Endothelial dysfunction in vascular complications of diabetes: a comprehensive review of mechanisms and implications

Front Endocrinol (Lausanne). 2024 Apr 5:15:1359255. doi: 10.3389/fendo.2024.1359255. eCollection 2024.

Abstract

Diabetic vascular complications are prevalent and severe among diabetic patients, profoundly affecting both their quality of life and long-term prospects. These complications can be classified into macrovascular and microvascular complications. Under the impact of risk factors such as elevated blood glucose, blood pressure, and cholesterol lipids, the vascular endothelium undergoes endothelial dysfunction, characterized by increased inflammation and oxidative stress, decreased NO biosynthesis, endothelial-mesenchymal transition, senescence, and even cell death. These processes will ultimately lead to macrovascular and microvascular diseases, with macrovascular diseases mainly characterized by atherosclerosis (AS) and microvascular diseases mainly characterized by thickening of the basement membrane. It further indicates a primary contributor to the elevated morbidity and mortality observed in individuals with diabetes. In this review, we will delve into the intricate mechanisms that drive endothelial dysfunction during diabetes progression and its associated vascular complications. Furthermore, we will outline various pharmacotherapies targeting diabetic endothelial dysfunction in the hope of accelerating effective therapeutic drug discovery for early control of diabetes and its vascular complications.

Keywords: atherosclerotic; diabetes; endothelial dysfunction; therapies; vascular diseases.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Diabetic Angiopathies* / etiology
  • Diabetic Angiopathies* / metabolism
  • Diabetic Angiopathies* / pathology
  • Diabetic Angiopathies* / physiopathology
  • Endothelium, Vascular* / metabolism
  • Endothelium, Vascular* / pathology
  • Endothelium, Vascular* / physiopathology
  • Humans
  • Oxidative Stress / physiology

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This research was funded by PROJECT ENDOCRINE AND METABOLIC TALENT RESEARCH, grant number 2022-N-02-14, Shenzhen Overseas High-Level Talent (Peacock Plan) Project Research Initiation Programme, grant number 827000745 and Shenzhen Municipal Science and Technology Innovation Commission Stability Support Program for Higher Education Institutions (20231120180418002).