Evidence map›Paper›PMID 30249002›Full record

ArticleInternational journal of molecular sciences2018

Chronic Insulin Infusion Down-Regulates Circulating and Urinary Nitric Oxide (NO) Levels Despite Molecular Changes in the Kidney Predicting Greater Endothelial NO Synthase Activity in Mice.

Maurice B Fluitt, Sophia Rizvi, Lijun Li, Ashley Alunan, Hwal Lee, Swasti Tiwari, Carolyn M Ecelbarger

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Oxidative medicine and cellular longevity · 2019
    Trial
  2. Article
  3. Article
  4. Review
  5. 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

7 authors at 3 institutions in 2 countries.

Maurice B FluittDivision of Endocrinology and Metabolism, Department of Medicine, Georgetown University, Washington, DC 20057, USA. mbf79@georgetown.edu.
Sophia RizviDivision of Endocrinology and Metabolism, Department of Medicine, Georgetown University, Washington, DC 20057, USA. sophiarizvi@health.usf.edu.
Lijun LiDivision of Endocrinology and Metabolism, Department of Medicine, Georgetown University, Washington, DC 20057, USA. lil@georgetown.edu.
Ashley AlunanDivision of Endocrinology and Metabolism, Department of Medicine, Georgetown University, Washington, DC 20057, USA. amalunan@willamette.edu.
Hwal LeeDivision of Endocrinology and Metabolism, Department of Medicine, Georgetown University, Washington, DC 20057, USA. hwal.lee17@gmail.com.
Swasti TiwariDepartment of Molecular Medicine & Biotechnology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow 226014, India. tiwari_pgi@yahoo.com.ORCID 0000-0002-1701-2636
Carolyn M EcelbargerDivision of Endocrinology and Metabolism, Department of Medicine, Georgetown University, Washington, DC 20057, USA. ecelbarc@georgetown.edu.
Georgetown University · USSanjay Gandhi Post Graduate Institute of Medical Sciences · INWillamette University · US

Funding

Translational Biomedical Science Training GrantTL1TR001431 · NCATS · GEORGETOWN UNIVERSITY · PI LEE, DEXTER L, SANDBERG, KATHRYN L · 2015 to 2024
$4.8M
NCATS NIH HHS TL1 TR001431
6 · The paper itself

Abstract

Insulin therapy is often needed to overcome insulin receptor resistance in type 2 diabetes; however, the impact of providing additional insulin to already hyperinsulinemic subjects is not clear. We infused male TALLYHO/Jng (TH) mice (insulin resistant) with insulin (50 U/kg·bw/d) or vehicle (control) by osmotic minipump for 14 days. One group of insulin-infused mice was switched to 4% NaCl diet (high-sodium diet, HSD) in the second week. Blood chemistry revealed a significantly higher anion gap and blood sodium concentrations with insulin infusion, i.e., relative metabolic acidosis. Systolic BP and heart rate were slightly (~5 mm Hg) higher in insulin-infused versus control mice. HSD resulted in a modest and transient rise in mean arterial blood pressure (BP), relative to control or insulin-infused, normal-NaCl-fed mice. In kidney, insulin infusion: (1) increased total and phosphorylated (serine-1177) endothelial nitric oxide synthase (eNOS) band densities; (2) reduced band density of the uncoupled form of eNOS; and (3) increased renal homogenate nitric oxide synthase (NOS) activity. Despite this, plasma and urine levels of nitrates plus nitrites (NOx) fell with insulin infusion, by day 14 (40⁻50%) suggesting worsening of resistance. Overall, insulin infusion ramps up the cellular means in kidney to increase vasodilatory and natriuretic NO, but in the long term may be associated with worsening of insulin receptor resistance.

Indexed as

Gene Expression Regulation, EnzymologicInsulin ResistanceAnimalsHeart RateHypoglycemic AgentsInfusions, IntravenousInsulinKidneyMaleMiceMice, Inbred C57BLNitric OxideNitric Oxide Synthase Type IIIHypoglycemic AgentsInsulinNitric OxideNitric Oxide Synthase Type IIIblood pressureheart ratehypertensionmetabolic syndromeoxidative stress

Identifiers

PMID30249002
PMCPMC6213653
OpenAlexW2891972833

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.