Reciprocal regulation of endothelin-1 and nitric oxide: relevance in the physiology and pathology of the cardiovascular system

Int Rev Cytol. 2001:209:241-72. doi: 10.1016/s0074-7696(01)09014-3.

Abstract

The endothelium plays a crucial role in the regulation of cardiovascular structure and function by releasing several mediators in response to biochemical and physical stimuli. These mediators are grouped into two classes: (1) endothelium-derived constricting factors (EDCFs) and (2) endothelium-derived relaxing factors (EDRFs), the roles of which are considered to be detrimental and beneficial, respectively. Endothelin-1 (ET-1) and nitric oxide (NO) are the prototypes of EDCFs and EDRFs, respectively, and their effects on the cardiovascular system have been studied in depth. Numerous conditions characterized by an impaired availability of NO have been found to be associated with enhanced synthesis of ET-1, and vice versa, thereby suggesting that these two factors have a reciprocal regulation. Experimental studies have provided evidence that ET-1 may exert a bidirectional effect by either enhancing NO production via ETB receptors located in endothelial cells or blunting it via ETA receptors prevalently located in the vascular smooth muscle cells. Conversely, NO was found to inhibit ET-1 synthesis in different cell types. In vitro and in vivo studies have started to unravel the molecular mechanisms involved in this complex interaction. It has been clarified that several factors affect in opposite directions the transcription of preproET-1 and NO-synthase genes, nuclear factor-KB and peroxisome proliferator-activated receptors playing a key role in these regulatory mechanisms. ET-1 and NO interplay seems to have a great relevance in the physiological regulation of vascular tone and blood pressure, as well as in vascular remodeling. Moreover, an imbalance between ET-1 and NO systems may underly the mechanisms involved in the pathogenesis of systemic and pulmonary hypertension and atherosclerosis.

Publication types

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

MeSH terms

  • Animals
  • Arteriosclerosis / physiopathology
  • Cardiovascular Physiological Phenomena*
  • Endothelin-1 / genetics
  • Endothelin-1 / metabolism*
  • Endothelium, Vascular / metabolism
  • Gene Expression Regulation
  • Humans
  • Hypertension, Pulmonary / physiopathology
  • Models, Biological
  • NF-kappa B / metabolism
  • Nitric Oxide / genetics
  • Nitric Oxide / metabolism*
  • Protein Precursors / genetics
  • Protein Precursors / metabolism
  • Receptor, Endothelin A
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Receptors, Endothelin / metabolism
  • Signal Transduction / physiology
  • Transcription Factors / metabolism

Substances

  • Endothelin-1
  • NF-kappa B
  • Protein Precursors
  • Receptor, Endothelin A
  • Receptors, Cytoplasmic and Nuclear
  • Receptors, Endothelin
  • Transcription Factors
  • Nitric Oxide