Interplay of Angiotensin Peptides, Vasopressin, and Insulin in the Heart: Experimental and Clinical Evidence of Altered Interactions in Obesity and Diabetes Mellitus

Int J Mol Sci. 2024 Jan 21;25(2):1310. doi: 10.3390/ijms25021310.

Abstract

The present review draws attention to the specific role of angiotensin peptides [angiotensin II (Ang II), angiotensin-(1-7) (Ang-(1-7)], vasopressin (AVP), and insulin in the regulation of the coronary blood flow and cardiac contractions. The interactions of angiotensin peptides, AVP, and insulin in the heart and in the brain are also discussed. The intracardiac production and the supply of angiotensin peptides and AVP from the systemic circulation enable their easy access to the coronary vessels and the cardiomyocytes. Coronary vessels and cardiomyocytes are furnished with AT1 receptors, AT2 receptors, Ang (1-7) receptors, vasopressin V1 receptors, and insulin receptor substrates. The presence of some of these molecules in the same cells creates good conditions for their interaction at the signaling level. The broad spectrum of actions allows for the engagement of angiotensin peptides, AVP, and insulin in the regulation of the most vital cardiac processes, including (1) cardiac tissue oxygenation, energy production, and metabolism; (2) the generation of the other cardiovascular compounds, such as nitric oxide, bradykinin (Bk), and endothelin; and (3) the regulation of cardiac work by the autonomic nervous system and the cardiovascular neurons of the brain. Multiple experimental studies and clinical observations show that the interactions of Ang II, Ang(1-7), AVP, and insulin in the heart and in the brain are markedly altered during heart failure, hypertension, obesity, and diabetes mellitus, especially when these diseases coexist. A survey of the literature presented in the review provides evidence for the belief that very individualized treatment, including interactions of angiotensins and vasopressin with insulin, should be applied in patients suffering from both the cardiovascular and metabolic diseases.

Keywords: angiotensin; diabetes mellitus; heart failure; hypertension; hypoxia; insulin; obesity; vasopressin.

Publication types

  • Review

MeSH terms

  • Angiotensin II* / metabolism
  • Arginine Vasopressin / metabolism
  • Diabetes Mellitus* / drug therapy
  • Diabetes Mellitus* / metabolism
  • Humans
  • Insulin* / metabolism
  • Obesity* / drug therapy
  • Obesity* / metabolism
  • Receptors, Angiotensin / metabolism
  • Receptors, Vasopressin
  • Vasopressins* / metabolism

Substances

  • Angiotensin II
  • Arginine Vasopressin
  • Insulin
  • Receptors, Angiotensin
  • Receptors, Vasopressin
  • Vasopressins

Grants and funding

This study was supported by the Medical University of Warsaw Scientific Projects (1MA/N/2022). The work did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.