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  • Type 1 (insulin-dependent) diabetes  (2)
  • 95.55.Ym  (1)
  • Activity index  (1)
  • Calcium ionophore  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Rheumatology international 15 (1995), S. 31-37 
    ISSN: 1437-160X
    Keywords: Rheumatoid arthritis ; IL-1β ; TNFα ; IFN-γ ; Activity index
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Serum cytokines such as interleukin 1β (IL-1β), interferon γ (IFN-γ), and tumor necrosis factor α (TNFα) were measured in 40 patients with rheumatoid arthritis (RA). In the 40 patients studied, serum IL-1β was detected in 5 patients, IFN-γ in 10 patients, and TNFα in 20 patients. The IL-1β-positive group showed increased values of activity indices compared to the IL-1β-negative group. Values of serum IFN-γ correlated well with the number of peripheral blood lymphocytes and CD3+ cells and with the percentage of CD3+ CD26+ cells. Values of serum TNFα correlated positively with the number of peripheral blood monocytes and the percentage of CD3+ HLA-DR+ and CD3+ CD25+ cells. These results indicated that serum IL-1β in RA patients reflects the activity of RA, while the serum IFN-γ and TNFα in RA patients may be related to circulating activated lymphocytes and monocytes, respectively.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0649
    Keywords: 04.80.Nn ; 07.60.Ly ; 95.55.Ym
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract We describe preliminary experimental results concerning the operation of a 3 m arm-length Michelson interferometer with two Fabry-Perot cavities whose mirrors and beam splitter are suspended independently by wires. The reflected light beams from the two Fabry-Perot cavities are recombined to obtain interference at a photo-detector; this scheme is necessary for future power-recycled laser interferometers used to detect gravitational waves. The fundamental properties of the interferometer are presented, including the power spectral density of the displacement noise.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-0533
    Keywords: Calcium ionophore ; Plasma membrane ; Freeze fracture ; Skeletal muscle ; Muscular dystrophy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The present study was undertaken to investigate changes in the muscle fiber when treated with calcium ionophore. Muscles treated with ionophore showed disruption of the plasma membrane of the muscle fiber, delta lesions, marked contraction of the myofibrills, and dissolution of Z lines and I bands. Black granules of calcium pyroantimonate were observed inside the plasma membrane in ionophoretreated muscle fibers without alteration of the other muscle organelles. The density of the intramembranous particles was less in muscle treated with calcium ionophore than in the control muscle. These results support the previous hypothesis that the increased concentration of intracellular calcium activates calcium-activated neutral protease and induces necrosis of the myofiber. The mechanism for the decrease in the density of intramembranous particles is unsolved. However, the disruption of the plasma membrane may not be a direct effect of calcium ionophore on it, but a secondary phenomenon which occurs after the calcium-induced necrosis of the muscle fibers.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-0428
    Keywords: Islet cell antibodies ; Type 1 (insulin-dependent) diabetes ; Epstein-Barr virus ; peripheral blood lymphocytes ; transformation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Islet cell antibodies are usually detected in the sera of almost all Type 1 (insulin-dependent) diabetic patients within several months after onset of the disease. The antibodies then disappear quite early during the course of the disease. The present study was undertaken to detect islet cell antibody-producing clones in peripheral blood lymphocytes of Type 1 diabetic patients whose islet cell antibodies could not be detected in sera. Epstein-Barr virus-transformed lymphocytes were employed to enhance the production of antibodies and to detect the clones from peripheral blood lymphocytes. Peripheral blood lymphocytes were obtained from 40 islet cell antibody-negative Type 1 diabetic patients, 10 antibody-positive Type 1 diabetic patients, 30 Type 2 (non-insulin-dependent) diabetic patients and 40 normal control subjects. Epstein-Barr virus-transformed lymphocytes were cultured for 4 weeks and the culture supernatants were used for assay of islet cell antibodies. Islet cell antibody assays were performed by immunohistochemical methods using peroxidase-labelled protein A for IgG antibodies, peroxidase-labelled anti-human IgM antibodies for IgM antibodies and fresh frozen human pancreatic tissue. IgG-islet cell antibodies were detected in 26 islet cell antibody-negative patients (65%), eight antibody-positive patients (80%) and one Type 2 diabetic patient (3%) in the culture supernatants. Islet cell antibodies in the supernatants could not be detected in any of the control subjects. IgM-islet cell antibodies could not be detected in any of the patients or control subjects. These findings indicate that islet cell antibody-producing clones exist in peripheral blood lymphocytes from Type 1 diabetic patients whose islet cell antibodies cannot be detected in their sera and IgG-islet cell antibodies might be a specific characteristic of Type 1 diabetes. The detection of islet cell antibodies from Epstein-Barr virus-transformed lymphocytes may be useful in examining the role of autoimmune mechanisms in the development of disease.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-0428
    Keywords: Islet cell antibody (ICA) ; Type 1 (insulin-dependent) diabetes ; peroxidase-labeled protein A ; incidence of ICA ; ICA titres
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We have developed a new method of detecting islet cell antibodies using peroxidase-labeled protein A, and have determined the incidence of ICA in Type 1 (insulin-dependent) diabetes in Japan. In our method, fresh frozen sections of human pancreas and serum samples were incubated and then treated with peroxidase-labeled protein A at room temperature. Conjugates of peroxidase and protein A were subjected to Sephadex G-200 column chromatography, and only the 80,000 dalton peak was employed. The treated sections were allowed to react with haematoxylin and eosin (HE) to confirm the localization of islet cells. With this method, human pancreatic tissues can be used regardless of age and blood type, and the stained sections can be stored for more than 5 years. Serum samples obtained from 52 patients with Type 1 diabetes, 54 with Type 2 (non-insulin-dependent) diabetes and 100 control subjects were examined. In patients with Type 1 diabetes, islet cell antibodies were detected in 14 of 14 (0.5 years after onset), 3 of 6 (0.5–1 years after onset), 7 of 16 (1–5 years after onset) and 2 of 16 (more than 5 years after onset). In contrast, only 4 of 54 patients with Type 2 diabetes and none of the controls were ICA positive. It is concluded that, with our newly developed method using peroxidase-labeled protein A, ICA is present in all Japanese Type 1 diabetic patients whose diabetic manifestations are less than 0.5 years duration from onset.
    Type of Medium: Electronic Resource
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