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Interrelationship between diabetes mellitus and heart failure: the role of peroxisome proliferator-activated receptors in left ventricle performance

机译:糖尿病和心力衰竭之间的相互关系:过氧化物体增殖物激活受体在左心室性能中的作用

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Heart failure (HF) is a common cardiac syndrome, whose pathophysiology involves complex mechanisms, some of which remain unknown. Diabetes mellitus (DM) constitutes not only a glucose metabolic disorder accompanied by insulin resistance but also a risk factor for cardiovascular disease and HF. During the last years though emerging data set up, a bidirectional interrelationship between these two entities. In the case of DM impaired calcium homeostasis, free fatty acid metabolism, redox state, and advance glycation end products may accelerate cardiac dysfunction. On the other hand, when HF exists, hypoperfusion of the liver and pancreas, b-blocker and diuretic treatment, and autonomic nervous system dysfunction may cause impairment of glucose metabolism. These molecular pathways may be used as therapeutic targets for novel antidiabetic agents. Peroxisome proliferator-activated receptors (PPARs) not only improve insulin resistance and glucose and lipid metabolism but also manifest a diversity of actions directly or indirectly associated with systolic or diastolic performance of left ventricle and symptoms of HF. Interestingly, they may beneficially affect remodeling of the left ventricle, fibrosis, and diastolic performance but they may cause impaired water handing, sodium retention, and decompensation of HF which should be taken into consideration in the management of patients with DM. In this review article, we present the pathophysiological data linking HF with DM and we focus on the molecular mechanisms of PPARs agonists in left ventricle systolic and diastolic performance providing useful insights in the molecular mechanism of this class of metabolically active regiments.
机译:心力衰竭(HF)是一种常见的心脏综合征,其病理生理学涉及复杂的机制,其中一些仍然是未知的。糖尿病(DM)不仅构成伴有胰岛素抵抗的葡萄糖代谢疾病,而且是心血管疾病和HF的危险因素。在过去几年中,虽然新兴数据设置,这两个实体之间的双向相互关系。在DM受损的钙稳态,游离脂肪酸代谢,氧化还原状态和预先糖化末端产物可能会加速心脏功能障碍。另一方面,当HF存在时,肝脏和胰腺的低血压,B阻滞剂和利尿处理,并且自主神经系统功能障碍可能导致葡萄糖代谢的损害。这些分子途径可用作新型抗糖尿病剂的治疗靶标。过氧化物体增殖剂活化受体(PPAR)不仅改善胰岛素抵抗和葡萄糖和脂质代谢,而且表现出与左心室的收缩或舒张性能和HF症状的分类或间接相关的分化。有趣的是,它们可能有利地影响左心室,纤维化和舒张性性能的重塑,但它们可能导致患有患者的水递减,钠保留和反作一定,这应该考虑到DM患者的管理。在本综述文章中,我们提出了将HF与DM连接的病理生理学数据,我们专注于左心室收缩和舒张性能的PPAR激动剂的分子机制,提供了这种代谢活性团的分子机制的有用见解。

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