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Potent antihyperglycaemic property of a new imidazoline derivative S-22068(PMS 847) in a rat model of NIDDM

机译:新型咪唑啉衍生物S-22068(PMS 847)在NIDDM大鼠模型中的有效抗高血糖特性

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摘要

Recent data suggest that some imidazoline derivatives can lower plasma glucose in experimental animal models of diabetes. We studied the activity of an imidazoline S-22068, in rat model of non- insulin-dependent diabetes mellitus(NIDDM) produced with a low dose of streptozotocin(35 mg kg~-1, i.v.) in the adult. The respective increase over basal value in glucose(ΔG) and insulin(ΔI), and the rate of glucose Disappearance (K), were measured during a 30 min intravenous glucose tolerance test. After an Intraperitoneal injection of S-22068 (24 mg kg~-1), ΔG(mM min~-1) was decreased (91.67±5.83 vs 120.5±3.65; P<0.001), whereas K was increased (1.74 ±0.09 vs 1.18±0.05; P<0.001). although insulinaemia was increased at time-point 0 of the test, ΔI was unchanged.
机译:最近的数据表明,某些咪唑啉衍生物可以降低糖尿病实验动物模型中的血浆葡萄糖。我们研究了在成人低剂量链脲佐菌素(35 mg kg〜-1,i.v.)产生的非胰岛素依赖型糖尿病(NIDDM)大鼠模型中咪唑啉S-22068的活性。在30分钟静脉葡萄糖耐量试验中,分别测量了葡萄糖(ΔG)和胰岛素(ΔI)的基础值各自增加,以及葡萄糖消失率(K)。腹腔注射S-22068(24 mg kg〜-1)后,ΔG(mM min〜-1)降低(91.67±5.83 vs 120.5±3.65; P <0.001),而K增加(1.74±0.09 vs. 1.18±0.05; P <0.001)。尽管在测试的时间点0时胰岛素血症增加,但ΔI不变。

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