A mammalian functional nitrate reductase that regulates nitrite and nitric oxide homeostasis

Nat Chem Biol. 2008 Jul;4(7):411-7. doi: 10.1038/nchembio.92. Epub 2008 May 30.

Abstract

Inorganic nitrite (NO(2)(-)) is emerging as a regulator of physiological functions and tissue responses to ischemia, whereas the more stable nitrate anion (NO(3)(-)) is generally considered to be biologically inert. Bacteria express nitrate reductases that produce nitrite, but mammals lack these specific enzymes. Here we report on nitrate reductase activity in rodent and human tissues that results in formation of nitrite and nitric oxide (NO) and is attenuated by the xanthine oxidoreductase inhibitor allopurinol. Nitrate administration to normoxic rats resulted in elevated levels of circulating nitrite that were again attenuated by allopurinol. Similar effects of nitrate were seen in endothelial NO synthase-deficient and germ-free mice, thereby excluding vascular NO synthase activation and bacteria as the source of nitrite. Nitrate pretreatment attenuated the increase in systemic blood pressure caused by NO synthase inhibition and enhanced blood flow during post-ischemic reperfusion. Our findings suggest a role for mammalian nitrate reduction in regulation of nitrite and NO homeostasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Allopurinol / pharmacology
  • Animals
  • Blood Pressure / drug effects
  • Disease Models, Animal
  • Female
  • Homeostasis* / drug effects
  • Homeostasis* / physiology
  • Humans
  • Liver / drug effects
  • Liver / enzymology
  • Liver / metabolism
  • Male
  • Mice
  • Middle Aged
  • Nitrate Reductase / metabolism
  • Nitrate Reductase / physiology*
  • Nitrates* / blood
  • Nitrates* / pharmacology
  • Nitrates* / therapeutic use
  • Nitric Oxide / metabolism*
  • Nitric Oxide Synthase / metabolism
  • Nitrites / blood
  • Nitrites / metabolism*
  • Organ Specificity
  • Oxidation-Reduction
  • Rats
  • Reperfusion Injury / drug therapy
  • Reperfusion Injury / enzymology
  • Reperfusion Injury / metabolism
  • Xanthine Dehydrogenase / metabolism

Substances

  • Nitrates
  • Nitrites
  • Nitric Oxide
  • Allopurinol
  • sodium nitrate
  • Nitric Oxide Synthase
  • Xanthine Dehydrogenase
  • Nitrate Reductase

Associated data

  • PubChem-Substance/49737746
  • PubChem-Substance/49737747
  • PubChem-Substance/49737748
  • PubChem-Substance/49737749
  • PubChem-Substance/49737750
  • PubChem-Substance/49737751
  • PubChem-Substance/49737752