Maksimenko A V, Grigor'eva E L, Bezrukavnikova L M, Petrov A D, Tishchenko E G, Arkhipova O G, Torchilin V P
Biull Eksp Biol Med. 1991 Sep;112(9):265-7.
The present paper dwells on biomedical study of aldehyde dextran modified superoxide dismutase. Pharmacokinetic data demonstrated that modification of superoxide dismutase increased its half-time. A rat model of experimental silicosis showed that aldehyde dextran modified superoxide dismutase inhibited evolving fibrosis in the lungs. The same dose of native enzyme produced no therapeutic effect. Thus, superoxide dismutase can be considered as a potential agent for treatment of fibrosis due to its modification.
本文详述了醛基葡聚糖修饰超氧化物歧化酶的生物医学研究。药代动力学数据表明,超氧化物歧化酶的修饰增加了其半衰期。实验性矽肺大鼠模型显示,醛基葡聚糖修饰的超氧化物歧化酶可抑制肺部正在发展的纤维化。相同剂量的天然酶未产生治疗效果。因此,由于其修饰作用,超氧化物歧化酶可被视为治疗纤维化的潜在药物。