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首页> 外文期刊>Diabetology and Metabolic Syndrome >Effect of combination treatment of S–amlodipine with peroxisome proliferator-activated receptor agonists on metabolic and cardiovascular parameters in Zucker fa/fa rats
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Effect of combination treatment of S–amlodipine with peroxisome proliferator-activated receptor agonists on metabolic and cardiovascular parameters in Zucker fa/fa rats

机译:S-氨氯地平与过氧化物酶体增殖物激活受体激动剂联合治疗对Zucker fa / fa大鼠代谢和心血管指标的影响

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Background 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. Methods 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. Results 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. Conclusions 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.
机译:背景技术2型糖尿病是一种复杂的代谢紊乱,其特征为高血糖,糖耐量降低和与血脂异常和高血压相关的胰岛素抵抗。现有的药物作为单一疗法或联合疗法在降低心血管疾病风险和恢复与2型糖尿病相关的正常葡萄糖代谢方面不够有效。本研究研究了抗高血压药(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Ragaglitazar)对老年糖尿病和胰岛素抵抗性Zucker fa的心血管危险因素的联合作用/ fa大鼠。方法联合治疗14天后,测量血压,血糖,总胆固醇和甘油三酸酯。进行了主动脉环研究,以确定联合治疗对去氧肾上腺素诱导的血管收缩和乙酰胆碱(Ach)诱导的血管舒张的作用。结果S-氨氯地平和吡格列酮合用可显着降低血糖(115.1±±6.6 vs. 81.7±±4.2),BP(184.4±±5.0 vs. 155.1±±5.0),血清甘油三酸酯(362.5±±)。与接受媒介物处理的Zucker fa / fa大鼠相比,葡萄糖耐受不良率为[47.5 vs. 211.1±±23.7]。除血清葡萄糖外,S-氨氯地平和拉格列扎的组合观察到了相似的结果(甘油三酸酯,362.5±±47.5 vs. 252.34±±27.86; BP,184.4±±5.0 vs. 159.0±±8.0)。与单独治疗相比,两种组合的ACh诱导的主动脉环血管舒张作用也都更好。此外,在Zucker fa / fa大鼠中,S-氨氯地平和吡格列酮组合的体重增加和食物摄入较少。通过口服葡萄糖耐量试验观察到,S-氨氯地平本身可导致血糖显着降低(115.1±±6.6比89.7±±2.7)和BP(184.4±±5.0与156.1±±4.0),胰岛素敏感性得到改善。 。结论结果表明,PPAR激动剂和S-氨氯地平联用可改善心血管危险因素,例如降低与慢性2型糖尿病有关的甘油三酸酯水平,因此有部分益处,因此可以用作解决其中一些问题的方法。破坏性代谢综合征的并发症。

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