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格列氟胺,一种新型高效口服抗糖尿病药物。

Gliflumide, a new oral antidiabetic of high potency and efficacy.

作者信息

Blumenbach L, Gerhards E, Gutsche H, Klein W, Loge O, Losert W, Schillinger E, Speck U, Vetter H, Wendt H

出版信息

Int J Clin Pharmacol Biopharm. 1975 Jul;12(1-2):141-51.

PMID:809367
Abstract

Gliflumide is an optically active sulfonylaminopyrimidine. In rats, the drug exhibited a long-lasting hypoglycemic effect following oral as well as intravenous administration. This effect resembled the action of glibenclamide, but was brought about by doses 5-10 times lower. In healthy volunteers, oral administration (0.0125 mg/kg) or intravenous injection (0.01mg/kg) of gliflumide resulted in a 30-40 per cent decrease of blood glucose characterized by slow onset and long duration. The stimulation of insulin secretion was studied after intravenous injection of gliflumide (0.01 mg/kg) and compared to the action of glibenclamide (0.01 mg/kg) and tolbutamide (10 mg/kg). Although the effect of these doses, measured by the area above the initial level, was similar, a different time course of action was found. Gliflumide and glibenclamide, compared with tolbutamide, produced a delayed and prolonged response. These characteristics were more pronounced with gliflumide. Maximal serum insulin levels were found after 3, 23, and 90 minutes for tolbutamide, glibenclamide, and gliflumide, respectively. In maturity-onset diabetics requiring glibenclamide or glibenclamide + biguanide, gliflumide was shown to have about the same efficacy as glibenclamide, the corresponding doses being 1.5-5 (generally 3) times lower.

摘要

格列氟胺是一种旋光性磺酰氨基嘧啶。在大鼠中,该药物经口服和静脉给药后均呈现出持久的降血糖作用。这种作用类似于格列本脲,但产生该作用的剂量要低5 - 10倍。在健康志愿者中,口服(0.0125mg/kg)或静脉注射(0.01mg/kg)格列氟胺会导致血糖降低30 - 40%,其特点是起效缓慢且持续时间长。静脉注射格列氟胺(0.01mg/kg)后研究了胰岛素分泌的刺激情况,并与格列本脲(0.01mg/kg)和甲苯磺丁脲(10mg/kg)的作用进行了比较。尽管以初始水平以上的面积衡量,这些剂量的作用相似,但发现作用的时间进程不同。与甲苯磺丁脲相比,格列氟胺和格列本脲产生的反应延迟且持续时间长。格列氟胺的这些特征更为明显。甲苯磺丁脲、格列本脲和格列氟胺分别在3分钟、23分钟和90分钟后达到最大血清胰岛素水平。在需要格列本脲或格列本脲 + 双胍类药物治疗的成年型糖尿病患者中,格列氟胺显示出与格列本脲大致相同的疗效,相应剂量低1.5 - 5倍(一般为3倍)。

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