Endogenous NO regulates plasminogen activator inhibitor-1 during angiotensin-converting enzyme inhibition

Nancy J. Brown*, James A S Muldowney, Douglas E. Vaughan

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

To test the hypothesis that NO contributes to effects of angiotensin-converting enzyme inhibitors on fibrinolysis, fibrinolytic balance was assessed in 17 normal subjects during placebo and after randomized, double-blind 4-week treatment with the NO precursor L-arginine (3 g TID), ramipril (10 mg QD), or L-arginine+ramipril. Neither L-arginine nor ramipril alone affected basal plasminogen activator inhibitor-1 or tissue-type plasminogen activator (t-PA) antigen in these salt-replete subjects in whom plasma renin activity was suppressed (mean±SD 0.7±0.5 ng angiotensin I/mL per hour). In contrast, L-arginine+ramipril reduced morning plasminogen activator inhibitor-1 antigen (10.8±9.5 ng/mL) and the molar ratio of plasminogen activator inhibitor-1:t-PA (2.3±1.6) compared with placebo (13.5±10.8 ng/mL, P=0.006; ratio 2.9±2.1, P=0.015) or ramipril alone (15.2±13.2 ng/mL, P=0.009; ratio 3.7±3.3, P=0.005). L-arginine and ramipril synergistically increased D-dimers (23.1±31.5, 29.7±50.0, 35.1±50.0, and 57.1±144.8 ng/mL during placebo, L-arginine, ramipril, and L-arginine+ramipril, respectively; P<0.05 for L-arginine+ramipril versus any other group). During ramipril, the NO synthase inhibitor L-NG-nitro-arginine-methyl-ester (2 mg/kg) significantly increased plasminogen activator inhibitor-antigen after 2 hours (from 9.4±8.6 ng/mL during vehicle to 13.5±11.0 ng/mL during L-N G-nitro-arginine-methyl-ester; P=0.020), consistent with an effect on expression but rapidly increased t-PA activity (from 0.4±0.3 to 0.5±0.4 IU/mL; P=0.031), consistent with an effect on release. Both effects of L-NG-nitro-arginine-methyl-ester were reversed by L-arginine. During angiotensin-converting enzyme inhibition, endogenous NO decreases plasminogen activator inhibitor-1 antigen and improves fibrinolytic balance in normotensive salt-replete subjects.

Original languageEnglish (US)
Pages (from-to)441-448
Number of pages8
JournalHypertension
Volume47
Issue number3
DOIs
StatePublished - Mar 2006

Keywords

  • Angiotensin
  • Nitric oxide
  • Nitric oxide synthase
  • Plasminogen
  • Renin

ASJC Scopus subject areas

  • Internal Medicine

Fingerprint Dive into the research topics of 'Endogenous NO regulates plasminogen activator inhibitor-1 during angiotensin-converting enzyme inhibition'. Together they form a unique fingerprint.

Cite this