Department of Clinical Neuroscience, University of Calgary, 3330 Hospital Drive, NW, Calgary, Alberta T2N4N1, Canada.
Diabetol Metab Syndr. 2014 Mar 28;6(1):45. doi: 10.1186/1758-5996-6-45.
Type 2 diabetes is a complex metabolic disorder characterized by hyperglycemia, impaired glucose tolerance and insulin resistance associated with dyslipidemia and hypertension. The available drugs are not sufficiently efficacious in reducing cardiovascular risk and restoring normal glucose metabolism associated with type 2 diabetes as a mono- or a combination therapy. The present study examined the combined effects of an antihypertensive (S-Amlodipine) and an insulin-sensitizing agent, peroxisome proliferator-activated receptor (PPAR) agonists (Pioglitazone and Ragaglitazar), on cardiovascular risk factors in aged diabetic and insulin-resistant Zucker fa/fa rats.
Following combination treatment for 14 days, blood pressure (BP), serum glucose, total cholesterol and triglycerides were measured. Aortic ring study was conducted to determine the effect of combination treatments on phenylephrine-induced vasoconstriction and acetylcholine (Ach)-induced vasorelaxation.
In combination, S-Amlodipine and Pioglitazone significantly reduced blood glucose (115.1 ± 6.6 vs. 81.7 ± 4.2), BP (184.4 ± 5.0 vs. 155.1 ± 5.0), serum triglycerides (362.5 ± 47.5 vs. 211.1 ± 23.7) and glucose intolerance when compared with vehicle treated Zucker fa/fa rats. Similar results were observed with the combination of S-Amlodipine and Ragaglitazar (Triglycerides, 362.5 ± 47.5 vs. 252.34 ± 27.86; BP, 184.4 ± 5.0 vs. 159.0 ± 8.0) except for serum glucose. ACh-induced vasorelaxation in aortic rings was also superior with both of the combinations compared to individual treatment. Furthermore, there was less body weight gain and food intake with S-Amlodipine and Pioglitazone combination in Zucker fa/fa rats. S-Amlodipine itself caused significant reduction in glucose (115.1 ± 6.6 vs. 89.7 ± 2.7) and BP (184.4 ± 5.0 vs. 156.1 ± 4.0) with improvement in insulin sensitivity observed through oral glucose tolerance test.
The results suggest that a combination of PPAR agonists and S-Amlodipine has partial benefits in improving the cardiovascular risk factors such as reduction in triglyceride levels, associated with chronic type 2 diabetes, and therefore may be utilized as an approach for addressing some of these devastating metabolic syndrome complications.
2 型糖尿病是一种复杂的代谢紊乱疾病,其特征为高血糖、葡萄糖耐量受损和胰岛素抵抗,同时伴有血脂异常和高血压。现有的药物在降低心血管风险和恢复 2 型糖尿病患者的正常葡萄糖代谢方面的疗效并不理想,无论是单药治疗还是联合治疗。本研究旨在探讨抗高血压药物(S-氨氯地平)和胰岛素增敏剂(过氧化物酶体增殖物激活受体 [PPAR] 激动剂吡格列酮和罗格列酮)联合应用对老龄糖尿病和胰岛素抵抗 Zucker fa/fa 大鼠心血管危险因素的影响。
联合治疗 14 天后,测量血压(BP)、血清葡萄糖、总胆固醇和甘油三酯。进行主动脉环研究,以确定联合治疗对苯肾上腺素诱导的血管收缩和乙酰胆碱(Ach)诱导的血管舒张的影响。
与 vehicle 处理的 Zucker fa/fa 大鼠相比,S-氨氯地平与吡格列酮联合使用可显著降低血糖(115.1±6.6 对 81.7±4.2)、血压(184.4±5.0 对 155.1±5.0)、血清甘油三酯(362.5±47.5 对 211.1±23.7)和葡萄糖耐量。S-氨氯地平与拉格列酮联合使用也有类似的结果(甘油三酯,362.5±47.5 对 252.34±27.86;血压,184.4±5.0 对 159.0±8.0),但血清葡萄糖除外。与单独治疗相比,两种联合治疗均可显著改善主动脉环中 Ach 诱导的血管舒张作用。此外,与 S-氨氯地平与吡格列酮联合使用相比,S-氨氯地平本身可显著降低 Zucker fa/fa 大鼠的体重增加和食物摄入。S-氨氯地平本身可显著降低血糖(115.1±6.6 对 89.7±2.7)和血压(184.4±5.0 对 156.1±4.0),并通过口服葡萄糖耐量试验观察到胰岛素敏感性的改善。
这些结果表明,PPAR 激动剂与 S-氨氯地平联合使用在改善心血管危险因素方面具有一定的益处,例如降低与慢性 2 型糖尿病相关的甘油三酯水平,因此可能被用作解决这些破坏性代谢综合征并发症的一种方法。