免疫调节剂2-氰氮嘧啶azimexone和bm41.332对小鼠不稳定血红蛋白形成的影响。

B Isert, K Mengel, U Bicker, K D Friedberg
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引用次数: 5

摘要

单次剂量20mg /kg后,Azimexone引起小鼠不稳定血红蛋白的形成。另一种2-氰氮吡啶类免疫调节药物bm41.332仅在单次口服500 mg/kg后才诱导这些不稳定的血红蛋白。随着不稳定血红蛋白的形成,我们观察到亨氏小体的发展。2-氰氮吡啶的这些作用既不是由血红蛋白的形成引起的,也不是由保护血红蛋白抗氧化成分(G6PD、过氧化氢酶、谷胱甘肽)的损害引起的。消除脾脏中改变的血红蛋白之后,可以测量脾脏中铁含量的升高。
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The influence on the formation of unstable haemoglobin by the immunomodulating 2-cyanaziridines azimexone and BM 41.332 in mice.

Azimexone causes in mice the formation of unstable haemoglobins after a single dose of 20 mg/kg. BM 41.332, another immunomodulating drug of the 2-cyanaziridine class, induces these unstable haemoglobins only after a single oral administration of 500 mg/kg. Subsequently to the formation of unstable haemoglobins we observed a development of Heinz bodies. These effects of the 2-cyanaziridines were elicited neither by methaemoglobin formation nor by an impairment of the components protecting haemoglobin against oxidation (G6PD, catalase, glutathione). The elimination of the altered haemoglobin in the spleen could be followed by measurement of the rise in the iron content of the spleen.

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