71 research outputs found

    The systematic investigations of high-pressure polymorphs in shocked L type ordinary chondrites

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    第6回極域科学シンポジウム[OA] 南極隕石11月16日(月) 国立国語研究所 2階 講

    Petrography of Yamato 984028 lherzolitic shergottite and its melt vein: Implications for its shock metamorphism and origin of the vein

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    AbstractYamato 984028 (Y984028) is a newly identified lherzolitic shergottite, recovered from the Yamato Mountains, Antarctica, in 1999. As part of a consortium study, we conducted petrographic observations of Y984028 and its melt vein in order to investigate its shock metamorphism. The rock displays the typical non-poikilitic texture of lherzolitic shergottite, characterized by a framework of olivine, minor pyroxene (pigeonite and augite), and interstitial maskelynite. Shock metamorphic features include irregular fractures in olivine and pyroxene, shock-induced twin-lamellae in pyroxene, and the complete conversion of plagioclase to maskelynite, features consistent with those found in other lherzolitic shergottites. The melt vein is composed of coarse mineral fragments (mainly olivine) entrained in a matrix of fine-grained euhedral olivine (with several modes of compositional zoning) and interstitial glassy material. Some coarse olivine fragments consist of an assemblage of fine-grained euhedral to subhedral olivine crystals, suggesting shock-induced fragmentation, recrystallization, and/or a process of sintering. The implication is that the fine-grained olivine crystals in the matrix of the melt vein represent complicated crystallization environments and histories

    The investigation of back-transformation mechanisms of ringwoodite and majorite in the Yamato 75267 H6

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    The Tenth Symposium on Polar Science/Special session: [OA] Antarctic meteorites, Thur. 5 Dec. / 3F Multipurpose conference room, National Institute of Polar Researc

    A Feasibility Study of Postoperative Adjuvant Therapy of Carboplatin and Weekly Paclitaxel for Completely Resected Non-small Cell Lung Cancer

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    IntroductionRecent clinical trials have shown significant survival benefits from postoperative adjuvant therapy for respectable nonsmall cell lung cancer (NSCLC). However, evaluation of adjuvant chemotherapy with carboplatin combination is still uncertain. The purpose of the study was to test the feasibility of adjuvant chemotherapy with carboplatin and separate weekly paclitaxel after complete resection of pStage IB, II, IIIA NSCLC in a multicenter study.MethodsThe study was conducted from 2001 to 2006 in the outpatient setting. A total of 61 patients were enrolled. Patients received adjuvant chemotherapy with 4 cycles of carboplatin (AUC 5) on day 1 and paclitaxel (70 mg/m2) on day 1, 8, and 15 every 4 weeks. Primary endpoints were toxicity and chemotherapy compliance. Secondary endpoints were disease-free survival and overall survival.ResultsMore than 65% of eligible patients had pStage IIIA. The median number of chemotherapy cycles was 4 (range 1–4). Grade 3 or 4 toxicities of neutropenia were 34% (grade 4: 2%). Other hematologic adverse effects were extremely less frequent. Regarding the nonhematologic adverse effect, hair loss was frequent; however, peripheral neuralgia was less frequent. Treatment-related death was not registered. During median follow-up of 21 months, 24 patients developed recurrent disease. Estimated disease-free survival and overall survival at 2 years was 51.2% and 84.6%, respectively.ConclusionsPostoperative carboplatin and weekly paclitaxel showed favorable feasibility and acceptable toxicity in comparison with the cisplatin-containing regimen. Consequently, it is desirable that this regimen would be validated in a phase III clinical trial for NSCLC after curative resection

    Inhibition of Phospholipase A2 and Platelet Aggregation by Grycyrrhizin, an Anti-inframmation Drug

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    We studied the effect of glycyrrhizin, a compound known as an anti-inflammatory and antiallergic drug, on the membrane permeability change induced by phospholipase A2 (PLA2) and on platelet aggregation. Glycyrrhizin was found to inhibit the PLA2-induced carboxyfluorescein (CF) release from D,L-dipalmitoyl phosphatidylcholine (DPPC) liposomes. Part of this inhibitory effect of glycyrrhizin on PLA2 is accounted for by the physical state of the substrate, the DPPC liposome membrane. Glycyrrhizin also inhibited collagen-induced platelet aggregation in a concentration dependent manner, which may in part account for its inhibitory effect on PLA2.</p

    Purification of enzymatically inactive peptidylarginine deiminase type 6 from mouse ovary that reveals hexameric structure different from other dimeric isoforms

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    The murine peptidylarginine deiminase (PAD) has five isoforms encoded by different genes and partici- pates in a variety of cellular functions through the citrullination of target proteins. The crystal structure of human PAD4 with a dimeric form was previously solved because of the enzyme’s relevance to rheuma- toid arthritis. PAD6, abundant in mouse oocytes and eggs, is believed to take part in early events of embryogenesis, but its biochemical properties are little understood. Here we have purified and charac- terized a recombinant PAD6. A PAD6 cDNA was cloned from mouse ovary RNA and expressed in Escherichia coli through pET29 and pGEX vectors. When benzoyl-L-arginine ethyl ester was used as a substrate, no appreciable activity was detected with a cell homogenate under conditions where a human PAD4 cDNA caused significant activity. Both pro- teins were affinity-purified to near homogeneity. The circular dichroism spectra of PAD6 and human PAD4 were similar in the far ultraviolet region. On molecular sieving, PAD6 was eluted faster than human PAD4. The cross-linking of PAD6 with dime- thyl suberimidate clearly showed six bands on an sodium dodecyl sulfate-polyacrylamide gel. These results indicate that PAD6 can constitute a hexameric structure. The purified PAD6 still showed no enzy- matic activity. This unique structure and loss in enzymatic activity is strongly suggested to favor the formation of egg cytoplasmic sheets as the architectu- ral protein

    Hydration study of slag-blended cement based on thermodynamic considerations

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    Thermodynamic calculations, using the geochemical code PHREEQC coupled with empirical equations for kinetics of cement hydration and slag reaction, were carried out to predict the compositions of the hydrate assemblage and pore solutions of hydrating Portland cement and cement blended with slag and the blended cement containing limestone. The predicted compositions of hydration products and element concentrations in pore solutions compared well with experimental data reported in literature. The calculation results showed the varying Ca/Si and Al/Si ratios of calcium aluminosilicate hydrate (C-A-S-H)(1) in the hydration products due to hydration and slag addition. Limitations on the equation for reaction of slag and the importance of a C-A-S-H solid solution model in prediction of hydration products are discussed
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