AI Article Synopsis

  • - Cardiometabolic disorders significantly contribute to cardiovascular diseases, with sphingosine-1-phosphate (S1P) and its receptors (S1PRs) playing crucial roles in maintaining heart health through complex signaling pathways.
  • - S1P is transported in the bloodstream by carriers such as high-density lipoprotein and albumin, allowing it to influence various essential processes like cardiac contractility, inflammation, and angiogenesis.
  • - The review highlights the roles of S1P/S1PRs in heart diseases and explores therapeutic potential, including the drug Fingolimod, while discussing the challenges of developing new treatments that target these receptors.

Article Abstract

Cardiometabolic disorders contribute to the global burden of cardiovascular diseases. Emerging sphingolipid metabolites like sphingosine-1-phosphate (S1P) and its receptors, S1PRs, present a dynamic signalling axis significantly impacting cardiac homeostasis. S1P's intricate mechanisms extend to its transportation in the bloodstream by two specific carriers: high-density lipoprotein particles and albumin. This intricate transport system ensures the accessibility of S1P to distant target tissues, influencing several physiological processes critical for cardiovascular health. This review delves into the diverse functions of S1P and S1PRs in both physiological and pathophysiological conditions of the heart. Emphasis is placed on their diverse roles in modulating cardiac health, spanning from cardiac contractility, angiogenesis, inflammation, atherosclerosis and myocardial infarction. The intricate interplays involving S1P and its receptors are analysed concerning different cardiac cell types, shedding light on their respective roles in different heart diseases. We also review the therapeutic applications of targeting S1P/S1PRs in cardiac diseases, considering existing drugs like Fingolimod, as well as the prospects and challenges in developing novel therapies that selectively modulate S1PRs.

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Source
http://dx.doi.org/10.1002/1873-3468.14973DOI Listing

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