14 research outputs found

    A Molecular Line Observation toward Massive Clumps Associated with Infrared Dark Clouds

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    We have surveyed the N2H+ J=1-0, HC3N J=5-4, CCS J_N=4_3-3_2, NH3 (J, K) = (1, 1), (2, 2), (3, 3), and CH3OH J=7-6 lines toward the 55 massive clumps associated with infrared dark clouds by using the Nobeyama Radio Observatory 45 m telescope and the Atacama Submillimeter Telescope Experiment 10 m telescope. The N2H+, HC3N, and NH3 lines are detected toward most of the objects. On the other hand, the CCS emission is detected toward none of the objects. The [CCS]/[N2H+] ratios are found to be mostly lower than unity even in the Spitzer 24 micron dark objects. This suggests that most of the massive clumps are chemically more evolved than the low-mass starless cores. The CH3OH emission is detected toward 18 out of 55 objects. All the CH3OH-detected objects are associated with the Spitzer 24 micron sources, suggesting that star formation has already started in all the CH3OH-detected objects. The velocity widths of the CH3OH J_K=7_0-6_0 A+ and 7_{-1}-6_{-1} E lines are broader than those of N2H+ J=1-0. The CH3OH J_K=7_0-6_0 A+ and 7_{-1}-6_{-1} E lines tend to have broader linewidth in the MSX dark objects than in the others, the former being younger or less luminous than the latter. The origin of the broad emission is discussed in terms of the interaction between an outflow and an ambient cloud.Comment: Accepted to Ap

    A Proteomic Approach for the Diagnosis of ‘Oketsu’ (blood stasis), a Pathophysiologic Concept of Japanese Traditional (Kampo) Medicine

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    ‘Oketsu’ is a pathophysiologic concept in Japanese traditional (Kampo) medicine, primarily denoting blood stasis/stagnant syndrome. Here we have explored plasma protein biomarkers and/or diagnostic algorithms for ‘Oketsu’. Sixteen rheumatoid arthritis (RA) patients were treated with keishibukuryogan (KBG), a representative Kampo medicine for improving ‘Oketsu’. Plasma samples were diagnosed as either having an ‘Oketsu’ (n = 19) or ‘non-Oketsu’ (n = 29) state according to Terasawa's ‘Oketsu’ scoring system. Protein profiles were obtained by surface-enhanced laser desorption/ionization time-of-flight mass spectrometry (SELDI-TOF MS) and hierarchical clustering and decision tree analyses were performed. KBG treatment for 4 or 12 weeks decreased the ‘Oketsu’ scores significantly. SELDI protein profiles gave 266 protein peaks, whose expression was significantly different between the ‘Oketsu’ and ‘non-Oketsu’ states. Hierarchical clustering gave three major clusters (I, II, III). The majority (68.4%) of ‘Oketsu’ samples were clustered into one cluster as the principal component of cluster I. The remaining ‘Oketsu’ profiles constituted a minor component of cluster II and were all derived from patients cured of the ‘Oketsu’ state at 12 weeks. Construction of the decision tree addressed the possibility of developing a diagnostic algorithm for ‘Oketsu’. A reduction in measurement/pre-processing conditions (from 55 to 16) gave a similar outcome in the clustering and decision tree analyses. The present study suggests that the pathophysiologic concept of Kampo medicine ‘Oketsu’ has a physical basis in terms of the profile of blood proteins. It may be possible to establish a set of objective criteria for diagnosing ‘Oketsu’ using a combination of proteomic and bioinformatics-based classification methods
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