Why the endothelium? The endothelium as a target to reduce diabetes-associated vascular disease
Chris R Triggle1, Hong Ding1, Isra Marei1
1Departments of Pharmacology and Medical Education, Weill Cornell Medical College, Doha, Qatar.
Insights
The endothelium, once viewed as a simple barrier, is now recognized as a vital endocrine-like organ regulating cardiovascular health. Its signaling molecules and therapeutic targeting are crucial for managing vascular disease, especially in diabetes.
Area of Science:
- Cardiovascular Biology
- Endothelial Function
- Vascular Medicine
Background:
- Historically, the endothelium was considered a passive barrier between blood and vascular smooth muscle.
- Significant advancements over 66 years have revealed its active role in cardiovascular regulation.
- Pioneering work by scientists like Rudolf Altschul and Robert Furchgott shaped our understanding.
Abstract:
Over the past 66 years, our knowledge of the role of the endothelium in the regulation of cardiovascular function and dysfunction has advanced from the assumption that it is a single layer of cells that serves as a barrier between the blood stream and vascular smooth muscle to an understanding of its role as an essential endocrine-like organ. In terms of historical contributions, we pay particular credit to (1) the Canadian scientist Dr. Rudolf Altschul who, based on pathological changes in the appearance of the endothelium, advanced the argument in 1954 that "one is only as old as one's endothelium" and (2) the American scientist Dr. Robert Furchgott, a 1998 Nobel Prize winner in Physiology or Medicine, who identified the importance of the endothelium in the regulation of blood flow. This review provides a brief history of how our knowledge of endothelial function has advanced and now recognize that the endothelium produces a plethora of signaling molecules possessing paracrine, autocrine, and, arguably, systemic hormone functions. In addition, the endothelium is a therapeutic target for the anti-diabetic drugs metformin, glucagon-like peptide I (GLP-1) receptor agonists, and inhibitors of the sodium-glucose cotransporter 2 (SGLT2) that offset the vascular disease associated with diabetes.
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