Woo L C, Yuen V G, Thompson K H, McNeill J H, Orvig C
Department of Chemistry, University of British Columbia, Vancouver, Canada.
J Inorg Biochem. 1999 Sep 30;76(3-4):251-7. doi: 10.1016/s0162-0134(99)00152-x.
Vanadium has well-documented blood-glucose-lowering properties both in vitro and in vivo. The design of new oxovanadium(IV) coordination compounds, intended for use as insulin-enhancing agents in the treatment of diabetes mellitus, can potentially benefit from a synergistic approach, in which the whole complex has more than an additive effect from its component parts. Biguanides, most importantly metformin, are oral hypoglycemic agents used today to treat type 2 diabetes mellitus. In this study, biguanide, metformin, and phenformin, all biguanides, were coordinated to oxovanadium(IV) to form potential insulin-enhancing compounds. Highly colored, air-stable, bis(biguanidato)oxovanadium(IV), [VO(big)2], bis(N'N'-dimethylbiguanidato)oxovanadium(IV), [VO(metf)2], and bis(beta-phenethyl-biguanidato)oxovanadium(IV), [VO(phenf)2], were prepared. Solvation with dimethylsulfoxide occurred with VO(metf)2 to form a six-coordinate complex. Precursor ligands and oxovanadium(IV) coordination complexes were characterized by infrared spectroscopy, mass spectrometry, elemental analyses, magnetic susceptibility, and, where appropriate, 1H NMR spectroscopy. Biological testing with VO(metf)2, a representative compound, for insulin-enhancing potential included acute (72 h) administration, both by intraperitoneal (i.p.) injection and by oral gavage (p.o.) in streptozotocin (STZ)-diabetic rats. VO(metf)2 administration resulted in significant blood-glucose lowering at doses of 0.12 mmol kg-1 i.p. and 0.60 mmol kg-1 p.o. (previously established as ED50 doses for organically chelated oxovanadium(IV) complexes); however, no positive associative effects due to the presence of biguanide in the complex were apparent.
钒在体外和体内均具有充分文献记载的降血糖特性。旨在用作治疗糖尿病的胰岛素增强剂的新型氧钒(IV)配位化合物的设计,可能受益于一种协同方法,即整个配合物具有超过其组成部分的加和效应。双胍类药物,最重要的是二甲双胍,是目前用于治疗2型糖尿病的口服降糖药。在本研究中,双胍、二甲双胍和苯乙双胍这三种双胍类药物与氧钒(IV)配位形成潜在的胰岛素增强化合物。制备了高显色性、空气稳定的双(双胍基)氧钒(IV)[VO(big)₂]、双(N'N'-二甲基双胍基)氧钒(IV)[VO(metf)₂]和双(β-苯乙基双胍基)氧钒(IV)[VO(phenf)₂]。VO(metf)₂发生二甲基亚砜溶剂化反应形成六配位配合物。前体配体和氧钒(IV)配位配合物通过红外光谱、质谱、元素分析、磁化率以及在适当情况下通过¹H NMR光谱进行表征。对代表性化合物VO(metf)₂进行的胰岛素增强潜力的生物学测试包括在链脲佐菌素(STZ)诱导的糖尿病大鼠中通过腹腔注射(i.p.)和灌胃(p.o.)进行急性(72小时)给药。以0.12 mmol kg⁻¹ i.p.和0.60 mmol kg⁻¹ p.o.的剂量给予VO(metf)₂可导致显著的血糖降低(先前已确定为有机螯合氧钒(IV)配合物的ED50剂量);然而,由于配合物中存在双胍而产生的正向协同效应并不明显。