Potenza Maria Assunta, Nacci Carmela, De Salvia Maria Antonietta, Sgarra Luca, Collino Massimo, Montagnani Monica
Department of Biomedical Sciences and Human Oncology-Pharmacology Section, Medical School-University of Bari "Aldo Moro", Bari, Italy.
Department of Emergency and Organ Transplantation-Section of Cardiovascular Diseases, Medical School-University of Bari "Aldo Moro", Bari, Italy.
Pharmacol Res. 2017 Jun;120:226-241. doi: 10.1016/j.phrs.2017.04.009. Epub 2017 Apr 10.
The association of obesity and diabetes, termed "diabesity", defines a combination of primarily metabolic disorders with insulin resistance as the underlying common pathophysiology. Cardiovascular disorders associated with diabesity represent the leading cause of morbidity and mortality in the Western world. This makes diabesity, with its rising impacts on both health and economics, one of the most challenging biomedical and social threats of present century. The emerging comprehension of the genes whose alteration confers inter-individual differences on risk factors for diabetes or obesity, together with the potential role of genetically determined variants on mechanisms controlling responsiveness, effectiveness and safety of anti-diabetic therapy underlines the need of additional knowledge on molecular mechanisms involved in the pathophysiology of diabesity. Endothelial cell dysfunction, resulting from the unbalanced production of endothelial-derived vascular mediators, is known to be present at the earliest stages of insulin resistance and obesity, and may precede the clinical diagnosis of diabetes by several years. Once considered as a mere consequence of metabolic abnormalities, it is now clear that endothelial dysfunctional activity may play a pivotal role in the progression of diabesity. In the vicious circle where vascular defects and metabolic disturbances worsen and reinforce each other, a low-grade, chronic, and 'cold' inflammation (metaflammation) has been suggested to serve as the pathophysiological link that binds endothelial and metabolic dysfunctions. In this paradigm, it is important to consider how traditional antidiabetic treatments (specifically addressing metabolic dysregulation) may directly impact on inflammatory processes or cardiovascular function. Indeed, not all drugs currently available to treat diabetes possess the same anti-inflammatory potential, or target endothelial cell function equally. Perspective strategies pointing at reducing metaflammation or directly addressing endothelial dysfunction may disclose beneficial consequences on metabolic regulation. This review focuses on existing and potential new approaches ameliorating endothelial dysfunction and vascular inflammation in the context of diabesity.
肥胖与糖尿病的关联,即“糖尿病型肥胖症”,定义了以胰岛素抵抗为潜在共同病理生理学特征的主要代谢紊乱的组合。与糖尿病型肥胖症相关的心血管疾病是西方世界发病和死亡的主要原因。这使得糖尿病型肥胖症对健康和经济的影响日益增加,成为本世纪最具挑战性的生物医学和社会威胁之一。对那些基因改变会导致个体间糖尿病或肥胖风险因素差异的基因的新认识,以及基因决定的变体在控制抗糖尿病治疗的反应性、有效性和安全性机制中的潜在作用,凸显了我们需要更多关于糖尿病型肥胖症病理生理学中涉及的分子机制的知识。由内皮衍生的血管介质产生失衡导致的内皮细胞功能障碍,已知在胰岛素抵抗和肥胖的最早阶段就已存在,并且可能在糖尿病临床诊断前数年就已出现。内皮功能障碍活动曾经被认为仅仅是代谢异常的结果,现在很清楚,它可能在糖尿病型肥胖症的进展中起关键作用。在血管缺陷和代谢紊乱相互恶化和强化的恶性循环中,一种低度、慢性和“冷”炎症(代谢性炎症)被认为是连接内皮功能障碍和代谢功能障碍的病理生理学纽带。在这种模式下,重要的是要考虑传统抗糖尿病治疗(专门针对代谢失调)如何可能直接影响炎症过程或心血管功能。事实上,目前并非所有用于治疗糖尿病的药物都具有相同的抗炎潜力,或者对内皮细胞功能的靶向作用相同。旨在减少代谢性炎症或直接解决内皮功能障碍的前瞻性策略可能会揭示对代谢调节的有益影响。本综述重点关注在糖尿病型肥胖症背景下改善内皮功能障碍和血管炎症的现有及潜在新方法。