Evidence map›Paper›PMID 22338086›Full record

ArticleAmerican journal of physiology. Renal physiology2012

Nicorandil as a novel therapy for advanced diabetic nephropathy in the eNOS-deficient mouse.

Katsuyuki Tanabe, Miguel A Lanaspa, Wataru Kitagawa, Christopher J Rivard, Makoto Miyazaki, Jelena Klawitter, George F Schreiner, Moin A Saleem, Peter W Mathieson, Hirofumi Makino and 2 more

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.4field-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

28 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
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  5. American journal of physiology. Renal physiology · 2024
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  12. [Nicorandil improves cognitive dysfunction in mice with streptozotocin-induced diabetes].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2018
    Article
  13. Article
  14. Article
  15. Antiangiogenic Therapy for Diabetic Nephropathy.BioMed research international · 2017
    Review
  16. Aging-associated renal disease in mice is fructokinase dependent.American journal of physiology. Renal physiology · 2016
    Article
  17. Article
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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

12 authors at 4 institutions in 4 countries.

Katsuyuki TanabeDivision of Renal Diseases and Hypertension, University of Colorado Denver, C281, 12900E 19th Ave., Aurora, CO 80045, USA.
Miguel A Lanaspa
Wataru Kitagawa
Christopher J Rivard
Makoto Miyazaki
Jelena Klawitter
George F Schreiner
Moin A Saleem
Peter W Mathieson
Hirofumi Makino
Richard J Johnson
Takahiko Nakagawa
Metabolism and Renal Physiology · FRUniversity of Bristol · GBOkayama University · JPUniversity of Colorado Denver · US

Funding

Medical Research Council G0800200NIDDK NIH HHS DK-5212
6 · The paper itself

Abstract

Nicorandil is an orally available drug that can act as a nitric oxide donor, an antioxidant, and an ATP-dependent K channel activator. We hypothesized that it may have a beneficial role in treating diabetic nephropathy. We administered nicorandil to a model of advanced diabetic nephropathy (the streptozotocin-induced diabetes in mice lacking endothelial nitric oxide synthase, eNOSKO); controls included diabetic eNOS KO mice without nicorandil and nondiabetic eNOS KO mice treated with either nicorandil or vehicle. Mice were treated for 8 wk. Histology, blood pressure, and renal function were determined. Additional studies involved examining the effects of nicorandil on cultured human podocytes. Here, we found that nicorandil did not affect blood glucose levels, blood pressure, or systemic endothelial function, but significantly reduced proteinuria and glomerular injury (mesangiolysis and glomerulosclerosis). Nicorandil protected against podocyte loss and podocyte oxidative stress. Studies in cultured podocytes showed that nicorandil likely protects against glucose-mediated oxidant stress via the ATP-dependent K channel as opposed to its NO-stimulating effects. In conclusion, nicorandil may be beneficial in diabetic nephropathy by preserving podocyte function. We recommend clinical trials to determine whether nicorandil may benefit diabetic nephropathy or other conditions associated with podocyte dysfunction.

Indexed as

Severity of Illness IndexAnimalsAntioxidantsApoptosisBlood PressureCells, CulturedDiabetes Mellitus, ExperimentalDiabetic NephropathiesDisease Models, AnimalDisease ProgressionHumansMaleMiceMice, Inbred C57BLMice, KnockoutNicorandilAntioxidantsNicorandilNitric Oxide DonorsNitric Oxide Synthase Type IIIReactive Oxygen SpeciesStreptozocin

Identifiers

PMID22338086
PMCPMC3362173
OpenAlexW2096275714

What OpenQuestion holds

Textmetadata
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.