肝素固定化EDA(+)纤维连接蛋白吸附剂的实验研究。

M. Yonekawa, M. Tanaka, A. Kawamura, K. Kukita, T. Tamaki, J. Meguro, E. Sakashita, M. Sawamoto
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引用次数: 1

摘要

EDA(+)纤维连接蛋白可能参与免疫疾病的发病和/或进展,通过冷冻过滤有效地从血浆中去除;然而,冷冻过滤不仅去除EDA(+)纤维连接蛋白,还去除其他蛋白质。因此,我们开发了一种新的吸附剂,利用其与肝素的高亲和力。本研究的目的是评价EDA(+)纤维连接蛋白(OHC-20)吸附剂在实验性关节炎中的作用。通过注射0.5 mg丁酸分枝杆菌诱导Lewis大鼠实验性关节炎。将大鼠分为4组;1个非治疗组,3个治疗组。各治疗组分别于第1、3、5天进行吸附治疗3次;B组第7、9、11天;第13、15、17天,B、c组大鼠的步行姿势由拖行变为踮脚行走,后足体积的增大受到抑制。由此可见,肝素固定化吸附剂可能在免疫疾病治疗中具有良好的应用前景。
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Experimental study using heparin-immobilized adsorbent of EDA(+)fibronectin.
EDA(+)fibronectin, which might participate in the pathogenesis and/or progress of immune diseases, is efficiently removed from plasma by cryofiltration; however, cryofiltration removes not only EDA(+)fibronectin, but also other proteins. We thus developed a new adsorbent by using its high affinity with heparin. The purpose of this study was to evaluate the efficacy of the adsorbent of EDA(+)fibronectin (OHC-20) in experimental arthritis. The experimental arthritis was induced by injection of 0.5 mg of Mycobacterium butyricum in Lewis rats. Rats were divided into 4 groups; 1 nontreatment group, and 3 treatment groups. Adsorption therapy in treatment groups was performed three times: on Days 1, 3, and 5 in Group A; Days 7, 9, and 11 in Group B; and Days 13, 15, and 17 in Group C. The walking postures of rats improved from dragging to walking on tiptoe, and the increase of hind-foot volume was suppressed in Groups B and C. We conclude that heparin-immobilized adsorbent might be promising for immune diseases.
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