Etiology-specific endothelin-1 clearance in human precapillary pulmonary hypertension

Chest. 2006 Mar;129(3):689-95. doi: 10.1378/chest.129.3.689.

Abstract

Study objectives: Endothelin (ET)-1 is a mediator of vascular remodeling seen in human pulmonary hypertension (PH), and it is normally cleared via endothelial ET-B receptors. Increased levels of ET-1 are found in precapillary PH, partly from increased synthesis. We hypothesized that the endothelial dysfunction and vascular remodeling seen in human precapillary PH would also reduce ET-1 clearance.

Design and setting: Case series from a single institutional PH center.

Patients: Thirty-four patients with pulmonary arterial hypertension (PAH; idiopathic [IPAH], n = 19; connective tissue disease [CTD], n = 15) and 11 patients with chronic thromboembolic PH were studied.

Measurements and results: Using indicator dilution methods, the first-pass extraction of radiolabeled ET-1 through the pulmonary circulation, and permeability surface (PS) area, an index of functional microvascular surface available for ET-1 clearance, were determined. Mean extraction for IPAH and thromboembolic PH groups was normal, but it was reduced in PAH from CTD; 69% of all patients studied had normal extraction. The mean PS product was reduced significantly for all three etiologies as compared to normal, but 58% of IPAH patients and 40% of CTD-related PAH patients had normal PS products.

Conclusions: Receptor-mediated ET-1 extraction and functional vascular surface area for clearance vary between etiologies of PAH. However, contrary to our hypothesis, endothelial ET-B receptor-mediated extraction is preserved in many patients. The scientifically significant finding of our study is that high ET-1 levels seen in patients with PAH must be predominantly due to excess synthesis rather than reduced clearance. The finding that endothelial ET-B receptors are still present and functional in PAH may also be of relevance to the choice of selective vs nonselective ET receptor antagonists.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclohexanones
  • Endothelin-1 / metabolism*
  • Endothelium, Vascular / physiopathology
  • Female
  • Glucosides
  • Humans
  • Hypertension, Pulmonary / etiology
  • Hypertension, Pulmonary / metabolism*
  • Indicator Dilution Techniques
  • Male
  • Microcirculation / physiology
  • Pulmonary Diffusing Capacity
  • Thermodilution

Substances

  • Cyclohexanones
  • Endothelin-1
  • Glucosides
  • precarthamin