Department of Pharmacology, Toxicology and Clinical Pharmacology, Iuliu Hatieganu University of Medicine and Pharmacy, 400337 Cluj-Napoca, Romania.
Department of Diabetes, and Nutrition Diseases, Iuliu Hatieganu University of Medicine and Pharmacy, 400006 Cluj-Napoca, Romania.
Int J Mol Sci. 2023 Feb 8;24(4):3385. doi: 10.3390/ijms24043385.
Atherosclerotic cardiovascular disease is the most common cause of morbidity and mortality worldwide. Diabetes mellitus increases cardiovascular risk. Heart failure and atrial fibrillation are associated comorbidities that share the main cardiovascular risk factors. The use of incretin-based therapies promoted the idea that activation of alternative signaling pathways is effective in reducing the risk of atherosclerosis and heart failure. Gut-derived molecules, gut hormones, and gut microbiota metabolites showed both positive and detrimental effects in cardiometabolic disorders. Although inflammation plays a key role in cardiometabolic disorders, additional intracellular signaling pathways are involved and could explain the observed effects. Revealing the involved molecular mechanisms could provide novel therapeutic strategies and a better understanding of the relationship between the gut, metabolic syndrome, and cardiovascular diseases.
动脉粥样硬化性心血管疾病是全世界发病率和死亡率的最常见原因。糖尿病会增加心血管风险。心力衰竭和心房颤动是相关的合并症,它们具有共同的主要心血管危险因素。基于肠促胰岛素的治疗方法的应用,促使人们认为激活替代信号通路可有效降低动脉粥样硬化和心力衰竭的风险。肠道来源的分子、肠道激素和肠道微生物群代谢物在心代谢疾病中既有积极作用,也有不良作用。尽管炎症在代谢疾病中起着关键作用,但还涉及其他细胞内信号通路,这可以解释观察到的作用。揭示相关的分子机制可以提供新的治疗策略,并更好地了解肠道、代谢综合征和心血管疾病之间的关系。