdioxopiperazine compounds (Biz)’, is systematically studied for its absorption, distribution and excretion in mice bearing Lewis lung carcinoma by a radioactivity-detective method in this investigation. It is found that the 14C-Pro concentrations in different normal organs of mice at 2 hrs are very high and dramatically declined at 24 and 48 hrs. However, Pro concentrations in metastatic foci are slightly changed at the same time. Almost no change of Pro concentrations is observed in pulmonary metastatic nodules within 48 hrs. This evidence can be used to explain the characteristics of good metastatic inhibition by Biz compounds. The radioactivity in brain is relatively low because Pro can hardly penetrate into the blood-brain-barrier to eliminate brain tumors. The excretion of 14C-Pro is observed at the same ratios from both urine and feces and also at constant rates. These data are much useful for better understanding of the general pharmacological characters and possible antimetastatic mechanisms of actions of probimane and other Biz compounds from a new perspective and research angles