157 research outputs found
Peroxidase as the Major Protein Constituent in Areca Nut and Identification of Its Natural Substrates
Numerous reports illustrate the diverse effects of chewing the areca nut, most of which are harmful and have been shown to be associated with oral cancer. Nearly all of the studies are focused on the extract and/or low molecular weight ingredients in the areca nut. The purpose of this report is to identify the major protein component in the areca nut. After ammonium sulfate fractionation, the concentrated areca nut extract is subjected to DEAE-cellulose chromatography. A colored protein is eluted at low NaCl concentration and the apparently homogeneous eluent represents the major protein component compared to the areca nut extract. The colored protein shares partial sequence identity with the royal palm tree peroxidase and its peroxidase activity is confirmed using an established assay. In the study, the natural substrates of areca nut peroxidase are identified as catechin, epicatechin, and procyanidin B1. The two former substrates are similarly oxidized to form a 576 Da product with concomitant removal of four hydrogen atoms. Interestingly, oxidation of procyanidin B1 occurs only in the presence of catechin or epicatechin and an additional product with an 864 Da molecular mass. In addition, procyanidin B1 is identified as a peroxidase substrate for the first time.</jats:p
Emodin Induces Apoptotic Death in Murine Myelomonocytic Leukemia WEHI-3 Cells In Vitro
Emodin is one of major compounds in rhubarb (Rheum palmatum L.), a plant used as herbal medicine in Chinese population. Although many reports have shown that emodin exhibits anticancer activity in many tumor cell types, there is no available information addressing emodin-affected apoptotic responses in the murine leukemia cell line (WEHI-3) and modulation of the immune response in leukemia mice. We investigated that emodin induced cytotoxic effects in vitro and affected WEHI-3 cells in vivo. This study showed that emodin decreased viability and induced DNA fragmentation in WEHI-3 cells. Cells after exposure to emodin for 24 h have shown chromatin condensation and DNA damage. Emodin stimulated the productions of ROS and Ca2+ and reduced the level of ΔΨm by flow cytometry. Our results from Western blotting suggest that emodin triggered apoptosis of WEHI-3 cells through the endoplasmic reticulum (ER) stress, caspase cascade-dependent and -independent mitochondrial pathways. In in vivo study, emodin enhanced the levels of B cells and monocytes, and it also reduced the weights of liver and spleen compared with leukemia mice. Emodin promoted phagocytic activity by monocytes and macrophages in comparison to the leukemia mice group. In conclusions, emodin induced apoptotic death in murine leukemia WEHI-3 cells and enhanced phagocytosis in the leukemia animal model
Excavatoids O and P, New 12-Hydroxybriaranes from the Octocoral Briareum excavatum
Two new 12-hydroxybriarane diterpenoids, designated as excavatoids O (1) and P (2), were isolated from the octocoral Briareum excavatum. The structures of briaranes 1 and 2 were established on the basis of extensive spectral data analysis. Excavatoid P (2) is the first metabolite which possesses a 6β -chlorine atom in briarane analogues
Novel Quinazolinone MJ-29 Triggers Endoplasmic Reticulum Stress and Intrinsic Apoptosis in Murine Leukemia WEHI-3 Cells and Inhibits Leukemic Mice
The present study was to explore the biological responses of the newly compound, MJ-29 in murine myelomonocytic leukemia WEHI-3 cells in vitro and in vivo fates. We focused on the in vitro effects of MJ-29 on ER stress and mitochondria-dependent apoptotic death in WEHI-3 cells, and to hypothesize that MJ-29 might fully impair the orthotopic leukemic mice. Our results indicated that a concentration-dependent decrease of cell viability was shown in MJ-29-treated cells. DNA content was examined utilizing flow cytometry, whereas apoptotic populations were determined using annexin V/PI, DAPI staining and TUNEL assay. Increasing vital factors of mitochondrial dysfunction by MJ-29 were further investigated. Thus, MJ-29-provaked apoptosis of WEHI-3 cells is mediated through the intrinsic pathway. Importantly, intracellular Ca2+ release and ER stress-associated signaling also contributed to MJ-29-triggered cell apoptosis. We found that MJ-29 stimulated the protein levels of calpain 1, CHOP and p-eIF2α pathways in WEHI-3 cells. In in vivo experiments, intraperitoneal administration of MJ-29 significantly improved the total survival rate, enhanced body weight and attenuated enlarged spleen and liver tissues in leukemic mice. The infiltration of immature myeloblastic cells into splenic red pulp was reduced in MJ-29-treated leukemic mice. Moreover, MJ-29 increased the differentiations of T and B cells but decreased that of macrophages and monocytes. Additionally, MJ-29-stimulated immune responses might be involved in anti-leukemic activity in vivo. Based on these observations, MJ-29 suppresses WEHI-3 cells in vitro and in vivo, and it is proposed that this potent and selective agent could be a new chemotherapeutic candidate for anti-leukemia in the future
Energy dissipation of composite multifilamentary superconductors for high-current ramp-field magnet applications
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Nuclear Engineering, 1993.Includes bibliographical references.by Chen Yu-Gung.Ph.D
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Cryostat with Foil and MLI
Induction cores are used to accelerate heavy ion beam array, which are built around the outer diameter of the cryostat housing the superconducting quadruple array. Compact cryostat is highly desirable to reduce the cost of the induction cores. Recent experiences in fabrication of a cryostat for single beam transport revealed that it is possible to reduce the spacing in the cryostat vacuum jacket by using low-emissivity thermal insulation material instead of conventional MLI. However, it is labor-intensive to install the new type of insulation as compared with using MLI. It is promising to build a cost-effective compact cryostat for quadruple magnet array for heavy ion beam array transport by using low-emissivity material combined with conventional MLI as radiation insulation. A matrix of insulation designs and tests will be performed as the feasibility study and for the selection of the optimal thermal insulation as the Phase I work. The selected mixed insulation will be used to build prototype compact cryostats in the Phase II project, which are aiming for housing quadruple doublet array. In this STTR phase I study, a small cryostat has been designed and built to perform calorimetric characterization of the heat load in a liquid helium vessel insulated with a vacuum layer with a nominal clearance of 3.5 mm. The vacuum clearance resembled that used in the warm-bore beam tube region in a prototype cryostat previously built for the heavy ion beam transport experiment. The vacuum clearance was geometrically restricted with a heater shell with the temperature controlled at near 300 K. Various combinations of radiation and thermal shields were installed in the tight vacuum clearance for heat load measurements. The measured heat loads are reported and compared with previous test result using a compact vacuum layer. Further developments of the thermal insulations used in the present study are discussed. The compact cryostat with foil and MLI insulation may be used in the superconducting magnets for a wide range of applications including particle accelerators, fusion energy research, NMR, NMI, laboratory high field experiments and industrial magnets, compact feed through for general-purpose cryostat, etc. Combination of low emissivity thermal insulation material with the conventional MLI has a great potential to build cost-effective compact cryostats for heavy ion fusion beam array transport and other more general-purpose applications
Exploring 3D-QSAR pharmacophore mapping of azaphenanthrenone derivatives for mPGES-1 inhibition Using HypoGen technique
Application of High Voltage Insulation on the Magnet Feeder Superconducting Joints During ITER Machine Assembly
The ITER Magnet Feeders are composed of three main sections which are connected together on the ITER site. During this process, the superconducting busbars which carry the electrical current to the ITER magnets are connected together via superconducting joints. As the magnet system operates under high voltage, it is necessary to apply high voltage insulation over the joints and seamlessly connect it to the existing high voltage insulation on the superconducting busbars. This paper describes the materials and detailed techniques used to apply the high voltage insulation on the superconducting joints in the ITER assembly environment. Prior to performing the work on-site, the entire process was qualified on mock-ups, and a process put in place to qualify the technicians who perform the work. These provisions were put in place so as to ensure the quality of the on-site work
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