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新型抗糖尿病药物BTS 67 582的胰岛素释放作用

Insulin-releasing action of the novel antidiabetic agent BTS 67 582.

作者信息

McClenaghan N H, Flatt P R, Bailey C J

机构信息

School of Biomedical Sciences, University of Ulster, Coleraine.

出版信息

Br J Pharmacol. 1998 Feb;123(3):400-4. doi: 10.1038/sj.bjp.0701631.

Abstract
  1. BTS 67582 (1,1-dimethyl-2-(2-morpholinophenyl)guanidine fumarate) is a novel antidiabetic agent with a short-acting insulin-releasing effect. This study examined its mode of action in the clonal B-cell line BRIN-BD11. 2. BTS 67582 increased insulin release from BRIN-BD11 cells in a concentration-dependent manner (10[-8] to 10[-4] M) at both non-stimulating (1.1 mM) and stimulating (16.7 mM) concentrations of glucose. 3. BTS 67582 (10[-4] M) potentiated the insulin-releasing effect of a depolarizing concentration of K+ (30 mM), whereas the K+ channel openers pinacidil (400 microM) and diazoxide (300 microM) inhibited BTS 67582-induced release. 4. Suppression of Ca+ channel activity with verapamil (20 microM) reduced the insulin-releasing effect of BTS 67582 (10[-4] M). 5. BTS 67582 (10[-4] M) potentiated insulin release induced by amino acids (10 mM), and enhanced the combined stimulant effects of glucose plus either the fatty acid palmitate (10 mM), or agents which raise intracellular cyclic AMP concentrations (25 microM forskolin and 1 mM isobutylmethylxanthine), or the cholinoceptor agonist carbachol (100 microM). 6. Inhibition of glucose-stimulated insulin release by adrenaline or noradrenaline (10 microM) was partially reversed by BTS 67582 (10[-4] M). 7. These data suggest that the insulin-releasing effect of BTS 67582 involves regulation of ATP-sensitive K+ channel activity and Ca2+ influx, and that the drug augments the stimulant effects of nutrient insulin secretagogues and agents which enhance adenylate cyclase and phospholipase C. BTS 67582 may also exert insulin-releasing effects independently of ATP-sensitive K+ channel activity.
摘要
  1. BTS 67582(富马酸1,1 - 二甲基 - 2 -(2 - 吗啉代苯基)胍)是一种具有短效胰岛素释放作用的新型抗糖尿病药物。本研究检测了其在克隆B细胞系BRIN - BD11中的作用模式。2. 在非刺激浓度(1.1 mM)和刺激浓度(16.7 mM)的葡萄糖条件下,BTS 67582均以浓度依赖性方式(10[-8]至10[-4] M)增加BRIN - BD11细胞的胰岛素释放。3. BTS 67582(10[-4] M)增强了去极化浓度的K +(30 mM)的胰岛素释放作用,而K +通道开放剂吡那地尔(400 microM)和二氮嗪(300 microM)抑制了BTS 67582诱导的释放。4. 用维拉帕米(20 microM)抑制Ca +通道活性降低了BTS 67582(10[-4] M)的胰岛素释放作用。5. BTS 67582(10[-4] M)增强了氨基酸(10 mM)诱导的胰岛素释放,并增强了葡萄糖与脂肪酸棕榈酸(10 mM)、或提高细胞内环状AMP浓度的药物(25 microM福斯高林和1 mM异丁基甲基黄嘌呤)、或胆碱能受体激动剂卡巴胆碱(100 microM)联合刺激的作用。6. 肾上腺素或去甲肾上腺素(10 microM)对葡萄糖刺激的胰岛素释放的抑制作用被BTS 67582(10[-4] M)部分逆转。7. 这些数据表明,BTS 67582的胰岛素释放作用涉及对ATP敏感性K +通道活性和Ca2 +内流的调节,并且该药物增强了营养性胰岛素促分泌剂以及增强腺苷酸环化酶和磷脂酶C的药物的刺激作用。BTS 67582也可能独立于ATP敏感性K +通道活性发挥胰岛素释放作用。

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