Shechter Yoram, Tsubery Haim, Fridkin Mati
Department of Biological Chemistry, The Weizmann Institute of Science, Rehovot, 76100, Israel.
Biochem Biophys Res Commun. 2003 May 30;305(2):386-91. doi: 10.1016/s0006-291x(03)00715-0.
Exendin-4, a glucagon-like peptide-1 agonist, is a relatively short-lived species in the circulatory system in vivo. We have linked three moieties of 2-sulfo-9-fluorenylmethoxycarbonyl (FMS) to the three amino functions of exendin-4. FMS(3)-exendin-4 thus obtained has about 0.1% the glucose-lowering potency of the native peptide. Upon in vitro incubation at physiological conditions, the FMS moieties undergo hydrolysis generating the parent fully active, exendin-4. A single subcutaneous administration of FMS(3)-exendin-4 to healthy and type II diabetic mice has induced a glucose-lowering profile that exceeds in length several times that obtained by the native peptide. The reduction of blood glucose level began 1h after administration and was maximal 3-4h later. The blood glucose level returned to pre-administered values with t(1/2) of 12+/-0.7, 26+/-2, and 44+/-3h with doses of 1, 10, and 100 micro g/mouse, respectively. In sum, we have synthesized and characterized FMS(3)-exendin-4, a prodrug derivative of the native insulinotropic peptide, and found it to facilitate a prolonged and stable, glucose-lowering action in healthy and diabetic mice.
艾塞那肽-4是一种胰高血糖素样肽-1激动剂,在体内循环系统中是一种相对半衰期较短的物质。我们将三个2-磺基-9-芴甲氧羰基(FMS)部分连接到艾塞那肽-4的三个氨基上。由此得到的FMS(3)-艾塞那肽-4的降血糖效力约为天然肽的0.1%。在生理条件下进行体外孵育时,FMS部分会发生水解,生成具有完全活性的母体艾塞那肽-4。对健康小鼠和II型糖尿病小鼠单次皮下注射FMS(3)-艾塞那肽-4后,其降血糖曲线的时长超过天然肽数倍。给药后1小时血糖水平开始下降,3 - 4小时后降至最低。血糖水平分别在给药后12±0.7小时、26±2小时和44±3小时恢复到给药前水平,对应的给药剂量分别为1、10和100μg/小鼠。总之,我们合成并表征了FMS(3)-艾塞那肽-4,一种天然促胰岛素肽的前药衍生物,并发现它能在健康小鼠和糖尿病小鼠中促进长效且稳定的降血糖作用。