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4. Poster display IV experimental and instrumentation

Author

Masoli, O. Osvaldo, Redruello, M., Ogresta, F., Collaud, C., Koslowski, P., Baliño, N. Perez, Eleta, M., Arce, P., Vidal, L., Kardash, O., Maroz-Vadalajskaya, N. Natalia, Vanhove, C. Christian, Lahoutte, T., Defrise, M., Andreyev, A., Bossuyt, A., Franken, P. R., Franken, P. R. Philippe, Lahoutte, T., Maskali, F., Vanhove, C., Nloga, J., Tran, N., Marie, P. Y., Peix, A. Amalia, Garcia-Barreto, D., Ponce, F., Cabrera, L. O., Valiente, J., Tornes, F., Guerrero, I., Heres, F., Garcia, E. J., Cabale, B., Bindslev, L. Lene, Bisgaard, K. B. Kirsten, Haack-Soerensen, M. H. S. Mandana, Mortensen, S. M. Steen, Kragh, L. K. Linda, Kjaer, A. K. Andreas, Kastrup, J. K. Jens, Hesse, B. H. Birger, Aboul-Enein, F. Fatma, Battah, A., Fattah, A. Abdel, Atty, A. Abdel, Allam, A., Riou, L. Laurent, Broisat, A., Ghezzi, C., Lartizien, C., Berthonneche, C., Toufektsian, M. C., Maitrejean, S., Janier, M., Vanzetto, G., Fagret, D., Rouzet, F. Francois, Daou, D., Lebtahi, R., Frank, R., Leenhardt, A., Slama, M., Guludec, D. Le, Sarda-Mantel, L. Laure, Michel, J. B., Rouzet, F., Martet, G., Meulemans, A., Vrigneaud, J. M., Guludec, D. Le, Daou, D. Doumit, Coaguila, C., Benada, A., Razzouk, M., Idy-Peretti, I., Guludec, D. Le, Vilain, D., Lebtahi, R., Guludec, D. Le, Stegger, L. Lars, Schäfers, K., Flögel, U., Schrader, J., Schober, O., Levkau, B., Schäfers, M., Kies, P. Peter, Wichter, T., Schäfers, K. P., Schäfers, M., Wielepp, J. P. Peter, Baller, D., Pulawski, E., Weise, R., Fricke, E., Horstkotte, D., Burchert, W., Eckert, S., Dongas, A., Horstkotte, D., Burchert, W., Nekolla, S. G. Stephan, Martinez, M. J., Howe, W., Kehren, F., Ziegler, S. I., Vassiliadis, I. Ioannis, Souretis, G., Komporozos, C., Fountos, A., Papademetriou, A., Spanos, A., Antoniou, A., Strembelas, P., Moralidis, E. Efstratios, Arsos, G., Boundas, D., Georga, S., Karatzas, N., Karakatsanis, K., Prassopoulos, V. Vassilios, Parthenakis, F., Patrianakos, A., Koukouraki, S., Velidaki, A., Karkavitsas, N., Vardas, P., Velidaki, A. Antigone, Perisinakis, K., Koukouraki, S., Koutsikos, J., Prassopoulos, V., Vardas, P., Karkavitsas, N., Sundaraiya, S. Sumati, Sumati, S., Sambhasivam, KA., David, S., Zakavi, S. R. Seyed Rasoul, Kakhki, V. R. Dabagh, Jabari, H., Zingerman, B., Bendayan, D., Sagie, A., Solodky, A., Mats, I., Shapira, Y., Kremer, M. R., Zafrir, N. Nili, Rimini, M. L. Maria Luisa De, Catalano, M., Bonzani, G., Scalzone, A., Merenda, R., Monteforte, I., Monda, V., Muto, P., Carboni, G. P. Gian Piero, Miglionico, M., Tavolozza, M., Marcassa, C. Claudio, Campini, R., Calza, P., Giannuzzi, P., Eleuteri, E., Marcassa, C. Claudio, Campini, R., Scapellato, F., Temporelli, P. L., Giannuzzi, P., Pellegrino, T., Storto, G., Sorrentino, A. R., Silvestri, A., Filardi, P. Perrone, Brevetti, G., Cuocolo, A. Alberto, Cho, K. Keiichi, Kumita, S., Seino, K., Nakajo, H., Toba, M., Kumazaki, T., Muramatsu, T. Toshihiro, Yamazaki, T., Seki, K., Kawanami, J., Nakajima, T., Yamada, Y., Suga, T., Matsumoto, K., Nishimura, S., Taki, J. Junichi, Higuchi, T., Kawashima, A., Nakajima, K., Muramori, A., Matsunari, I., Tait, J. F., Vanderheyden, J. L., Strauss, H. W., Tonami, N., Adachi, I. Itaru, Shimomura, H., Kintaka, T., Komori, T., Ogura, Y., Kitaura, Y., Narabayashi, I., Iida, H. Hidehiro, Zeniya, T., Kim, K. M., Watabe, H., Teramoto, N., Yamamichi, Y., Alexanderson, E. Erick, Ricalde, A., Vargas, A., Meave, A., Amigo, M. C., Misko, J., Dziuk, M. Miroslaw, Warczynska, A., Skrobowska, E., Vasconcelos, M. Mariana, Martins, E., Faria, T., Oliveira, A., Pardal, N., Macedo, F., Pereira, J., Rocha-Gonçalves, F., Cantinho, G. Guilhermina, Pena, H., Freire, L., Veiga, A., Gonçalves, P., Godinho, F., Chua, T. Terrance, Lee, C. Y., Keng, F., Ding, Z. P., Koh, T. H., Awamleh, P. Paula, Talavera, P., Torres, V., Balsa, M. A., González, O., Alberca, M. T., Miguel, R., Cosío, F. G., Lomsky, M. Milan, Richter, J., Johansson, L., El-Ali, H., Åström, K., Ljungberg, M., Edenbrandt, L., Hung, G. U. Guang-Uei, Lee, K. W., Chen, C. P., Yang, K. T., Pekindil, G., Sarikaya, A. Ali, Ege, T., Salihoglu, S., Entok, E. Emre, Cavusoglu, Y., Ak, I., Vardareli, E., Timuralp, B., Tout, D. Deborah, Loong, C. Y., Naidoo, V. V., Aswegen, A. Van, Underwood, S. R., Thorley, P. J. Penelope, Goris, M. Michael, ZHU, H. J., Clements, I. P. Ian, Mullan, B. P., O’Connor, M. K., Breen, J. F., McGregor, C. G. A., Liu, Y. H. Yi-Hwa, Li, S., Bourke, B., Weyman, C., Sinusas, A. J., Ramakrishna, G. Gautam, Miller, T. D., O’Connor, M. K., Gibbons, R. J., Tsatkin, V., Wackers, F. J. T. H., Liu, Y. H. Yi-Hwa, Tsatkin, V., Prior, J. O. John, Facta, A. D., Schindler, T. H., Oxilia-Estigarribia, M. A., Hernandez-Pampaloni, M., Campisi, R., Zhang, X., Bischof-Delaloye, A., Nathan, L., Schelbert, H. R., Gullberg, G. T. Grant, Huesman, R. H., Reutter, B. W., Sitek, A., Veress, A. I., Weiss, J. A., Qi, J., Yang, Y., Gordi, T. Toufigh, Olmsted, A., Lieu, H., and Belardinelli, L.

Published
2005
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8. The dual frequency RV-coupling coefficient: a novel measure for quantifying cross-frequency information transactions in the brain

Author

Pascual-Marqui, RD, Faber, P, Kinoshita, T, Kitaura, Y, Kochi, K, Milz, P, Nishida, K, Yoshimura, M, and University of Zurich

Subjects
Methodology (stat.ME), FOS: Computer and information sciences, FOS: Biological sciences, Quantitative Biology - Neurons and Cognition, 10054 Clinic for Psychiatry, Psychotherapy, and Psychosomatics, Neurons and Cognition (q-bio.NC), 610 Medicine & health, Statistics - Methodology, 10074 The KEY Institute for Brain-Mind Research
Abstract

Identifying dynamic transactions between brain regions has become increasingly important. Measurements within and across brain structures, demonstrating the occurrence of bursts of beta/gamma oscillations only during one specific phase of each theta/alpha cycle, have motivated the need to advance beyond linear and stationary time series models. Here we offer a novel measure, namely, the "dual frequency RV-coupling coefficient", for assessing different types of frequency-frequency interactions that subserve information flow in the brain. This is a measure of coherence between two complex-valued vectors, consisting of the set of Fourier coefficients for two different frequency bands, within or across two brain regions. RV-coupling is expressed in terms of instantaneous and lagged components. Furthermore, by using normalized Fourier coefficients (unit modulus), phase-type couplings can also be measured. The dual frequency RV-coupling coefficient is based on previous work: the second order bispectrum, i.e. the dual-frequency coherence (Thomson 1982; Haykin & Thomson 1998); the RV-coefficient (Escoufier 1973); Gorrostieta et al (2012); and Pascual-Marqui et al (2011). This paper presents the new measure, and outlines relevant statistical tests. The novel aspects of the "dual frequency RV-coupling coefficient" are: (1) it can be applied to two multivariate time series; (2) the method is not limited to single discrete frequencies, and in addition, the frequency bands are treated by means of appropriate multivariate statistical methodology; (3) the method makes use of a novel generalization of the RV-coefficient for complex-valued multivariate data; (4) real and imaginary covariance contributions to the RV-coherence are obtained, allowing the definition of a "lagged-coupling" measure that is minimally affected by the low spatial resolution of estimated cortical electric neuronal activity., technical report, pre-print, 2016-03-16

Published
2016

11. Intracellular viral localization in murine coxsackievirus-B3 myocarditis. Ultrastructural study by electron microscopic in situ hybridization

Author

Ukimura, A., Deguchi, H., Kitaura, Y., Fujioka, S., Hirasawa, M., Kawamura, K., and Hirai, K.

Subjects
Male, Mice, Inbred C3H, Time Factors, viruses, Macrophages, Myocardium, virus diseases, Coxsackievirus Infections, Heart, Immunohistochemistry, Enterovirus B, Human, Mice, Microscopy, Electron, Myocarditis, Animals, RNA, Viral, Lymphocytes, In Situ Hybridization, Research Article
Abstract

Group B Coxsackieviruses are a common cause of myocarditis. To detect the viral genome and its localization in the myocardium, we examined C3H/He mice with Coxsackievirus B3 (CVB3) myocarditis on days 5, 8, and 14 after inoculation by the reverse transcriptase polymerase chain reaction and by in situ hybridization. Sense and antisense CVB3 RNA were detected in the myocardium of all mice up to day 14 by reverse transcriptase polymerase chain reaction. Light microscopic in situ hybridization with a cDNA probe for CVB3 showed clusters of positive signals in the areas of myocardial necrosis and cell infiltration. With electron microscopic in situ hybridization, CVB3 RNA was detected in the cytoplasm of cardiocytes, between the myofibrils, near the mitochondria, and in tubular or vesicular structures. Viral RNA was also detected in necrotic debris, in the cytoplasm of macrophages, and in the cytoplasm of interstitial fibroblasts. These findings suggest that CVB3 RNA is replicated in the cytoplasm of cardiocytes, transferred into tubular or vesicular structures, released into the interstitium, and phagocytosed by macrophages. Some positive signals were also detected in the cytoplasm of cardiocytes showing close contact with infiltrating lymphocytes, suggesting that the lymphocytes recognized virus-infected cardiocytes and caused cell-mediated immune cardiocyte damage.

Published
1997

31. Effect of NbC addition on mechanical properties of dual two-phase Ni3Al–Ni3V intermetallic alloy

Author

Kitaura, Y., Kaneno, Y., and Takasugi, T.

Subjects
*INTERMETALLIC compounds, *ALUMINUM alloys, *MECHANICAL properties of metals, *HIGH temperature metallurgy, *METAL microstructure, *HEAT treatment of metals, *FRACTURE mechanics
Abstract

Abstract: Dual two-phase intermetallic alloy that has an alloy composition of Ni75Al9V13Nb3 and is composed of geometrically close packed (GCP) Ni3Al (L12) and Ni3V (D022) phases was studied, focusing on the effect of NbC addition on high-temperature tensile properties. The two-phase microstructures defined by primary Ni3Al precipitates and eutectoid region consisting of Ni3Al and Ni3V phases were kept and were dispersed by Nb2C particles regardless of NbC content. EPMA analysis showed that alloy compositions in matrix of the NbC added alloy were different from those in the base alloy. The positive temperature dependence of flow strength was observed for all NbC added alloys. In low temperature range the maximum strengthening took place at 1at.% NbC content. On the other hand, tensile elongation increased with increasing NbC content up to 1at.% NbC content and gradually decreased at NbC content over 1at.% content in whole temperature ranges. Also, the NbC addition resulted in change of the fracture mode from brittle transgranular fracture to ductile transgranular fracture in low temperature range, and from brittle intergranular fracture to ductile transgranular in high temperature range. Possible mechanisms responsible for the strengthening and ductilization by NbC addition were discussed, based on the behavior of C solutes in the matrix, which were released from the charged NbC carbides. [Copyright &y& Elsevier]

Published
2010
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32. Suppression of inflammation in rat autoimmune myocarditis by S100A8/A9 through modulation of the proinflammatory cytokine network.

Author

Otsuka K, Terasaki F, Ikemoto M, Fujita S, Tsukada B, Katashima T, Kanzaki Y, Sohmiya K, Kono T, Toko H, Fujita M, Kitaura Y, Otsuka, Kaoru, Terasaki, Fumio, Ikemoto, Masaki, Fujita, Shuichi, Tsukada, Bin, Katashima, Takashi, Kanzaki, Yumiko, and Sohmiya, Koichi

Abstract

Aims: S100A8/A9 is expressed in activated monocytes/macrophages and assumed to be heavily involved in the pathogenesis of acute inflammation. Although several studies have asserted that S100A8/A9 has a proinflammatory function, the exact biological function of S100A8/A9 is yet to be described. We examined the anti-inflammatory effects of S100A8/A9 on experimental autoimmune myocarditis (EAM) in rats.Methods and Results: Experimental autoimmune myocarditis was induced in Lewis rats by immunization with porcine cardiac myosin. The recombinant (R-) S100A8/A9 was injected intraperitoneally into EAM rats. R-S100A8/A9 attenuated the severity of myocarditis, as evidenced by echocardiographic and histological findings. In addition, we found that not only the mRNA expression of proinflammatory cytokines [interleukin (IL)-1beta, IL-6, and tumour necrosis factor (TNF)-alpha] in the myocardium, but also their serum concentrations were suppressed in EAM rats treated with R-S100A8/A9. Nuclear factor-kappa B expression in inflammatory cells was also suppressed in the treated rats. To elucidate the mechanistic function of S100A8/A9 on proinflammatory cytokines in vivo, we used an ELISA on the supernatant of homogenized heart tissue treated with R-S100A8/A9. The findings revealed high-affinity binding of R-S100A8/A9 with IL-1beta, IL-6, and TNF-alpha in the myocardium, suggesting the trapping of proinflammatory cytokines by R-S100A8/A9.Conclusion: S100A8/A9 attenuates EAM through modulation of the proinflammatory cytokine network. [ABSTRACT FROM AUTHOR]

Published
2009
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34. Coxsackie B Virus Infection in Idiopathic Dilated Cardiomyopathy: Clinical and Pharmacological Implications.

Author

Fujioka, S. and Kitaura, Y.

Subjects
*CARDIOMYOPATHIES, *COXSACKIEVIRUSES, *POLYMERASE chain reaction
Abstract

Idiopathic dilated cardiomyopathy (IDC) is a myocardial disease characterised by ventricular dilatation, impaired contractility, and the symptoms of congestive heart failure. Although the causes of IDC remain uncertain, much interest has been focused on the enteroviral infection in the myocardium in the pathogenesis of this disease. Enteroviral RNA has been demonstrated in the myocardium at all stages of IDC. Recent studies using sequence analysis of enteroviral polymerase chain reaction (PCR) products have shown that the viruses detected in hearts of patients with IDC are coxsackie B. In addition, active coxsackieviral RNA replication in the myocardium has been demonstrated by strand-specific detection of viral RNA. Viral antigen has also been found in hearts with IDC by immunohistochemical techniques. In tissue culture experiments and transgenic mice, it has been shown that restricted coxsackieviral RNA replication, and not infectious virus progeny, in the myocardium can impair cardiac contractile function and lead to dilated cardiomyopathy. Coxsackieviral RNA in the myocardium can be a marker of a poor clinical outcome after partial left ventriculectomy, and might influence prognosis after heart transplantation. Therefore, there is a therapeutic need to detect replicating coxsackieviral RNA in the myocardium, and a specific therapy for coxsackie B viruses is indicated in the management of patients with virus-positive IDC. [ABSTRACT FROM AUTHOR]

Published
2001
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35. Increased digitalis-like immunoreactive substances in patients with hypertrophic cardiomyopathy.

Author

Hayashi, T, Ijiri, Y, Toko, H, Shimomura, H, Okabe, M, Terasaki, F, Kitaura, Y, and Kawamura, K

Abstract

Aims Although increased digitalis-like immunoreactive substances have been found in cases of hypertension and heart failure, no information is available about digitalis-like immunoreactive substances in patients with hypertrophic cardiomyopathy. We investigated digitalis-like immunoreactive substances in the plasma and biopsied specimens of patients with hypertrophic cardiomyopathy.Methods and Results In 40 patients with hypertrophic cardiomyopathy (27 with the non-obstructive type and 13 with the obstructive type), the plasma concentration of digitalis-like immunoreactive substances was studied by fluorescence polarization immunoassay. Right ventricular endomyocardial biopsy specimens were analysed immunohistochemically, using a monoclonal antibody against digoxin. An increase in digitalis-like immunoreactive substances of more than 0·2ng.ml−1in plasma was found in six of 27 patients with non-obstructive hypertrophic cardiomyopathy (22·2%) and five of 13 with obstructive hypertrophic cardiomyopathy (38·4%). Under light microscopy, positive staining against the antibody was observed heterogeneously on some cardiocytes. In non-obstructive hypertrophic cardiomyopathy, digitalis-like immunoreactive substances in the plasma correlated with the left atrial dimension and inversely with the cardiac index. In obstructive hypertrophic cardiomyopathy, plasma and myocardial digitalis-like immunoreactive substances were positively correlated; they also correlated with left ventricular end-diastolic pressures. Under electron microscopy, digitalis-like immunoreactive substances were detected at the sarcolemma in the free wall, T-tubules, intercalated discs and Z-bands of cardiocytes.Conclusions Increased digitalis-like immunoreactive substances in plasma and cardiocytes, which may have been caused by pressure and/or volume overload, were found in patients with hypertrophic cardiomyopathy. Digitalis-like immunoreactive substances may act on the sarcolemma of cardiocytes and be transported into the cytoplasm. [ABSTRACT FROM PUBLISHER]

Published
2000
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43. Myocardial inflammatory cell infiltrates in cases of dilated cardiomyopathy: light microscopic, immunohistochemical, and virological analyses of myocardium specimens obtained by partial left ventriculectomy.

Author

Terasaki, Fumio, Okabe, Makoto, Hayashi, Tetsuya, Fujioka, Shigekazu, Suwa, Michihiro, Hirota, Yuzo, Kitaura, Yasushi, Kawamura, Keishiro, Isomura, Tadashi, Suma, Hisayoshi, Terasaki, F, Okabe, M, Hayashi, T, Fujioka, S, Suwa, M, Hirota, Y, Kitaura, Y, Kawamura, K, Isomura, T, and Suma, H

Published
1999
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49. Spontaneous myocarditis in DBA/2 mice. Light microscopic study with transmission and X-ray analytical electron microscopic studies.

Author

Hirasawa, M., Kitaura, Yasushi, Deguchi, Hirofumi, Ukimura, Akira, Kawamura, Keishiro, Kitaura, Y, Deguchi, H, Ukimura, A, and Kawamura, K

Abstract

DBA/2 inbred mice spontaneously develop myocarditis and a unique form of subepicardial inflammation of the right ventricle characterized by a prominent eosinophilic infiltrate with calcinosis. We studied this myocarditis using light microscopy and both transmission and analytical X-ray electron microscopy, paying particular attention to eosinophil-associated cardiocyte injury. At 5 weeks of age, many eosinophils and mononuclear cells (MNCs) were seen in the subepicardium of the right ventricle. Electron microscopy showed that cardiocytes underwent degenerative changes, including myofibrillar lysis, accumulation of Z-band material and mitochondrial inclusions, and rupture of plasma membranes. The infiltrating eosinophils appeared to be activated, and cells with cytoplasmic vacuoles, suggestive of degranulation, were noted. The myocardial injury was most severe in the 7th week and healed with myocardial fibrosis and calcinosis by the 8th week. Analytical X-ray electron microscopy showed that the calcinosis was initiated in mitochondrial inclusions of injured cardiocytes. The peripheral eosinophil count did not increase during the course of the disease, but there was a positive correlation between the ratio of eosinophils to infiltrated white blood cells (Eo/WBCs) in the right ventricle and the severity of myocardial damage. Eosinophils may play a significant part in subepicardial cardiocyte injury seen in DBA/2 mice. [ABSTRACT FROM AUTHOR]

Published
1998
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