Goodwill Adam G, Mather Kieren J, Conteh Abass M, Sassoon Daniel J, Noblet Jillian N, Tune Johnathan D
Department of Cellular & Integrative Physiology, Indiana University School of Medicine, 635 Barnhill Drive, Indianapolis, IN, 462025111, USA.
Rev Endocr Metab Disord. 2014 Sep;15(3):209-17. doi: 10.1007/s11154-014-9290-z.
Glucagon-like peptide-1 (GLP-1) is an incretin hormone that has been shown to have hemodynamic and cardioprotective capacity in addition to its better characterized glucoregulatory actions. Because of this, emerging research has focused on the ability of GLP-1 based therapies to drive myocardial substrate selection, enhance cardiac performance and regulate heart rate, blood pressure and vascular tone. These studies have produced consistent and reproducible results amongst numerous laboratories. However, there are obvious disparities in findings obtained in small animal models versus those of higher mammals. This species dependent discrepancy calls to question, the translational value of individual findings. Moreover, few studies of GLP-1 mediated cardiovascular action have been performed in the presence of a pre-existing comorbidities (e.g. obesity/diabetes) which limits interpretation of the effectiveness of incretin-based therapies in the setting of disease. This review addresses cardiovascular and hemodynamic potential of GLP-1 based therapies with attention to species specific effects as well as the interaction between therapies and disease.
胰高血糖素样肽-1(GLP-1)是一种肠促胰岛素激素,除了具有其已被充分表征的血糖调节作用外,还被证明具有血流动力学和心脏保护能力。因此,新兴研究聚焦于基于GLP-1的疗法驱动心肌底物选择、增强心脏功能以及调节心率、血压和血管张力的能力。这些研究在众多实验室中产生了一致且可重复的结果。然而,在小动物模型与高等哺乳动物模型中获得的研究结果存在明显差异。这种物种依赖性差异使得个别研究结果的转化价值受到质疑。此外,很少有关于GLP-1介导的心血管作用的研究是在存在预先存在的合并症(如肥胖/糖尿病)的情况下进行的,这限制了对基于肠促胰岛素的疗法在疾病背景下有效性的解读。本综述探讨了基于GLP-1的疗法的心血管和血流动力学潜力,关注物种特异性效应以及疗法与疾病之间的相互作用。