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Research Article

Dietary inorganic nitrate reverses features of metabolic syndrome in endothelial nitric oxide synthase-deficient mice

Mattias Carlström, Filip J. Larsen, Thomas Nyström, Michael Hezel, Sara Borniquel, Eddie Weitzberg, and Jon O. Lundberg
PNAS October 12, 2010 107 (41) 17716-17720; https://doi.org/10.1073/pnas.1008872107
Mattias Carlström
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Filip J. Larsen
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Thomas Nyström
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Michael Hezel
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Sara Borniquel
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Eddie Weitzberg
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  • For correspondence: eddie.weitzberg@ki.se jon.lundberg@ki.se
Jon O. Lundberg
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  • For correspondence: eddie.weitzberg@ki.se jon.lundberg@ki.se
  1. Edited* by Louis J. Ignarro, University of California Los Angeles School of Medicine, Los Angeles, CA, and approved September 7, 2010 (received for review June 23, 2010)

  2. ↵1E.W. and J.O.L. contributed equally to this work.

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Abstract

The metabolic syndrome is a clustering of risk factors of metabolic origin that increase the risk for cardiovascular disease and type 2 diabetes. A proposed central event in metabolic syndrome is a decrease in the amount of bioavailable nitric oxide (NO) from endothelial NO synthase (eNOS). Recently, an alternative pathway for NO formation in mammals was described where inorganic nitrate, a supposedly inert NO oxidation product and unwanted dietary constituent, is serially reduced to nitrite and then NO and other bioactive nitrogen oxides. Here we show that several features of metabolic syndrome that develop in eNOS-deficient mice can be reversed by dietary supplementation with sodium nitrate, in amounts similar to those derived from eNOS under normal conditions. In humans, this dose corresponds to a rich intake of vegetables, the dominant dietary nitrate source. Nitrate administration increased tissue and plasma levels of bioactive nitrogen oxides. Moreover, chronic nitrate treatment reduced visceral fat accumulation and circulating levels of triglycerides and reversed the prediabetic phenotype in these animals. In rats, chronic nitrate treatment reduced blood pressure and this effect was also present during NOS inhibition. Our results show that dietary nitrate fuels a nitrate–nitrite–NO pathway that can partly compensate for disturbances in endogenous NO generation from eNOS. These findings may have implications for novel nutrition-based preventive and therapeutic strategies against cardiovascular disease and type 2 diabetes.

  • glucose
  • insulin
  • s-nitrosothiol
  • obesity
  • bacteria

Footnotes

  • 2To whom correspondence may be addressed. E-mail: eddie.weitzberg{at}ki.se or jon.lundberg{at}ki.se.
  • Author contributions: M.C., F.J.L., T.N., E.W., and J.O.L. designed research; M.C., F.J.L., T.N., M.H., and S.B. performed research; M.H. contributed new reagents/analytic tools; M.C., F.J.L., T.N., M.H., S.B., E.W., and J.O.L. analyzed data; and M.C., E.W., and J.O.L. wrote the paper.

  • Conflict of interest: E.W. and J.O.L. are named coinventors on a patent application related to the therapeutic use of nitrate and nitrite salts. This application was filed in 2007.

  • ↵*This Direct Submission article had a prearranged editor.

  • This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1008872107/-/DCSupplemental.

Freely available online through the PNAS open access option.

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Dietary inorganic nitrate reverses features of metabolic syndrome in endothelial nitric oxide synthase-deficient mice
Mattias Carlström, Filip J. Larsen, Thomas Nyström, Michael Hezel, Sara Borniquel, Eddie Weitzberg, Jon O. Lundberg
Proceedings of the National Academy of Sciences Oct 2010, 107 (41) 17716-17720; DOI: 10.1073/pnas.1008872107

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Dietary inorganic nitrate reverses features of metabolic syndrome in endothelial nitric oxide synthase-deficient mice
Mattias Carlström, Filip J. Larsen, Thomas Nyström, Michael Hezel, Sara Borniquel, Eddie Weitzberg, Jon O. Lundberg
Proceedings of the National Academy of Sciences Oct 2010, 107 (41) 17716-17720; DOI: 10.1073/pnas.1008872107
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