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Impact of chronic congestive heart failure on pharmacokinetics and vasomotor effects of infused nitrite
Author(s) -
Maher Abdul R,
Arif Sayqa,
Madhani Melanie,
Abozguia Khalid,
Ahmed Ibrar,
Fernandez Bernadette O,
Feelisch Martin,
O'Sullivan AG,
Christopoulos Arthur,
Sverdlov Aaron L,
Ngo Doan,
Dautov Rustem,
James Philip E,
Horowitz John D,
Frenneaux Michael P
Publication year - 2013
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/bph.12152
Subject(s) - medicine , heart failure , hemodynamics , anesthesia , brachial artery , heart rate , cardiology , blood pressure
Background and Purpose Nitrite ( NO 2 − ) has recently been shown to represent a potential source of NO , in particular under hypoxic conditions. The aim of the current study was to compare the haemodynamic effects of NO 2 − in healthy volunteers and patients with stable congestive heart failure ( CHF ). Experimental Approach The acute haemodynamic effects of brachial artery infusion of NO 2 − (0.31 to 7.8 μmol·min −1 ) was assessed in normal subjects ( n = 20) and CHF patients ( n = 21). Key Results NO 2 − infusion was well tolerated in all subjects. Forearm blood flow ( FBF ) increased markedly in CHF patients at NO 2 − infusion rates which induced no changes in normal subjects ( anova : F = 5.5; P = 0.02). Unstressed venous volume ( UVV ) increased even with the lowest NO 2 − infusion rate in all subjects (indicating venodilation), with CHF patients being relatively hyporesponsive compared with normal subjects ( anova : F = 6.2; P = 0.01). There were no differences in venous blood pH or oxygen concentration between groups or during NO 2 − infusion. Venous plasma NO 2 − concentrations were lower in CHF patients at baseline, and rose substantially less with NO 2 − infusion, without incremental oxidative generation of nitrate, consistent with accelerated clearance in these patients. Plasma protein‐bound NO concentrations were lower in CHF patients than normal subjects at baseline. This difference was attenuated during NO 2 − infusion. Prolonged NO 2 − exposure in vivo did not induce oxidative stress, nor did it induce tolerance in vitro . Conclusions and Implications The findings of arterial hyper‐responsiveness to infused NO 2 − in CHF patients, with evidence of accelerated transvascular NO 2 − clearance (presumably with concomitant NO release) suggests that NO 2 − effects may be accentuated in such patients. These findings provide a stimulus for the clinical exploration of NO 2 − as a therapeutic modality in CHF .