Differential changes in endothelin-1 and endothelial nitric oxide synthase gene expression in rats with a chronic high pulmonary flow

J Cardiovasc Pharmacol. 2004 Nov:44 Suppl 1:S341-5. doi: 10.1097/01.fjc.0000166266.09550.a7.

Abstract

The expressions of endothelin-1 (ET-1) and endothelial nitric oxide synthase were assessed in the lung of adult Wistar rats (n = 6/group) undergoing an abdominal aortocaval shunt to increase pulmonary blood flow for 4, 8 or 12 weeks. The shunt resulted in significant medial hypertrophy of the pulmonary artery without significant increases in pulmonary and systemic arterial pressure. A competitive reverse transcriptase-polymerase chain reaction demonstrated significant increases in pulmonary preproET-1 mRNA at 12 weeks (mean +/- standard error of the mean; shunt, 1.82 +/- 0.12; sham, 1.00 +/- 0.15; P < 0.05) and in pulmonary endothelial nitric oxide synthase mRNA at both 8 weeks (shunt, 1.57 +/- 0.12; sham, 1.00 +/- 0.18; P < 0.05) and 12 weeks (shunt, 1.89 +/- 0.18; sham, 1.00 +/- 0.13; P < 0.05). In addition, western blot analysis showed increases in pulmonary endothelial nitric oxide synthase protein by 126% and 164% at 8 and 12 weeks, respectively, in the shunt animals. However, the plasma ET-1 concentrations and the lung ET-1 contents were unchanged. These results indicate that endothelial nitric oxide synthase gene expression was upregulated, prior to that of ET-1, at the transcriptional level during pulmonary vascular remodeling in this chronic shunt model.

MeSH terms

  • Animals
  • Aorta, Abdominal / surgery
  • Arteriovenous Shunt, Surgical
  • Endothelin-1 / genetics*
  • Endothelin-1 / metabolism
  • Gene Expression Regulation, Enzymologic
  • Male
  • Nitric Oxide Synthase Type II / genetics
  • Nitric Oxide Synthase Type II / metabolism
  • Nitric Oxide Synthase Type III
  • Protein Precursors / genetics*
  • Protein Precursors / metabolism
  • Pulmonary Artery / enzymology*
  • Pulmonary Artery / physiopathology
  • Pulmonary Circulation*
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Time Factors
  • Transcription, Genetic
  • Venae Cavae / surgery

Substances

  • Endothelin-1
  • Protein Precursors
  • RNA, Messenger
  • Nitric Oxide Synthase Type II
  • Nitric Oxide Synthase Type III
  • Nos3 protein, rat