Malaisse-Lagae F, Malaisse W J
Laboratory of Experimental Medicine, Brussels Free University, Erasmus Medical School, Belgium.
Acta Diabetol. 1996 Dec;33(4):298-300. doi: 10.1007/BF00571569.
The fate of 3H- and 14C-labelled A-4166 was examined in rat pancreatic islets. The net uptake of the meglitinide analogue by islets incubated for 60 min in the presence of 0.1 mM A-4166 and then submitted to repeated washes was close to 0.1 pmol/islet. It was significantly increased when the concentration of D-glucose in the incubation medium was raised from 2.8 to 16.7 mM. No sizeable internalization of tritiated A-4166 into insulin-producing cells could be detected by autoradiography. These findings suggest that the interaction of A-4166 with the beta-cell may be restricted to its insertion on the plasma membrane and binding to sulphonylurea receptors.
在大鼠胰岛中研究了3H和14C标记的A - 4166的命运。在0.1 mM A - 4166存在下孵育60分钟,然后反复洗涤的胰岛对瑞格列奈类似物的净摄取量接近0.1 pmol/胰岛。当孵育培养基中D - 葡萄糖的浓度从2.8 mM提高到16.7 mM时,摄取量显著增加。通过放射自显影未检测到氚标记的A - 4166大量内化到胰岛素产生细胞中。这些发现表明,A - 4166与β细胞的相互作用可能仅限于其插入质膜并与磺酰脲受体结合。