6533b7ddfe1ef96bd1275343

RESEARCH PRODUCT

Plasma concentration of asymmetric dimethylarginine, an endogenous inhibitor of nitric oxide synthase, is elevated in hyperthyroid patients.

Gloria SegarraSalvador LluchJosé M. VilaMarta PeiroCarlos HermenegildoPascual MedinaJoaquín Ortega

subject

AdultMalemedicine.medical_specialtyendocrine system diseasesEndotheliumEndocrinology Diabetes and MetabolismClinical BiochemistryArginineNitric OxideBiochemistryHyperthyroidismNitric oxidechemistry.chemical_compoundEndocrinologyHypothyroidismGriess testReference ValuesInternal medicineBlood plasmamedicineHumansNitriteNitritesAgedNitratesbiologyBiochemistry (medical)Osmolar ConcentrationMiddle AgedNitric oxide synthaseEndocrinologymedicine.anatomical_structurechemistrybiology.proteinFemaleNitric Oxide SynthaseAsymmetric dimethylarginineHormone

description

Cardiovascular manifestations are frequent findings in patients with thyroid hormone disorders. Nitric oxide (NO) plays a key role in vascular, endothelial-mediated relaxation. NO is synthesized from L-arginine by NO synthase, an enzyme inhibited by endogenous compounds, mainly asymmetric dimethylarginine [asymmetric N(G),N(G)-dimethyl-L-arginine (ADMA)]. The aim of our work was to investigate whether plasma L-arginine and dimethylarginine concentrations and NO production are altered in hypo- and hyperthyroid patients, compared with control subjects. L-arginine, ADMA and symmetric dimethylarginine were analyzed by HPLC. NO was measured as plasma nitrite plus nitrate (NO(x)) concentration by a colorimetric method based on Griess reagent. L-arginine, ADMA, and symmetric dimethylarginine plasma levels in the hypothyroid group were similar to those of the control group; whereas in hyperthyroidism, these values were significantly increased. However, the L-arginine/ADMA ratio was decreased in hyperthyroid patients, resulting in diminished NO(x) production. When all subjects were analyzed together, free T(4) levels were directly correlated with ADMA and inversely correlated with NO(x).

10.1210/jc.2002-020905https://pubmed.ncbi.nlm.nih.gov/12466365