Literature DB >> 17536885

Effects of losartan and delapril on the fibrinolytic system in patients with mild to moderate hypertension.

Salvatore Paterna1, Vincenzo Di Garbo, Gino Avellone, Pietro Di Pasquale, Antonina Cacia, Antonio Tuttolomondo, Giuseppe Follone, Antonietta Cardinale, Tiziana Maniscalchi, Giuseppe Licata.   

Abstract

BACKGROUND AND OBJECTIVES: Angiotensin-converting enzyme (ACE) probably influences the fibrinolytic system at a central point by converting angiotensin I to angiotensin II, which increases plasminogen activator inhibitor-1 (PAI-1) activity. This effect appears to be mediated in humans via the angiotensin II type 1 (AT(1)) receptor. The objective of this study was to evaluate, in patients with mild to moderate hypertension, the change in tissue plasminogen activator (t-PA) and PAI-1 plasma levels after treatment with an AT(1)-receptor blocker (losartan 50 mg/day) or an ACE inhibitor (delapril 60 mg/day). PATIENTS AND METHODS: 30 hypertensive patients and 15 controls were enrolled. Essential hypertension was established by a medical history, physical examination and the absence of clinical findings suggestive of a secondary form of hypertension. Preliminary investigations, routine biochemical tests (including clearance of creatinine and oral glucose tolerance test), chest x-ray, standard and 24-hour ECG monitoring, M- and B-mode echocardiography and fundus oculi examinations were performed. No patients had previously received ACE inhibitors or AT(1)-receptor blockers. After a 14-day run-in period with placebo, patients were randomised in a double-blind fashion into two groups: 15 patients were randomised to losartan 50 mg/day (group 1), 15 patients were randomised to delapril 60 mg/day (group 2), and 15 healthy subjects were used as controls (group 3). Plasma PAI-1 and t-PA antigen were determined by enzyme-linked immunosorbent assay and a photometric method at the end of the run-in period and after 6 months of treatment.
RESULTS: There were no significant differences among the three groups regarding age, sex, body mass index and smoking. After 6 months, both groups of patients showed a reduction in blood pressure values. The losartan group did not demonstrate significant changes in PAI-1 levels (96.52 +/- 23.73 and 99.89 +/- 22.18 mug/L, pre- and post-treatment, respectively) or in t-PA antigen levels (26.17 +/- 6.18 and 27.32 +/- 5.91 mug/L, pre- and post-treatment, respectively). The delapril group showed no significant changes in PAI-1 levels (97.73 +/- 25.75 and 86.12 +/- 13.12 mug/L, pre- and post-treatment, respectively), but did show a statistically significant difference (p < 0.005) in t-PA antigen levels (25.71 +/- 6.40 and 32.24 +/- 5.31 mug/L, pre- and post-treatment, respectively). The losartan group demonstrated significantly higher post-treatment PAI-1 values than the delapril group (p = 0.048).
CONCLUSION: The study showed that losartan does not affect fibrinolytic parameters, while delapril resulted in an insignificant reduction in PAI-1 and a significant increase in t-PA levels. Further studies are clearly required in order to establish whether these different effects on the fibrinolytic system between ACE inhibitors and AT(1)-receptor blockers may have clinical relevance.

Entities:  

Year:  2003        PMID: 17536885     DOI: 10.2165/00044011-200323110-00004

Source DB:  PubMed          Journal:  Clin Drug Investig        ISSN: 1173-2563            Impact factor:   2.859


  38 in total

Review 1.  The plasminogen activator/plasmin system.

Authors:  J D Vassalli; A P Sappino; D Belin
Journal:  J Clin Invest       Date:  1991-10       Impact factor: 14.808

Review 2.  The kallikrein-kinin and the renin-angiotensin systems have a multilayered interaction.

Authors:  Alvin H Schmaier
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2003-07       Impact factor: 3.619

3.  Potentiation of bradykinin-induced tissue plasminogen activator release by angiotensin-converting enzyme inhibition.

Authors:  C Labinjoh; D E Newby; M P Pellegrini; N R Johnston; N A Boon; D J Webb
Journal:  J Am Coll Cardiol       Date:  2001-11-01       Impact factor: 24.094

4.  Plasminogen activator inhibitor-1 expression is regulated by the angiotensin type 1 receptor in vivo.

Authors:  S Nakamura; I Nakamura; L Ma; D E Vaughan; A B Fogo
Journal:  Kidney Int       Date:  2000-07       Impact factor: 10.612

5.  Angiotensin II and IV stimulate expression and release of plasminogen activator inhibitor-1 in cultured human coronary artery endothelial cells.

Authors:  J L Mehta; D Y Li; H Yang; M K Raizada
Journal:  J Cardiovasc Pharmacol       Date:  2002-06       Impact factor: 3.105

6.  Role of the angiotensin AT(1) receptor in rat aortic and cardiac PAI-1 gene expression.

Authors:  H C Chen; J L Bouchie; A S Perez; A C Clermont; S Izumo; J Hampe; E P Feener
Journal:  Arterioscler Thromb Vasc Biol       Date:  2000-10       Impact factor: 8.311

7.  Effects of angiotensins II and IV on blood pressure, renal function, and PAI-1 expression in the heart and kidney of the rat.

Authors:  Christian T Abrahamsen; Mark A Pullen; Christine G Schnackenberg; Eugene T Grygielko; Richard M Edwards; Nicholas J Laping; David P Brooks
Journal:  Pharmacology       Date:  2002-09       Impact factor: 2.547

8.  Angiotensin induction of PAI-1 expression in endothelial cells is mediated by the hexapeptide angiotensin IV.

Authors:  D M Kerins; Q Hao; D E Vaughan
Journal:  J Clin Invest       Date:  1995-11       Impact factor: 14.808

9.  Marked bradykinin-induced tissue plasminogen activator release in patients with heart failure maintained on long-term angiotensin-converting enzyme inhibitor therapy.

Authors:  Fraser N Witherow; Pamela Dawson; Christopher A Ludlam; Keith A A Fox; David E Newby
Journal:  J Am Coll Cardiol       Date:  2002-09-04       Impact factor: 24.094

10.  GISSI-3: effects of lisinopril and transdermal glyceryl trinitrate singly and together on 6-week mortality and ventricular function after acute myocardial infarction. Gruppo Italiano per lo Studio della Sopravvivenza nell'infarto Miocardico.

Authors: 
Journal:  Lancet       Date:  1994-05-07       Impact factor: 79.321

View more
  1 in total

1.  Angiotensin-converting enzyme inhibition and novel cardiovascular risk biomarkers: results from the Trial of Angiotensin Converting Enzyme Inhibition and Novel Cardiovascular Risk Factors (TRAIN) study.

Authors:  Matteo Cesari; Stephen B Kritchevsky; Hal H Atkinson; Brenda W Penninx; Mauro Di Bari; Russell P Tracy; Marco Pahor
Journal:  Am Heart J       Date:  2009-02       Impact factor: 4.749

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.