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The novel imidazoline compound BL11282 potentiates glucose-induced insulin secretion in pancreatic β-cells in the absence of modulation of K_ATP channel activity

机译:新型咪唑啉化合物BL11282在不调节K_ATP通道活性的情况下增强胰岛β细胞中葡萄糖诱导的胰岛素分泌

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摘要

The insulinotropic activity of the novel imidazoline com- pound BL11282 was investigated. Intravenous adminis- tration of BL11282(0.3 mg.kg~-1. min~-1)to anesthetized rats did not changes blood glucose and insulin levels un- der basal conditions, but produced a higher increase in blood insulin levels and a faster glucose removal from the blood after glucose infusion. Similarly, in isolated Wistar rat pancreatic islets, 0.1-100 μ-mol/l BL11282 Potently stimulated glucose-induced insulin secretion But did not modulate basal insulin secretion.
机译:研究了新型咪唑啉化合物BL11282的促胰岛素活性。麻醉大鼠静脉注射BL11282(0.3 mg.kg〜-1.min〜-1)并没有改变基础条件下的血糖和胰岛素水平,但是使血糖水平增加了较高的速度,并且血糖更快了葡萄糖输注后从血液中清除。同样,在离体的Wistar大鼠胰岛中,0.1-100μmol/ l BL11282有效刺激葡萄糖诱导的胰岛素分泌,但不调节基础胰岛素的分泌。

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