187 research outputs found

    Research on Two-stage Rotary Compressor with Refrigerant Injection for Cold Climate Heat Pump

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    As an promising heating application of environmental conservation and energy conservation, air-source heat pump systems has been spreading. However, conventional heat pump systems have problems remaining, such as inadequate heating capacity and reduced performance under low environmental temperature condition. To solve these problems, we developed a two-stage rotary compressor for household R32 air-source heat pump system. We analyzed the thermodynamic characteristics of two-stage rotary compressor with refrigerant injection used in heat pump system with economizer. It is found that the two-stage rotary compressor can enhance heating capacity and performance of R32 heat pump under cold climate markedly

    Theoretical and Experimental Research on The Optimal Displacement Ratio of Rotary Two-Stage Inverter Compressor With Vapor Injection

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    Displacement ratio is one of the most important parameters of designing rotary two-stage inverter compressor with vapor injection, which decides the COP (Coefficient of Performance) of the compressor. The optimal displacement ratio can bring about the highest COP. The mathematical model of the optimal displacement ratio of rotary two-stage inverter compressor with vapor injection has been developed and verified with the test data. It can be seen from theoretical and experimental research that the optimal displacement ratio of compressors in different working conditions can be obtained accurately by the mathematical model introduced in this paper

    The Effect of Fecal Microbiota Transplantation on a Child with Tourette Syndrome

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    Tourette syndrome is a neuropsychiatric disorder with onset in childhood. New therapies are needed to effectively manage and treat this condition. Gut microbiota can affect central physiology and function via the microbiota-gut-brain axis. Here, we report a case in which fecal microbiota transplantation (FMT) is used to treat a child with Tourette syndrome, whose symptoms ameliorated dramatically in the following eight weeks

    A Wheat Cinnamyl Alcohol Dehydrogenase TaCAD12 Contributes to Host Resistance to the Sharp Eyespot Disease

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    peer reviewedSharp eyespot, caused mainly by the necrotrophic fungus Rhizoctonia cerealis, is a destructive disease in hexaploid wheat (Triticum aestivum L.). In Arabidopsis, certain cinnamyl alcohol dehydrogenases (CADs) have been implicated in monolignol biosynthesis and in defense response to bacterial pathogen infection. However, little is known about CADs in wheat defense responses to necrotrophic or soil-borne pathogens. In this study, we isolate a wheat CAD gene TaCAD12 in response to R. cerealis infection through microarray-based comparative transcriptomics, and study the enzyme activity and defense role of TaCAD12 in wheat. The transcriptional levels of TaCAD12 in sharp eyespot-resistant wheat lines were significantly higher compared with those in susceptible wheat lines. The sequence and phylogenetic analyses revealed that TaCAD12 belongs to IV group in CAD family. The biochemical assay proved that TaCAD12 protein is an authentic CAD enzyme and possesses catalytic efficiencies toward both coniferyl aldehyde and sinapyl aldehyde. Knock-down of TaCAD12 transcript significantly repressed resistance of the gene-silenced wheat plants to sharp eyespot caused by R. cerealis, whereas TaCAD12 overexpression markedly enhanced resistance of the transgenic wheat lines to sharp eyespot. Furthermore, certain defense genes (Defensin, PR10, PR17c, and Chitinase1) and monolignol biosynthesis-related genes (TaCAD1, TaCCR, and TaCOMT1) were up-regulated in the TaCAD12-overexpressing wheat plants but down-regulated in TaCAD12-silencing plants. These results suggest that TaCAD12 positively contributes to resistance against sharp eyespot through regulation of the expression of certain defense genes and monolignol biosynthesis-related genes in wheat.Nationa l“KeySci-Tech” Projec

    Apelin-13 Suppresses Neuroinflammation Against Cognitive Deficit in a Streptozotocin-Induced Rat Model of Alzheimer’s Disease Through Activation of BDNF-TrkB Signaling Pathway

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    Alzheimer’s disease (AD), a progressive neurodegenerative disease characterized by impairments of cognitive function as a result of synaptic deficits and neuronal loss, is associated with inflammation. Apelin-13, a predominant neuropeptide with inhibiting effect on inflammation, has beneficial effects on cognition memory and neuronal damage. However, whether apelin-13 can protect neurons to ameliorate cognitive deficits in AD by inhibiting the inflammatory response remains largely unknown. To test this hypothesis, rats were intracerebroventricularly (ICV) injected with streptozotocin (3 mg/kg) alone or in combination with apelin-13 (2 μg). And tyrosine receptor kinase B (TrkB) blocker K252a (200 nM) was administrated 10 min before apelin injection. Furthermore, cognitive performance was assessed by new object recognition (NOR) and Y-maze tests. Protein expression of apelin, APJ, microglial marker (IBA1), astroglia marker (GFAP), interleukin 1 beta (IL-1β), tumor necrosis factor-α (TNF-α), synaptophysin (SYP), brain-derived neurotrophic factor (BDNF), TrkB, phospho-TrkB (p-TrkB) in the hippocampus were examined by western blotting or immunohistochemistry. And the gene expression of IBA1, GFAP, IL-1β, TNF-α, and SYP were detected by real-time quantitative polymerase chain reaction (PCR). Inflammatory disorder in the hippocampus was tested by hematoxylin and eosin (H&E) staining. The enzyme-linked immunosorbent assay (ELISA) was used to study the expression level of acetylcholine. And the activity of acetylcholinesterase was detected by Acetylcholinesterase Assay Kit. We observed that apelin/APJ signaling was downregulated in the hippocampus of rats administrated with STZ. Apelin-13 was found to significantly ameliorate STZ-induced AD-like phenotypes including congnitive deficit, cholinergic disfunction and the damage of neuron and synaptic plasticity. Moreover, apelin-13 inhibited microglia and astrocyte activation, reduced IL-1β and TNF-α expression and hippocampal BDNF/TrkB expression deficit in AD rats. Finally, apelin-13-mediated effects were blocked by TrkB receptor antagonist K252a. These results suggest that apelin-13 upregulates BDNF/TrkB pathway against cognitive deficit in a STZ-induced rat model of sporadic AD by attenuating inflammation

    miRNA-135a promotes breast cancer cell migration and invasion by targeting HOXA10

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    <p>Abstract</p> <p>Background</p> <p>miRNAs are a group of small RNA molecules regulating target genes by inducing mRNA degradation or translational repression. Aberrant expression of miRNAs correlates with various cancers. Although miR-135a has been implicated in several other cancers, its role in breast cancer is unknown. <it>HOXA10 </it>however, is associated with multiple cancer types and was recently shown to induce p53 expression in breast cancer cells and reduce their invasive ability. Because <it>HOXA10 </it>is a confirmed miR-135a target in more than one tissue, we examined miR-135a levels in relation to breast cancer phenotypes to determine if miR-135a plays role in this cancer type.</p> <p>Methods</p> <p>Expression levels of miR-135a in tissues and cells were determined by poly (A)-RT PCR. The effect of miR-135a on proliferation was evaluated by CCK8 assay, cell migration and invasion were evaluated by transwell migration and invasion assays, and target protein expression was determined by western blotting. GFP and luciferase reporter plasmids were constructed to confirm the action of miR-135a on downstream target genes including <it>HOXA10</it>. Results are reported as means ± S.D. and differences were tested for significance using 2-sided Student"s t-test.</p> <p>Results</p> <p>Here we report that miR-135a was highly expressed in metastatic breast tumors. We found that the expression of miR-135a was required for the migration and invasion of breast cancer cells, but not their proliferation. <it>HOXA10</it>, which encodes a transcription factor required for embryonic development and is a metastasis suppressor in breast cancer, was shown to be a direct target of miR-135a in breast cancer cells. Our analysis showed that miR-135a suppressed the expression of <it>HOXA10 </it>both at the mRNA and protein level, and its ability to promote cellular migration and invasion was partially reversed by overexpression of <it>HOXA10</it>.</p> <p>Conclusions</p> <p>In summary, our results indicate that miR-135a is an onco-miRNA that can promote breast cancer cell migration and invasion. <it>HOXA10 </it>is a target gene for miR-135a in breast cancer cells and overexpression of <it>HOXA10 </it>can partially reverse the miR-135a invasive phenotype.</p

    A Kinetic View on Proximity-dependent Selectivity of Carbon Dioxide Reduction on Bifunctional Catalysts

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    Multifunctional catalysts with distinct functional components are known to have much improved selectivity. However, the well-known proximity-dependent selectivity observed in several high profile experiments is yet to be understood. Here, we reveal that such dependence is closely associated with the kinetics involved. Based on reaction-diffusion dynamics together with kinetic Monte Carlo simulation on a coarse-grained model, one famous example of bifunctional catalysis, namely the proximity-dependent selectivity from carbon dioxide to liquid fuels on a bifunctional catalyst composed of HZSM-5 and In2O3, has been systematically examined. It is found that the diffusion kinetics of the intermediate methanol generated on In2O3 plays a decisive role for the selectively. For different In2O3/HZSM-5 proximities, the local methanol concentration induce a shift of the dominant process for subsequent methanol-to-hydrocarbon reactions inside HZSM-5, resulting in a preferred reaction window to generate favorable liquid fuels with profound high selectivity. Our findings emphasize the importance of the largely overlooked kinetic in the design of multifunctional catalysts

    Ground surface temperature and the detection of permafrost in the rugged topography on NE Qinghai-Tibet Plateau

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    The thermal regime of permafrost in the rugged topography on parts of the Qinghai-Tibet Plateau (QTP) remains ambiguous, due to general inaccessibility and inconvenient investigations with geophysical prospecting. While the relatively easy implementations of monitoring ground surface temperature (GST) may facilitate the investigations of permafrost thermal state. Here, surface freezing and thawing and the relationship between GST and permafrost temperature are investigated in the Bayan Har Mountains, NE QTP on the basis of 22 monitoring sites. Results demonstrate that, unlike the air temperature (Ta) mainly controlled by elevation, the GST is complicately influenced by elevation and the surface characteristics, such as vegetation, local soil textures, as well as the exposure to solar radiation. Mean annual GST (MAGST) ranges from 1.1 °C to −3.1 °C and is averaged at −0.8 °C. MAGST generally decreases at a lapse rate of 1.1 °C/100 m in relation to elevation. Surface freezing and thawing processes depend on topography and local surface characteristics. The onset of unstable thawing, stable thawing, unstable freezing, and stable freezing are averaged at 6 April 2015, 15 May 2015, 14 October 2015, and 21 October 2015. Based on the relationship between MAGST and the ground temperature at the depth of zero annual amplitude, GST likely serves as a reliable indicator of the thermal state of permafrost. For the 22 sites, it is estimated that the lowest TZAA of permafrost is −3.4 °C and the thickest permafrost is 106.2 m. However, detailed investigations of subsurface characteristics are indispensable for the accurate inference of permafrost.</p
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