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Primulina guarouba, a new species from the limestone area of northern Guangxi, China, is described and illustrated. According to the maximum likelihood (ML) and Bayesian inference (BI) analysis, it nests in a strongly supported clade (BP = 99%) that includes P. cordifolia, P. repanda and P. huangii. Of these, P. guarouba is similar to the P. cordifolia in morphology, but it is easily distinguished from the latter by some of the distinct characters in leaf blade, peduncles, bracts, calyx, corolla, pistil. [ABSTRACT FROM AUTHOR]

Extracellular vesicles (EVs) play a crucial role in triggering tumour‐aggressive behaviours. However, the energetic process by which tumour cells produce EVs remains poorly understood. Here, we demonstrate the involvement of β‐hexosaminidase B (HEXB) in mediating EV release in response to oxidative stress, thereby promoting the development of hepatocellular carcinoma (HCC). Mechanistically, reactive oxygen species (ROS) stimulate the nuclear translocation of transcription factor EB (TFEB), leading to the upregulation of both HEXB and its antisense lncRNA HEXB‐AS. HEXB‐AS can bind HEXB to form a protein/RNA complex, which elevates the protein stability of HEXB. The stabilized HEXB interacts with lysosome‐associated membrane glycoprotein 1 (LAMP1), disrupting lysosome‐multivesicular body (MVB) fusion, which protects EVs from degradation. Knockdown of HEXB efficiently inhibits EV release and curbs HCC growth both in vitro and in vivo. Moreover, targeting HEXB by M‐31850 significantly inhibits HCC growth, especially when combined with GW4869, an inhibitor of exosome release. Our results underscore the critical role of HEXB as a modulator that promotes EV release during HCC development. [ABSTRACT FROM AUTHOR]

cAMP responsive element binding protein 3 (CREB3), belonging to bZIP family, was reported to play multiple roles in various cancers, but its role in hepatocellular carcinoma (HCC) is still unclear. cAMP responsive element binding protein 3 like 3 (CREB3L3), another member of bZIP family, was thought to be transcription factor (TF) to regulate hepatic metabolism. Nevertheless, except for being TFs, other function of bZIP family were poorly understood. In this study, we found CREB3 inhibited growth and metastasis of HCC in vitro and in vivo. RNA sequencing indicated CREB3 regulated AKT signaling to influence HCC progression. Mass spectrometry analysis revealed CREB3 interacted with insulin receptor (INSR). Mechanistically, CREB3 suppressed AKT phosphorylation by inhibiting the interaction of INSR with insulin receptor substrate 1 (IRS1). In our study, CREB3 was firstly proved to affect activation of substrates by interacting with tyrosine kinase receptor. Besides, CREB3 could act as a TF to transactivate RNA‐binding motif protein 38 (RBM38) expression, leading to suppressed AKT phosphorylation. Rescue experiments further confirmed the independence between the two functional manners. In conclusion, CREB3 acted as a tumor suppressor in HCC, which inhibited AKT phosphorylation through independently interfering interaction of INSR with IRS1, and transcriptionally activating RBM38. [ABSTRACT FROM AUTHOR]

Loss of E‐cadherin (ECAD) is required in tumor metastasis. Protein degradation of ECAD in response to oxidative stress is found in metastasis of hepatocellular carcinoma (HCC) and is independent of transcriptional repression as usually known. Mechanistically, protein kinase A (PKA) senses oxidative stress by redox modification in its β catalytic subunit (PRKACB) at Cys200 and Cys344. The activation of PKA kinase activity subsequently induces RNF25 phosphorylation at Ser450 to initiate RNF25‐catalyzed degradation of ECAD. Functionally, RNF25 repression induces ECAD protein expression and inhibits HCC metastasis in vitro and in vivo. Altogether, these results indicate that RNF25 is a critical regulator of ECAD protein turnover, and PKA is a necessary redox sensor to enable this process. This study provides some mechanistic insight into how oxidative stress‐induced ECAD degradation promotes tumor metastasis of HCC. [ABSTRACT FROM AUTHOR]

N6‐methyladenosine (m6A) modification orchestrates cancer formation and progression by affecting the tumor microenvironment (TME). For hepatocellular carcinoma (HCC), immune evasion and angiogenesis are characteristic features of its TME. The role of YTH N6‐methyladenosine RNA binding protein 2 (YTHDF2), as an m6A reader, in regulating HCC TME are not fully understood. Herein, it is discovered that trimethylated histone H3 lysine 4 and H3 lysine 27 acetylation modification in the promoter region of YTHDF2 enhanced its expression in HCC, and upregulated YTHDF2 in HCC predicted a worse prognosis. Animal experiments demonstrated that Ythdf2 depletion inhibited spontaneous HCC formation, while its overexpression promoted xenografted HCC progression. Mechanistically, YTHDF2 recognized the m6A modification in the 5′‐untranslational region of ETS variant transcription factor 5 (ETV5) mRNA and recruited eukaryotic translation initiation factor 3 subunit B to facilitate its translation. Elevated ETV5 expression induced the transcription of programmed death ligand‐1 and vascular endothelial growth factor A, thereby promoting HCC immune evasion and angiogenesis. Targeting YTHDF2 via small interference RNA‐containing aptamer/liposomes successfully both inhibited HCC immune evasion and angiogenesis. Together, this findings reveal the potential application of YTHDF2 in HCC prognosis and targeted treatment. [ABSTRACT FROM AUTHOR]

Background: Disrupted protein homeostasis (proteostasis) has been demonstrated to facilitate the progression of various diseases. The cytosolic T‐complex protein‐1 ring complex (TRiC/CCT) was discovered to be a critical player in orchestrating proteostasis by folding eukaryotic proteins, guiding intracellular localisation and suppressing protein aggregation. Intensive investigations of TRiC/CCT in different fields have improved the understanding of its role and molecular mechanism in multiple physiological and pathological processes. Main body: In this review, we embark on a journey through the dynamic protein folding cycle of TRiC/CCT, unraveling the intricate mechanisms of its substrate selection, recognition, and intriguing folding and assembly processes. In addition to discussing the critical role of TRiC/CCT in maintaining proteostasis, we detail its involvement in cell cycle regulation, apoptosis, autophagy, metabolic control, adaptive immunity and signal transduction processes. Furthermore, we meticulously catalogue a compendium of TRiC‐associated diseases, such as neuropathies, cardiovascular diseases and various malignancies. Specifically, we report the roles and molecular mechanisms of TRiC/CCT in regulating cancer formation and progression. Finally, we discuss unresolved issues in TRiC/CCT research, highlighting the efforts required for translation to clinical applications, such as diagnosis and treatment. Conclusion: This review aims to provide a comprehensive view of TRiC/CCT for researchers to inspire further investigations and explorations of potential translational possibilities. [ABSTRACT FROM AUTHOR]

BRAF V600E attracts wide attention in the treatment of colorectal cancer (CRC) as stratifying and predicting a refractory classification of CRC. Recent evidence indicates that Wnt/β‐catenin signaling is broadly activated and participates in the refractoriness of BRAF V600E CRC, but the underlying molecular mechanism needs to be elucidated. Here, heat shock 70 kDa protein 8 (HSPA8), an essential regulator in chaperone‐mediated autophagy (CMA), is identified as a potential therapeutic target for advanced BRAF V600E CRC. These results show that HSPA8 is transcriptionally upregulated in BRAF V600E CRC, which promotes CMA‐dependent degradation of caveolin‐1 (CAV1) to release β‐catenin into the nucleus and thus activates the Wnt/β‐catenin pathway, contributing to metastasis and progression of BRAF V600E CRC. Of note, HSPA8 directly interacts with the KIFSN motif on CAV1, the interaction can be enhanced by p38 MAPK‐mediated CAV1 S168 phosphorylation. Furthermore, pharmacological targeting HSPA8 by VER155008 exhibits synergistic effects with BRAF inhibitors on CRC mouse models. In summary, these findings discover the important role of the HSPA8/CAV1/β‐catenin axis in the development of refractory BRAF V600E CRC and highlight HSPA8 as a predictive biomarker and therapeutic target in clinical practice. [ABSTRACT FROM AUTHOR]

In this letter, a novel true random number generator (TRNG) with high energy‐efficient and throughput is proposed for cryptographic systems. The current starve based ring oscillator (CSRO) is biased in the subthrehold region as an entropy source. An individual ring oscillator (RO) is sampled using multiple sampling points of the CSRO working in the sub‐threshold region to obtain a multi‐channel sequence output, thereby fully exploiting the randomness of the entropy source. The proposed TRNG is implemented using a standard 40nm CMOS technology and the simulation results show that it provides high‐quality and 20.66 Mbps random sequences while only consuming 11.46 μW at 1.1 V, 25°C. In addition, the proposed TRNG passes the NIST SP 800‐22 and the NIST SP 800‐90B tests without post‐processing and outperforms the state‐of‐the‐art in terms of energy consumption per bit of the output bitstream, reaching 0.555pJ/bit. [ABSTRACT FROM AUTHOR]

Respiratory tract infections are associated with the most common diseases transmitted among people and remain a huge threat to global public health. Rapid and sensitive diagnosis of causative agents is critical for timely treatment and disease control. Here, we developed a novel method based on recombinase polymerase amplification (RPA) combined with CRISPR‐Cas12a to detect three viral pathogens, including SARS‐CoV‐2, influenza A, and influenza B, which cause similar symptom complexes of flu cold in the respiratory tract. The detection method can be completed within 1 h, which is faster than other standard detection methods, and the limit of detection is approximately 102 copies/μL. Additionally, this detection system is highly specific and there is no cross‐reactivity with other common respiratory tract pathogens. Based on this assay, we further developed a more simplified RPA/CRISPR‐Cas12a system combined with lateral flow assay on a manual microfluidic chip, which can simultaneously detect these three viruses. This low‐cost detection system is rapid and sensitive, which could be applied in the field and resource‐limited areas without bulky and expensive instruments, providing powerful tools for the point‐of‐care diagnostic. [ABSTRACT FROM AUTHOR]

To achieve high charge density for the triboelectric polymer is a crucial task for fabricating triboelectric nanogenerators (TENGs). This work has developed a quenching polarization (QP) method to create ultrahigh and long‐persistent triboelectric charge on the triboelectric polymer with weak dipole polarity. The Ethylene chlorotrifluoroethylene copolymer (ECTFE) film can reach a charge density of 391 µC m−2 in the vertical contact mode by using this QP treatment, which is 200% higher than the result achieved by the most widely used method of corona polarization. The mechanism of the improvement through QP on the triboelectric properties is studied on the basis of the polarization induced grain refinement and interfacial trapping. The QP‐treated ECTFE can maintain ultra‐high charge density for both solid‐solid and solid‐liquid TENG. More interestingly, the charge induced by QP treatment is so persistent that it produces a recoverable discharging phenomenon for solid‐liquid TENG, which has never been observed before. This QP method provides a different approach for fabricating high‐performance triboelectric materials, while the QP‐induced changes in crystallization and tribo‐charge density can help to complete the physical understanding of the electrification mechanism of triboelectric polymer. [ABSTRACT FROM AUTHOR]

Bone is the second leading metastatic site for hepatocellular carcinoma (HCC). Patients with HCC and bone metastasis suffer poor quality of life and reduced survival time. Extracellular vesicles (EVs) are widely involved in HCC formation and metastasis. However, the communication between primary HCC and bone lesions mediated by EVs remains unclear and the possible effect of bone metastasis on the progression of HCC remains largely unknown. Here, bone‐metastasized HCC‐derived EVs (BM‐EVs) are found to localize to orthotropic HCC cells and promote HCC progression. Mechanistically, miR‐3190‐5p (miR‐3190) is upregulated in intracellular HCC cells isolated from bone lesions as well as in their derived EVs. miR‐3190 in BM‐EVs is transferred into orthotopic tumor cells and enhances their metastatic capacity by downregulating AlkB homolog 5 (ALKBH5) expression. Decreased level of ALKBH5 exacerbates the prometastatic characteristics of HCC by modulating gene expression in N6‐methyladenosine‐dependent and ‐independent ways. Finally, antagomir‐miR‐3190‐loaded liposomes with HCC affinity successfully suppress HCC progression in mice treated with BM‐EVs. These findings reveal that BM‐EVs initiate prometastatic cascades in orthotopic HCC by transferring ALKBH5‐targeting miR‐3190 and miR‐3190 is serving as a promising therapeutic target for inhibiting the progression of HCC in patients with bone metastasis. [ABSTRACT FROM AUTHOR]

Conductive polymer composites with segregated structure (s‐CPCs) are widely used in the electronics industry. Achieving selective distribution of the conductive fillers in the polymer matrix is an effective way to construct s‐CPCs. In this work, the starch was used as the matrix and the carbon nanotube (CNT) was used as the conductive fillers to fabricate multifunctional s‐CPCs, via simple mechanical mixing and compression molding. During the processing, the starch underwent partial gelatinization, which was conducive to the fusion of the starch granules and the selective distribution of the CNT. Scanning electron microscope and atomic force microscope images showed that the CNT was attached to the surface of the starch granules to form a segregated structure. The starch/CNT composites exhibited a significant percolation, with a percolation threshold of 0.24 vol%. When the CNT content was 3.05 vol%, the starch/CNT composites exhibited a high electromagnetic interference (EMI) shielding effectiveness of 33.12 dB, which was commercially applicable in EMI shielding devices. The starch/CNT composites also possess good thermal management properties and can be used as thermal conductors and electro‐thermal conversion devices. This work manifests the application prospect in the field of the electronics industry and broadens the application potential of starch. [ABSTRACT FROM AUTHOR]

Acute compartment syndrome (ACS) is a life‐threatening orthopedic emergency, which can even result in amputation. Ferroptosis is an iron‐dependent form of nonapoptotic cell death. This study investigated the mechanism of ferroptosis in ACS, explored candidate markers, and determined effective treatments. This study identified pathways involved in the development of ACS through gene set enrichment analysis (GSEA), Gene Ontology, Kyoto Encyclopedia of Genes and Genomes (KEGG), and GSEA of heme oxygenase 1 (Hmox1). Bioinformatics methods, combined with real‐time quantitative polymerase chain reaction, western blot analysis, and iron staining, were applied to determine whether ferroptosis was involved in the progression of ACS and to explore the mechanism of nuclear factor erythroid‐2‐related factor 2 (Nfe2l2)/Hmox1 in ferroptosis regulation. Optimal drugs for the treatment of ACS were also investigated using Connectivity Map. The ferroptosis pathway was enriched in GSEA, KEGG of DEGs, and GSEA of Hmox1. After ACS, the reactive oxygen species content, tissue iron content, and oxidative stress level increased, whereas glutathione peroxidase 4 protein expression decreased. The skeletal muscle was swollen and necrotized; the number of mitochondrial cristae became fewer or even disappeared, and Nfe2l2/Hmox1 expression increased at the transcriptional and protein levels. Hmox1 was highly expressed in ACS, indicating that Hmox1 is a possible marker for ACS. we could predict 12 potential target drugs for the treatment of ACS. In conclusion, Hmox1 was a potential candidate marker for ACS diagnosis. Ferroptosis was involved in the progression of ACS. It was speculated that ferroptosis is inhibited by the Nfe2l2/Hmox1 signaling pathway. [ABSTRACT FROM AUTHOR]

Metformin, a well‐known antidiabetic drug, has been repurposed for cancer treatment; however, recently observed drug resistance and tumor metastasis have questioned its further application. Here, we found that long‐term metformin exposure led to metabolic adaptation of hepatocellular carcinoma (HCC) cells, which was characterized by an obvious epithelial–mesenchymal transition (EMT) phenotype and compensatory elevation of oxidative phosphorylation (OXPHOS). TOMM34, a translocase of the outer mitochondrial membrane, was upregulated to promote tumor metastasis in response to metformin‐induced metabolic stress. Mechanistically, TOMM34 interacted with ATP5B to preserve F1FO‐ATPase activity, which conferred mitochondrial OXPHOS and ATP production. This metabolic preference for OXPHOS suggested a large requirement of energy supply by cancer cells to survive and spread in response to therapeutic stress. Notably, disturbing the interaction between TOMM34 and ATP5B using Gboxin, a specific OXPHOS inhibitor, increased sensitivity to metformin and suppressed tumor progression both in vitro and in vivo. Overall, this study demonstrates a molecular link of the TOMM34/ATP5B‐ATP synthesis axis during metformin adaptation and provides promising therapeutic targets for metformin sensitization in cancer treatment. Synopsis: Adaptation to metformin is frequently observed during long‐term tumor treatment. Here, during this adaptation process, TOMM34 was upregulated to enhance OXPHOS by interacting with ATP5B. Disruption of the TOMM34‐ATP5B interaction using Gboxin synergized with metformin to suppress HCC. HCC cells exhibited an EMT phenotype and a compensatory elevation of respiration rate during metformin adaptation.TOMM34 upregulation preserved OXPHOS and ATP production during metformin adaptation.TOMM34 interacted with ATP5B to maintain OXPHOS and ATP production.Gboxin disrupted TOMM34/ATP5B interaction and prevented metformin adaptation. [ABSTRACT FROM AUTHOR]

(S)‐equol, the most active metabolite of the soybean isoflavones in vivo, has exhibited various biological activities and clinical benefits. Existing studies on the heterologous biosynthesis of (S)‐equol via the engineered E. coli constructed have been significantly progressed. In the present study, the engineered E. coli was further improved to be more suitable for (S)‐equol production. The four enzymes involved in the biosynthesis of (S)‐equol and another GDH for NADPH regeneration were combined to construct the recombinant E. coli BL21(DE3). The optimal conditions for (S)‐equol production were explored, respectively. The yield of equol reached 98.05% with 1 mM substrate daidzein and 4% (wt/vol) glucose. Even when the substrate concentration increased to 1.5 mM, (S)‐equol could maintain a high yield of 90.25%. Based on the 100 ml one‐pot reaction system, (S)‐equol was produced with 223.6 mg/L in 1.5 h. The study presented a more suitable engineered E. coli for the production of (S)‐equol. [ABSTRACT FROM AUTHOR]

Epithelial–mesenchymal transition (EMT) is a program wherein epithelial cells lose their junctions and polarity while acquiring mesenchymal properties and invasive ability. Originally defined as an embryogenesis event, EMT has been recognized as a crucial process in tumor progression. During EMT, cell–cell junctions and cell–matrix attachments are disrupted, and the cytoskeleton is remodeled to enhance mobility of cells. This transition of phenotype is largely driven by a group of key transcription factors, typically Snail, Twist, and ZEB, through epigenetic repression of epithelial markers, transcriptional activation of matrix metalloproteinases, and reorganization of cytoskeleton. Mechanistically, EMT is orchestrated by multiple pathways, especially those involved in embryogenesis such as TGFβ, Wnt, Hedgehog, and Hippo, suggesting EMT as an intrinsic link between embryonic development and cancer progression. In addition, redox signaling has also emerged as critical EMT modulator. EMT confers cancer cells with increased metastatic potential and drug resistant capacity, which accounts for tumor recurrence in most clinic cases. Thus, targeting EMT can be a therapeutic option providing a chance of cure for cancer patients. Here, we introduce a brief history of EMT and summarize recent advances in understanding EMT mechanisms, as well as highlighting the therapeutic opportunities by targeting EMT in cancer treatment. [ABSTRACT FROM AUTHOR]

As an ordinary alteration mineral in the process of fluid–rock interaction, chlorite (most especially its chemical composition) has the potential to become an effective tool to reveal the physicochemical conditions during alteration and help exploration. However, its elemental characteristics during the chloritization process are yet to be clearly understood. The Dehua‐Youxi‐Yongtai (DYY) ore district in south‐east China is one of the potential areas of gold and polymetallic deposits. Lying in the north‐west section of the DYY ore district, the Donghua area is notable for its remarkable metallogenic potential, and porphyry‐epithermal systems might have developed in the area. This study focuses on the elemental characteristics of chlorite in the Donghua area as footprints of the alteration process and mineralization vectoring. According to the geological features and occurrences, the chlorite from Donghua can be divided into two generations: (a) Chlorite I is closely related to chloritization developed in intrusive and volcanic rocks (Permian quartz monzobiorite and Jurassic volcanic rocks of Changlin Formation), and (b) chlorite II is accompanied by superimposed hydrothermal overprinting. The alteration process suggested by overprinting chlorite II can be regarded as almost coeval with the ca. 154–153 Ma magmatic event, and chlorite II is later than chlorite I generation. According to the geothermometry of the chlorite in Donghua, chlorite I might have crystallized on the temperature of 180–240°C with a peak of ~200°C, and the overprinting chlorite II might have experienced two episodes of hydrothermal/epithermal fluid pulsing. The mineral geochemistry of the trace elements in the two generations of the chlorite in Donghua shows different characteristics. The replacement of Mg2+ by Fe2+ plays an important role for ionic substitution in the octahedral position, especially for chlorite II. The other occasion might be Mg and Fe jointly entering the octahedral position as well as Mg‐ and Fe‐AlVI substitution mechanisms. The enrichment of Mg especially in chlorite II suggests low‐grade oxidation and acid conditions, which might be beneficial for the transportation of metallogenic substances. The obvious differences of Co and Ni are remarkable aspects of the trace elements of chlorite in Donghua, resulted by the ion substitution and function of different octahedral site preference energy. The mineral chemistry of chlorite II from Donghua can be helpful for targeting and exploration vectoring in the DYY ore district. [ABSTRACT FROM AUTHOR]

Cancer cells reprogram their copper metabolism to adapt to adverse microenvironments, such as oxidative stress. The copper chelator elesclomol has been reported to have considerable anticancer efficacy, but the underlying mechanisms remain largely unknown. In this study, we found that elesclomol‐mediated copper overload inhibits colorectal cancer (CRC) both in vitro and in vivo. Elesclomol alone promotes the degradation of the copper transporter copper‐transporting ATPase 1 (ATP7A), which retards the proliferation of CRC cells. This property distinguishes it from several other copper chelators. Combinational treatment of elesclomol and copper leads to copper retention within mitochondria due to ATP7A loss, leading to reactive oxygen species accumulation, which in turn promotes the degradation of SLC7A11, thus further enhancing oxidative stress and consequent ferroptosis in CRC cells. This effect accounts for the robust antitumour activity of elesclomol against CRC, which can be reversed by the administration of antioxidants and ferroptosis inhibitors, as well as the overexpression of ATP7A. In summary, our findings indicate that elesclomol‐induced copper chelation inhibits CRC by targeting ATP7A and regulating ferroptosis. [ABSTRACT FROM AUTHOR]

Three‐dimensional graphene materials have greatly expanded the market space of graphene, but their economical fabrication remains a challenge. Herein, we report a facile and low‐cost method for the preparation of high‐performance graphene hydrogels by adding ammonium‐modified graphene oxide into low‐dielectric constant organic solvents. By forming ammonium salts or through a re‐protonation process, the graphene sheets are assembled together by electrostatic attraction or hydrogen bonding interactions, along with π‐π interactions. The unique structure‐aligned few‐layer graphene sheets, abundant surface functional groups and multifarious pores‐enables prepared hydrogels with both superior charge storage capability (207.6 F g−1 at 1 A g−1) and excellent high‐rate performance (83.2 % capacitance retention when the discharge current density is increased from 0.5 to 10 A g−1). In this study, we present some achievements in capacitive energy storage but, while they are encouraging, graphene‐based materials prepared by this feasible and efficient route can also be applied to other advanced applications likenew‐generation rechargeable batteries, sensors, biomedical engineering, and water purification. [ABSTRACT FROM AUTHOR]

In this paper, a novel E‐plane waveguide bandpass filter with multiple transmission zeros is proposed in W‐band. The center frequency and bandwidth of this filter can be flexibly designed. Stripe line resonators and L‐shaped resonators are used in the filter. The filter contains four resonators, two of which are used to generate transmission zeros in the upper stopband, and the other two are used to generate transmission zeros in the lower stopband. These transmission zeros can enhance the out‐of‐band suppression and selectivity of the filter. And the position of the transmission zeroes can be flexibly changed as required. One sample is fabricated and measured to verify the proposed filter. The minimum insertion loss in passband is 0.6 dB. Good agreements between the simulated and measured results are achieved. [ABSTRACT FROM AUTHOR]

The electric and dielectric properties of Na0.5Bi4.50+xTi4Oy (x = −0.02, 0, 0.02) prepared by conventional mixed oxide route have been investigated by impedance spectroscopy (IS) over a wide temperature range. Single‐phase bismuth layer‐structured perovskite patterns were observed through X‐ray diffraction of the three samples Na0.5Bi4.5Ti4O15, Na0.5Bi4.48Ti4Oy, and Na0.5Bi4.52Ti4Oy. The results show that the relative permittivity (εr) increases with the increase in temperature and reaches its maximum at about 675℃. With the continuous increase in temperature, the permittivity decreases gradually. Both relative permittivity and dielectric loss show great stability at the low‐temperature zone. The ceramic of x = 0.02 with Ea of 1.09 eV has the maximum oxygen ionic transport number between 600 and 800℃ for all samples. And at this time, it has the maximum electrical conductivity. All the results indicated that Na0.5Bi4.50+xTi4Oy (x = −0.02, 0, 0.02) ceramics were promising base materials for high‐temperature capacitor because of their high dielectric properties. [ABSTRACT FROM AUTHOR]

Small nucleolar RNA (snoRNA) plays important role in various histogenesis. Whether snoRNA plays a role in adipogenesis is unknown. SNORD126 is a C/D box snoRNA. We previously demonstrated that SNORD126 promoted hepatocellular carcinoma cell growth by activating the phosphoinositide 3‐kinase–protein kinase B (Akt) pathway through upregulating fibroblast growth factor receptor 2 expression. In the present study, we found that the expression of SNORD126 was downregulated in the obesity‐related tissues in high‐fat diet‐fed rats. Overexpression of SNORD126 in 3T3‐L1 cells promoted adipocytes differentiation. SNORD126 significantly increased the expression of CCAAT/enhancer‐binding protein α, fatty acid‐binding protein 4, peroxisome proliferative‐activated receptor‐γ, and the phosphorylation of Akt and p70S6K. Overexpression of SNORD126 in human adipose‐derived stem cells stimulated adipogenesis and increased phosphorylation of Akt. Meanwhile, SNORD126 increased the messenger RNA and protein levels of cyclin D1 and cyclin‐dependent kinase 2, which promoted mitotic clonal expansion progression during the early stage of 3T3‐L1 cell differentiation. We further found that SNORD126 accelerated the growth of the groin fat pad and increased phosphorylation of Akt and p70S6K in rats. Overall, our results suggested that SNORD126 promoted adipocyte differentiation through increasing phosphorylation of Akt and p70S6K both in vitro and in vivo. [ABSTRACT FROM AUTHOR]

Myocardial ischemia/reperfusion (I/R) injury greatly contributes to myocardial tissue damage in patients with coronary disease, which eventually leads to heart failure. Long noncoding RNAs (lncRNAs) have an emerging role in the process of myocardial I/R injury. Our previous work revealed the protective role of miR‐374a‐5p against myocardial I/R injury. In this study, we explored the role of lncRNA TTTY15 and its potential interaction mechanisms with miR‐374a‐5p in myocardial I/R injury. The expression of TTTY15 was increased both in vitro and in vivo after myocardial I/R injury models according to quantitative real‐time polymerase chain reaction. Various assays were conducted to evaluate the regulatory relationship among TTTY15, miR‐374a‐5p, FOXO1, and autophagy in H9c2 and HL‐1 cells. The results showed that TTTY15 suppresses autophagy and myocardial I/R injury by targeting miR‐374a‐5p. We found that TTTY15 regulates miR‐374a‐5p, thus affecting FOXO1 expression and autophagy in myocytes during I/R. Furthermore, in an in vivo mouse model of myocardial I/R injury, suppression of TTTY15 successfully alleviated myocardial I/R injury. Our results reveal a novel feedback mechanism in which TTTY15 regulates miRNA processing and a potential target in myocardial I/R injury. TTTY15 is a promising therapeutic target for treating myocardial I/R injury. [ABSTRACT FROM AUTHOR]

Morphology control of polymer alloys is an attractive topic for investigators due to its ability to improve the performance of products for years. However, it is hard to control the morphology of immiscible polymer blends during melt processing. Herein, we studied the morphology evolution of poly(lactic acid) (PLA)/poly(butylene succinate) (PBS) with the inclusion of ethylene‐methyl acrylate‐glycidyl methacrylate (EGMA). Scanning electron microscopy of both cryo‐fractured and etched cryo‐fractured samples indicates that the in situ reaction among PLA, PBS, and EGMA can induce the morphology change and result in a novel 3D star‐like structure. Rheology behaviors of the samples under different angular frequencies were used to validate the formation of 3D networks in the samples. Tensile stiffness reinforcements at both room temperature and high temperature were provided through dynamic mechanical analysis. In addition, a 10‐fold improvement in impact strength is also monitored by the unnotched impact test to indicate the superior toughening effect. Furthermore, the crystalline behavior and thermal properties of the blends were also studied. It is believed that our work not only gives a deeper understanding of the reaction‐induced morphology evolution of the PLA/PBS/EGMA blends but also reveals an avenue toward morphology control by melt processing. [ABSTRACT FROM AUTHOR]

It remains a challenge to rational design of a new metal–organic framework (MOF) as highly efficient direct electrocatalysts for the oxygen evolution reaction (OER). Herein, we developed a simple and effective method to explore a new pillared‐layered MOF with syringic acid as a promising OER electrocatalyst. The isostructural mono‐, heterobimetallic MOF and N,S co‐doped MOF by mixing thiourea were quickly synthesized in a high yield under solvothermal condition. Moreover, the optimized N,S co‐doped MOF exhibits the lowest overpotential of 254 mV at 10 mA cm−2 on a glass carbon electrode and a small Tafel slope of 50 mV dec−1, especially, this catalyst also possesses long‐term electrochemical durability for at least 16 h. According to the characterization, the incorporation of N and S atoms into this heterobimetallic CoFe‐based MOF could modify its pore structure, tune the electronic structure, accordingly, improve the mass and electron transportation, and facilitate the formation of active species, as a consequence, the improved activity of this new N,S co‐doped MOF for OER should be mainly be ascribed to higher electrochemical activation toward the active species via in situ surface modification during the OER process. [ABSTRACT FROM AUTHOR]

The tree shrew (Tupaia belangeri chinensis) is the closest living relative of primates. Yet, little is known about the anatomical distribution of tyrosine hydroxylase (TH)‐immunoreactive (ir) structures in the hypothalamus of the tree shrew. Here, we provide the first detailed description of the distribution of TH‐ir neurons in the hypothalamus of tree shrews via immunohistochemical techniques. TH‐ir neurons were widely distributed throughout the hypothalamus of tree shrew. The majority of hypothalamic TH‐ir neurons were found in the paraventricular hypothalamic nucleus (PVN) and supraoptic nucleus (SON), as was also observed in the human hypothalamus. In contrast, rare TH‐ir neurons were localized in the PVN and SON of rats. Vasopressin (AVP) colocalized with TH‐ir neurons in the PVN and SON in a large number of neurons, but oxytocin and corticotropin‐releasing hormone did not colocalize with TH. In addition, colocalization of TH with AVP was also observed in the other hypothalamic regions. Moreover, TH‐ir neurons in the PVN and SON of tree shrews expressed other dopaminergic markers (aromatic l‐amino acid decarboxylase and vesicular monoamine transporter, Type 2), further supporting that TH‐ir neurons in the PVN and SON were catecholaminergic. These findings provide a detailed description of TH‐ir neurons in the hypothalamus of tree shrews and demonstrate species differences in the distribution of this enzyme, providing a neurobiological basis for the participation of TH‐ir neurons in the regulation of various hypothalamic functions. [ABSTRACT FROM AUTHOR]

This study evaluated the interaction of Chrysanthemum indicum (CI) flavonoids (luteolin, acacetin, and buddleoside) with α‐amylase. Surface plasmon resonance (SPR) assay showed their equilibrium dissociation constants (KD) are 1.9695 ± 0.12, 2.9240 ± 0.20, and 3.2966 ± 0.08 mM at pH 6.0, respectively. Furthermore, their binding affinities were influenced by KCl, MgCl2, and CaCl2. Enzymatic kinetic studies revealed that three flavonoids exhibited noncompetitive α‐amylase inhibitory activity. The inhibitory sequence is luteolin > acacetin > buddleoside, which was in accordance with the results of binding affinity from SPR. 1,1‐diphenyl‐2‐picryl hydrazyl radical assay demonstrated that antioxidant activities of three flavonoids were inhibited significantly with α‐amylase. Meanwhile, the study reveals that hydroxyl on C′‐4, C′‐5, and C‐7 of flavonoids play an important role on the interaction of three flavonoids with α‐amylase. Also, SPR could be used as sensor for rapid screening inhibitors of α‐amylase and provide useful information for the application of C. indicum flavonoids in food and pharmaceutical area. [ABSTRACT FROM AUTHOR]

Formononetin is a natural isoflavone compound found mainly in Chinese herbal medicines such as astragalus and red clover. It is considered to be a typical phytooestrogen. In our previous experiments, it was found that formononetin has a two‐way regulatory effect on endothelial cells (ECs): low concentrations promote the proliferation of ECs and high concentrations have an inhibitory effect. To find a specific mechanism of action and provide a better clinical effect, we performed a structural transformation of formononetin and selected better medicinal properties for formononetin modifier J1 and J2 from a variety of modified constructs. The MTT assay measured the effects of drugs on human umbilical vein endothelial cell (HUVEC) activity. Scratch and transwell experiments validated the effects of the drugs on HUVEC migration and invasion. An in vivo assessment effect of the drugs on ovariectomized rats. Long‐chain non‐coding RNA for EWSAT1, which is abnormally highly expressed in HUVEC, was screened by gene chip, and the effect of the drug on its expression was detected by PCR after the drug was applied. The downstream factors and their pathways were analysed, and the changes in the protein levels after drug treatment were evaluated by Western blot. In conclusion, the mechanism of action of formononetin, J1 and J2 on ECs may be through EWSAT1‐TRAF6 and its downstream pathways. [ABSTRACT FROM AUTHOR]

As the direct entrapment of camptothecin (CPT) into conventionally used polymeric materials is extremely difficult due to its high crystallization property, CPT‐derived prodrugs are widely used to increase drug‐polymer compatibility. However, the rapid CPT conversion from prodrugs is still a challenge due to the high steric hindrance around the hydroxyl of CPT. To address this, we reported here a fragile lactyl carbonate (LC) linker, which could be instantly cleaved to release CPT from LC‐linked lipophilic prodrugs under physiological conditions. Furthermore, such instantly‐cleaved CPT prodrugs could be stably encapsulated in methoxy poly(ethylene glycol)‐block‐poly(actic acid) (mPEG‐PLA) micelles, thus to achieve indirect CPT entrapment with a potent in vitro cytotoxicity as a result of the rapid CPT conversion. The strategy of entrapping instantly‐cleaved prodrugs in polymeric micelles displayed an excellent potential to broaden the scope of application of polymeric materials in drug delivery. [ABSTRACT FROM AUTHOR]

The cerebellum is involved in the control of movement, emotional responses, and reward processing. The tree shrew is the closest living relative of primates. However, little is known not only about the systematic nomenclature for the tree shrew cerebellum but also about the detailed neurochemical characterization and afferent projections. In this study, Nissl staining and acetylcholinesterase histochemistry were used to reveal anatomical features of the cerebellum of tree shrews (Tupaia belangeri chinensis). The cerebellar cortex presented a laminar structure. The morphological characteristics of the cerebellum were comprehensively described in the coronal, sagittal, and horizontal sections. Moreover, distributive maps of calbindin‐immunoreactive (‐ir) cells in the Purkinje cell layer of the cerebellum of tree shrews were depicted using coronal, sagittal, and horizontal schematics. In addition, 5th cerebellar lobule (5Cb)‐projecting neurons were present in the pontine nuclei, reticular nucleus, spinal vestibular nucleus, ventral spinocerebellar tract, and inferior olive of the tree shrew brain. The anterior part of the paramedian lobule of the cerebellum (PMa) received mainly strong innervation from the lateral reticular nucleus, inferior olive, pontine reticular nucleus, spinal trigeminal nucleus, pontine nuclei, and reticulotegmental nucleus of the pons. The present results provide the first systematic nomenclature, detailed atlas of the whole cerebellum, and whole‐brain mapping of afferent projections to the 5Cb and PMa in tree shrews. Our findings provide morphological support for tree shrews as an alternative model for studies of human cerebellar pathologies. Here we provided acetylcholinesterase‐stained section showing the cerebellar subregions in tree shrews. Schematic drawings showing the morphological characteristics of the cerebellum in the sagittal plane. [ABSTRACT FROM AUTHOR]

ABSTRACT: In this study, various poly(ethylene terephthalate) (PET) and linear low‐density polyethylene (LLDPE) with maleic anhydride‐grafted LLDPE (LLDPE‐g‐MAH) compatibilizer were melt blended under an elongational flow. A novel extrusion device, eccentric rotor extruder (ERE), was developed to supply such flow during the process. Including morphology, mechanical properties, melting behavior, and rheological behavior were studied. The morphological study showed that the compatibility between LLDPE and PET was greatly improved with LLDPE loading up to 80 wt %. Mechanical tests indicated that LLDPE could toughen PET to some extent. Moreover, a comparison of samples prepared between ERE and conventional extruder was made and demonstrated the sample prepared by ERE can exhibit better mechanical properties. Differential scanning calorimetry results revealed that PET can promote the crystallinity of LLDPE. Rheological behavior indicated that the complex viscosity of the blends exhibited strong shear thinning phenomenon with increasing LLDPE content, particularly in high‐frequency range blend with the LLDPE weight ratio of 80 wt % was more sensitivity to shear rate than neat LLDPE. The G′‐G″ curves of the blends also revealed that the microstructure of the blends changed significantly with the addition of LLDPE which was consistent with the scanning electron micrographs that PET particles became smaller and distributed more uniform with increasing LLDPE content. Furthermore, the blends showed similar stress relaxation mechanism with adding LLDPE content from 60 to 100 wt %. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018, 135, 46489. [ABSTRACT FROM AUTHOR]

We report the isolation of a novel diterpene, designated as `amethane', from Isodon amethystoides (Lamiaceae). The diterpene [amethinol A; systematic name: (4aR,4bR,7R,10aS)‐4b,7‐dihydroxy‐7‐isopropyl‐1,1‐dimethyl‐9‐oxododecahydrobenzo[a]azulene‐4a(2H)‐carboxylic acid], possesses a unique skeleton containing a six/five/seven‐membered tricyclic system. Intermolecular O—H…O close contacts were found to the carboxyl, carbonyl and hydroxy groups, connecting molecules into a two‐dimensional structure. A possible biosynthetic pathway has been proposed. In addition, the compound was evaluated for its biological activities against different disease targets, and was found to significantly attenuate RORγt‐dependent autoimmune responses. [ABSTRACT FROM AUTHOR]

Development of chemoresistance, which limits the efficiency of anticancer agents, has long been a major problem in cancer therapy and urgently needs to be solved to improve clinical outcomes. Factors contributing to chemoresistance are various, but a key factor is the cell's capability for stress management. Autophagy, a favored survival strategy that organisms employ to get over many kinds of stress, is emerging as a crucial player in drug resistance. It has been shown that autophagy facilitates the resistance of tumor cells to anticancer agents, and abrogation of autophagy could be therapeutically beneficial in some cases, suggesting autophagy could be a promising target for cancer treatments. Thus, defining the roles of autophagy in chemoresistance, and the mechanisms involved, will be critical to enhance the efficiency of chemotherapy and develop novel anticancer strategy interventions. [ABSTRACT FROM AUTHOR]

A one-pot method for the fast synthesis of a 3D nanochain network (NNC) of PdCu alloy without any surfactants is described. The composition of the as-prepared PdCu alloy catalysts can be precisely controlled by changing the precursor ratio of Pd to Cu. First, the Cu content changes the electronic structure of Pd in the 3D NNC of PdCu alloy. Second, the 3D network structure offers large open pores, high surface areas, and self-supported properties. Third, the surfactant-free strategy results in a relatively clean surface. These factors all contribute to better electrocatalytic activity and durability towards ethanol oxidation. Moreover, the use of copper in the alloy lowers the price of the catalyst by replacing the noble metal palladium with non-noble metal copper. The composition-optimized Pd80Cu20 alloy in the 3D NNC catalyst shows an increased electrochemically active surface area (80.95 m2 g−1) and a 3.62-fold enhancement of mass activity (6.16 A mg−1) over a commercial Pd/C catalyst. [ABSTRACT FROM AUTHOR]

ABSTRACT A novel mixer-vane mixer which is based on elongation flow was used to prepare high-density polyethylene (HDPE)/montmorillonite (MMT) nanocomposites without any additives. The effect of elongation flow on MMT intercalating in HDPE matrix was studied in terms of rotor speed and mixing time. X-ray diffraction and transmission electron microscope analyses showed that exfoliated and intercalated nanostructures were obtained when the rotor speed was 40 and 50 rpm, and mixing time was 6 minutes. For all samples prepared by vane mixer, MMT layers showed fine intercalation in the nanocomposites. Differential scanning calorimetry and thermogravimetric analysis were used to study the thermal properties of the nanocomposites. The results showed that the addition of MMT can improve the crystallization of the HDPE. Tensile test revealed the relationships between the mechanical properties and process parameters. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 42600. [ABSTRACT FROM AUTHOR]

An intermediate-template-directed method has been developed for the synthesis of quasi-one-dimensional Au/PtAu heterojunction nanotubes by the heterogeneous nucleation and growth of Au on Te/Pt core-shell nanostructures in aqueous solution. The synthesized porous Au/PtAu bimetallic nanotubes (PABNTs) consist of porous tubular framework and attached Au nanoparticles (AuNPs). The reaction intermediates played an important role in the preparation, which fabricated the framework and provided a localized reducing agent for the reduction of the Au and Pt precursors. The Pt7Au PABNTs showed higher electrocatalytic activity and durability in the oxygen-reduction reaction (ORR) in 0.1 M HClO4 than porous Pt nanotubes (PtNTs) and commercially available Pt/C. The mass activity of PABNTs was 218 % that of commercial Pt/C after an accelerated durability test. This study demonstrates the potential of PABNTs as highly efficient electrocatalysts. In addition, this method provides a facile strategy for the synthesis of desirable hetero-nanostructures with controlled size and shape by utilizing an intermediate template. [ABSTRACT FROM AUTHOR]

Proteins implement most of the vital molecular functions of living organisms, including structural support, energy generation, biomolecule sensing, and chemical catalysis, storage, and degradation. While capturing proteins in materials could create devices that mimic these functions, this process is challenging due to the sensitivity of protein structure to the chemical environment. Using recombinant DNA methods, specific functions can be incorporated by fusing the gene encoding a self-assembling protein and the desired functional protein, to produce a single polypeptide that self-assembles into functionalized materials. However, the functional protein has the potential to disrupt protein production, protein assembly, and/or the structure and mechanical properties of the resulting materials. 24 fusion proteins are created based on Ultrabithorax, a Drosophila transcription factor that self-assembles into materials in vitro. The appended proteins dictate the solubility and purification yield of the corresponding protein fusions. Any loss of solubility and yield can be mitigated by fusing a third protein that is highly soluble. All protein fusions self-assemble equally well to produce materials with similar morphologies. Fusing enhanced green fluorescent protein to Ultrabithorax influences mechanical properties of the resulting fibers. It is concluded that a far wider range of proteins can be successfully incorporated into elastomeric protein-based materials than originally anticipated. [ABSTRACT FROM AUTHOR]

NaSr2Nb5O15 piezoelectric ceramics were sintered at different temperatures with or without atmospheric powder. The effects of atmospheric powder and sintering temperature on the dielectric, piezoelectric, and ferroelectric properties of the ceramics were analyzed. According to the modified Curie-Weiss law, we know that all these ceramics show an intermediate relaxor-like behavior between the normal and ideal relaxor ferroelectrics. Atmospheric powder affects significantly the properties of ceramics because the ceramics sintered without atmospheric powder lose lots of sodium. Furthermore, sintering temperature also significantly affects the properties of ceramics because the relative density of ceramics is enhanced when sintering temperature is increased. [ABSTRACT FROM AUTHOR]

The aim of this study was to investigate the effect of neutral microporous resin hemoperfusion on oxygenation improvement, removal of inflammatory cytokines in plasma and bronchoalveolar lavage, and mortality in acute lung injury induced by extrapulmonary sepsis. Forty-six patients with acute lung injury induced by extrapulmonary sepsis were randomized to HA type hemoperfusion treatment ( N = 25) or standard therapy ( N = 21). Those undergoing hemoperfusion treatment received HA330 hemoperfusion. We measured the plasma and bronchoalveolar lavage concentrations of TNF-α and IL-1, and the following parameters were compared between the control group and the hemoperfusion group on days 0, 3 and 7: lung injury measurements (arterial oxygen tension/fractional inspired oxygen ratio, lung injury score, chest X-ray score); interstitial edema of lung (extravascular lung water). Duration of mechanical ventilation, hospital, 28-day, and intensive care unit mortality were also observed. Patients treated with HA hemoperfusion showed a significant removal of plasma and bronchoalveolar lavage TNF-α and IL-1 over time while in the study. Patients in the HA group also demonstrated not only significant improvement of PaO2/FiO2, but also decreased Lung Injury Score and chest X-ray score at days 3 and 7. Furthermore, the measurements of the arterial oxygen tension/fractional inspired oxygen ratio, lung injury score and extravascular lung water (EVLWI) significantly correlated with and the concentration of cytokines in the plasma (all P < 0.05). The HA hemoperfusion treatment group had a significant reduction in duration of mechanical ventilation, length of intensive care unit stay, and intensive care unit mortality. Significant removal of inflammatory cytokines from circulation and lung by hemoperfusion treatment using the HA type cartridge may contribute to the improvement of lung injury and intensive care unit outcome in extrapulmonary septic patients. [ABSTRACT FROM AUTHOR]

Processed xenegeneic cancellous bone represents an alternative to bone autograft. In order to observe the effects of present prion inactivation treatments on the natural properties of xenogeneic cancellous bones, we treated bovine bone granules with sodium hydroxide ( NaOH), sodium hypochlorite ( NaOCl), and gaseous hydrogen peroxide (g H2O2) respectively in this study. The microstructure, composition, and mineral content of the granules were evaluated by scanning electron micrograph, energy dispersive X-ray spectroscopy, ash analysis, and micro-computed tomography. The biomechanical property was analyzed by a materials testing machine. The cytocompatibility was evaluated by using a mouse fibroblast cell line (3 T3). The microstructure, organic content, and mechanical strength were dramatically altered at the surface of bone in both NaOH- and NaOCl-treated groups, but not in the g H2O2-treated group. Compared with the g H2O2-treated group, attachment and proliferation of 3 T3 were reduced in either NaOH- or NaOCl-treated groups. As the consequence, g H2O2 treatment may be a useful approach of disinfection for the preparation of natural cancellous bone with well-preserved structural, mechanical, and biological properties. [ABSTRACT FROM AUTHOR]

Mitochondrial DNA (mtDNA) mutations are associated with a large number of neuromuscular diseases. Myoclonus epilepsy with ragged-red fibers (MERRF) syndrome is a mitochondrial disease inherited through the maternal lineage. The most common mutation in MERRF syndrome, the A8344G mutation of mtDNA, is associated with severe defects in mitochondrial protein synthesis, which impair the assembly and function of the respiratory chain. We have previously shown that there is a decreased level of heat shock protein 27 (HSP27) in lymphoblastoid cells derived from a MERRF patient and in cytoplasmic hybrids (cybrids) harboring the A8344G mutation of mtDNA. In the present study, we found a dramatic decrease in the level of phosphorylated HSP27 (p-HSP27) in the mutant cybrids. Even though the steady-state level of p-HSP27 was reduced in the mutant cybrids, normal phosphorylation and dephosphorylation were observed upon exposure to stress, indicating normal kinase and phosphatase activities. To explore the roles that p-HSP27 may play, transfection experiments with HSP27 mutants, in which three specific serines were replaced with alanine or aspartic acid, showed that the phosphomimicking HSP27 desensitized mutant cybrids to apoptotic stress induced by staurosporine (STS). After heat shock stress, p-HSP27 was found to enter the nucleus immediately, and with a prolonged interval of recovery, p-HSP27 returned to the cytoplasm in wild-type cybrids but not in mutant cybrids. The translocation of p-HSP27 was correlated with cell viability, as shown by the increased number of apoptotic cells after p-HSP27 returned to the cytoplasm. In summary, our results demonstrate that p-HSP27 provides significant protection when cells are exposed to different stresses in the cell model of MERRF syndrome. Therapeutic agents targeting anomalous HSP27 phosphorylation might represent a potential treatment for mitochondrial diseases. [ABSTRACT FROM AUTHOR]

The aim of this study is to evaluate the impact of neutral microporous resin hemoperfusion on hemodynamic improvement, removal of inflammatory cytokines, and mortality in critical care patients with severe sepsis. Forty-four patients with severe sepsis or septic shock were randomized to HA type hemoperfusion treatment ( N = 24) or standard therapy ( N = 20). Those undergoing hemoperfusion treatment received HA330 hemoperfusion. We measured the plasma concentrations of IL-6 and IL-8 at the start of every hemoperfusion treatment, and the following parameters were compared between the control group and the hemoperfusion group on days 3, 7, and 14: hemodynamics (cardiac index, systemic vascular resistance index, heart rate, and mean arterial pressure); change of hematology and coagulation function; organ function; and the sequential organ failure assessment (SOFA) score. Hospital, 28-day, and ICU mortality were also observed. Patients treated with HA hemoperfusion showed a significant removal of plasma IL-6 and IL-8 over time while in the study. Patients in the HA group also demonstrated significant increases in cardiac index, systemic vascular resistant index, fast withdrawal of vasoactive agents and decreases in heart rate compared with the controls at days 3 and 7. Although there was no significant difference between the groups in organ dysfunction as assessed by SOFA scores from day 0 (baseline) to day 7, significant improvement can be demonstrated in the hemoperfusion group at day 14. There was no significant difference between the groups in 28-day mortality, hospital mortality, or length of hospital stay, but ICU mortality and the length of ICU stay in the HA group were markedly reduced. Hemoperfusion treatment using the HA type cartridge in sepsis is safe and it may improve organ dysfunction, ICU mortality, and shorten the length of ICU stay. Clinical significant removal of inflammatory cytokines such as IL-6 and IL-8 from circulation by hemoperfusion may contribute to improving a patient's outcome in an ICU. [ABSTRACT FROM AUTHOR]

Much of the evidence from the West has shown links between children's developing self-control (executive function), their social experiences, and their social understanding (Carpendale & Lewis, 2006, chapters 5 and 6), across a range of cultures including China. This chapter describes four studies conducted in three Oriental cultures, suggesting that the relationships among social interaction, executive function, and social understanding are different in these cultures, implying that social and executive skills are underpinned by key cultural processes. [ABSTRACT FROM AUTHOR]