Wan Andrea, Rodrigues Brian
Faculty of Pharmaceutical Sciences, The University of British Columbia, 2405 Wesbrook Mall, Vancouver, BC, Canada V6T 1Z3.
Faculty of Pharmaceutical Sciences, The University of British Columbia, 2405 Wesbrook Mall, Vancouver, BC, Canada V6T 1Z3
Cardiovasc Res. 2016 Aug 1;111(3):172-83. doi: 10.1093/cvr/cvw159. Epub 2016 Jun 10.
The incidence of diabetes is increasing globally, with cardiovascular disease accounting for a substantial number of diabetes-related deaths. Although atherosclerotic vascular disease is a primary reason for this cardiovascular dysfunction, heart failure in patients with diabetes might also be an outcome of an intrinsic heart muscle malfunction, labelled diabetic cardiomyopathy. Changes in cardiomyocyte metabolism, which encompasses a shift to exclusive fatty acid utilization, are considered a leading stimulus for this cardiomyopathy. In addition to cardiomyocytes, endothelial cells (ECs) make up a significant proportion of the heart, with the majority of ATP generation in these cells provided by glucose. In this review, we will discuss the metabolic machinery that drives energy metabolism in the cardiomyocyte and EC, its breakdown following diabetes, and the research direction necessary to assist in devising novel therapeutic strategies to prevent or delay diabetic heart disease.
全球糖尿病发病率正在上升,心血管疾病导致了大量与糖尿病相关的死亡。虽然动脉粥样硬化性血管疾病是这种心血管功能障碍的主要原因,但糖尿病患者的心力衰竭也可能是心肌内在功能异常的结果,即糖尿病性心肌病。心肌细胞代谢的变化,包括转向仅利用脂肪酸,被认为是这种心肌病的主要刺激因素。除心肌细胞外,内皮细胞(ECs)在心脏中占很大比例,这些细胞中的大部分ATP由葡萄糖提供。在本综述中,我们将讨论驱动心肌细胞和内皮细胞能量代谢的代谢机制、糖尿病后其功能的破坏,以及为设计预防或延缓糖尿病性心脏病的新治疗策略所必需的研究方向。