DPP-4抑制剂的非肠促胰岛素效应:比较研究

A.S.A.Bhatti, Aliya Shabbir, Abdul Waheed Shehzad, M.A.Bhatti
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引用次数: 0

摘要

背景:糖尿病是一种代谢综合征,对身体各部分尤其是心血管系统都有不良影响。二肽基肽酶-4 (DPP-4)是一种多功能蛋白,其抑制作用多种多样。抑制DPP-4可提高小鼠心肌梗死后的存活率。在实验模型中观察到DPP-4抑制剂有益的心肌代谢作用。DPP-4抑制剂的心血管结局试验显示不同的不良心血管事件。目的:本实验旨在研究DPP-4抑制剂对大鼠慢性(心率,HR)、肌力(心尖力和心肌力)的直接心血管效应;dP/dt(max)、ECG和冠状动脉血流(C.F),并检测其对心血管参数的潜在有益和有害影响。方法:观察西格列汀(10-9 ~ 10-6M)和维格列汀(10-6M)梯度剂量(10-9 ~ 10-6M)对兔离体心脏逆行灌注加温Krebs-Henseliet溶液对radnoi工作心脏系统的影响。54只家兔分为9组:I(S1)、II(S2)、III(S3)、IV(S4)、V(S5)、VI(S6)、VII(V1)、VIII(V2)和IX(V3)各由6只动物组成(n=6)。观察实验药物对大鼠慢性(HR)、肌力(顶力)和LVP(峰值上升率)的影响;dP/dt(max)和冠状动脉血流(CF)。使用Graph Pad Grism对结果进行统计分析,必要时采用配对或非配对“t”检验。结论:西格列汀和维格列汀对HR均有抑制作用。西格列汀有正性肌力作用,维格列汀有负性肌力作用。两种药物(10-8 - 10-6M);降低冠状动脉血流,但对心电图无明显影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Non Incretin Effects of DPP-4 Inhibitors: Comparative Study
Background: Diabetes mellitus is a metabolic syndrome that adversely affects all parts of the body especially the cardiovascular system. Dipeptidyl peptidase-4 (DPP-4) is a multifunctional protein and its inhibition has diverse effects. DPP-4 inhibition was shown to improve the survival rate after myocardial infarction in mice. Beneficial myocardial metabolic effects of DPP-4 inhibitors have been observed in experimental models. Cardiovascular outcome trials of DPP-4 inhibitors show variable adverse cardiovascular events. Objective: This experimental study was aimed to study the direct cardiovascular effects of DPP-4 Inhibitors on chronotropicity (Heart Rate, HR), inotropicity (Apical Force and; dP/dt(max), ECG and Coronary Flow(C.F) and detect its potential useful and harmful effects on cardiovascular parameters. Methods: The effects of graded doses (10-9 - 10-6M) of Sitagliptin (S) and Vildagliptin(V) were observed on retrograde perfused isolated rabbit hearts with warm Krebs-Henseliet solution on Radnoti working heart system. Fifty four(54) rabbits were grouped into nine groups i.e ; I(S1), II(S2), III(S3), IV(S4), V(S5), VI(S6), VII(V1), and VIII(V2) and IX(V3) each comprising of six animals(n=6).Effects of experimental drugs were observed on chronotropicity(HR), inotropicity (Apical Force and Peak rate of rise of LVP i.e; dP/dt(max) and Coronary flow(CF). The results were statistically analyzed with Graph Pad Grism and wherever necessary paired or unpaired “t” test was applied. Conclusion: Sitagliptin and Vildagliptin both have suppressant effects on HR. Sitagliptin has positive and Vildagliptin had negative inotropic effects. Both drugs (10-8 - 10-6M); decrease coronary flow but have no significant effect on ECG.
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