Comparative Study of 1.5-Hour and 48-Hour Homologous Passive Cutaneous Anaphylaxis in the Mouse Ear
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概要
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To characterize passive cutaneous anaphylaxis (PCA) in the mouse ear, reactions caused by non-heated and heated antiserum were compared to those caused by monoclonal immunoglobulin E antibody (mc-IgE) and monoclonal immunoglobulin G_1 antibody (mc-IgG_1). Heat treatment at 56℃ did not alter the activity of antiserum or mc-IgG_1 to elicit the 1.5-h PCA. The 1.5-h PCA mediated by mc-IgE and 48-h PCA's mediated by both antiserum and mc-IgE were abrogated almost completely by heating at 56℃ for 2 h. The 48-h PCA was not elicited by mc-IgG_1. The sensitized state persisted at least for 7 d when mice were sensitized with non-heated antiserum or mc-IgE. In contrast, the sensitized state disappeared rapidly in cases of heated antiserum and mc-IgG_1. In 48-h PCA's mediated by antiserum and mc-IgE, extravasated dye in the ear was detected 5 min after challenge and the reaction was terminated in 15 min. In contrast, in the 1.5-h PCA mediated by heated antiserum, the accumulation of dye in the ear was delayed slightly when compared to the 48-h PCA. In mc-IgG_1-mediated 1.5-h PCA, the delay was significant. Both 1.5-h PCA's mediated by heated antiserum and mc-IgG_1,and the 48-h PCA's mediated by antiserum and mc-IgE were not observed in WBB6 F_1-W/W^v mice, which lack mast cells. All these PCA's were inhibited equally by tranilast, an inhibitor of mediator release from mast cells. The 1.5-h PCA was abrogated completely when heated antiserum was absorbed with a rabbit anti-mouse IgG_1 serum coupled-Sepharose 4B. On the other hand, the 48-h PCA was abrogated completely by absorption of the antiserum with goat anti-mouse IgE serum coupled-Sepharose 4B. These results indicated that the 48-h PCA in mice sensitized with antiserum is mediated by IgE antibody. In the 1.5-h PCA in mice sensitized with heated antiserum, it is considered that IgG_1 antibody plays a major role to elicite PCA. However, it is also considered that the reaction is modified by other serum components.
- 公益社団法人日本薬学会の論文
著者
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Koda Akihide
岐阜薬科大学 薬
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Inagaki Naoki
Department Of Electrical And Computer Engineering Nagoya Institute Of Technology
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Nagai Hiroichi
Department Of Clinical Pharmacology Gifu Pharmaceutical University
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Koda Akihide
Department Of Pharmacology Gifu College Of Pharmacy
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NAKATOMI Ichiro
Department of Pharmacology, Gifu Pharmaceutical University
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Inagaki Naoki
Departmen T Of Pharmacology Gifu Pharmaceutical University
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Inagaki Naoki
Laboratory Of Bioresponses And Regulation United Graduate School Of Drug Discovery And Medical Information Science Gifu University
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Nagai Hiroichi
Department Of Applied Pharmacology Graduate School Of Medicine And Pharmaceutical Sciences University Of Toyama
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