258 research outputs found

    Numerical Geodynamic Modeling of Continental Convergent Margins

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    Cardiovascular medicin

    Quality Changes of Pre-fried Fish during Frozen and Reheating Process

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    To solve the problem of taste loss of new retail prepared fish after freezing and reheating. The changes of moisture content, water holding capacity, water distribution, and microstructure in pre-fried fish were analyzed during frying, freezing and reheating processes. The results showed that with the increase of freezing-thawing cycles, a significant decrease of the moisture content (P<0.05) and water holding capacity of pre-fried fish were observed, while the degree of fat oxidation, protein degradation, and muscle fiber destruction were increased significantly (P<0.05)ļ¼Œas well as the flavor changes were displayed in all the samples. After reheating, the taste of pre-fried fish at 1 freezing-thawing cycle was similar to the unfrozen group. However, lower sensory scores were gained after 2 freezing-thawing cycles. Also, in comparation with the samples without freezing, the contents of myofibrillar fragmentation index, TBARS and TCA-soluble peptide increased by 24.44%, 225.84% and 52.85%, respectively. In conclusion, the edible quality and consumer acceptance of the pre-fried fish are significantly reduced when the number of freezing-thawing cycles are more than 2 times in the process of storage and transportation

    Uplift of the Longmen Shan range and the Wenchuan earthquake

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    ABSTRACT: The 12 May 2008 Wenchuan earthquake (M-s,=8.0) struck on the Longmen Shan foreland thrust zone. The event took place within the context of long-term uplift of the Longmen Shan range is a result of the extensive eastward-extrusion of crustal materials from the Tibetan plateau against the rheologically strong crust of the Sichuan Basin. The Longmen Shan range is characterized by a Pre-Sinian crystalline complex constrained by the Maoxian-Wenchuan-Kangding ductile detachment at the western margin and the Yingxiu-Beichuan-Luding ductile thrust at the eastern margin. The Longmen Shan uplift was initiated by intracontinental subduction between the Songpan-Ganzi terrane and the Yangtze block during the Pre-Cenozoic. The uplift rate was increased considerably by the collision between the Indian and Eurasian plates since similar to 50 Ma. The Wenchuan earthquake resulted in two major NE-striking coseismic ruptures (i.e., the similar to 275 km long Yingxiu-Beichuan-Qingchuan fault and the similar to 100 km long Anxian-Guanxian fault). Field investigations combined with focal solutions and seismic reflection profiles suggest that the coseismic ruptures are steeply dipping close-to-pure reverse or right reverse oblique slip faults in the similar to 15 km thick tipper crust. These faults are unfavorably oriented for frictional slip in the horizontally compressional regime, so that they need a long recurrence interval to accumulate the tectonic stress and fluid pressure to critically high levels for the formation of strong earthquakes at a given locality. It is also found that all the large earthquakes (M-s>7.0) occurred in the fault zones across which the horizontal movement velocities measured by the GPS are markedly low (<3 mm/yr). The faults, which constitute the northeastern fronts of the enlarging Tibetan plateau against the strong Sichuan Basin, Ala Shan and Ordos blocks, are very destructive, although their average recurrence intervals are generally long

    Quantum-Enhanced Diamond Molecular Tension Microscopy for Quantifying Cellular Forces

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    The constant interplay and information exchange between cells and their micro-environment are essential to their survival and ability to execute biological functions. To date, a few leading technologies such as traction force microscopy, have been broadly used in measuring cellular forces. However, the considerable limitations, regarding the sensitivity and ambiguities in data interpretation, are hindering our thorough understanding of mechanobiology. Herein, we propose an innovative approach, namely quantum-enhanced diamond molecular tension microscopy (QDMTM), to precisely quantify the integrin-based cell adhesive forces. Specifically, we construct a force sensing platform by conjugating the magnetic nanotags labeled, force-responsive polymer to the surface of diamond membrane containing nitrogen vacancy (NV) centers. Thus, the coupled mechanical information can be quantified through optical readout of spin relaxation of NV centers modulated by those magnetic nanotags. To validate QDMTM, we have carefully performed corresponding measurements both in control and real cell samples. Particularly, we have obtained the quantitative cellular adhesion force mapping by correlating the measurement with established theoretical model. We anticipate that our method can be routinely used in studying important issues like cell-cell or cell-material interactions and mechanotransduction.Comment: 51 pages, 20 figure

    ADAR2-dependent RNA editing of GluR2 is involved in thiamine deficiency-induced alteration of calcium dynamics

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    BACKGROUND: Thiamine (vitamin B1) deficiency (TD) causes mild impairment of oxidative metabolism and region-selective neuronal loss in the central nervous system (CNS). TD in animals has been used to model aging-associated neurodegeneration in the brain. The mechanisms of TD-induced neuron death are complex, and it is likely multiple mechanisms interplay and contribute to the action of TD. In this study, we demonstrated that TD significantly increased intracellular calcium concentrations [Ca2+]i in cultured cortical neurons. RESULTS: TD drastically potentiated AMPA-triggered calcium influx and inhibited pre-mRNA editing of GluR2, a Ca2+-permeable subtype of AMPA receptors. The Ca2+ permeability of GluR2 is regulated by RNA editing at the Q/R site. Edited GluR2 (R) subunits form Ca2+-impermeable channels, whereas unedited GluR2 (Q) channels are permeable to Ca2+ flow. TD inhibited Q/R editing of GluR2 and increased the ratio of unedited GluR2. The Q/R editing of GluR2 is mediated by adenosine deaminase acting on RNA 2 (ADAR2). TD selectively decreased ADAR2 expression and its self-editing ability without affecting ADAR1 in cultured neurons and in the brain tissue. Over-expression of ADAR2 reduced AMPA-mediated rise of [Ca2+]i and protected cortical neurons against TD-induced cytotoxicity, whereas down-regulation of ADAR2 increased AMPA-elicited Ca2+ influx and exacerbated TD-induced death of cortical neurons. CONCLUSIONS: Our findings suggest that TD-induced neuronal damage may be mediated by the modulation of ADAR2-dependent RNA Editing of GluR2
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