Tahara Atsuo, Matsuyama-Yokono Akiko, Nakano Ryosuke, Someya Yuka, Hayakawa Masahiko, Shibasaki Masayuki
Drug Discovery Research, Astellas Pharma Inc, Tsukuba, Ibaraki, Japan.
Eur J Pharmacol. 2009 Mar 1;605(1-3):170-6. doi: 10.1016/j.ejphar.2008.12.040. Epub 2009 Jan 10.
Several combination therapies have been investigated in an effort to achieve and maintain glycemic control in patients with type 2 diabetes. In this study, we combined the novel dipeptidyl peptidase (DPP)-IV inhibitor ASP8497 with the antidiabetic drugs metformin, glibenclamide, voglibose, rosiglitazone, and insulin to examine the effects of each combination on glucose tolerance in streptozotocin-nicotinamide-induced mildly diabetic mice. Single treatments with ASP8497 (1 mg/kg), metformin (300 mg/kg), glibenclamide (3 mg/kg), voglibose (0.3 mg/kg), rosiglitazone (10 mg/kg), or insulin (0.2 IU/kg) significantly improved glucose tolerance during the liquid meal tolerance test. In addition, combination treatment with ASP8497 and each antidiabetic drug additively improved glucose tolerance. Among these, the combination of ASP8497 and glibenclamide or insulin additively ameliorated glucose tolerance with an additive increase in the plasma insulin level; however, it did not affect the fasting blood glucose lowering effects of glibenclamide or insulin. These profiles indicate that the combination of ASP8497 with existing antidiabetic drugs could be useful for correcting the postprandial hyperglycemia seen with type 2 diabetes.
为了实现并维持2型糖尿病患者的血糖控制,人们已经对几种联合疗法进行了研究。在本研究中,我们将新型二肽基肽酶(DPP)-IV抑制剂ASP8497与抗糖尿病药物二甲双胍、格列本脲、伏格列波糖、罗格列酮和胰岛素联合使用,以研究每种联合用药对链脲佐菌素-烟酰胺诱导的轻度糖尿病小鼠糖耐量的影响。在液体餐耐量试验期间,单独使用ASP8497(1毫克/千克)、二甲双胍(300毫克/千克)、格列本脲(3毫克/千克)、伏格列波糖(0.3毫克/千克)、罗格列酮(10毫克/千克)或胰岛素(0.2国际单位/千克)均能显著改善糖耐量。此外,ASP8497与每种抗糖尿病药物联合治疗可累加改善糖耐量。其中,ASP8497与格列本脲或胰岛素联合用药可累加改善糖耐量,并使血浆胰岛素水平呈累加性升高;然而,这并不影响格列本脲或胰岛素降低空腹血糖的作用。这些结果表明,ASP8497与现有抗糖尿病药物联合使用可能有助于纠正2型糖尿病患者的餐后高血糖。