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Sivakumar Subramanian,A. S. Sekhar,B. V. S. S. S. Prasad 대한기계학회 2015 JOURNAL OF MECHANICAL SCIENCE AND TECHNOLOGY Vol.29 No.6
Leakage characteristics, influenced by centrifugal and thermal radial growth are determined computationally for a generic rotating labyrinthseal used in the gas turbine secondary air system. Three seal locations, namely, R25, R50 and R75 are represented by means ofvarying the rotor radius mimicking different radial positions of the seal from the shaft axis. The combined influence of seal location andits radial (Centrifugal and thermal) growth on the leakage performance is investigated for a wide-ranging speeds from 1000 to 3000 rad/s,temperatures ranging from 200 to 450 oC and pressure ratios varying from 1.1 to 2.5, for a chosen initial clearance of 500 micron. Acomparison of the effect of rotation and temperature gradient among different rotors shows that the radial growth and leakage flow ratessignificantly vary with the increasing radius.
( Sivakumar Lingappa ),( Muthugounder Subramanian Shivakumar ),( Thamilarasan Manivasagam ),( Somasundaram Thirugnanasambandan Somasundaram ),( Palaniappan Seedevi ) 한국미생물생명공학회(구 한국산업미생물학회) 2021 Journal of microbiology and biotechnology Vol.31 No.6
Epalrestat (EPS) is a brain penetrant aldose reductase inhibitor, an approved drug currently used for the treatment of diabetic neuropathy. At near-plasma concentration, EPS induces glutathione biosynthesis, which in turn reduces oxidative stress in the neuronal cells. In this study, we found that EPS reduces neurodegeneration by inhibiting reactive oxygen species (ROS)-induced oxidative injury, mitochondrial membrane damage, apoptosis and tauopathy. EPS treatment up to 50 μM did not show any toxic effect on SH-SY5Y cell line (neuroblastoma cells). However, we observed toxic effect at a concentration of 100 μM and above. At 50 μM concentration, EPS showed better antioxidant activity against H<sub>2</sub>O<sub>2</sub> (100 μM)-induced cytotoxicity, ROS formation and mitochondrial membrane damage in retinoic acid-differentiated SH-SY5Y cell line. Furthermore, our study revealed that 50 μM of EPS concentration reduced the glycogen synthase kinase-3 β (GSK3-β) expression and total tau protein level in H<sub>2</sub>O<sub>2</sub> (100 μM)-treated cells. Findings from this study confirms the therapeutic efficacy of EPS on regulating Alzheimer's disease (AD) by regulating GSK3- β and total tau proteins phosphorylation, which helped to restore the cellular viability. This process could also reduce toxic fibrillary tangle formation and disease progression of AD. Therefore, it is our view that an optimal concentration of EPS therapy could decrease AD pathology by reducing tau phosphorylation through regulating the expression level of GSK3-β.