Literature DB >> 1905595

Concurrent hydralazine administration prevents nitroglycerin-induced hemodynamic tolerance in experimental heart failure.

J A Bauer1, H L Fung.   

Abstract

BACKGROUND: Organic nitrates such as nitroglycerin and isosorbide dinitrate are useful in the treatment of congestive heart failure (CHF), but tolerance develops rapidly during continuous administration. Because combination therapy of nitrate and hydralazine has been shown to provide both short- and long-term benefit but nitrate alone produces hemodynamic tolerance, we questioned whether hydralazine can preserve the favorable preload effects of nitroglycerin. METHODS AND
RESULTS: Using an in vivo model of nitroglycerin tolerance in the CHF rat, we examined the effects of hydralazine bolus dosing during continuous nitroglycerin infusion. Continuous infusion of nitroglycerin alone (10 micrograms/min) produced initial reductions in left ventricular end-diastolic pressure of 40-50%, which returned to baseline by 8 hours (tolerance development). Coadministration of hydralazine (2 x 0.1 mg) maintained the effects of nitroglycerin infusion on left ventricular end-diastolic pressure (45% reduction at 10 hours). This hydralazine dose alone reduced left ventricular peak systolic pressure by approximately 12 +/- 3% but had no effect on left ventricular end-diastolic pressure. Hydralazine dosing did not affect steady-state plasma concentrations of nitroglycerin or metabolites, and hydralazine was unable to prevent nitroglycerin tolerance induced in vitro.
CONCLUSIONS: The beneficial interaction of hydralazine on the preload effects of nitroglycerin may explain the long-term clinical efficacy of hydralazine/nitrate combination in CHF. Our results also suggest that the mechanism of in vivo nitrate tolerance in CHF may be systemic rather than vascular in origin.

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Year:  1991        PMID: 1905595     DOI: 10.1161/01.cir.84.1.35

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  16 in total

1.  Application of pharmacodynamic modeling for designing time-variant dosing regimens to overcome nitroglycerin tolerance in experimental heart failure.

Authors:  J A Bauer; J P Balthasar; H L Fung
Journal:  Pharm Res       Date:  1997-09       Impact factor: 4.200

2.  The role of nitric oxide in heart failure. Potential for pharmacological intervention.

Authors:  P Macdonald; C Schyvens; D Winlaw
Journal:  Drugs Aging       Date:  1996-06       Impact factor: 3.923

Review 3.  Pharmacological treatment of chronic heart failure.

Authors:  Rachele Adorisio; Leonardo De Luca; Joseph Rossi; Mihai Gheorghiade
Journal:  Heart Fail Rev       Date:  2006-06       Impact factor: 4.214

4.  Hydralazine prevents nitroglycerin tolerance by inhibiting activation of a membrane-bound NADH oxidase. A new action for an old drug.

Authors:  T Münzel; S Kurz; S Rajagopalan; M Thoenes; W R Berrington; J A Thompson; B A Freeman; D G Harrison
Journal:  J Clin Invest       Date:  1996-09-15       Impact factor: 14.808

5.  Effect of apparent elimination half-life on nitroglycerin-induced hemodynamic rebound in experimental heart failure.

Authors:  J A Bauer; H L Fung
Journal:  Pharm Res       Date:  1993-09       Impact factor: 4.200

6.  Hydralazine and organic nitrates restore impaired excitation-contraction coupling by reducing calcium leak associated with nitroso-redox imbalance.

Authors:  Raul A Dulce; Omer Yiginer; Daniel R Gonzalez; Garrett Goss; Ning Feng; Meizi Zheng; Joshua M Hare
Journal:  J Biol Chem       Date:  2013-01-14       Impact factor: 5.157

Review 7.  Organic nitrate metabolism and action: toward a unifying hypothesis and the future-a dedication to Professor Leslie Z. Benet.

Authors:  Nathaniel A Page; Ho-Leung Fung
Journal:  J Pharm Sci       Date:  2013-05-13       Impact factor: 3.534

8.  The prevention of cardiovascular disease in cancer survivors.

Authors:  Iyad N Daher; Tina R Daigle; Nirmanmoh Bhatia; Jean-Bernard Durand
Journal:  Tex Heart Inst J       Date:  2012

9.  Lack of bioequivalence between different formulations of isosorbide dinitrate and hydralazine and the fixed-dose combination of isosorbide dinitrate/hydralazine: the V-HeFT paradox.

Authors:  S William Tam; Michael L Sabolinski; Manuel Worcel; Milton Packer; Jay N Cohn
Journal:  Clin Pharmacokinet       Date:  2007       Impact factor: 6.447

10.  Lack of tolerance in forearm blood vessels in man to glyceryl trinitrate.

Authors:  A R Cheesman; N Benjamin
Journal:  Br J Clin Pharmacol       Date:  1994-05       Impact factor: 4.335

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