Noblía Pabla, Vieites Marisol, Torre María H, Costa-Filho Antonio J, Cerecetto Hugo, González Mercedes, Lavaggi María Laura, Adachi Yusuke, Sakurai Hiromu, Gambino Dinorah
Cátedra de Química Inorgánica, Facultad de Química, Universidad de la República, Gral. Flores 2124, C.C. 1157, 11800 Montevideo, Uruguay.
J Inorg Biochem. 2006 Feb;100(2):281-7. doi: 10.1016/j.jinorgbio.2005.11.012. Epub 2006 Jan 4.
As a contribution to the development of novel vanadyl complexes with potential insulin-mimetic activity, three new oxovanadium(IV) complexes with the formula VO(L)(2), where L are 3-amino-quinoxaline-2-carbonitrile N(1),N(4)-dioxide derivatives, have been synthesized. Complexes have been characterized by elemental and thermal analyses, fast atom bombardment mass spectroscopy (FAB-MS), conductivity measurements and electronic, Fourier transform infrared (FTIR) and electron paramagnetic resonance (EPR) spectroscopies. The in vitro insulin-mimetic activity of the vanadyl complexes has been estimated by lipolysis inhibition tests, in which the inhibition of the release of free fatty acid from isolated rat adipocytes treated with epinephrine was determined. All the complexes showed inhibitory effects on free fatty acid release. [V(IV)O(3-amino-6(7)-bromoquinoxaline-2-carbonitrile N(1),N(4)-dioxide)(2)] exhibited higher in vitro insulin-mimetic activity than the very active bis(6-methylpicolinato)oxovanadium(IV), VO(6mpa)(2). This new vanadyl complex is expected to exhibit a higher blood glucose lowering activity than VO(6mpa)(2) in diabetic animals.
作为对具有潜在胰岛素模拟活性的新型钒氧配合物开发的贡献,已合成了三种新的通式为VO(L)(2)的氧钒(IV)配合物,其中L为3-氨基喹喔啉-2-甲腈N(1),N(4)-二氧化物衍生物。通过元素分析、热分析、快原子轰击质谱(FAB-MS)、电导率测量以及电子、傅里叶变换红外(FTIR)和电子顺磁共振(EPR)光谱对配合物进行了表征。通过脂解抑制试验评估了钒氧配合物的体外胰岛素模拟活性,该试验测定了用肾上腺素处理的分离大鼠脂肪细胞中游离脂肪酸释放的抑制情况。所有配合物均对游离脂肪酸释放显示出抑制作用。[V(IV)O(3-氨基-6(7)-溴喹喔啉-2-甲腈N(1),N(4)-二氧化物)(2)]表现出比活性很高的双(6-甲基吡啶甲酸根)氧钒(IV),VO(6mpa)(2)更高的体外胰岛素模拟活性。预计这种新的钒氧配合物在糖尿病动物中比VO(6mpa)(2)表现出更高的降血糖活性。