Evidence map›Paper›PMID 25696116›Full record

ArticleDiabetes & vascular disease research2015

Oral nitrite therapy improves vascular function in diabetic mice.

Amy L Sindler, Kimberly Cox-York, Lauren Reese, Nathan S Bryan, Douglas R Seals, Christopher L Gentile

Abstract read
In one paragraph

Article in Diabetes & vascular disease research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 20% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
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 4 institutions in 1 country.

Amy L SindlerDepartment of Integrative Physiology, University of Colorado, Boulder, Boulder, CO, USA Department of Health and Human Physiology, University of Iowa, Iowa City, IA, USA.
Kimberly Cox-YorkDepartment of Food Science and Human Nutrition, Colorado State University, Fort Collins, CO, USA.
Lauren ReeseDepartment of Food Science and Human Nutrition, Colorado State University, Fort Collins, CO, USA.
Nathan S BryanTexas Therapeutics Institute, Brown Foundation Institute of Molecular Medicine, University of Texas Health Science Center at Houston, Houston, TX, USA.
Douglas R SealsDepartment of Integrative Physiology, University of Colorado, Boulder, Boulder, CO, USA.
Christopher L GentileDepartment of Food Science and Human Nutrition, Colorado State University, Fort Collins, CO, USA Christopher.gentile@colostate.edu.
Colorado State University · USBrown Foundation · USUniversity of Colorado Boulder · USUniversity of Iowa · US

Funding

PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Paul S. Maclean · 1995 to 2026
$32.6M
University of Colorado Aging Training GrantT32AG000279 · NIA · UNIVERSITY OF COLORADO DENVER · PI Kerrie Moreau · 2001 to 2026
$10.1M
SODIUM RESTRICTION &ARTERIAL COMPLIANCE IN OLDER HUMANSR01AG013038 · NIA · UNIVERSITY OF COLORADO AT BOULDER · PI SEALS, DOUGLAS R · 1996 to 2018
$4.0M
Human Aging, Exercise &FMD: Translational PhysiologyR37AG013038 · NIA · UNIVERSITY OF COLORADO AT BOULDER · PI SEALS, DOUGLAS R · 2004 to 2013
$3.0M
The Role of Endoplasmic Reticulum Stress in Obesity-Related Endothelial DysfunctiK01DK087777 · NIDDK · COLORADO STATE UNIVERSITY · PI GENTILE, CHRISTOPHER L · 2010 to 2013
$550k
NIA NIH HHS AG000279NIA NIH HHS AG013038NIA NIH HHS R01 AG013038NIA NIH HHS R37 AG013038NIA NIH HHS T32 AG000279NIDDK NIH HHS DK087777NIDDK NIH HHS K01 DK087777NIDDK NIH HHS P30 DK048520NIDDK NIH HHS P30DK048520
6 · The paper itself

Abstract

aimWe tested the hypothesis that short-term oral sodium nitrite supplementation would improve vascular dysfunction in obese, diabetic mice. METHODS AND

resultsVascular function was determined in control mice and in db/db mice receiving drinking water with or without sodium nitrite (50 mg/L) for 5 weeks. Nitrite supplementation increased plasma nitrite concentrations in db/db mice (0.19±0.02 µM vs 0.80±0.26 µM; p < 0.05). Db/db mice had lower endothelium-dependent dilation (EDD) in response to increasing doses of acetylcholine versus heterozygous control mice (71.2% ± 14.3% vs 93% ± 7.0%; p < 0.05), and sodium nitrite supplementation restored endothelium-dependent dilation to control levels (92.9% ± 2.3% vs 93% ± 7.0%; p < 0.05). The improvement in endothelial function was accompanied by a reduction in intrinsic stiffness, but not by alterations in plasma or vascular markers of inflammation.

conclusionThese data suggest that sodium nitrite may be a novel therapy for treating diabetes-related vascular dysfunction; however, the mechanisms of improvement are unknown.

Indexed as

Administration, OralAnimalsDiabetes Mellitus, Type 2Diabetic AngiopathiesDisease Models, AnimalDose-Response Relationship, DrugHeterozygoteHomozygoteMice, Inbred C57BLMice, Mutant StrainsPoint MutationReceptors, LeptinSodium NitriteVascular StiffnessVasodilationVasodilator Agentsleptin receptor, mouseReceptors, LeptinSodium NitriteVasodilator AgentsdiabetesEndothelial functionnitrite

Identifiers

PMID25696116
PMCPMC5027127
OpenAlexW2123490974

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.