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PMID: 20026772 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Nitrite potently inhibits hypoxic and inflammatory pulmonary arterial hypertension and smooth muscle proliferation via xanthine oxidoreductase-dependent nitric oxide generation.

Circulation ·Vol. 121 ·No. 1 ·2010-01-05 ·Pages 98-109

Zuckerbraun BS, Shiva S, Ifedigbo E, Mathier MA, Mollen KP, Rao J, Bauer PM, Choi JJ, Curtis E, Choi AM, Gladwin MT

Abstract

Pulmonary arterial hypertension is a progressive proliferative vasculopathy of the small pulmonary arteries that is characterized by a primary failure of the endothelial nitric oxide and prostacyclin vasodilator pathways, coupled with dysregulated cellular proliferation. We have recently discovered that the endogenous anion salt nitrite is converted to nitric oxide in the setting of physiological and pathological hypoxia. Considering the fact that nitric oxide exhibits vasoprotective properties, we examined the effects of nitrite on experimental pulmonary arterial hypertension. We exposed mice and rats with hypoxia or monocrotaline-induced pulmonary arterial hypertension to low doses of nebulized nitrite (1.5 mg/min) 1 or 3 times a week. This dose minimally increased plasma and lung nitrite levels yet completely prevented or reversed pulmonary arterial hypertension and pathological right ventricular hypertrophy and failure. In vitro and in vivo studies revealed that nitrite in the lung was metabolized directly to nitric oxide in a process significantly enhanced under hypoxia and found to be dependent on the enzymatic action of xanthine oxidoreductase. Additionally, physiological levels of nitrite inhibited hypoxia-induced proliferation of cultured pulmonary artery smooth muscle cells via the nitric oxide-dependent induction of the cyclin-dependent kinase inhibitor p21(Waf1/Cip1). The therapeutic effect of nitrite on hypoxia-induced pulmonary hypertension was significantly reduced in the p21-knockout mouse; however, nitrite still reduced pressures and right ventricular pathological remodeling, indicating the existence of p21-independent effects as well. These studies reveal a potent effect of inhaled nitrite that limits pathological pulmonary arterial hypertrophy and cellular proliferation in the setting of experimental pulmonary arterial hypertension.

MeSH Terms
Administration, Inhalation Animals Cell Division/drug effects Cells, Cultured Chronic Disease Cyclin-Dependent Kinase Inhibitor p21/genetics,metabolism Disease Models, Animal Hypertension, Pulmonary/chemically induced,drug therapy,metabolism Hypoxia/drug therapy,metabolism Male Mice Mice, Inbred C57BL Mice, Knockout Monocrotaline/toxicity Myocytes, Smooth Muscle/cytology,drug effects,enzymology Nitric Oxide/metabolism Pulmonary Artery/cytology Rats Rats, Sprague-Dawley Sodium Nitrite/pharmacokinetics,pharmacology Xanthine Dehydrogenase/antagonists & inhibitors,metabolism
Chemicals
Cdkn1a protein, mouse Cdkn1a protein, rat Cyclin-Dependent Kinase Inhibitor p21 Nitric Oxide Monocrotaline Xanthine Dehydrogenase Sodium Nitrite
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Zuckerbraun Brian S
Department of Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
Shiva Sruti
Ifedigbo Emeka
Mathier Michael A
Mollen Kevin P
Rao Jayashree
Bauer Philip M
Choi Justin J W
Curtis Erin
Choi Augustine M K
Gladwin Mark T
Article Info
Journal
Circulation
Abbr.
Circulation
ISSN
1524-4539
Published
2010-01-05
Epub
2009-00-21
Pages
98-109
Language
English
Region
United States
NLM ID
0147763
Subset
IM
Grants
NHLBI NIH HHS · R01 HL085134 · United States
NHLBI NIH HHS · R01 HL085134-04 · United States
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