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咪唑啉酮是一种新型晚期糖基化终产物,在链脲佐菌素诱导的糖尿病大鼠肾脏中含量很高。

Imidazolone, a novel advanced glycation end product, is present at high levels in kidneys of rats with streptozotocin-induced diabetes.

作者信息

Niwa T, Katsuzaki T, Ishizaki Y, Hayase F, Miyazaki T, Uematsu T, Tatemichi N, Takei Y

机构信息

Nagoya University Daiko Medical Center, Higashi-ku, Japan.

出版信息

FEBS Lett. 1997 May 5;407(3):297-302. doi: 10.1016/s0014-5793(97)00362-1.

Abstract

We produced a monoclonal antibody to imidazolones A and B, novel advanced glycation end products formed from the reaction of 3-deoxyglucosone (3-DG) with the guanidino group of arginine. Liquid chromatography/mass spectrometry demonstrated that the formation of imidazolone A by incubating 3-DG with arginine is very rapid, reaching a maximum concentration within 24 h, but the formation of imidazolone B is very slow and low in quantity even after 2 weeks. Thus, at physiological conditions the formation of imidazolone A is dominant, while that of imidazolone B is negligible. Immunochemistry demonstrated that the imidazolone content in the kidneys of streptozotocin-induced diabetic rats was significantly higher than in the control rats. Serum levels of 3-DG in the diabetic rats were also significantly higher than in control rats. 3-DG attacks the arginine residues of the tissue proteins, producing imidazolone at high levels in the kidneys affected by diabetic nephropathy.

摘要

我们制备了一种针对咪唑啉酮A和B的单克隆抗体,咪唑啉酮A和B是由3-脱氧葡萄糖酮(3-DG)与精氨酸的胍基反应形成的新型晚期糖基化终产物。液相色谱/质谱分析表明,3-DG与精氨酸孵育形成咪唑啉酮A的过程非常迅速,在24小时内达到最大浓度,但即使在2周后,咪唑啉酮B的形成也非常缓慢且产量很低。因此,在生理条件下,咪唑啉酮A的形成占主导地位,而咪唑啉酮B的形成可忽略不计。免疫化学分析表明,链脲佐菌素诱导的糖尿病大鼠肾脏中的咪唑啉酮含量显著高于对照大鼠。糖尿病大鼠血清中的3-DG水平也显著高于对照大鼠。3-DG攻击组织蛋白的精氨酸残基,在受糖尿病肾病影响的肾脏中高水平产生咪唑啉酮。

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