Japanese Journal of Allergology
Online ISSN : 1347-7935
Print ISSN : 0021-4884
ISSN-L : 0021-4884
Volume 49, Issue 1
Displaying 1-16 of 16 articles from this issue
  • Article type: Cover
    2000Volume 49Issue 1 Pages Cover1-
    Published: January 30, 2000
    Released on J-STAGE: February 10, 2017
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  • Article type: Cover
    2000Volume 49Issue 1 Pages Cover2-
    Published: January 30, 2000
    Released on J-STAGE: February 10, 2017
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  • Article type: Appendix
    2000Volume 49Issue 1 Pages App1-
    Published: January 30, 2000
    Released on J-STAGE: February 10, 2017
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  • Article type: Appendix
    2000Volume 49Issue 1 Pages App2-
    Published: January 30, 2000
    Released on J-STAGE: February 10, 2017
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  • Sei Sasaki
    Article type: Article
    2000Volume 49Issue 1 Pages 1-4
    Published: January 30, 2000
    Released on J-STAGE: February 10, 2017
    JOURNAL FREE ACCESS
  • Shinpei Torii
    Article type: Article
    2000Volume 49Issue 1 Pages 5-8
    Published: January 30, 2000
    Released on J-STAGE: February 10, 2017
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  • Junichi Yata
    Article type: Article
    2000Volume 49Issue 1 Pages 9-11
    Published: January 30, 2000
    Released on J-STAGE: February 10, 2017
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  • Toshiaki Sakai, Atushi Inoue, Chang-Sung Koh, Shu-ich Ikeda
    Article type: Article
    2000Volume 49Issue 1 Pages 12-18
    Published: January 30, 2000
    Released on J-STAGE: February 10, 2017
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    Free radicals are molecules that contain at least one unpaired electron and by nature are highly reactive and potentially destructive. Free radical damage can play an important role of demyelination. Glutathione peroxidase, which plays a role in free radical defenses, and myeloperoxidase and lactoferrin, which are considered to reflet the strength of oxidative stress, were examined by monoclonal antibody-based enzyme immunoassay on serum samples taken from patients with neuroimmunological disorders, namely, 35 multiple sclerosis(MS), and 2 Balo disease, 10 Guillain-Barre syndrome(GBS), and 25 human T-lymphotropic virus type-1 associated myelopathy (HAM). The levels of glutathione peroxidase in active phase of MS (8.37±5.59μg / ml: p<0.05)were increased rather than in inactive phase (5.05±2.44μg / ml) and control (5.41±1.40μg / ml), the levels of myeloperoxidase in HAM (95.5±89.1ng / ml: p<0.05) were increased rather than in controls (21.5±4.1ng / ml), and the levels of lactoferrin were not significantly increased than in other disease and control. Moreover the levels of myeloperoxidase and lactoferrin are increased in Balo disease (myeloperoxidase 487,762ng / ml; not signigicant, lactoferrin 2.58, 2.77ng / ml; not significant) than in control (myeloperoxidase 21.5±4.1ng / ml, lactoferrin 0.69±0.32ng / ml). In conclusion, we have here first demonstrated that the levels of these enzyme were not paralleled in MS and Balo diseases. In GBS the levels of all these enzyme were not increased. Thus, these findings suggest that these enzyme may play an important role of the disease activity of Balo, and may reflect the activity of the defense of MS.
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  • Fumio Kokubu, Shigenori Nakajima, Kouji Ito, Souhei Makino, Satoshi Ki ...
    Article type: Article
    2000Volume 49Issue 1 Pages 19-31
    Published: January 30, 2000
    Released on J-STAGE: February 10, 2017
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    We examined an effectiveness of a new asthma telemedicine system in reducing hospitalizations using a multi-site randomized control study. In this program, a nurse under physician supervision monitors the patient's airway status at home and provides instructions to individuals via the telephone, helping them manage exacerbations as well as reinforcing proper use of a zone-controlled management plan. Patients with a high risk for hospitalization were screened based on the numbers of emergency room visits and hopsitalizations found in a previous study and randomly assigned to either and telemedicine or control group. After a six-month study period, an 83% reduction in hospitalization was demonstrated in the telemedicine group versus the control group, with a P value of 0.01. Improvement of peak expiratory flow and symptoms were also shown in the study group. We conclude that the key success factors in home asthma management for poorly controlled asthma patients are early detection of exacerbations through daily peak flow monitoring, compliance with prescribed daily prophylactic anti-inflammatory steroid medications, and immediate action as specified by a zone-controlled action plan upon the first signs of deterioration.
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  • Yasuhiro Nakano, Masao Toda, Minoru Yoshida, Hironori Sagara
    Article type: Article
    2000Volume 49Issue 1 Pages 32-39
    Published: January 30, 2000
    Released on J-STAGE: February 10, 2017
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    Asthma is associated with a chronic remodeling of the airways, but it remains to be elucidated whether repeated bronchoconstriction (BC) influences any structural attributes of the lungs. To investigate the role of repeated BC on the morphology of the airways, we chronically exposed guinea pigs to an aerosol of acetylcholine (ACH) over a period of 6 months. The guinea pigs were challenged with either ACH or saline daily for 10 days and thereafter were challenged once a week. To compare repeated BC with a chronic model of allergic inflammation, an additional group of animals were sensitized to aerosolized ovalbumin (OA) and subsequently exposed with OA. The airway wall area and basement membrane (BM) thickness were measured by standard morphometric techniques. Both airway wall area and BM thickness were significantly increased in OA exposed guinea pigs compared with both saline control and AHC-exposed guinea pigs. Our result suggest that persistent bronchoconstriction and / or allergic airway inflammation in asthmatics may contribute to the thickness of the airway wall observed in this disorder. However, repeated acute bronchoconstriction events may not contribute to the increase in the airway wall or BM thickness.
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  • Tomoki Kubota, Kazuyosi Koga, Hayao Araki, Hirosi Odajima, Sankei Nish ...
    Article type: Article
    2000Volume 49Issue 1 Pages 40-51
    Published: January 30, 2000
    Released on J-STAGE: February 10, 2017
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    β-adrenaline receptors exist on peripheral mononuclear leukocytes as well as in lung tissue. We assessed the relationships of plasma catecholamine release by exercise to aerobic capacity and to exercise-induced asthma (EIA) in asthmatic children (Study 1). We then measured mononuclear leukocyte β-aderenergic receptor densities at rest and asessed the relationships of the number of receptors to aerobic capacity, EIA, and bronchial responsiveness to acetylcholine (Study 2). Study 1: Eleven children (9 males, 2 females ; 11〜16 years old) with bronchial asthma participated in this study. The subjects underwent an incremental aerobic exercise test on a cycle ergometer to determine their aerobic capacity at the lactic threshold (LT) and Vo_2max. Each subject underwent an EIA test of which the intensity was 175% of LT, and plasma catecholamine concentrations were measured before and after exercise. A significant negative relationship was found between the degree of EIA and % change of plasma adrenaline concentrations to rest level (p<0.05), and a significant positive relationship was found between Vo@S22@E2max / wt and % change of plasma adrenaline concentrations (p<0.05). Study 2: Twelve asthmatic children (10 males, 2 females; 11〜16 years old) participated in this study. Aerobic capacity, and degree of EIA were also measured in each subject by the same method as that used in Study. 1. The number of mononuclear leukocyte β-adrenergic receptors at rest was determined by (-) [^<125>I]-iodocyanopindolol binding in each subject. A significant negative relationship was found between the number of adrenergic receptors and Max. % fall in FEV_<1.0> (p<0.01), and a significant positive relationship was found between the number of adrenergic receptors and Vo_2max / kg (p<0.01). These results suggested that a reduced adrenaline production and a reduced number of β-receptors contributed to the pathogenesis of EIA.
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  • Article type: Appendix
    2000Volume 49Issue 1 Pages 52-
    Published: January 30, 2000
    Released on J-STAGE: February 10, 2017
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  • Article type: Appendix
    2000Volume 49Issue 1 Pages 53-
    Published: January 30, 2000
    Released on J-STAGE: February 10, 2017
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  • Article type: Appendix
    2000Volume 49Issue 1 Pages 54-55
    Published: January 30, 2000
    Released on J-STAGE: February 10, 2017
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  • Article type: Appendix
    2000Volume 49Issue 1 Pages 56-59
    Published: January 30, 2000
    Released on J-STAGE: February 10, 2017
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  • Article type: Cover
    2000Volume 49Issue 1 Pages Cover3-
    Published: January 30, 2000
    Released on J-STAGE: February 10, 2017
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