
Evidence for Dysregulation of Dimethylarginine Dimethylaminohydrolase I in Chronic Hypoxia–Induced Pulmonary Hypertension
Author(s) -
Lesley J. Millatt,
Guy Whitley,
Dechun Li,
James Leiper,
Helmy M. Siragy,
Robert M. Carey,
Roger A. Johns
Publication year - 2003
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/01.cir.0000089087.25930.ff
Subject(s) - asymmetric dimethylarginine , pulmonary hypertension , hypoxia (environmental) , medicine , western blot , endocrinology , nitric oxide , nitric oxide synthase , lung , hypoxic pulmonary vasoconstriction , enzyme , chemistry , arginine , biochemistry , oxygen , amino acid , organic chemistry , gene
Chronic hypoxia-induced pulmonary hypertension is associated with increased pulmonary expression of nitric oxide synthase (NOS) enzymes. Nevertheless, some reports have indicated decreased pulmonary production of NO in the disease. To address this paradox, we determined pulmonary concentrations of the endogenous NOS inhibitor asymmetric dimethylarginine (ADMA) in the hypoxia-induced pulmonary hypertension rat model. In addition, we determined whether dysregulation of the ADMA-metabolizing enzyme dimethylarginine dimethylaminohydrolase I (DDAH I) plays a role in this disease.
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