Evidence map›Paper›PMID 25727730›Full record

ArticleNitric oxide : biology and chemistry2015

Skeletal muscle as an endogenous nitrate reservoir.

Barbora Piknova, Ji Won Park, Kathryn M Swanson, Soumyadeep Dey, Constance Tom Noguchi, Alan N Schechter

Open access · greenAbstract read
In one paragraph

Article in Nitric oxide : biology and chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 3 pooled it
4.7field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

55 citing papers in PubMed, 3 syntheses or guidelines pooled it, 104 citations in OpenAlex.

  1. The Effects of Dietary Nitrate Supplementation on Explosive Exercise Performance: A Systematic Review.International journal of environmental research and public health · 2022
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  13. Effect of pre-exercise dietary nitrate on skeletal muscle blood flow in a rat model of pulmonary hypertension.American journal of physiology. Regulatory, integrative and comparative physiology · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Barbora PiknovaMolecular Medicine Branch, NIDDK, NIH, Bethesda, MD 20892, USA. Electronic address: piknovab@mail.nih.gov.
Ji Won ParkMolecular Medicine Branch, NIDDK, NIH, Bethesda, MD 20892, USA.
Kathryn M SwansonMolecular Medicine Branch, NIDDK, NIH, Bethesda, MD 20892, USA.
Soumyadeep DeyMolecular Medicine Branch, NIDDK, NIH, Bethesda, MD 20892, USA.
Constance Tom NoguchiMolecular Medicine Branch, NIDDK, NIH, Bethesda, MD 20892, USA.
Alan N SchechterMolecular Medicine Branch, NIDDK, NIH, Bethesda, MD 20892, USA.
National Institutes of Health · US

Funding

Receptor Mediated Metabolic Response to Cerebral ErythropoietinZIADK025061 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI NOGUCHI, CONSTANCE · 2009 to 2025
$16.2M
Nitric Oxide Transport By HemoglobinZIADK025093 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI SCHECHTER, ALAN · 2009 to 2022
$7.2M
Role of erythropoietin in skeletal muscle and bone maintenance and repairZIADK025103 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI NOGUCHI, CONSTANCE · 2009 to 2015
$2.2M
Intramural NIH HHS Z99 DK999999
6 · The paper itself

Abstract

The nitric oxide synthase (NOS) family of enzymes form nitric oxide (NO) from arginine in the presence of oxygen. At reduced oxygen availability NO is also generated from nitrate in a two step process by bacterial and mammalian molybdopterin proteins, and also directly from nitrite by a variety of five-coordinated ferrous hemoproteins. The mammalian NO cycle also involves direct oxidation of NO to nitrite, and both NO and nitrite to nitrate by oxy-ferrous hemoproteins. The liver and blood are considered the sites of active mammalian NO metabolism and nitrite and nitrate concentrations in the liver and blood of several mammalian species, including human, have been determined. However, the large tissue mass of skeletal muscle had not been generally considered in the analysis of the NO cycle, in spite of its long-known presence of significant levels of active neuronal NOS (nNOS or NOS1). We hypothesized that skeletal muscle participates in the NO cycle and, due to its NO oxidizing heme protein, oxymyoglobin has high concentrations of nitrate ions. We measured nitrite and nitrate concentrations in rat and mouse leg skeletal muscle and found unusually high concentrations of nitrate but similar levels of nitrite, when compared to the liver. The nitrate reservoir in muscle is easily accessible via the bloodstream and therefore nitrate is available for transport to internal organs where it can be reduced to nitrite and NO. Nitrate levels in skeletal muscle and blood in nNOS(-/-) mice were dramatically lower when compared with controls, which support further our hypothesis. Although the nitrate reductase activity of xanthine oxidoreductase in muscle is less than that of liver, the residual activity in muscle could be very important in view of its total mass and the high basal level of nitrate. We suggest that skeletal muscle participates in overall NO metabolism, serving as a nitrate reservoir, for direct formation of nitrite and NO, and for determining levels of nitrate in other organs.

Indexed as

AnimalsMaleMiceMice, Inbred C57BLMice, KnockoutMuscle, SkeletalNitratesNitric OxideNitric Oxide SynthaseRatsRats, WistarNitratesNitric OxideNitric Oxide SynthaseFunctional hyperemiaMammalian nitrate reductasesNitrateNitriteXanthine oxidoreductase

Identifiers

PMID25727730
PMCPMC4439352
OpenAlexW2022265373

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.