Evidence map›Paper›PMID 11248117›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

Insulin promotes rapid delivery of N-methyl-D- aspartate receptors to the cell surface by exocytosis.

V A Skeberdis, J Lan, X Zheng, R S Zukin, M V Bennett

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 147 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
147citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

147 citing papers in PubMed, 1 synthesis or guideline pooled it, 308 citations in OpenAlex.

  1. Obesity and episodic memory function.The journal of physiological sciences : JPS · 2018
    Pooled it
  2. Central Nervous Insulin Signaling in Sleep-Associated Memory Formation and Neuroendocrine Regulation.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2016
    Trial
  3. Trial
  4. Caloric restriction improves memory in elderly humans.Proceedings of the National Academy of Sciences of the United States of America · 2009
    Trial
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Exploring the Role of Metabolic Hormones in Amyotrophic Lateral Sclerosis.International journal of molecular sciences · 2024
    Article
  18. Article
  19. Review
  20. Article

87 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

V A SkeberdisDepartment of Neuroscience, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
J Lan
X Zheng
R S Zukin
M V Bennett
Albert Einstein College of Medicine · USYeshiva University · US

Funding

PURIFICATION OF NEUROBLASTOMA OPIATE RECEPTORSR01NS020752 · NINDS · YESHIVA UNIVERSITY · PI ZUKIN, R. SUZANNE · 1985 to 2009
$3.6M
GLUTAMATE RECEPTOR GENE EXPRESSION IN ISCHEMIAR01NS031282 · NINDS · YESHIVA UNIVERSITY · PI ZUKIN, R. SUZANNE · 1996 to 2000
$574k
NINDS NIH HHS NS 20752NINDS NIH HHS NS 31282
6 · The paper itself

Abstract

Insulin potentiates N-methyl-d-aspartate receptors (NMDARs) in neurons and Xenopus oocytes expressing recombinant NMDARs. The present study shows that insulin induced (i) an increase in channel number times open probability (nP(o)) in outside-out patches excised from Xenopus oocytes, with no change in mean open time, unitary conductance, or reversal potential, indicating an increase in n and/or P(o); (ii) an increase in charge transfer during block of NMDA-elicited currents by the open channel blocker MK-801, indicating increased number of functional NMDARs in the cell membrane with no change in P(o); and (iii) increased NR1 surface expression, as indicated by Western blot analysis of surface proteins. Botulinum neurotoxin A greatly reduced insulin potentiation, indicating that insertion of new receptors occurs via SNARE-dependent exocytosis. Thus, insulin potentiation occurs via delivery of new channels to the plasma membrane. NMDARs assembled from mutant subunits lacking all known sites of tyrosine and serine/threonine phosphorylation in their carboxyl-terminal tails exhibited robust insulin potentiation, suggesting that insulin potentiation does not require direct phosphorylation of NMDAR subunits. Because insulin and insulin receptors are localized to glutamatergic synapses in the hippocampus, insulin-regulated trafficking of NMDARs may play a role in synaptic transmission and plasticity, including long-term potentiation.

Indexed as

AnimalsBiological TransportCell MembraneElectric ConductivityElectrophysiologyEnzyme ActivationExocytosisFemaleGene ExpressionInsulinIon Channel GatingMiceOocytesPatch-Clamp TechniquesPhosphorylationRatsInsulinNR1 NMDA receptorNR2A NMDA receptorReceptor, InsulinReceptors, N-Methyl-D-AspartateTyrosine

Identifiers

PMID11248117
PMCPMC30692
OpenAlexW2107406042

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.