Evidence map›Paper›PMID 27388219›Full record

ArticleDiabetes2016

NMDA Receptors as Potential Therapeutic Targets in Diabetic Nephropathy: Increased Renal NMDA Receptor Subunit Expression in Akita Mice and Reduced Nephropathy Following Sustained Treatment With Memantine or MK-801.

Hila Roshanravan, Eun Young Kim, Stuart E Dryer

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 38 citations in OpenAlex.

  1. N-methyl-D-aspartate receptor inhibition protects against obesity-induced kidney disease.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2026
    Article
  2. The CaPediatric nephrology (Berlin, Germany) · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Non-voltage-gated CaAmerican journal of physiology. Renal physiology · 2024
    Review
  7. Urinary podocyte markers in diabetic kidney disease.Kidney research and clinical practice · 2024
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Therapeutic Potential of Polyphenols in the Management of Diabetic Neuropathy.Evidence-based complementary and alternative medicine : eCAM · 2021
    Review
  13. Article
  14. Review
  15. Article
  16. Polyphenols for diabetes associated neuropathy: Pharmacological targets and clinical perspective.Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2019
    Review
  17. Hydrogen sulfide inhibits CaAmerican journal of physiology. Endocrinology and metabolism · 2019
    Article
  18. Article
  19. Trpc6 inactivation confers protection in a model of severe nephrosis in rats.Journal of molecular medicine (Berlin, Germany) · 2018
    Article
  20. 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

3 authors at 1 institution in 1 country.

Hila RoshanravanDepartment of Biology and Biochemistry, University of Houston, Houston, TX.
Eun Young KimDepartment of Biology and Biochemistry, University of Houston, Houston, TX.
Stuart E DryerDepartment of Biology and Biochemistry, University of Houston, Houston, TX Division of Nephrology, Baylor College of Medicine, Houston, TX sdryer@uh.edu.
University of Houston · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

N-methyl-d-aspartate (NMDA) receptors are expressed throughout the kidney, and the abundance of these receptors and some of their endogenous agonists are increased in diabetes. Moreover, sustained activation of podocyte NMDA receptors induces Ca(2+) influx, oxidative stress, loss of slit diaphragm proteins, and apoptosis. We observed that NMDA receptor subunits and their transcripts are increased in podocytes and mesangial cells cultured in elevated glucose compared with controls. A similar increase in NMDA subunits, especially NR1, NR2A, and NR2C, was observed in glomeruli and tubules of Akita mice. Sustained continuous treatment with the strong NMDA receptor antagonist dizocilpine (MK-801) for 28 days starting at 8 weeks of age reduced 24-h albumin excretion and mesangial matrix expansion and improved glomerular ultrastructure in Akita mice. MK-801 did not alleviate reduced Akita mouse body weight and had no effect on kidney histology or ultrastructure in DBA/2J controls. The structurally dissimilar NMDA antagonist memantine also reduced diabetic nephropathy, although it was less effective than MK-801. Inhibition of NMDA receptors may represent a valid therapeutic approach to reduce renal complications of diabetes, and it is possible to develop well-tolerated agents with minimal central nervous system effects. Two such agents, memantine and dextromethorphan, are already in widespread clinical use.

Indexed as

AnimalsBody WeightDiabetic NephropathiesDizocilpine MaleateExcitatory Amino Acid AntagonistsKidneyKidney GlomerulusKidney TubulesMemantineMesangial CellsMicePodocytesReceptors, N-Methyl-D-AspartateDizocilpine MaleateExcitatory Amino Acid AntagonistsMemantineNR1 NMDA receptorNR2A NMDA receptorNR2C NMDA receptorReceptors, N-Methyl-D-Aspartate

Identifiers

PMID27388219
PMCPMC5033270
OpenAlexW2466224676

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.